Introduction

Homeodomain transcription factors (HD TFs) play a fundamental role in vertebrate development. Members of the HD TF family are characterized by the presence of a highly conserved 60 amino acid helix-turn-helix DNA-binding domain known as the homeodomain (HD). The HD is one of the most studied eukaryotic DNA-binding motifs since its discovery in Drosophila homeotic transformations^1,2. Hundreds of HD TFs have subsequently been documented in regulating gene expression programs important for body plan specification, pattern formation and cell fate determination^1,2. Mutations in HD TFs have been linked to many human diseases, including neuropsychiatric and neurodegenerative conditions^3,4. Although significant progress has been made in understanding HD-DNA interactions, uncovering the pathogenetic mechanisms of disease-causing missense mutations in HD have proven challenging.

The retina has long been used as a model system to study the role of HD TFs in normal central nervous system (CNS) development and in neurological diseases⁵. During retinogenesis, HD TFs play essential roles in the patterning of neuroepithelium, specification of retinal progenitors and differentiation of all retinal cell classes that derive from a common progenitor⁶. Importantly, many HD TFs are shared between the brain and the retina during development and mutations in these TFs can lead to disease manifestation in both tissues^7–12. The accessibility and wealth of available molecular tools makes the retina a valuable tool to decipher the pathogenic mechanisms of HD TF mutations associated with neurological diseases.

Here, we study CRX, a HD TF essential for photoreceptor cells in the retina, as a model to understand how single amino acid substitutions in the HD impact TF functions and cause blinding diseases. Photoreceptors are the most numerous neurons in the retina and are specialized to sense light and initiate vision through a process called phototransduction. Animal studies have demonstrated that Crx is first expressed in post-mitotic photoreceptor precursors¹³ and maintained throughout life^14,15. Loss of CRX results in impaired photoreceptor gene expression, failure of maturation and rapid degeneration of immature, non-functional photoreceptors¹⁶. Protein-coding sequence variants in human CRX have been associated with inherited retinal diseases (IRDs) that affect photoreceptors: Leber congenital amaurosis (LCA), cone-rod dystrophy (CoRD), and retinitis pigmentosa (RP) (OMIM:602225). However, the recessive phenotype observed in Crx knockout mouse models fails to recapitulate many dominant human CRX mutations that arise de novo¹⁶.

CRX contains two functional domains – the N-terminal HD and C-terminal activation domain (AD) (Figure 1A), both are required for proper activation of target genes and maintenance of normal Crx mRNA transcript abundance^17,18. To understand how CRX HD mutations cause diseases, we have previously reported a mutation knock-in mouse model carrying a hypomorphic mutation p.R90W (R90W) in CRX HD^19,20. We found that R90W mutation produces a recessive loss-of-function phenotype very similar to that of Crx knockout mice.

Figure 1.

Intriguingly, several missense mutations within the same HD recognition helix as R90W, including p.E80A (E80A) and p.K88N (K88N), are linked to severe dominant IRDs^21–23 (Figures 1A and 1B). Here, we utilized a multi-omics approach to investigate the functional consequences of the E80A and K88N mutations on CRX regulatory activities and photoreceptor development (Figure S1). Comparison of the in vitro HD-DNA binding models of CRX and disease variants generated by Spec-seq revealed unique specificity changes of each mutant protein. Introduction of each mutation into the endogenous Crx locus generated knock-in mouse models Crx^E80A and Crx^K88N that reproduced dCoRD- and dLCA-like phenotypes. ChIP-seq analysis of CRX binding in vivo revealed mutation-specific changes in CRX targetome, consistent with mutation-specific DNA binding changes in vitro. Retinal RNA-seq analysis uncovered two distinct mechanisms by which the two HD missense mutations contribute to altered gene expression programs during photoreceptor differentiation and maturation. Our results highlight the importance of residues E80 and K88 in CRX-mediated transcriptional regulation during photoreceptor development and the diverse mechanisms by which HD missense mutations can affect TF functions and lead to severe dominant neurological diseases.

Results

K88N but not E80A mutation alters CRX HD DNA-binding specificity in vitro

CRX belongs to the paired-like HD TF family that recognize a 6-bp DNA motif in a stereotypic way^24–30. Extensive studies of the HD have revealed a canonical HD-DNA recognition model where recognition of the 3’ region (bases 4-6) of the HD DNA binding site is mediated by specificity determinants within the conserved HD recognition helix, corresponding to CRX residues 80-96^{24–27,30,31} (Figure 1B). In particular, HD residue 50, equivalent to CRX K88 residue (Figure 1A), is the major specificity determinant in paired-like HD TF-DNA interactions^25,26. Since the three disease-associated HD missense mutations, E80A, K88N and R90W, are located within the CRX HD recognition helix, we wondered if these mutations change CRX HD DNA-binding specificity.

We adapted a high-throughput in vitro assay, Spec-seq, that determines protein-DNA-binding specificity by sequencing^32–34. Spec-seq was developed based on the traditional electrophoretic mobility shift assay (EMSA) to measure protein-DNA interactions. Spec-seq allows us to measure the relative binding affinities (i.e., specificity) for a library of HD binding motifs in parallel and generate quantitative binding models for different CRX HDs (Figures 1C). Based on the HD-DNA interaction model, we designed and tested a Spec-seq library containing all possible monomeric HD motifs (TAANNN) (Figure 1D).

We first obtained the wild-type (WT) CRX HD DNA binding model with Spec-seq using bacterially-expressed and affinity-purified HD peptides (Figures 1E-1G, Methods). Relative binding energies of CRX WT HD from two experiments showed strong correlation (r: 0.984) and noise level (0.114 kT) within the expected range in typical Spec-seq data (Figure 1F). Binding energy model of WT HD was then generated by applying multiple linear regressions on the relative binding energies of all sequences within two base-pair mismatches to the WT CRX consensus (TAATCC)¹⁴ (Figure 1G, Methods). A clear preference for CC bases at the 3’ end of the motif is consistent with known CRX binding preference in vitro and in vivo^35,36.

We next sought to understand how disease mutations affect CRX DNA-binding specificity. We purified all mutant HD peptides following the same protocol as WT HD peptides and verified their DNA binding (Figures S2A-S2D)¹⁸. Comparison of the relative binding energies between each pair of mutant and WT HD revealed distinct effects (Figures 1H-1J). By definition, the consensus DNA binding motif of a testing peptide has a relative binding energy of 0kT. The relative binding energy difference between nucleotide variants and the consensus motif correlates with the DNA binding specificity of the testing peptide. We found that R90W HD and E80A HD both prefer the same consensus motif as WT (Figures 1K and 1L). R90W HD bound with slightly higher specificity than WT, as demonstrated by most data points falling above the identity line (Figures 1H and 1K), suggesting that R90W HD is more sensitive than WT to binding sequence variations. In contrast, when comparing E80A HD with WT HD, many data points fell below the identity line and the relative binding energies regressed towards 0 on the E80A axis (Figures 1I and 1L). This suggests that E80A HD bound with lower specificity than WT HD and thus was more tolerant to base variations in the HD DNA motif. Different from R90W and E80A, K88N mutation dramatically altered CRX HD DNA-binding specificity (r: 0.160) (Figures 1J and 1M). The K88N preferred binding sequence (TAAT/ATT/A) is referred to as N88 HD motif hereafter. K88N HD also had the largest degree of discrimination from its preferred to the weakest binding motif, suggesting that it is most sensitive to variants in the HD DNA motif. As a control, we tested a second library with the TAANNN sites on the reverse strand and obtained similar results (Figures S2E-S2L). Together, these results indicate that while E80A mutation does not affect CRX HD DNA binding specificity, the K88N mutation dramatically alters the specificity in vitro.

E80A protein binds to WT sites while K88N occupies novel genomic regions with N88 HD motifs in vivo

Next, we asked if changes in DNA-binding specificity affected mutant CRX chromatin binding in developing photoreceptors. We first created two human mutation knock-in mouse models, Crx^E80A and Crx^K88N, each carrying a single base substitution at the endogenous Crx locus (Figures S3A and S3B, Methods). We confirmed that Crx mRNA was expressed at comparable levels in WT and mutant retinas (Figure S3C), and the full-length CRX proteins were readily detectable in the nuclear extracts from all samples (Figure S3D). We then obtained genome-wide binding profiles for each CRX variant by chromatin immunoprecipitation followed by sequencing (ChIP-seq) on mouse retinas at P14, a time when all retinal cell types are born, photoreceptor specification is completed in WT animals, and prior to any observed cell death in other CRX mutants previously characterized^19,37. To focus on changes specific to each mutant CRX protein, only homozygous animals were used for ChIP-seq profiling.

Unsupervised clustering of all CRX binding sites revealed two major clusters (Figure 2A, Methods). Cluster 1 consisted of canonical WT CRX binding sites that are also occupied by CRX E80A protein (Figures 2A and 2B). Similar to WT CRX, CRX E80A binding in vivo was mostly enriched in intronic, followed by intergenic and TSS regions (Figure 3D). In contrast, CRX R90W, that also showed similar consensus preference to WT in vitro, failed to produce significant DNA binding in vivo (Figures 2A-2C, Methods). This suggests that the retinopathy phenotype of Crx^R90W/W is likely due to loss of binding at canonical WT CRX binding sites. Intriguingly, while CRX K88N showed loss of binding at canonical CRX binding sites, it gained a small set of binding sites (Cluster 2, Figures 2A-2C). De novo motif searching with DREME³⁸ under CRX peaks in each genotype revealed enrichment of monomeric HD motifs (Figure 2E) consistent with those found in Spec-seq (Figures 1G and 1K-1M), highlighted by a change in enriched HD motif from WT CRX HD type to N88 HD type in the Crx^K88N/N retinas. Consistency with in vitro binding models suggests that in vivo changes in CRX chromatin binding were at least in part driven by the intrinsic changes in HD-DNA binding specificity by each individual mutation.

Figure 2.

Figure 3.

E80A and K88N mutations affected the expression of CRX-dependent activated genes in opposite directions in a critical time window of photoreceptor differentiation

To understand how different CRX mutations affected gene expression at canonical and de novo binding sites and how these changes impair photoreceptor differentiation, we turned to bulk RNA-seq analysis from the developing retinas at P10. At P10, photoreceptors have started to differentiate, and the expression of many photoreceptor genes undergo exponential increase^39,40. To focus on the most relevant expression changes, we first defined a set of genes that most likely depend on CRX activity nearby for expression (Figure S4A, Methods). Briefly, we associated each CRX ChIP-seq peak to the nearest gene, filtered only genes with nearby CRX ChIP-seq peaks, and further narrowed the list of genes to those significantly down-regulated in the loss of function mutant Crx^R90W/W. Gene ontology (GO) analysis confirmed that this putative CRX-dependent gene set is associated with biological processes related to photoreceptor development and functions (Figure S4B). This set of putative CRX-dependent genes also showed developmental dependent gain in expression, consistent with CRX’s primary function as a transcriptional activator (Figure S4C). As a control, CRX-independent genes were constitutively expressed and largely involved in general cellular processes (Figures S4D-S4F). Therefore, the CRX-dependent gene set comprises genes important for photoreceptor differentiation and functional maturation and are dependent on CRX for activation. We denote these genes as “CRX-dependent activated genes” (CRX-DAGs).

Next, we sought to understand how each mutation affected photoreceptor differentiation. One way of measuring the progression of photoreceptor differentiation is to determine the similarity in CRX-DAG expression in a given sample with that of known developmental ages in WT control animals. We thus performed sample-wise correlation of CRX-DAG expression obtained in our P10 samples with a previously published RNA-seq dataset of normal mouse retinal development (Figure 3A)³⁹. As expected, our P10 WT sample showed strong correlations with all developmental ages in the published WT control dataset. A stronger correlation with early ages (P3, P7, P10) and a weaker correlation with later ages (P14, P21) is also an indication of ongoing photoreceptor differentiation at P10. Unlike the WT sample, Crx^E80A/+ and Crx^E80A/Asamples both showed a stronger correlation with later developmental ages (P14, P21) but a weaker correlation with earlier postnatal ages (P3, P7). Since the CRX-DAGs are normally developmentally upregulated, this shift in correlation towards later developmental ages suggested that these genes were prematurely upregulated in the P10 Crx^E80A mutant retinas. In contrast, Crx^K88N/+ and Crx^K88N/N samples both showed a weaker correlation with all developmental ages when compared with WT samples in our dataset. This suggests that early photoreceptor differentiation was compromised in both Crx^K88N mutants, consistent with their association with early-onset LCA²³. Importantly, Crx^R90W/W, also associated with LCA-like phenotype^19,22, displayed strong correlation with earlier ages (P3, P7) similar to WT, but only showed moderate correlation with later ages (P14, P21). This suggests loss of CRX function at canonical binding sites does not affect the initiation of photoreceptor differentiation, but WT CRX activity at these sites is required to sustain differentiation. Since CRX-DAG expression was more severely affected in Crx^K88N mutants than in Crx^R90W/W, the photoreceptor differentiation deficits seen in the Crx^K88N mutants cannot be explained solely by the loss of regulatory activity at canonical CRX binding sites. Overall, our sample-wise correlation analysis with normal retinal development dataset suggests that E80A and K88N mutations affected the expression CRX-dependent activated genes in opposite directions, implicating novel and distinct pathogenic mechanisms from the loss-of-function R90W mutation.

Crx^E80A retinas show up-regulation of rod genes but down-regulation of cone genes, underlying CoRD-like phenotype

Upon closer examination, we noted that not all CRX-DAGs were up-regulated in Crx^E80A mutants (Figure 3B). Hierarchical clustering of all CRX-DAGs using expression changes revealed two major groups (Methods). In aggregate, when compared to WT, Group 1 genes were up-regulated in Crx^E80A mutants while Group 2 genes were down-regulated. We noted genes indicative of the two photoreceptor subtypes, rods and cones, could partially define the two groups (Figures 3C and 3D). For example, Esrrb⁴¹ and Nrl⁴² in Group 1 are important regulators of rod differentiation. Other genes in Group 1 are components of the phototransduction cascade in rods, including Rcvrn⁴³, Rho⁴⁴, Gnat1^45,46, Pde6g⁴⁷, Abca4^48,49, Gnb1⁵⁰, Rdh12⁵¹, Cngb1⁵², Rp1^53,54. Mis-regulations of many of these genes have been associated with diseases that affect rod development, function, and long-term survival. The increased activation of these genes likely underlies the stronger correlation with later developmental ages in Crx^E80A+/and Crx^E80A/A retinas (Figure 3A). In contrast, Group 2 genes, many down-regulated in Crx^E80A mutants, were implicated in cone development and functions. For example, Gnat2^55,56, Pde6c⁵⁷, and Pde6h^58,59 all act in the cone phototransduction cascade. Mis-regulation of these genes has also been implicated in different retinal dystrophies that primarily affect cone photoreceptors. Comparison of ChIP-seq signal revealed that peaks associated with Group 2 genes showed lower occupancy compared to Group 1 genes in the Crx^E80A/A retinas (Mann-Whitney U test p-value: 9.51e-07) while no difference was observed in WT retinas (Mann-Whitney U test p-value: 0.541), suggesting loss of CRX activity likely underlies the down-regulation of Group 2 genes in the Crx^E80A mutants (Figure S5A). Collectively, the selective down-regulation of cone genes in Group 2 may explain the CoRD-like phenotype in adult Crx^E80Amutant mice described later.

Additionally, we noticed that a subset of genes not affected in Crx^R90W/W(CRX-independent genes) were also down-regulated in Crx^E80A mutants (Figures S5B-S5D). Among these genes were transcription regulators important for early photoreceptor development, such as Ascl1⁶⁰, Rax⁶¹, Sall3⁶², and Pias3⁶³. The down-regulation of these factors coincided with the up-regulation of mature rod genes in P10 Crx^E80A retinas, suggesting that the E80A mutation might hamper the proper timing of photoreceptor differentiation.

Crx^K88N retinas display greater reduction of rod and cone genes than the loss-of-function mutants

Crx^K88N retinas had the most severe gene expression changes among all mutants with down-regulation of both Group 1 (rod) and Group 2 (cone) genes (Figures 3B-3D). The heterozygous Crx^K88N/+ retina displayed a similar degree of expression reduction as homozygous Crx^R90W/W, consistent with its association with dLCA²³. Given the normal phenotype of heterozygous loss-of-function mutants - Crx^+/-and Crx^R90W/+19, these results suggest that mutant CRX K88N not only failed to activate WT target genes, but also functionally antagonized WT CRX regulatory activity in differentiating photoreceptors. This antagonism might be associated with ectopic CRX K88N activity when bound to regulatory regions with N88 HD DNA motifs (Figures 2A and 2E). In the absence of WT CRX, Crx^K88N/N retina displayed a more severe expression reduction of CRX-DAG than Crx^R90W/W, raising the possibility that CRX K88N also antagonized the activity of other transcriptional regulators important for photoreceptor differentiation. Supporting this possibility, a set of CRX-independent genes were also mis-regulated in both heterozygous and homozygous Crx^K88N mutants. We noted that a number of these down-regulated genes are also involved in photoreceptor functional development (Figures S5B, S5E, and S5F). Overall, CRX K88N is associated with greater gene expression changes than other CRX HD mutants, which is likely attributed to ectopic regulatory activity.

Both E80A and K88N mutants show compromised rod/cone terminal differentiation in young adults

Since Crx^+/- and Crx^R90W/+ mutant mouse models showed a late-time recovery in photoreceptor gene expression and function²⁰, we sought to determine the degree of photoreceptor differentiation in Crx^E80A and Crx^K88N mutants at P21. At this age, the normal retina has largely completed terminal differentiation with photoreceptor gene expression reaching a plateau⁶⁴. However, when P21 CRX HD mutant retinas were examined for the expression of genes under the GO term detection of light stimulus (GO:0009583), which comprises genes in both rod and cone phototransduction cascades, many genes failed to reach WT levels, despite variable degrees of impact across different HD mutants (Figure 4A). Crx^E80A mutants, in contrast to the increased rod gene expression at P10, displayed a deficiency in both cone and rod phototransduction genes at P21 (Figure 4B, Supplementary Table 6). This suggests that mutant CRX E80A transcriptional activity fails to sustain photoreceptor terminal differentiation and ultimately results in non-functional and severely affected photoreceptors. In comparison, Crx^K88N mutants showed severely reduced expression of rod/cone phototransduction genes at both P10 and P21 (Figures 3B-3D and 4B).

Figure 4.

To assess retinal morphology and photoreceptor subtype-specific gene expression at the cellular level, we performed immunohistochemistry analysis on P21 retinal sections. In WT animals, a hallmark of photoreceptor maturation is the outgrowth of photoreceptor outer segments (OS) filled with proteins necessary for the phototransduction. We thus performed hematoxylin and eosin (H&E) staining on P21 sagittal retinal sections to visualize changes in retinal layer organization, focusing on photoreceptor layers – outer nuclear layer (ONL) and OS. Compared to the well-organized ONL in WT retinas (Figure 5A), all mutants showed variable degrees of ONL disorganization, forming waves, whorls, and rosettes (Figures 5B-5E). The ONL disorganization was more severe in homozygotes than in heterozygotes for both mutations and Crx^K88Nmutants were more severely affected than Crx^E80A mutants. Photoreceptor OS layer was formed in the Crx^E80A/+ retinas, but absent in Crx^E80A/A, Crx^K88N/+, and Crx^K88N/N mutant retinas. Inner retinal layers, including inner plexiform layer (IPL) and ganglion cell layer (GCL) were not as severely affected as the outer retinal layers, supporting a model that the mutant morphological abnormalities largely originated from the diseased photoreceptors. These morphological abnormalities were distinct from the degenerative phenotypes of other Crx mutant models reported previously^19,65,66.

Figure 5.

Next, we sought to determine the expression of the rod-specific visual pigment rhodopsin (RHO) and cone arrestin (mCAR) in the P21 mouse retinas. In WT retinas, RHO is trafficked to the rod OS while mCAR is present in the cone OS and IS (inner segment), cell body, and synaptic terminals (Figure 5F). Unlike WT retina, all mutants lacked mCAR immunoreactivity (Figures 5G-5J), consistent with the loss of cone gene expression shown by RNAseq (Figure 4B). In Crx^E80A/+ retinas, RHO staining was localized to the OS layer; in Crx^E80A/A and Crx^K88N/+retinas, positive RHO staining was observed within the whorls and rosettes; in Crx^K88N/N mutant retinas, RHO staining was completely absent. Importantly, we did not observe mis-localized RHO staining in the inner retinal layers (INL) suggesting that the developmental programs of other retinal cell types were not directly affected by E80A or K88N mutation. Overall, abnormalities in the cone/rod gene expression matched the corresponding human disease diagnosis^21,23, and the phenotypic severity correlated with the degree of mis-regulation of CRX target genes in the corresponding RNAseq dataset. Thus, these results support a model that CRX HD mutation-mediated mis-regulation of gene expression disrupts photoreceptor terminal differentiation and leads to defects in retinal layer organization and OS formation.

E80A and K88N mouse models show visual function deficits that recapitulate human diseases

To understand the consequences of disrupted photoreceptor differentiation on visual function, we measured electroretinogram (ERG) responses to light stimuli for WT and mutant mice at one month of age (Figures 5K-M). In response to incremental changes of light intensities, WT animals showed corresponding amplitude increases in dark adapted A-waves (rod signals) and B-waves (rod-evoked bipolar cell signals), as well as in light-adapted B-waves (cone-evoked bipolar cell signals). The three severe mutants, Crx^E80A/A, Crx^K88N/+, and Crx^K88N/N had no detectable dark-adapted or light-adapted ERG responses, suggesting that these mice have no rod or cone function and are blind at young ages. The null ERG phenotype of the Crx^K88N animals is consistent with the clinical LCA phenotype in humans²³. In contrast, Crx^E80A/+ animals retained partial rod ERG responses as indicated by the reduced A-wave and B-wave amplitudes (Figures 5K and 5L). Yet, Crx^E80A/+ animals had no detectable cone ERG responses, which is consistent with the CoRD clinical phenotype in humans²¹ (Figure 5M). Taken together, the visual function impairment in each CRX HD mutant model, coincided with the morphological and molecular changes, suggesting that Crx^E80A and Crx^K88Nmouse models recapitulate the corresponding human diseases.

CRX E80A has increased transactivation activity and leads to precocious differentiation in Crx^E80A retinas

Lastly, we asked what might be the molecular mechanism that causes the mis-regulation of photoreceptor genes in the mutant retinas. Previous studies have established that reporter assays with the rhodopsin promoter in HEK293T cells can measure changes of CRX transactivation activity and inform the mechanisms by which photoreceptor genes are mis-regulated in CRX mutant retinas¹⁸. We thus tested the transactivation activity of the three CRX HD mutants on the pRho-Luc reporter in HEK293T cells (Figure 6A, Methods). Consistent with published studies, R90W mutant had significantly reduced activity compared to WT CRX¹⁸. K88N mutant showed a similarly reduced activity as R90W, consistent with K88N’s loss of binding at canonical CRX sites and failure to activate CRX-DAGs in vivo (Figures 2A, 2B, 3A-3C). In contrast, E80A mutant, which binds to canonical CRX sties, showed significantly increased transactivation activity on the Rho promoter. This hyperactivity of E80A protein at Rho promoter correlates with the upregulation of CRX-DAGs in the mutant retinas at P10 (Figures 3A-3C).

Figure 6.

A transition to the next developmental stage usually requires the expression of important developmental genes passing an abundance threshold. Based on the hyperactivity model, photoreceptor genes are activated stronger in Crx^E80A retinas and thus could reach the abundance threshold earlier. To determine the consequences of E80A hyperactivity on photoreceptor differentiation timing, we compared RHO protein expression during early postnatal retinal development using retinal section immunostaining (Figures 6B-6D). In WT retinas, most rods were born by P3 but had not differentiated (Figure 6B). Previous studies showed that RHO proteins were detected by IHC starting around P7 in WT retinas⁶⁴. In comparison, both Crx^E80A/+ and Crx^E80A/A retinas showed positive RHO staining at P3 (Figures 6C and 6D). RHO⁺ cells were largely seen in the outer portion of the ONBL layers in Crx^E80A/+ retinas, and strikingly spread throughout the large presumptive ONL layers in Crx^E80A/A retinas. The detection of RHO protein in P3 Crx^E80A mutant retinas indicates that photoreceptor differentiation program was precociously activated. Taken together, our results support a model that E80A and K88N mutations each perturbs CRX regulatory activity in a unique way, causes photoreceptor differentiation defects, and ultimately leads to distinct dominant disease phenotype that recapitulates human diseases.

Discussion

Through molecular characterization of mutant proteins, transcriptome, and cellular profiling of developing mutant mouse retinas and ERG testing of adult retinas, we have identified two novel pathogenic mechanisms of CRX HD mutations, E80A and K88N, that are associated with dominant CoRD and dominant LCA in human^21,22. Distinct from the previously characterized loss-of-function R90W mutation^19,20, E80A and K88N mutations produce altered CRX proteins with gain of regulatory functions - CRX E80A is associated with increased transcriptional activity and CRX K88N has altered DNA binding specificity. Both CRX E80A and CRX K88N proteins impair photoreceptor gene expression, development and produce structural and functional deficits in knock-in mouse models, recapitulating human diseases⁶⁵ (Figure 7). Thus, both target specificity and regulatory activity precision at the canonical CRX targets are essential for proper photoreceptor development and functional maturation.

Figure 7.

Although associated with distinct disease phenotypes, the E80A, K88N, and R90W mutations are located very close to each other in the CRX HD recognition helix. Extensive biochemical and structural studies on the HD-DNA complexes afford important insights into how these mutations could affect CRX HD-DNA interactions differently. Most distinctively, CRX K88 residue, at HD50 position, is the major contributor to HD-DNA binding specificity, with lysine making favorable interactions with both guanines in the CRX consensus TAATCC binding site^67,68. It is thus expected that K88N mutation drastically changes CRX DNA binding preference at the 3’ end of the HD motif, reminiscent of previous findings on novel HD DNA-binding specificity using bacterial one-hybrid (B1H) systems^31,69. Supporting the importance of K88 residue mediated CRX target specificity in regulating photoreceptor development, Crx^K88Nretinas show more severe perturbations in photoreceptor gene expression and development than in loss-of-function mutant Crx^R90W/W. Crx^K88N/+and Crx^K88N/N mice display the most severe photoreceptor morphological deficits observed in any Crx mouse models and show absence of visual functions in young adults. Thus, CRX target specificity is critical for photoreceptor development fidelity.

In developing WT mouse retinas, the HD motif preferred by HD TFs with a glutamine (Q) at HD50 position encodes quantitatively different activity than the CRX consensus suggesting functional difference between HD binding site variants^61,70. It is likely that the severe Crx^K88N phenotypes are attributed to both diminished activity at canonical CRX motifs and ectopic binding and transcriptional activity at N88 HD motifs. Since a functional copy of WT CRX is retained in Crx^K88N/+ retinas, the lack of WT activity alone cannot explain the severe developmental deficits. Alternatively, these results suggest involvement of additional regulatory mechanisms: CRX K88N activity at N88 HD motifs might (1) ectopically activate genes whose expression prevents the progression of development or inactivate genes required for development; (2) interfere with other HD TFs that also recognize N88 HD motifs; (3) lead to epigenetic alterations that antagonize normal CRX functions. Many other HD containing TFs are expressed in developing mouse retina, including OTX2, RAX, VSX2, PAX6, SIX3/6, and LHX family⁶. Different from CRX, these HD TFs are essential for gene regulation in retinal progenitor cells and/or in other retinal cell lineages. Alteration of CRX DNA binding specificity could mis-regulate genes originally targeted by these HD TFs and lead to severe perturbations in the retinal gene regulatory networks (GRNs). To date, most studies have focused on CRX activity at cis-regulatory sequences enriched for the WT CRX consensus motifs^71,72. Systematic comparison of regulatory activity at N88 HD motifs and WT consensus in the context of photoreceptor development in both WT and mutant retinas would be needed to substantiate the impact of mutant CRX K88N activity at different HD motifs. These experiments will also help clarify the pathogenic mechanisms in the Crx^K88Nmodels and extend our knowledge of CRX HD mediated regulatory grammar during photoreceptor development.

Different from CRX K88, the E80 and R90 residues, although the most common residues at HD42 and HD52 positions respectively, do not contact DNA directly and thus lacked in-depth investigations in prior studies. CRX R90 residue has been suggested to confer additional stability for the homeodomain fold besides the core residues and make contacts with the DNA backbone through bases in the TAAT core motif^67,68. Substitution of the basic R90 residue with a bulky, neutral tryptophan (W) potentially reduces overall CRX HD stability which in term reduces CRX HD DNA-binding affinity without affecting its binding preference. The potential reduction in CRX HD-DNA complex stability is in line with our observation that R90W mutation abolishes CRX binding across the genome resulting in global loss of CRX target gene activation. It also explains the association of CRX R90W mutation with recessive loss-of-function LCA phenotypes in human and mouse^22,65.

Structural studies suggest that CRX E80 residue plays a role in stabilizing the HD-DNA binding complex through intramolecular interactions with other HD residues^29,68, yet functional validations await further experiments. E80A mutation, replacing glutamic acid (E), which is acidic and polar, with alanine (A), which is neutral and non-polar, could render HD-DNA interactions more promiscuous as reflected in overall reduced magnitude of CRX E80A HD specificity (Figure 1I). Regulatory sequences of many photoreceptor genes contain both consensus and non-consensus CRX motifs^14,15,18,35. It is likely that the more promiscuous CRX E80A-DNA interaction increases the likelihood of non-consensus CRX HD motifs being bound and activated resulting in overall increased transcriptional output (hyperactivity) as seen both in luciferase assays and in developing Crx^E80A mouse retinas. The promiscuous TF-DNA-binding associated hyperactivity phenomenon has also been observed in a dominant disease mouse model harboring a missense mutation in the zinc finger TF Krüppel-like factor-1 (KLF1)⁷³. Yet, in adult Crx^E80A retinas, photoreceptor terminal differentiation is impaired, resulting in disrupted retinal morphology and defective visual functions. Photoreceptor differentiation is programmed via sequential and concerted gene expression programs within a defined time window^74,75. One explanation for adult Crx^E80A phenotypes is that CRX E80A hyperactivity precociously activates later stage genes in the absence of proper nuclear context and/or subcellular structures, which in turn negatively impacts early events in photoreceptor differentiation. These observations underscore the importance of precisely tuned CRX-mediated transcriptional activity during photoreceptor development.

Although a global increase in expression is expected in Crx^E80A retinas based on the hyperactivity model, a subset of CRX dependent activated genes implicated in cone photoreceptor development and functions is down-regulated in both differentiating and mature mutant retinas. While cones undergo terminal differentiation to develop into cone subtypes – M- or S-cones – in a similar postnatal window as rods, they were born prenatally in mice within an earlier time window than rods. At an early postnatal age, cells expressing RXRγ, a ligand-dependent nuclear hormone receptor normally expressed in developing cones^60,76–78, were observed in Crx^E80A retinas, suggesting cone photoreceptors were born in these mutant retinas (Figure S7A). One model for lack of cone markers in adult Crx^E80A retinas is that CRX E80A improperly activates later stage cone genes at a much earlier time window, disrupting cone terminal differentiation. Supporting this model, CRX E80A also hyperactivates the S-cone opsin promoter (Figure S7B). An alternative model is that cones might be more sensitive to perturbations in CRX activity. It is known that cones depend on a different repertoire of TFs than rods for subtype terminal differentiation⁶⁰. It is possible that cone TFs respond differently to mutant CRX E80A hyperactivity, leading to the distinct expression changes in Crx^E80A mutant retains. It is important to note that different point mutations at CRX E80 residue have been reported in dominant CoRD cases (ClinVar VCV000865803.1, VCV000007416.7, VCV000099599.6), emphasizing the importance of residue CRX E80 in regulating cone photoreceptor development. Since cones only make up a very small portion (3%) of photoreceptors in mouse retinas⁷⁹, quantitative characterization of CRX E80A molecular functions in a cone dominant retina warrants further study to understand its selective effect on the cone differentiation program and help elucidate WT CRX regulatory principles in early photoreceptor development.

Given that the spatial structures and HD-DNA contact models of HD proteins are evolutionarily conserved, our study of CRX provides valuable molecular insights for HD mutations implicated in other diseases. For example, p.E79K substitution (corresponds to CRX E80) in OTX2 HD is associated with dominant early-onset retinal dystrophy⁸⁰, heterozygous p.R89G (corresponds to CRX R90) mutation in OTX2 HD causes severe ocular malformations⁸¹, and missense mutations of the CRX K88 and R90 homologous residues in PITX2 HD are associated with dominant Rieger syndrome⁸². It is likely that these mutations affect HD activity in similar ways as observed in CRX, and the exact disease manifestation is determined by cell-type or tissue specific mechanisms. The retina is readily accessible, and a broad range of molecular tools are available for ex vivo and in vivo manipulations. We believe that CRX is an ideal model to study the pathogenic mechanisms of HD mutations and to test therapeutic regimens, which would ultimately benefit the study of HD TFs and their associated diseases in other tissues and organs.

One limitation of this work is that effects of E80A and K88N mutations on CRX HD-DNA interactions have been evaluated at monomeric HD motifs and with homogenous protein species both in vitro and in vivo. Further evaluation of WT and mutant CRX binding at dimeric motifs will be desirable, since selected dimeric HD motifs are known to mediate HD TF interactions to ensure gene expression fidelity during development^83,84. Relatedly, we also need to address how CRX WT and mutant E80A or K88N proteins interact at HD binding motifs – whether they cooperate or compete with each other, whether these interactions are HD motif sequence-dependent, and how gene expression is impacted by CRX cooperativity or competition. While CRX HD mediates both TF-DNA interactions and protein-protein interactions, evaluation of how E80A and K88N mutations impact CRX interaction with other important photoreceptor TFs and how perturbations in these interactions lead to disease phenotypes warrant further study.

Collectively, our findings support a unifying model in which precise CRX interaction with cis-regulatory sequences is essential for gene expression and functional maturation during photoreceptor development. Disease-associated mutations in CRX have been classified into two main groups – insertion/deletion-derived frameshift mutations in the activation domain (AD) and missense mutations in the homeodomain⁶⁵. Prior biochemical and mouse model studies of the first group have established that AD-truncated mutant proteins abolish CRX transcriptional activity and functionally interfere with the WT allele. As a result, the mutant retinas fail to activate or maintain robust cone/rod gene expression, resulting in incomplete photoreceptor differentiation and ultimately rapid degeneration of immature photoreceptors^16,19. In this study, we demonstrate that missense mutations in the CRX HD, by either a loss- or gain-of-function mechanism, alter CRX target specificity and/or CRX transactivation activity. These biochemical property changes impair CRX-mediated transcriptional regulation in vivo and lead to distinct morphological and functional deficits (Figures 7A-7D). Despite the difference in molecular mechanisms, both Crx^E80A and Crx^K88N mouse models develop whorls and rosettes in the ONL by P21, which are not observed in degenerative CRX mouse models¹⁹, suggesting distinct pathogenic mechanisms. Future cellular biology studies are needed to understand the formation mechanisms of these unique cellular phenotypes (ONL disorganization) and their impacts on the function and survival of photoreceptors and other retinal cell types over development.

Our study here also emphasizes the importance of tailoring gene therapy regimens to tackle individual pathogenic mechanisms. For instance, while supplementing WT CRX might be sufficient to rescue a hypomorphic/loss-of-function mutant, simultaneous elimination of a gain-of-function CRX product would be necessary to rescue dominant mutants, as exemplified in a recent report of allele-specific gene editing to rescue dominant CRX-associated LCA7 phenotypes in a retinal organoid model⁸⁵. We believe that this principle also applies to other dominant neurological diseases. Additionally, with the refinement of the CRX mechanistic model, when new disease mutations are identified, genetic counsellors can now provide more informed predictions of disease progression and future visual deficits. This information is important for individuals to be psychologically prepared and seek necessary assistance to improve their quality of life.

Author contributions

S. Chen conceived and supervised the study. S. Chen, P. Ruzycki, C. Sun and Y. Zheng designed the experiments. Y. Zheng performed Spec-seq and luciferase experiments; X. Zhang performed CRX ChIP-seq experiments; C. Sun performed immunochemistry and ERG experiments. Y. Zheng analyzed Spec-seq, CRX ChIP-seq, RNA-seq, and luciferase data; P. Ruzycki assisted in CRX ChIP-seq and RNA-seq data analysis; C. Sun analyzed immunochemistry and ERG data. Y. Zheng wrote the original draft; S. Chen, P. Ruzycki, C. Sun, and Y. Zheng revised the manuscript. All authors read and approved the final manuscript.

Acknowledgements

We thank Mingyan Yang and Guangyi Ling for technical assistance, Susan Penrose and Mike Casey from the Molecular Genetics Service Core for generating E80A and K88N mutation knock-in mice lines, Inez Oh for RNA-seq sample collection and processing, and J. Hoisington-Lopez and M. Crosby from DNA Sequencing Innovation Lab at the Center for Genome Sciences & Systems Biology for sequencing assistance. This work was supported by NIH grants EY012543 (to S. Chen), EY032136 (to S. Chen), EY002687 (to WU-DOVS), and the Stein Innovation Award (to SC) and unrestricted funds (to WU-DOVS) from Research to Prevent Blindness. We also thank Mr. Artur Widlak for the generous gift from Widłak Family CRX Research Fund.

Declaration of interests

The authors declare no competing interests.

Inclusion and diversity

We support inclusive, diverse, and equitable conduct of research.

Methods

Resource availability

Lead contact

Further information and requests for resources and reagents should be directed to and will be fulfilled by the lead contact Shiming Chen (chenshiming@wustl.edu).

Materials Availability

• ▪ All unique/stable reagents generated in this study are available from the lead contact with a completed materials transfer agreement.

Data and Code Availability

• ▪ The raw sequencing data and processed data generated in this study have been deposited at NCBI GEO.

• ▪ This paper does not report original code.

• ▪ Any additional information required to reanalyze the data reported in this paper is available from the lead contact upon request.

Animal study and sample collection

Ethics statement

All procedures involving mice were approved by the Animal Studies Committee of Washington University in St. Louis and performed under Protocol 21-0414 (to SC). Experiments were carried out in strict accordance with recommendations in the Guide for the Care and Use of Laboratory Animals of the National Institutes of Health (Bethesda, MD), the Washington University Policy on the Use of Animals in Research; and the Guidelines for the Use of Animals in Visual Research of the Association for Research in Ophthalmology and Visual Sciences. Every effort was made to minimize the animals’ suffering, anxiety and discomfort.

Mutation knock-in mouse model generation

CRISPR/Cas9 based genome editing was performed to generate the Crx^E80A and Crx^K88N mice as previously described⁸⁶. The Cas9 guide RNAs (gRNA) were designed based on proximity to the target amino acid and was synthesized using the MEGAshortscript™ T7 Transcription Kit (Thermo Fisher Scientific, Waltham, MA). The gRNAs were subsequently tested for cutting efficiency in cell culture by the Washington University Genome Engineering and iPSC Center. The validated gRNA and Cas9 protein were then microinjected into the pronuclei of C57Bl/6J-0.5-dpc (days post coitum) zygotes along with the donor DNA, a 190-bp single stranded oligodeoxynucleotide (ssODN) carrying either the c.239A>G substitution for p.E80A mutation or the c.264G>T substitution for p.K88N mutation⁸⁷. Embryos were then transferred into the oviduct of pseudo-pregnant female. Pups were generally delivered ∼20 days after microinjection. Tissues from 10-day postnatal (P10) pups were collected by toe biopsy/tail for identification of the targeted allele by restriction digest (HinfI) of PCR amplified DNA first and then confirmed by Sanger sequencing (Genewiz).

Founders carrying the correct alleles were then bred with wild-type C57BL/6J mice (Jackson Laboratories, Bar Harbor, ME, Strain #000664) to confirm transmission. All experimental animals used were backcrossed at least 10 generations. Genotyping of mutation knock-in mice follows cycling conditions: 95°C for 2 min, 94°C for 30 sec, 60°C for 30 sec, 68°C for 60 sec, repeat steps 2-4 for 34 cycles, 68°C for 7 min, and hold at 4°C. After PCR reaction, the amplified DNA fragments wee digested with HinfI. Sequences of gRNAs, ssODNs and genotyping primers can be found in Supplementary Table S3. A representative DNA gel of HinfI digested genotyping DNA fragments can be found at Figure S3B.

RNA-seq sample collection and library preparation

For each genotype, three biological replicates, two retinas per replicate from one male and one female mouse were analyzed. All retinas were processed for RNA simultaneously using TRIzol™ Reagent (Invitrogen, Waltham, MA) following the manufacturer’s protocol. The quantity and quality of the RNA was assayed using Bioanalyzer (Agilent, Santa Clara, CA). Samples with a minimum RNA integrity number (RIN) score of 8.0 were then selected for library construction as previously described²⁰.

Chromatin immunoprecipitation and library preparation

CRX chromatin immunoprecipitation was performed as previously published⁸⁸. Briefly, pooled nuclear extracts from 6 retinae were cross-linked with formaldehyde prior to immunoprecipitation with anti-CRX antibody A-9 (#sc-377138, Santa Cruz Biotechnology, Dallas, TX). Input controls were included as background. The libraries were prepared following the standard ChIP-seq protocol⁸⁹. The quantity and quality of the ChIP-seq libraries was assayed using Bioanalyzer (Agilent, Santa Clara, CA) prior to sequencing.

ERG and statistical analyses

ERGs were performed on 1-month-old mice using UTAS-E3000 Visual Electrodiagnostic System (LKC Technologies Inc., MD). Mice were dark-adapted overnight prior to the tests. Mouse body temperature was kept at 37 ± 0.5 °C during the tests. Pupils were dilated with 1% atropine sulfate solution (Bausch and Lomb). Platinum 2.0 mm loop electrodes were placed on the cornea of each eye. A reference electrode was inserted under the skin of the mouse’s head and a ground electrode was placed under the skin near mouse’s tail. Retinal response to full-field light flashes (10 μs) of increasing intensity were recorded; maximum flash intensity for dark-adapted testing was 0.895 cd*s/m2. Following dark adapted tests, mice were light-adapted under light condition (about 29.2 cd/mm) for 10 minutes and exposed to 10 μs light flashes of increasing intensity; maximum flash intensity for light-adapted testing was 2.672 cd*s/m2. ERG responses of biological replicates were recorded, averaged and analyzed using Graphpad Prism 8 (GraphPad Software, CA). The mean peak amplitudes of dark-adapted A and B waves and light-adapted B waves were plotted against log values of light intensities (cd*s/m2). The statistics were obtained by two-way ANOVA with multiple pairwise comparisons (Tukey’s).

Histology and immunohistology chemistry

Enucleated eyes were fixed at 4°C overnight for paraffin embedded sections. Each retinal cross-section was cut 5 microns thick on a microtome. Hematoxylin and Eosin (H&E) staining was performed to examine retinal morphology. For IHC staining, sections firstly went through antigen retrieval with citrate buffer, and blocked with a blocking buffer of 5% donkey serum, 1% BSA, 0.1% Triton X-100 in 1x PBS (pH-7.4) for 1 h. Sections were then incubated with primary antibodies at 4°C overnight. Sections were washed with 1x PBS containing 0.01% Triton X-100 (PBST) for 30 min, and then incubated with specific secondary antibodies for 1 h. Primary and secondary antibodies were applied with optimal dilution ratios. All slides were mounted with VECTASHIELD®HardSet™ Antifade Mounting Medium with DAPI (Vector Laboratories, Inc., CA). All images were taken on a Leica DB5500 microscope. All images were acquired at 1000 µm from ONH for ≥ P21 samples and at 500 µm from ONH for P0, P3, P10 samples.

Biochemistry

Protein expression

Expression plasmids for GST-WT, E80A, and R90W HDs were published previously¹⁸. Plasmid for GST-K88N HD was generated by site-directed mutagenesis from the pGEX4T2-CRX WT HD backbone. In vivo protein expression and purification was done as previously described¹⁸. Briefly, 0.05mM IPTG was added to E. coli BL-21 (DE3) cell cultures containing different CRX HD constructs at OD₆₀₀ = 0.6. The cultures were incubated for 2 hours or until OD₆₀₀ = 2.0 at 34°C and the cells were collected by centrifugation at 6000 rpm and 4°C for 15 minutes. Cell pellets were resuspended in 1x PBS (Corning, Corning, NY) and then lysed by sonication. 5mM DTT (Bio-Rad Laboratories, Inc., Hercules, CA) and 1% Triton X-100 (MilliporeSigma, Burlington, MA) was then added, and the mixtures were incubated with gentle shaking at 4°C for 30 minutes to maximize protein extraction. The separation of proteins from the cellular debris were then performed by centrifugation at 15 000 rpm for 10 minutes and filtered through a 0.45μm membrane. Glutathione Sepharose 4B resin (Cytiva, Marlborough, MA) was first equilibrated with PBS before adding to the supernatant. 5x Halt™ Protease Inhibitor Cocktail and PMSF was added to minimize degradation. The mixtures were incubated with gentle shaking at 4°C overnight before loading on GST Spintrap™ columns (Cytiva, Marlborough, MA). The peptides were eluted following the manufacturer’s protocol and buffer exchanged into CRX binding buffer⁹⁰ using Amicon centrifugal filters (MilliporeSigma, Burlington, MA). The protein stock was supplemented with 10% glycerol before aliquoted and stored at -80°C.

Protein quantification and visualization

The size and integrity of purified GST-CRX HDs were visualized with a native 12% Tris-Glycine SDS-PAGE gel in the absence any reducing agent. Protein concentration was measured by NanoDrop Oneᶜ Microvolume UV-Vis Spectrophotometers (ThermoFisher Scientific, Waltham, MA) and calculated using the equation: C = (1.55 * A₂₈₀) – (0.76 * A₂₆₀), where C is the concentration of the protein in mg/ml, A₂₈₀ and A₂₆₀ are the absorbance of protein samples at 280nm and 260nm respectively⁹¹. The protein concentrations obtained with this method were comparable with BCA protein quantification assays.

Spec-seq library synthesis and purification

Single-stranded Spec-seq library templates and IRDye 700-labeled reverse complement primers (Supplementary Table S1) were ordered directly from Integrated DNA Technologies (IDT, Coralville, Iowa). The synthesis and purification of the double-stranded libraries followed previously published protocols^33,34,91. Briefly, 100 pmol of template oligos and 125 pmol IRDye 700-labeled reverse complement primer F1 were mixed in Phusion® High-Fidelity PCR Master Mix (NEB, Ipswich, MA). A 15s denaturing at 95°C following a 10-minute extension at 52°C afforded duplex DNAs. Subsequently, the mixture was treated with 1ul Exonuclease I (NEB, Ipswich, MA) to remove excess ssDNA. The libraries were purified by MinElute PCR Purification Kit (QIAGEN, Hilden, Germany) and eluted in molecular biology graded water (Corning, Corning, NY).

EMSA and sample preparation for sequencing

The protein-DNA binding reactions was done in 1x CRX binding buffer (60mM KCl, 25mM HEPES, 5% glycerol, 1mM DTT)⁹⁰. A fixed amount (Supplementary Table S1) of IRDye-labelled DNA libraries were incubated on ice for 30 minutes with varying concentrations of wild type or mutant peptides in 20μl reaction volume. The reaction mixtures were run at 4°C in native 12% Tris-Glycine PAGE gel (Invitrogen, Waltham, MA) at 160V for 40min. The IRDye-labeled DNA fragments in the bound and unbound fractions were visualized by Odyssey® CLx and Fc Imaging Systems (LI-COR, Inc., Lincoln, NE). The visible bands were excised from the gels and DNAs were extracted with acrylamide extraction buffer (100mM NH₄OAc, 10mM Mg(OAc)₂, 0.1% SDS) then purified with MinElute PCR Purification Kit (QIAGEN, Hilden, Germany). The DNAs were amplified, barcoded by indexed Illumina primers. All indexed libraries were then pooled and sequenced on a single 1×50bp Miseq run at DNA Sequencing Innovation Lab at the Center for Genome Sciences & Systems Biology (CGS&SB, WashU).

qRT-PCR

For each replicate, RNA from 2 retinae of a mouse was extracted using the NucleoSpin® RNA kits (Takara Bio USA, Inc., San Jose, CA). RNA sample concentration and quality was determined with NanoDrop Oneᶜ Microvolume UV-Vis Spectrophotometers (ThermoFisher Scientific, Waltham, MA). 1 μg of RNA was used for cDNA synthesis with iScript cDNA Synthesis Kits (BioRad, Hercules, CA) in a 20μl reaction volume. Primers used in this study were listed in Supplementary Table S2. qRT-PCR reactions were assembled using SsoFast™ EvaGreen® Supermix with Low ROX (Bio-Rad Laboratories, Inc., Hercules, CA) following manufacturer’s protocol. Data was obtained from Bio-Rad CFX96 Thermal Cycler following a three-step protocol: 1 cycle of 95°C 3 min, 40 cycles of 95°C 10 sec and 60°C 30 sec. Data was exported and further processed with customized python script.

Western blot

Experiments were performed using two biological replicates with two retinas for each replicate. Nuclear extracts were prepared using the NE-PER Nuclear and Cytoplasmic Extraction Reagents (Thermo Fisher Scientific, Waltham, MA) following manufacturer’s instructions. 1x Roche cOmplete™ Mini Protease Inhibitor Cocktail (MilliporeSigma, Burlington, MA) was supplemented in all extraction reagents. 5mM of DTT was added immediately before sample denaturing and protein was separated by running on Invitrogen NuPAGE™ Novex 4-12% Bis-Tris MiniGels (Invitrogen, Waltham, MA). Membrane transfer was done with the Blot™ mini blot module (Invitrogen, Waltham, MA) following the manufacturer’s protocol. Membrane was probed with mouse monoclonal anti-CRX antibody M02 (1:1 000, Abnova Corp., Taipei City, Taiwan) and rabbit polyclonal anti-HDAC1 antibody H51 (1:1 000, Santa Cruz Biotechnology, Dallas, TX), visualized with IRDye® 680RD goat anti-rabbit IgG and IRDye® 800CW goat anti-mouse IgG secondary antibodies (1:10 000, LI-COR, Inc., Lincoln, NE). The membrane was then imaged using Odyssey® CLx and Fc Imaging Systems (LI-COR, Inc., Lincoln, NE).

Transient transfection luciferase reporter assays

HEK293T cells were cultured in Dulbecco’s Modified Eagle Medium supplemented with 10% fetal bovine serum (FBS) and Penicillin-Streptomycin following the manufacturer’s protocol. Cells were transfected with calcium phosphate transfection protocol in 6-well plates as previously described^18,19. Experimental plasmids and usage amount are described in Supplementary Table S1. Typically, 48 hours after transfection, cells were harvested, digested and assayed for luciferase activity using Dual-Luciferase Reporter Assay System (Promega, Madison, WI) following the manufacturer’s protocol. Data were collected using TD-20/20 Luminometer (Turner Designs, East Lyme, CT) and further processed with customized python scripts.

Data analysis

Homeodomain sequence alignment

The full-length protein sequences for the selected TFs were first aligned with Clustal Omega (EMBL-EBI, UK). Aligned sequences of the third homeodomain helix were then extracted to generate Figure 1B using Jalview (v2.11.1.7). A list of the accession numbers for the selected TFs can be found in Supplementary Table S1.

Determination of relative binding affinity with Spec-seq

For a biomolecular interaction between a protein P and a particular DNA sequence, S_i, the interaction can be diagrammed as:

where p · i_i refers to the protein-DNA complex. The affinity of the protein P to sequence S_i is defined as the association constant K_A, or its reciprocal, the dissociation constant K_D. The K_A of the protein-DNA interaction is determined by measuring the equilibrium concentrations of each reactant and the complex:

where […] refers to concentrations. As in a typical Spec-seq experiment, thousands of different DNA sequences compete for the same pool of proteins, their relative binding affinities (the ratio of their K_A) can be determined by measuring the concentrations of each sequence in the bound and unbound fractions without measuring the free protein concentrations, which is often the most difficult to measure accurately:

In a binding reaction involving TF and a library of DNAs, the concentration of bound and unbound species are directly proportional to the number of individual DNA molecules in each fraction which can be obtained directly from sequencing data. With enough counts in each fraction, we can accurately estimate the ratios of concentrations from counts with the relationship:

where N_U denotes counts in the unbound fraction and N_B denotes counts in the bound fraction. Therefore, the binding affinity of a sequence variant S_x relative to the reference sequence S_ref can be calculated by:

The natural logarithms of these ratios are the relative binding free energies in the units of kcal/mol. The relative free energy of the reference site for each CRX HD was set to 0.

Spec-seq data analysis and energy logo visualization

The sequencing results were first filtered and sorted based on conserved regions and barcodes. Reads with any mismatch in the conserved regions were discarded prior to further analysis as described previously^32,34,91. The ratio of individual sequence in bound and unbound reads was calculated as a measurement of relative binding affinity (Equation. 5) compared to the consensus sequence. The relative binding energy was then derived from the natural logarithm of the relative binding affinity and represented in kcal/mol units.

For wild type CRX HD and all the mutants, the energy weight matrices (ePWMs) were generated based on the regression of the TF’s binding energy to its reference sequence. Only sequences within two mismatches to the reference were used to generate the ePWMs. Energy logos were generated from ePWMs after normalizing the sum of energy on each position to 0 and the negative energy values were plotted such that preferred bases are on top. The sequence logos were generated from ePWMs with python package logomaker (v0.8). The ePWMs for all CRX HDs are listed in Supplementary Table S3.

ChIP-seq data analysis

2×150bp reads from Illumina NovaSeq were obtained for all samples with a minimum depth of 22M reads at Novogene (Beijing, China). For each sample, reads from two sequencing lanes were first concatenated and run through Trim Galore (v0.6.1)⁹² to remove adapter sequences and then QC by FastQC (v0.11.5)⁹³. The trimmed reads were then mapped to the mm10 genome using Bowtie2 (v 2.3.4.1)⁹⁴ with parameters -X 2000 --very-sensitive. Only uniquely mapped and properly paired reads were retained with samtools (v1.9)⁹⁵ with parameters -f 0×2 -q 30. Mitochondria reads were removed with samtools (v1.9)⁹⁵. Duplicated reads were marked and removed with Picard (v2.21.4)⁹⁶. Last, reads mapped to the mm10 blacklist regions were removed by bedtools (v2.27.1)⁹⁷ by intersect -v. bigWig files were generated with deeptools (v3.0.0)⁹⁸ with command bamCoverage --binSize 10 -e -- normalizeUsing CPM and visualized on IGV Web App⁹⁹. For each genotype, an average binding intensity bigWig file from two replicates was generated with deeptools (v3.0.0)⁹⁸ command bamCompare –operation mean with default parameters.

Peak-calling was done with MACS2 (v2.1.1.20160309)¹⁰⁰ on individual replicate with the default parameters. For each genotype, we then generated a genotype specific high confidence peakset by intersection of peaks called in two replicates. IDR framework (v2.0.4)¹⁰¹ were used to generate quality metrics for the processed ChIPseq data. R package DiffBind (v3.0.15)^102,103 and DEseq2 (v1.30.1)¹⁰⁴ were then used to re-center peaks to ±200bp regions surrounding summit, generate normalized binding intensity matrix, and differential binding matrix. We defined differentially bound peaks between each mutant and wild type sample if the absolute log₂FC is more than 1.0, corresponding to two-fold, and the FDR is smaller than 5e-2.

To associate peaks to genes, we used Genomic Regions Enrichment of Annotations Tool (GREAT v4.0.4)¹⁰⁵ through the R package rGREAT (v1.19.2)¹⁰⁶. Each peak was assigned to the closest TSS within 100kb.

Binding intensity heatmap and clustering

To generate the binding intensity heatmap in Figure 2A, we first compiled the genotype specific high confidence peakset for all genotypes into a single consensus peakset and only peaks with at least 5 cpm in all genotypes were retained. Python package fastcluster (v1.1.26)¹⁰⁷ was used to perform hierarchical clustering of the consensus peakset intensity matrix with parameters method=’single’, metric=’euclidean’. The genomic regions corresponding to the two major clusters were exported and used to generate binding intensity heatmaps with deeptools (v3.0.0)⁹⁸.

Genomic region enrichment of CRX peaks

Peak annotation in Figure 2D were obtained using annotatePeaks.pl from HOMER (v4.8).

De novo motif searching

The mm10 fasta sequences for each genotype specific peaks were obtained using R package BSgenome (v 1.58.0)¹⁰⁸. De novo motif enrichment analysis for each set of sequences were then performed with MEME-ChIP in MEME Suite (v5.0.4)¹⁰⁹ using order 1 Markov background model and default parameters. Since homeodomain motifs are relatively short and can be repetitive (e.g. K88N motif), we reported DREME³⁸ found motifs for Figure 2E, which is more sensitive than MEME to find short, repetitive motifs.

RNA-seq data analysis

2×150bp reads from Illumina NovaSeq were obtained for all samples with a minimum depth of 17 M reads at Novogene (Beijing, China). Sequencing reads were first run through Trim Galore (v0.6.1)⁹² to remove adapter sequences and then QC by FastQC (v0.11.5)⁹³. Trimmed reads were then mapped to the mm10 genome and quantified with kallisto (v0.46.2)¹¹⁰. Kallisto output transcript-level abundance matrices were then imported and summarized into gene-level matrices with R package tximport (v1.18.0)¹¹¹. DEseq2 (v1.30.1)¹⁰⁴ was then used for normalization and differential expression analysis. The normalized count and differential expression matrices were then exported and further processed with customized python scripts.

We defined differentially expressed genes between each mutant and wild type sample if the absolute log₂FC is more than 1.0, corresponding to two-fold, and the FDR is smaller than 1e-2. For comparison between heterozygous and homozygous mutants, we first filtered genes with at least 5 cpm and then those that were called differentially expressed compared with wild type in at least one mutant genotype. We retrieved gene names in Supplementary Tables S3-S5 from the Database for Annotation, Visualization and Integrated Discovery (DAVID, v6.8)¹¹².

Definition of CRX-dependent and -independent gene set

We first identified CRX peaks that were bound in the WT sample but lost in R90W/W sample (log₂FC < -1 and FDR < 5e-2). This yielded a total of 7677 peaks. We then found the genes associated with these peaks. We defined a gene to be CRX-dependent activated if its expression was down in adult (P21) R90W/W RNA-seq sample (log₂FC < -0.6 and FDR < 1e-5). Similarly, a gene is defined as CRX-dependent suppressed if its expression was up in adult R90W/W RNA-seq sample (log₂FC > 0.6 and FDR < 1e-5). A gene is defined as CRX-independent if its expression was not significantly affected in adult R90W/W RNA-seq samples. There were 617 CRX-dependent activated, 135 CRX-dependent suppressed, and 5565 CRX-independent genes. Manual inspection of the CRX-dependent suppressed genes revealed no clear association with photoreceptor development. Therefore, we did not further pursue this gene set. The complete list of CRX-dependent activated genes that showed differential expression in at least one of the HD mutant retinas can be found in Supplementary Table S5. The lists for CRX-independent genes that showed differential expression in Crx^E80Aor Crx^K88N mutant retinas can be found in Supplementary Tables S6 and S7 respectively.

Gene ontology analysis

Gene ontology analysis in Figures S4B, S4E, and S5F were performed using R package clusterProfiler (v4.0.5)^113,114 with the genome wide annotation package org.Mm.eg.db (v3.12.0)¹¹⁵. Redundant enriched GO terms were removed using simplify() function with parameters cutoff=0.7, by=“p.adjust”. The enrichment analysis results were then exported in table format and further processed for plotting with python.

Aldiri et al. RNA-seq data re-analysis

The RNA-seq data from Aldiri et al.³⁹ were obtained from GEO under accession numbers GSE87064. The reads were processed similarly as all other RNA-seq data generated in this study. For Figures S4C, S4F, S5C, S5E,S6A, S6B, expression row z-scores were calculated using average cpm from replicates at each age.

Statistical analysis

One-way ANOVA with Turkey honestly significant difference (HSD) test in Figures 6A, S3C, and S7D were performed with python packages scipy (v1.8.1)¹¹⁶ and scikit_posthocs (v0.7.0)¹¹⁷. Two-sided Mann-Whitney U test in Figure S5A was performed with python package scipy (v1.8.1)¹¹⁶.

Key resources table

Supplementary tables

Supplementary Table S1. HD TF accession numbers (related to Figure 1B)

Supplementary Table S2. Plasmids and primers for biochemistry experiments

Supplementary Table S3. Spec-seq ePWMs (related to Figures 1G, 1K, 1L, 1M, and S2I-S2L)

Supplementary Table S4. DNA sequences for mutation knock-in mice generation

Supplementary Table S5. CRX-dependent activated genes differentially expressed in at least one mutant mouse model (ordered as in Figure 3B)

Supplementary Table S6. CRX-independent genes mis-regulated in Crx^E80A mutants (ordered as in Figure S5C)

Supplementary Table S7. CRX-independent genes mis-regulated in Crx^K88N mutants (ordered as in Figure S5E)

Supplementary Table S8. Annotation for phototransduction genes in Figure 4B

Supplementary Table S9 Quantification and statistical analysis (related to Figures S3C and S5A)