The neuronal RNA binding protein NOVA regulates splicing, shuttles to the cytoplasm, and co-localizes with target transcripts in dendrites, suggesting links between splicing and local translation. Here we identified >200 transcripts showing NOVA-dependent changes in abundance, but, surprisingly, HITS-CLIP revealed NOVA binds these RNAs in introns rather than 3′ UTRs. This led us to discover NOVA-regulated splicing of cryptic exons within these introns. These exons triggered nonsense mediated decay (NMD), as UPF1 and protein synthesis were required for NOVA's effect on RNA levels. Their regulation was dynamic and physiologically relevant. The NMD exons were regulated by seizures, which also induced changes in Nova subcellular localization and mediated large changes in synaptic proteins, including proteins implicated in familial epilepsy. Moreover, Nova haploinsufficient mice had spontaneous epilepsy. The data reveal a hidden means of dynamic RNA regulation linking electrical activity to splicing and protein output, and of mediating homeostatic excitation/inhibition balance in neurons.https://doi.org/10.7554/eLife.00178.001
After the DNA in a gene has been transcribed into messenger RNA, portions of the mRNA called introns are removed, and the remaining stretches of mRNA, which are known as exons, are spliced together. Within eukaryotic cells, a process known as alternative splicing allows a single gene to encode for multiple protein variants by ensuring that some exons are included in the final, modified mRNA, while other exons are excluded. This modified mRNA is then translated into proteins.
Eukaryotic cells also contain proteins that bind to RNA to regulate alternative splicing. These RNA-binding proteins are often found in both the cytoplasm and nucleus of cells, and their involvement in splicing may be linked to other processes in the cell such as mRNA localization and translation. It has also become clear over the past two decades that certain types of RNA-binding proteins, including NOVA proteins, are only found in neurons, and that these proteins have been best characterized as alternative splicing regulators. Recent work has also suggested that they also have important roles in regulating neuronal activity and development, and that their actions in neuronal nuclei and cytoplasm might be coordinated.
Now Eom et al. use the predictive power of a high throughput sequencing and crosslinking method termed HITS-CLIP to show that NOVA proteins can indirectly regulate cytoplasmic mRNA levels by regulating the process of alternative splicing in the nucleus to produce ‘cryptic’ exons in the brains of mice. The presence of these exons in the mRNA leads to the production of premature termination codons in the cytoplasm. These codons trigger a process called nonsense-mediated decay that involves identifying mRNA transcripts that contain nonsense mutations, and then degrading them. These cryptic exons were seen in mice missing the NOVA proteins, where they are expressed in abnormally high levels; in normal mice, these exons have not been seen before, hence they were termed ‘cryptic’.
Eom et al. also show that these cryptic exons are physiologically relevant by inducing epileptic seizures in mice. Following the seizures, they find that the NOVA proteins up-regulate and down-regulate the levels of different cryptic exons, leading to changes in the levels of the proteins encoded by these mRNAs, including proteins that inhibit further seizures. Overall the results indicate that, by controlling the production of various proteins in neurons, these previously unknown cryptic exons have important roles in the workings of the brain.https://doi.org/10.7554/eLife.00178.002
RNA binding proteins (RNABPs) play critical roles in the brain to regulate neuronal development and activity, as underscored by the finding that dysregulation of RNABP function underlies a growing list of neurological disorders (Licatalosi and Darnell, 2006; Cooper et al., 2009; Poulos et al., 2011). This connection was first highlighted by the use of autoantibodies present in the paraneoplastic neurologic disorders (Darnell, 1996, 2004; Darnell and Posner, 2006, 2011) to discover that NOVA and ELAVL/Hu are neuron-specific RNABPs (Szabo et al., 1991; Buckanovich et al., 1993; Okano and Darnell, 1997; Kim et al., 2009; Dredge and Jensen, 2011). The characterization of these proteins, as well as a number of subsequently described mammalian RNABPs, including NeuN/RBFOX3 (Kim et al., 2009; Dredge and Jensen, 2011) and brPTB/nPTB/PTBP2 (Markovtsov et al., 2000; Polydorides et al., 2000), suggests that the brain, and neurons in particular, harbor unique sets of RNABPs to uniquely regulate RNA metabolism (Darnell, 2006).
NOVA proteins are among the best-studied mammalian tissue-specific RNABPs. Two paralogs, NOVA1 (Buckanovich et al., 1993) and NOVA2 (Yang et al., 1998), are present in mammals, with largely indistinguishable biochemical properties but largely reciprocal expression within the central nervous system (Darnell, 2006). They bind to YCAY-rich elements (Buckanovich and Darnell, 1997; Jensen et al., 2000a; Lewis et al., 2000; Ule et al., 2006) to regulate neuronal alternative splicing (Polydorides et al., 2000; Jensen et al., 2000b; Dredge and Darnell, 2003; Dredge et al., 2005; Ule et al., 2005b; Licatalosi et al., 2008) and mRNA transport of some target RNAs (Racca et al., 2010). NOVA-mediated RNA regulation is essential, as Nova DKO (Nova1−/− and Nova2−/−) mice die immediately at birth (Ruggiu et al., 2009), although the range of NOVA actions is still being enumerated (Zhang et al., 2010). For example, NOVA, like many other splicing factors (Huang and Steitz, 2005), shuttles between the nucleus and cytoplasm (Racca et al., 2010), reflecting the interesting but incompletely understood relationship between the regulation of RNA splicing, transport, stability, localization and translation (Maniatis and Reed, 2002; Huang and Steitz, 2005; Martin and Ephrussi, 2009; Darnell, 2010).
Several well-defined RNA elements mediate RNA stability and localization, such as 3′ UTR adenine/uridine-rich (ARE) elements recognized by the Elavl family of RNABPs (Levine et al., 1993; Myer et al., 1997; Peng et al., 1998; Brennan and Steitz, 2001; Kishore et al., 2010) and the zipcode recognized by ZBP1 (Chao et al., 2010). NOVA may play coordinate roles in the nucleus and cytoplasm, as HITS-CLIP studies have shown direct binding to introns and 3′ UTRs of GlyRa2 and Girk2 mRNA (Racca et al., 2010), and evidence of splicing and a role for localization in each. However, the extent and means by which NOVA might mediate actions in both compartments remains uncertain.
Here we explore the relationship between nuclear and cytoplasmic functions of NOVA by undertaking HITS-CLIP (Darnell, 2010) on each fraction separately, and comparing results with microarray analysis of RNA in Nova-null mice. NOVA crosslinks to many transcripts in both nuclear/intronic and cytoplasmic/3′ UTR clusters, suggesting an ordered set of cis-actions on target RNAs. Surprisingly, however, among 229 transcripts showing significant steady-state changes, NOVA binding was primarily present in intronic rather than cytoplasmic elements. This led us to hypothesize and identify previously unannotated exons or alternative splicing patterns near these intronic elements that introduced premature termination codons (PTC) able to mediate nonsense-mediated mRNA decay (NMD). Thus HITS-CLIP reveals that NOVA regulates otherwise cryptic NMD exons in the nucleus to indirectly regulate steady-state mRNA levels in the cytoplasm. We put this finding in a physiologic context, showing that these exons encode synaptic proteins, they are regulated by seizure activity, and that Nova itself is important in epilepsy, as the protein shifts from the neuronal nucleus to cytoplasm shortly after seizure, and Nova haploinsufficient mice have spontaneous epilepsy. Together, these data suggest a role for Nova in maintaining homeostasis after seizure, in part through the regulation of cryptic NMD exons.
Previous CLIP experiments have identified NOVA binding sites near alternative exons and poly(A) sites (Ule et al., 2003; Ule et al., 2005b, 2006; Licatalosi et al., 2008), but have not fully addressed whether NOVA might also regulate the steady-state level of some transcripts. To assess the degree to which NOVA might regulate this aspect of neuronal mRNA metabolism, we compared steady-state levels of total poly(A)+ mRNAs in four Nova WT and four Nova1−/−/2−/− (double KO; DKO) brains from P0 littermates (DKO mice die shortly after birth) with Affymetrix exon arrays. A total of 229 genes showing significant changes (|log2(WT/DKO)|>0.3; p < 0.05, Student's t-test) were identified (Figure 1A). Interestingly, this data indicated that NOVA had a disproportionate action to increase (rather than decrease) steady state levels of brain transcripts. Specifically, 215 of the 229 transcripts showed significant decreases in the absence of NOVA (NOVA-dependent ‘upregulation’ of steady-state mRNA levels; Figure 1A). 22 showed a >1.5-fold change, and 11 of these were validated experimentally by qRT-PCR (Figure 1B; Table 1). Only 14 transcripts showed comparable NOVA-dependent mRNA suppression of steady-state levels (five showing a greater than 1.5-fold change), and these were validated experimentally (Figure 1C and Table 1).
These observations do not indicate whether NOVA acts directly or indirectly on these 229 transcripts to regulate their levels. HITS-CLIP has proven to be a reliable means of defining sites of direct functional RNA–protein interactions (Licatalosi and Darnell, 2010). Analysis of prior CLIP data (Licatalosi et al., 2008; Zhang et al., 2010) demonstrated that many of the 229 transcripts showing NOVA-dependent changes in level had CLIP tags when whole brain extracts were crosslinked (see also below). Such changes could result from nuclear and/or cytoplasmic actions, and we have previously found evidence that NOVA may act in both compartments (Racca et al., 2010). Therefore, we undertook a systematic comparison of NOVA binding in each compartment.
To define NOVA-RNA interactions in the nucleus and cytoplasm separately, we crosslinked mouse brain cortex, ‘freezing’ RNA–protein complexes for analysis, and then subfractionated tissue into nuclear and cytoplasmic fractions. To assess the integrity of this fractionation, we performed immunoblot analysis with markers known to be specific for each fraction and antibodies to NOVA, demonstrating that each fraction was >90% pure, and that ∼60% of NOVA was nuclear and 40% cytoplasmic (Figure 1D, consistent with and detailed in a previous study (Racca et al., 2010)). While this fractionation scheme (based on salt extraction) gave a relatively clean separation between each compartment, we cannot exclude the possibility that some NOVA protein was not extracted from each compartment under these conditions. Nonetheless, these data suggested that highly enriched NOVA-RNA complexes present in subcellular compartments could be purified and analyzed.
We examined NOVA RNA binding maps to nuclear and cytoplasmic RNAs by analyzing HITS-CLIP results from each fraction (Figure 1E and Figure 1—figure supplement 1; see also Table 2). We defined NOVA CLIP tag clusters by grouping overlapping RNA tags identified in multiple biologic replicates (biologic complexity (BC) > 2) (Licatalosi et al., 2008) from four independent animals. These clusters were classified according to their locations within protein-coding transcripts, using annotations from cDNA/EST data and RefSeq and UCSC known genes (Zhang et al., 2010). By focusing on CLIP tags in robust clusters (BC = 4, peak height (PH) ≥ 4), we observed that nuclear HITS-CLIP tags were enriched in introns (90%) and cytoplasmic HITS-CLIP tags in 3′ UTR (63%, including ∼13% within 10 kb downstream of annotated transcripts; Figure 1F; see (Licatalosi et al., 2008)). NOVA cytoplasmic CLIP data also contained a significant number of intronic clusters, but many of these were derived from abundant non-coding RNA species, such as ribosomal RNAs (also evident in nuclear CLIP data). After we reanalyzed the clusters with repetitive sequences excluded, only 17% clusters were located in introns (Figure 1F). In addition, when we analyzed the distribution of clusters as a function of peak height (PH), we identified a large proportion of intronic clusters in nuclear CLIP data, while less than 5% of NOVA cytoplasmic CLIP tag clusters were intronic (at PH 12–14).
The proportion of apparent cytoplasmic NOVA binding sites in introns was nonetheless an unexpectedly high number, prompting us to repeat the cytoplasmic purification with an independent method (based upon differential centrifugation; data not shown) and then repeat HITS-CLIP analysis on mouse brain. This experiment independently confirmed the presence and position of NOVA2 cytoplasmic (R2 = 0.77) and nuclear (R2 = 0.77) CLIP tags between experiments. We have not studied the function of the small numbers of reproducible NOVA ‘cytoplasmic’ intronic clusters further, which most likely reflect remaining impurity of the cell fractionation, but could also reflect other processes, including NOVA binding to non-coding RNAs, stable processed introns, or unspliced transcripts. Taken together, our data suggest that NOVA binds predominantly to intronic elements in pre-mRNA in the nucleus and mature mRNA elements in the cytoplasm, but may have an unexpected role in binding intronic non-coding RNA elements in the cytoplasm as well.
We previously identified RNA transcripts bound by NOVA in the nucleus that also co-localize with (GlyRa2) or are localized by (Girk2) NOVA in neuronal processes (Racca et al., 2010), prompting us to compare the NOVA nuclear and cytoplasmic binding maps. We first compared the frequency and extent to which cytoplasmic NOVA clusters were also present in the same location in nuclear CLIP. There was a significant albeit small correlation between cytoplasmic and nuclear HITS-CLIP tags (R2 = 0.32, Figure 1—figure supplement 2) and robust clusters (BC = 4; R2 = 0.36, Figure 1—figure supplement 2). Moreover, when we relaxed the stringency of the nuclear clusters, we found that in most transcripts with robust cytoplasmic clusters, NOVA was already bound to those clusters in the nucleus. Among 504 transcripts with robust cytoplasmic clusters (BC ≥ 4, PH > 10), 235 had robust nuclear clusters (BC ≥ 4, PH > 10), and an additional 251 (46.6%) had weaker nuclear clusters. There were 18 unique cytoplasmic clusters (i.e. clusters not present in nuclear CLIP, but in transcripts which nonetheless had nuclear clusters in other locations), suggesting the possibility of a reassortment of NOVA binding sites in cis on individual transcripts; such a mechanism might allow nuclear and cytoplasmic functions like RNA localization or RNA stability to be linked (see Racca et al., 2010).
We analyzed the relationship between NOVA cytoplasmic and nuclear binding in transcripts whose levels are NOVA-dependent. One common mechanism by which transcript steady-state levels are regulated is through actions on stability elements within the 3′ UTR, either through the actions of miRNAs (Fabian et al., 2010) or through RNABP-RNA regulatory interactions via actions on conserved elements such as ARE sequences (Brennan and Steitz, 2001; Yang et al., 2003; Khabar, 2010). Surprisingly however, the distribution of NOVA CLIP tags within NOVA-regulated transcripts (specifically, in the 149 of 229 transcripts harboring ≥5 CLIP tags) revealed that the majority of NOVA CLIP tags (∼76%) were not present on the 3′ UTRs of NOVA-regulated transcripts. Instead the predominant location of NOVA CLIP tags on these transcripts was intronic (Figure 1G), suggesting the possibility that NOVA action on pre-mRNA might be linked to steady-state levels of NOVA target mRNAs.
To address the mechanism by which NOVA regulates mRNA steady-state levels, we analyzed individual targets in more detail. The transcript encoding Dlg3 (Sap102) showed the most significant NOVA-dependent upregulation (i.e. the largest decrease in steady state levels in NOVA DKO brain) in exon arrays (Figure 1B,C), which was confirmed in qRT-PCR studies (Table 1). The Dlg3 transcript had a large number of NOVA CLIP tags (Figure 2A), suggesting that it might be both directly bound and regulated by NOVA. Consistent with this possibility, we found a nearly 10-fold reduction in Dlg3 mRNA in NOVA DKO brain RNA samples by Northern blot analysis using two different probes and semi-quantitative RT-PCR (Figure 2B, Figure 2—figure supplement 1), with intermediate changes seen in single NOVA1 or NOVA2 KO mice (data not shown).
To assess whether these changes in mRNA levels led to corresponding changes in DLG3 protein levels, we analyzed protein extracts from NOVA WT vs DKO brain. Western blots demonstrated that DLG3 protein levels were severely reduced (∼90% reduction; Figure 2C) in DKO brain, closely reflecting the reduction in Dlg3 mRNA. We also examined DLG3 protein by immunofluorescence microscopy using anti-DLG3 antibodies. We co-cultured WT/DKO neurons together and stained for NOVA protein to distinguish WT from DKO neurons, using Neurofilament-M (NF-M) immunoreactivity as a positive control to stain all neurons. These experiments clearly showed that NOVA DKO neurons had very little DLG3 signal (Figure 2D). Taken together, these data demonstrate that the absence of NOVA protein in neurons is associated with a drastic reduction in Dlg3 mRNA levels and a concomitant reduction in DLG3 protein levels.
To address whether NOVA protein might directly regulate Dlg3 mRNA levels, we examined the specific locations of NOVA HITS CLIP tags along the Dlg3 transcript (Figure 2A). NOVA binding sites were present in both the 3′ UTR and introns, and in both locations these sites harbored NOVA binding elements (clusters of the sequence YCAY; (Zhang et al., 2010)). To assay the functional outcome of NOVA binding to the 3′ UTR elements, we generated a construct encoding a destabilized d1EGFP fused to either a 214 nt fragment (NOVA binding clusters in 3′ UTR shown in Figure 2A) from the wild-type Dlg3 3′ UTR or a mutant fragment which would disrupt NOVA binding (YCAY->YAAY; Figure 3—figure supplement 1). 24 hr after transfection of these constructs into Neuro2a (N2a) neuroblastoma cells, actinomycin D was added for 5 hr in order to block transcription, and Dlg3 mRNA levels were followed by qRT-PCR (Figure 3—figure supplement 2). These data revealed a relatively small but clear decrease in d1EGFP mRNA containing mutant YAAY NOVA binding sites (∼50% reduction) compared to transcripts harboring WT YCAY elements, indicating that NOVA binding to the 3′ UTR had a small effect on Dlg3 steady state levels. However, this interaction did not appear to be sufficient to explain the large effect NOVA had on transcript (see Table 1) and protein levels in neurons, prompting us to examine whether additional NOVA actions on Dlg3 intronic elements contributed to effects on steady-state RNA levels.
The NOVA nuclear HITS-CLIP results demonstrated NOVA intronic and 3′ UTR binding sites that were present only in nuclear and cytoplasmic HITS-CLIP, respectively, (Figure 2A), suggesting a hierarchy of NOVA action. To explore whether NOVA intronic binding sites might relate to an action on Dlg3 steady-state mRNA levels, we empirically searched for cryptic alternative splicing events in regions neighboring the largest intronic HITS-CLIP clusters, given previous observations indicating that NOVA intronic clusters predict alternative splicing outcomes (Dredge et al., 2005; Ule and Darnell, 2006; Licatalosi et al., 2008; Zhang et al., 2010). RT-PCR was performed in WT vs. NOVA DKO brain RNA using primers bounding introns harboring NOVA HITS-CLIP clusters (exons 14 (E14) and E18 in Figure 2A). In WT mouse brain two isoforms were detected and sequenced, and these were found to correspond to known alternative spliced isoforms, harboring what we refer to as E16, with or without E17, and a trace amount of a larger isoform. Remarkably, RT-PCR analysis of NOVA DKO mouse brain RNA revealed a marked increase of this larger isoform, and the presence of a previously unknown fourth, even larger form. Sequence analysis revealed the latter two isoforms correspond to the inclusion of an exon, E15, just downstream of the main Nova nuclear CLIP cluster, and a new combination of exons undetectable in WT brain, incorporating both E15 and E16 (as well as E17; termed Dlg3.15-16-17). E16 also has a second upstream intronic CLIP cluster, suggesting that the Nova binding sites upstream of E15 and E16 could normally act to suppress their dual inclusion, consistent with their inclusion in the DKO brain and with the Nova position-dependent splicing map (Licatalosi et al., 2008; Licatalosi and Darnell, 2010).
Interestingly, the previously unknown Dlg3 isoform (Dlg3.15-16-17) encoded a transcript harboring a PTC, formed by the inclusion of both E15 and E16 (see Figure 3A). This suggested that the marked reduction in DLG3 protein levels might relate to nonsense-mediated mRNA decay (NMD), an mRNA surveillance mechanism in which transcripts containing PTCs are recognized and degraded in association with early rounds of translation (Schoenberg and Maquat, 2012).
To assess whether NOVA acted on the Dlg3.15-16-17 through NMD, we examined the effect of blocking NMD on NOVA-dependent Dlg3 splicing using multiple approaches (Matsuda et al., 2008). First, we added emetine, a translational inhibitor, into primary neuronal cultures of neurons obtained from WT or NOVA DKO mouse brain, since a pioneering round of translation is necessary to activate the NMD pathway (Ni et al., 2007; Schoenberg and Maquat, 2012). After emetine treatment for 10 hr, RNA was isolated and Dlg3 splicing was assayed by RT-PCR. In WT neurons, emetine had no effect on Dlg3 splicing. However, in the absence of NOVA, emetine induced a dramatic increase in the NMD isoform Dlg3.15-16-17, and total Dlg3 mRNA levels increased by 3.5-fold (Figure 3B). This result establishes a link between the ability to detect NOVA-dependent splicing of Dlg3.15-16-17 and active translation, suggesting that this isoform is normally suppressed coordinately both by NOVA and NMD.
To more directly assess whether Dlg3.15-16-17 is regulated by NMD, we knocked down a core component of the NMD pathway, Upf1 (Mendell et al., 2002), with Upf1 siRNA. We first established that Upf1 siRNA was able to reduce UPF1 protein (by ∼90%) in N2a cells (Figure 4—figure supplement 1). We then transfected Upf1 siRNA into cultured primary neurons to readdress the possibility of coordinate regulation by NOVA and NMD. In primary neuronal cultures, transfection efficiency was lower, such that only about half of the cells were transfected, and we detected a concomitant ∼50% decrease in Upf1 transcript in qRT-PCR analysis (Figure 4—figure supplement 2). Hence to directly assess the effects of Upf1 knock-down on a per-cell basis, we transfected Upf1 siRNA into WT or DKO primary neuronal cultures, and monitored DLG3 and UPF1 protein levels in individual cells by immunofluorescence microscopy. These experiments revealed a reciprocal relationship between DLG3 protein and UPF1 protein levels in NOVA DKO neurons. DLG3 protein level was very low in untransfected DKO neurons that expressed UPF1 protein (see Figures 2D and 3C), whereas cells in which UPF1 signals were markedly reduced by Upf1 siRNA exhibited a markedly increased DLG3 signal. We interpret these results to indicate that when the NMD pathway was inhibited by Upf1 knock-down, mis-spliced Dlg3.15-16-17 mRNA led to accumulation of DLG3 protein that escape NMD degradation and accumulate at the protein level. This may have included truncated isoforms, as these experiments used an antibody against a Dlg3 N-terminal epitope; (see ‘Materials and methods’). More generally, these results demonstrate that NOVA regulation of a cryptic alternatively spliced exon is necessary to prevent NMD-mediated suppression of Dlg3 expression in the brain, and this can act in concert with 3′ UTR binding to maintain Dlg3 expression.
We next explored an example of the less common converse situation, in which microarray analysis revealed NOVA-dependent decreases in steady-state mRNA levels. We examined Scn9a mRNA, which showed the largest increase of 2.9-fold in NOVA DKO brain in the microarray data. We first independently validated this data, demonstrating that Scn9a mRNA level increased in NOVA DKO RNA by qRT-PCR (Table 1). We then determined whether the effects of NOVA on steady state Scn9a mRNA were reflected at the protein level. Western blot analysis revealed a marked reduction (∼12-fold) of SCN9a protein in NOVA DKO brain (Figure 4A,B), indicating that NOVA normally acts to suppress SCN9a expression at both the RNA and protein levels in the brain.
When we examined Scn9a transcripts for NOVA binding in HITS-CLIP data, we found no 3′ UTR tag clusters. Given that NOVA regulated Dlg3 mRNA through repression of the NMD pathway, we explored whether an action of NOVA on NMD might also explain its effect on Scn9a mRNA steady-state levels. We found that Scn9a did harbor a major tag cluster in an intron upstream of a previously uncharacterized but conserved exon (Figure 4D; based on one sequenced transcript; NCBI accession: AM905322). Empirically, we assayed mRNA expression in this region from WT vs DKO brain by RT-PCR (Figure 4C). Interestingly, in WT brain the Scn9a transcript had two isoforms, but in NOVA DKO brain the larger isoform was lost. Sequence analysis demonstrated that this larger isoform corresponded to an alternative exon 17, termed E17a, that was not represented in RefSeq (as it corresponded to a partial mRNA sequence only), and that E17a harbored a PTC (Figure 4D). Again, this data was consistent with the upstream position of the NOVA CLIP tag clusters relative to E17a (Figure 4C) predicting (Licatalosi et al., 2008; Licatalosi and Darnell, 2010) that NOVA would normally act to suppress E17a inclusion.
These findings suggested that in the WT brain, Nova-mediated inclusion of Scn9a E17a was normally used to produce transcripts that are likely degraded by NMD, and that E17a exclusion in the absence of NOVA activity could lead to an increase in steady state mRNA and protein level. To test the role of NMD in NOVA-mediated regulation of Scn9a levels, we applied emetine to primary WT neurons to inhibit translation and NMD. After 10 hr, RT-PCR was performed using primers bounding E17a. Emetine treatment increased the levels of E17a-included Scn9a transcripts compared to non-treated cells (∼75% increase; Figure 4E). In addition, we transfected Upf1 siRNA into WT primary neuronal cultures, and observed an increase in Scn9a E17a containing mRNA after siRNA KD (Figure 4F). Taken together, these observations indicate that Scn9a mRNA and consequently protein is held in balance by a NOVA-regulated NMD pathway.
To find additional NOVA-dependent NMD target mRNAs, we searched HITS-CLIP data and exon array data for target RNAs that had unexplained NOVA intronic CLIP tags (‘orphan clusters’) and whose steady-state level was NOVA-dependent. Since not all alternative exons and splicing patterns are fully annotated, particularly those associated with NMD, we empirically searched for cryptic exons in introns that had robust NOVA orphan clusters in nuclear CLIP experiments. Among 15 transcripts showing significant NOVA-dependent changes (Table 1), 11 transcripts harbored robust NOVA intronic CLIP tag clusters. We designed RT-PCR primers in exons bounding these orphan intronic NOVA binding sites and assessed whether cryptic NOVA-dependent NMD exons could be identified. We identified and sequenced cryptic NOVA-regulated exons, evident only in NOVA DKO brain RNA, in 9 of these 11 transcripts, as well as in an additional 2 transcripts (see Table 1, and Figure 3—source data 1), and found PTCs in each (Figure 5—figure supplement 1). In 7 transcripts splicing was consistent with NOVA-dependent inclusion of an NMD exon, such that these exons were absent in NOVA DKO brain, and in each case these correlated with increased steady-state mRNA levels in NOVA DKO brain. Conversely, in 4 transcripts splicing of these cryptic exons was consistent with NOVA-dependent suppression of an NMD exon and decreased steady-state levels in NOVA DKO brain.
To assess whether these transcripts were indeed regulated through NMD, we added emetine to primary neuronal cultures and examined the steady-state expression of the putative NMD-exons. After emetine treatment for 10 hr, qRT-PCR was performed on five transcripts in WT and DKO neurons. When we plotted normalized fold changes on a log2 scale, the results demonstrated that Dlg3, Rasgrf1 and Slc4a3 were degraded by NMD in DKO relative to WT mice, while Stx2 and Scn9a degradation by NMD in WT mice was alleviated in NOVA DKO animals (Figure 5B; Figure 5—figure supplement 2). Taken together, these data indicate the extensive use of NOVA in steady-state neurons to inhibit cryptic NMD exons, and, to a lesser degree, mediate inclusion of NMD exons, as a means to maintain or reduce, respectively, the steady-state levels of neuronal transcripts and proteins.
To assess whether NOVA-dependent regulation of NMD exons is dynamic and physiologically relevant, we examined the effects of inducing seizures in vivo on the utilization of these alternative exons. Mice were treated with pilocarpine or sham to induce acute generalized seizures, using previously established protocols (Turski et al., 1986). We assayed activity-dependent inclusion of NMD exons in Scn9a, Cdk5rap2 and Stx2, which we had found to be included by NOVA in the resting brain. In each transcript, pilocarpine induced seizures correlated with clear increases in utilization of the NMD exon (Figure 6A,B), suggesting that the levels of these transcripts can be dynamically altered by electrical activity altering NOVA action.
Pilocarpine can induce neuronal loss days after seizure (Turski et al., 1986), although this is unlikely to be the case in these experiments, as RNA was analyzed 2 hr after seizure, and direct examination of neurons by immunofluorescence microscopy gave no indication of neuronal loss (see below, Figure 7A). Nonetheless, to assess whether this protocol, which induces neuronal stress, affects splicing in a global or specific manner, we examined global and Nova-dependent splicing changes at various times after pilocarpine induced seizures (Table 3).
We first examined global changes in splicing using exon junction arrays at 4 hr and 24 hr after induction of pilocarpine seizure. Remarkably, there were very few splicing changes detected in the brain after pilocarpine seizure. Using stringent criteria (|ΔI| > 0.2), only 23 exons showed differential splicing 24 hr after pilocarpine treatment, with more changes (96) evident 4 hr after pilocarpine treatment (Supplementary file 1); by contrast, using the same stringency, 1,239 exons showed differential splicing in brain relative to thymus tissue (|ΔI| > 0.2; (Ule et al., 2005b)). These results indicate that the regulation of alternative splicing is not globally perturbed within 24 hr of epileptic seizure in the mouse brain.
We validated exons that did show seizure-induced splicing changes, and examined their relationship to Nova-regulated exons. We measured the ratio of alternate exon inclusion:exclusion by RT-PCR, validating 35 targets at 4 hr and 24 hr time points (Supplementary file 1). GO analysis revealed that transcripts showing these changes showed a 7.5-fold enrichment of synaptic proteins, and a 5.2-fold enrichment for proteins with serine/threonine kinase activity, including SNAP25 and BDNF, proteins shown to play important roles during synaptic activity (Yoshii and Constantine-Paton, 2010; Kennedy and Ehlers, 2011). We have previously found that NOVA regulates ∼800 alternate splicing events, about half of which are cassette exons (Zhang et al., 2010). We examined the 35 alternate exons that showed pilocarpine-dependent changes to see which were present on our list of Nova-dependent exons, and identified only eight as Nova-regulated (Supplementary file 1). These data indicate that only a small fraction of potential regulated alternate exons, including those regulated by Nova, are affected by seizure activity, and that pilocarpine does not appear to have a global impact on Nova splicing activity.
To further assess the relationship between Nova and epilepsy, we examined EEGs in Nova-null mice. However, Nova-null mice die by 2–3 weeks of birth, and we instead examined Nova-2 heterozygotes, which show partial defects (∼50% or less) changes in a number of NOVA regulated alternative exons (Ule et al., 2005b). Background cortical activity recorded in heterozygous mutants showed frequent bilateral synchronous cortical epileptiform discharges (Figure 6C) that were not seen in control +/+ mice (Figure 6D). A second abnormality observed was the spontaneous occurrence of generalized seizures (Figure 6E). Thus perturbing NOVA steady-state levels in vivo has relevant physiologic consequences, as haploinsufficiency is sufficient to give rise to spontaneous epilepsy in mice.
To further explore the relationship between electrical activity and NOVA action on splicing, we asked whether we could detect any acute effect of pilocarpine seizure on NOVA itself. We have previously demonstrated that NOVA shuttles between the nucleus and cytoplasm (Racca et al., 2010), and hence explored the possibility that electrical activity might affect the cellular distribution of the protein. We examined NOVA subcellular localization by immunofluorescence microscopy after sham or pilocarpine induced seizures. We consistently observed marked shifts of NOVA from the neuronal nucleus to the cytoplasm within 2–4 hr of pilocarpine-induced seizures, and that persisted in some animals for 24 hr (Figure 7A). This finding was evident in cortical neurons, and even more so in the CA1 pyramidal neurons of the hippocampus, where quantitation revealed over a 6-fold shift in the ratio of nuclear to cytoplasmic signal intensity at 4 hr after seizure (Figure 7B). Consistent with the cortical nature of epilepsy, we did not see this shift in NOVA localization in Purkinje neurons of the cerebellum (Figure 7A). These data suggest that there may in part be cell biologic mechanisms whereby pilocarpine affects the ability of NOVA to regulate splicing of some targets, but additional experiments will be required to fully understand their nature and consequences.
To further address the role NOVA plays in 3′ UTR regulation of mRNA steady-state levels, we searched for transcripts with a high percentage of 3′ UTR tags. We found that Synaptogyrin III (Syngr3), Glycine receptor B (Glrb) and the Gaba-B receptor1 (Gabbr1) had robust 3′ UTR CLIP tag clusters (Figure 8A). RNA levels quantitated by RT-PCR in WT or DKO brain demonstrated reduced levels of all three mRNAs in NOVA DKO (Figure 8B). Decrease of Syngr3 mRNA in NOVA DKO was confirmed by Northern blot (∼20% reduction; Figure 8C,D) and at the protein level by Western blot (∼35% reduction Figure 8E,F).
To address whether direct NOVA binding to the Syngr3 or other 3′ UTR (YCAY) elements could stabilize mRNA, we generated reporter constructs in which EGFP was generated from a transcript harboring WT or YAAY-mutated NOVA 3′ UTR binding sites defined by CLIP (Figure 3—figure supplement 1). After transfecting each construct into N2a cell lines, cells were treated with actinomycin D for 5 hr to block new RNA synthesis, and qRT-PCR was performed to measure mRNA levels of each construct. These data showed that transcripts containing 3′ UTR YCAY elements were stabilized relative to those harboring YAAY elements (by a factor of 25–65%) compared to YAAY elements (Figure 3—figure supplement 2). Taken together (Figure 8 and Figure 3—figure supplement 2), these data suggest NOVA protein is able to regulate mRNA levels through direct binding to 3′ UTR YCAY elements.
To investigate whether transcripts whose steady-state levels are NOVA-regulated are more enriched in certain functional classes of genes than others, we analyzed the functional annotations associated with 229 genes from exon array data (Figure 1A) using GO analysis (Table 4). We found that these transcripts encode proteins that regulate synaptic biology or transport. We compared this set of transcripts with those previously found to be regulated by NOVA at the level of alternative splicing but without changes in steady-state mRNA levels. Interestingly, while both sets of transcripts encode proteins related to synaptic function, only 18 genes overlap between the two sets (Figure 6—figure supplement 1). This implies that the set of functions NOVA regulates at steady-state level differ significantly from those functions NOVA regulated strictly at the level of alternative splicing.
Regulation of steady-state mRNA levels plays a key role in cellular and neuronal plasticity, allowing tunable and dynamic regulation of protein output. Such regulation is generally thought to be mediated by RNA–protein interactions in the 3′ UTR, which may involve interactions with a number of RNA binding proteins. For example, the balance of binding to AU-rich elements by AUF1, BRF1, KSRP, TTP or HuR (Meisner and Filipowicz, 2011), binding to UGUR elements by Pumillio (Crittenden et al., 2002; Quenault et al., 2011), or interactions between miRNAs and the Ago–RISC complex (Krol et al., 2010) all feed into pathways of deadenylation and mRNA decay. Our finding that transcripts showing NOVA-dependent steady-state regulation did not have NOVA binding sites in the 3′ UTR was therefore unexpected, and might have suggested that these were indirect targets of NOVA action. However, HITS-CLIP provides a powerful means of providing unambiguous and unbiased sites of RNA–protein interaction. Directed analysis of unbiased HITS-CLIP targets can reveal cryptic biology, as in the analysis of developmental HITS-CLIP maps to study NOVA interactions with transcripts of the Reelin pathway and thereby identify a previously unknown NOVA-dependent alternative exon necessary for proper neuronal migration (Yano et al., 2010). Here, we have used the predictive power of HITS-CLIP to identify seemingly irrelevant intronic NOVA binding sites on transcripts showing unexplained NOVA-dependent steady-state changes to predict the presence of cryptic alternative NMD exons.
NMD is an RNA surveillance mechanism that degrades mRNAs harboring premature termination codons (PTC), and is generally thought of as a means to protect cells from inadvertently producing truncated proteins that could be harmful to the cell. Such transcripts harbor downstream exon junction complex (EJC) proteins that, due to upstream PTCs, fail to be removed during an initial round of translation, leading to recruitment of NMD components (Schoenberg and Maquat, 2012). Recent studies have extended this view, indicating that NMD can function beyond a quality control mechanism, to serve as a mechanism for regulating gene expression disability (Huang and Wilkinson, 2012). NMD efficiency varies in different tissues, loss-of-function mutations in Upf genes in mice alter expression of a subset of transcripts, and loss-of-function mutations in Upf3b in humans are associated with intellectual disability (Tarpey et al., 2007).
Regulated alternative splicing of NMD exons has also been shown to act as a mechanism to regulate transcript levels, as in the case of autoregulation of splicing factors such as SC35, Ptbp1 and 9G8 (Lewis et al., 2003), as well as core components of the spliceosome (Saltzman et al., 2008). In addition, alternative splicing-coupled NMD has been shown to regulate expression levels of Arc (Giorgi et al., 2007), PSD95 (Zheng et al., 2012), and spermine acetyltransferase (Hyvönen et al., 2006), a process referred to as regulated unproductive splicing and translation (RUST) (Lewis et al., 2003). In yeast, a direct role for NMD was statistically inferred in the regulation of hundreds of transcripts involved in chromosomal and telomere maintenance and silencing (Guan et al., 2006). Cancer cells have been shown to utilize NMD, for example via actions on mutant cadherin transcripts (Chd1) that are associated with poor clinical outcome in hereditary diffuse gastric cancer. A full understanding of such pathways and means to manipulate them has been challenging because the factors regulating NMD-associated splicing are not generally known. Some well-studied exceptions have provided significant biologic insights, such as the autoregulation of the splicing factor PTBP1 (Wollerton et al., 2004) and its action on the paralogous transcript PTBP2, which mediates skipping of Ptbp2 exon 10, leading to NMD and suppression of neuronal differentiation (Boutz et al., 2007; Makeyev et al., 2007). Indeed, Makeyev and co-workers have identified PTBP1-dependent retained introns that suppress expression of neuronal transcripts in non-neuronal cells, allowing their expression as PTBP1 is downregulated during neuronal differentiation (Yap et al., 2012). We recently found that PTBP2 is expressed in neuronal progenitors, while NOVA is induced in post-mitotic neurons (Yano et al., 2010; Licatalosi et al., 2012); regulation of cryptic exon splicing may affect transcript levels in neurons and/or prevent spurious expression of transcripts in non-neural cells. Another point of interest will be to assess whether there is cell-type specific regulation of PTC exons in specific neuronal types within the adult brain in a manner analogous to PTBP1 regulation of expression within different tissues of the body.
Here we show the frequent use of trans-acting control by a single neuronal splicing factor, NOVA, to regulate an array of target transcripts. This mechanism is biologically rich, as it includes both the up- and down-regulation of target RNAs through alternative splicing coupled to NMD in neuron. The regulatory roles of these actions are underscored by our observation that the cryptic NMD exons NOVA acts upon are evolutionarily conserved (Zhang and Darnell, manuscript in preparation), suggesting a regulatory rather than quality-control NOVA function. Taken together, our data suggest a model in which NOVA regulation maintains a balance of transcript levels through NOVA-dependent alternative splicing coupled NMD and, to a lesser degree, through direct interaction with 3′ UTR binding elements (Figure 9).
We found that NOVA mediated NMD-coupled splicing can be dynamically regulated in the brain. This suggests in turn that NOVA activity may be regulated by such dynamic events, leading to changes in RNA regulation and ultimately changes in neuronal proteins. The mechanisms that regulate NOVA are largely unknown, but interestingly, NOVA may be phosphorylated by GSK3 (Dredge et al., 2005), which itself is known to be inactivated in response to various extracellular stimuli in the brain, stimulating pathways such as the PI3K/Akt pathway (Hur and Zhou, 2010), which are activated by electrical activity (Richter and Klann, 2009). Thus it is possible that neuronal cell dynamics lead to fine tuning of RNA processing and expression through RNA binding proteins that act as sensors of electrical activity.
There is growing interest in the relationship between alternative splicing and neuronal excitability in the brain, as underscored by the recent finding that loss of the splicing factor Rbfox1 results in increased susceptibility to seizures and concomitant splicing changes in transcripts encoding synaptic proteins (Gehman et al., 2011). Interestingly, NOVA interacts functionally with Rbfox1 (Zhang et al., 2010), and many of the proteins showing large Nova-dependent changes are also involved in synaptic regulation with links to epilepsy were also found to have NOVA-dependent NMD exons regulated after induction of seizures in mice. For example, NOVA regulation of NMD splicing controls the levels of DLG3, one of a family of postsynaptic density proteins, including PSD95, that transduce signals from the NMDA receptor. Increases in both PSD95 (Ying et al., 2004) and DLG3 (Qu et al., 2009) in cortex or post-synaptic fractions, respectively, have been described in brains of patients with focal cortical dysplasia and epilepsy. NOVA regulation of NMD splicing also controls the levels of SCN9a, a sodium channel initially thought to act primarily in dorsal root ganglia (Meisler et al., 2010) (neurons that do not express NOVA proteins (Buckanovich et al., 1993)), but more recently found to be mutated in human epilepsy (causing familial febrile seizures; (Singh et al., 2009)). Other NOVA-NMD related targets in which gene mutations have been implicated in human epilepsy include the anion transporters SLC4a10 and SLC4a3 (Table 1; (Gurnett et al., 2008; Sander et al., 2002)).
The observation that either induction or loss of the same protein activity may be associated with epilepsy, suggest that the proper stoichiometry of synaptic proteins (or protein activity), rather than their absolute amount, may be a key determinant in electrical balance (Figure 8). This correlates with our observation that NOVA haploinsufficiency is sufficient to induce spontaneous epilepsy (Figure 6), an observation also made with the neuronal RNABP Elavl3 and Elavl4 (Ince-Dunn et al., 2012). Moreover, NOVA control of NMD exons can act to either up or down-regulate protein levels generated from target transcripts, and, more specifically, to act after seizure to restore balance to synaptic proteins that would inhibit further seizure (e.g. increasing SCN9a, which would presumably be anti-epileptic). Hence the normal regulation of NOVA itself may provide an RNA-based means of regulating homeostatic plasticity in the face of electrical stress.
We have previously found that NOVA regulates neuronal alternative splicing, and that steady-state levels of these regulated transcripts are not significantly altered in Nova KO mice (Ule et al., 2005b; Licatalosi et al., 2008). The observation here of a significant set of transcripts undergoing NOVA-dependent regulation of steady-state levels on the surface therefore initially suggested that this was an independent set of NOVA actions. However, our finding that these were disproportionately NOVA-mediated actions to maintain neuronal transcript levels (215 vs 14) is consistent with an overall action linking alternative splicing suppression of NMD exons to steady-state transcript levels.
Interestingly, our data also suggested a more general link between splicing and mRNA stability. Among transcripts with NOVA 3′ UTR binding we observed a significant number also had intronic NOVA binding, suggesting a possible hierarchy of events in which nuclear binding precedes (and potentially determines) 3′ UTR binding. Such connections were originally suggested from studies in Drosophila, in demonstration of the coupling of the splicing and localization of Oskar mRNA (Hachet and Ephrussi, 2004), and the observation that the predominantly nuclear Hrb27c protein (whose mammalian homologue is the DAZAP1 splicing factor; (Goina et al., 2008)) also binds to and is required for localization of Grk mRNA (Goodrich et al., 2004). In mammalian cells, ZBP1 binds to actin mRNA in the nucleus and subsequently is required for its localization (Gu et al., 2002; Pan et al., 2007), and NOVA binds to transcripts (e.g. GlyRα2) in introns to regulate alternative splicing and is also associated with 3′ UTR and localization of the same mRNA in the neuronal dendrite (Racca et al., 2010).
One potential explanation for such observations, as well as for the link between nuclear and cytoplasmic NOVA tags seen here, would be reassortment of transcripts in cis on individual transcripts, providing a means of linking nuclear functions such as alternative splicing with cytoplasmic function such as RNA localization or RNA stability. For example, intronic NOVA binding to high affinity intronic clusters would allow a high local concentration of the protein upon individual transcripts, potentially allowing rearrangement in cis and binding of additional secondary RNA elements, including those within the 3′ UTR. However, it should be noted that HITS-CLIP provides data that is a population average of many individual RNA–protein interactions, so that such potential cis-actions on a single transcript can only be inferred. Nonetheless, it is noteworthy that such local concentration and one-dimensional rearrangements in cis are believed to play an important role in scanning and initiation of transcription (Blainey et al., 2006; Wang and Greene, 2011), and hence may plausibly act on pre-mRNAs to distribute RNABPs in cis to coordinate different aspects of post-transcriptional regulation. In this context, it is especially notable that NOVA localization changes after seizure, suggesting that the association of NOVA with newly transcribed and spliced transcripts may be coupled in an activity-sensitive manner with their localization and/or translational control.
We identified transcripts that show NOVA-dependent changes in steady-state levels in KO mice and used HITS-CLIP to drive the unexpected observation that what appeared to be functionless NOVA intronic binding sites in unregulated regions of these pre-mRNAs do function to regulate expression of cryptic NMD exons. These were enriched in transcripts encoding synaptic proteins, and their regulation mediated large changes in protein levels (up or down), including proteins implicated in familial epilepsy. The link between NOVA and regulation of excitation/inhibition balance was supported by finding that NOVA haploinsufficient mice had spontaneous epilepsy, and that pilocarpine-induced seizures regulated inclusion of a relatively small number of exons, a subset of which are regulated by Nova. Moreover, Nova redistributes from the nucleus to cytoplasm following pilocarpine seizure, and providing a possible mechanism underlying seizure-associated splicing changes involving Nova-regulated exons. Collectively, our data support a model in which changes in electrical activity affect the distribution of Nova, altering the splicing of cryptic exons that elicit NMD; these changes may provide a homeostatic means of regulating levels of transcripts and proteins associated with epilepsy.
YCAY elements were amplified by PCR and added into the pd1EGFP vector (Clontech, CA). Mutations to YCAY elements were made by using QuickChange site-directed mutagenesis kit (Stratagene, CA). Primers are listed in Supplementary file 2. RT-PCR products were cloned by using pGEM-T-easy Vector system (Promega, WI) and then sequenced (Genewiz, NJ).
Two fractionation methods were used. In the first, P13 wild type mouse cortex was, dissociated and then UV irradiated for CLIP (3 × 400 mJ/cm2) in a Stratalinker (Stratagene), and fractionation was performed as recommended with a commercial kit (BioVision, CA). In the second method, P13 mice were used. The brain cortex was dissected of white matter, chopped and irradiated (3 × 400 mJ/cm2) in HBSS (Invitrogen, NY) containing 0.01 M HEPES (pH 7.3) in a Stratalinker. Tissue was Dounce homogenized in cold gradient buffer (20 mM HEPES [pH 7.4], 150 mM NaCl, 5 mM MgCl2, 0.5 mM DTT, protease inhibitor [Roche, NJ] and RNasin Plus RNase inhibitor [Promega, WI]). The homogenized tissue was then treated with 0.5% NP-40 on ice and centrifuged 2× at 2000×g for 10 min, and the resultant supernatant was collected as the cytoplasmic fraction.
Protein extracts (nuclear/cytoplasmic fractions and WT vs DKO brain extracts from P13 and E18.5 whole brains, respectively) were resolved by 10% SDS-PAGE and transferred to PVDF membranes (Millipore, MA). Membrane was blocked and incubated with primary antibodies including goat anti-NOVA2; mouse anti-HSP90, mouse anti-HNRNP-C1, mouse anti-DLG3 (SAP102), mouse anti-SCN9a, rabbit anti-SYNGR3, rabbit anti-STX2 and mouse anti-γ-tubulin. Three different mouse brains were used as biological replicates as indicated throughout.
For estimating the level of brain transcripts, total RNAs from four E18.5 mouse brains were extracted using Trizol (Invitrogen, NY) and RNAeasy kit (Qiagen, CA) and mRNA was amplified and labeled by the method provided by Affymetrix. Mouse MoEx 1.0ST Arrays were used for measuring signal intensity of each exon in the samples. To process the signals from the array, quantile normalization (WT vs DKO) and PM-GCBG (signal adjustment based on the background with similar GC content) were applied.
Steady state RNA levels were assessed using Affymetrix Mouse MoEx 1.0ST Exon arrays (Affymetrix, CA), and analyzed with Affymetrix Power Tools using IterPLIER. IterPLIER was used for selecting appropriate ‘core exon’ probes to estimate gene-level intensities. Finally, median log2 values from four biological replicates are used to estimate level of transcripts in the E18.5 brain in WT vs DKO.
cDNA was generated by using random hexamers and Superscript III (Invitrogen, NY). Once the number of PCR cycle was tested for the linear range, 32P-dCTP was added into the PCR reactions for the last two cycles and then run onto denaturing gels (6% polyarylamide/7 M urea). It was exposed to X-ray film (Kodak, NY). Quantitative RT-PCR (qRT-PCR) was performed by using a MyiQ single-color real time PCR detection system (Biorad, CA), using mouse tubulin as an internal control, and relative mRNA level (WT vs DKO) was calculated by ΔΔCt values. All qRT-PCR was performed in RNA from at least three biological replicates. qRT-PCR and other PCR primers are listed in Supplementary file 2.
Total RNA (10 μg) was electrophoresed and transferred into the Nylon membrane (Ambion, CA). The cDNA fragments complementary to Dlg3 (digested by XmaI and BspE1), Syngr3 (primers as below) and Gapdh (Ambion, CA) were labeled with 32P-dCTP using prime II random label kit (Stratagene, CA). The membrane was hybridized with 32P-labeled probes at 45°C overnight. After several washes, the membrane was exposed to X-ray film (Kodak, NY).
NOVA HITS-CLIP was performed on subcellular fractions using previously described protocols (Ule et al., 2003, 2005a; Jensen and Darnell, 2008; Licatalosi et al., 2008). High-throughput sequencing was performed on an Illumina GAIIx. CLIP tags were analyzed as previously described (Licatalosi et al., 2008), with modifications as described below.
Sequencing reads were first filtered by the default Illumina pipeline. Filtered reads were then mapped by Eland using different sizes from 25 to 32 nt, with at most two mismatches (Zhang et al., 2010). A read is kept for analysis only if it was mapped to an unambiguous locus with at least one particular size. If unambiguous mapping was possible with different sizes, the one with largest size, yet without increasing number of mismatches was kept. Overall, 57% of reads are unambiguously mappable (Table 2).
For each individual CLIP experiments, we further collapsed reads with the same start genomic coordinates to remove potential RT-PCR artifacts. As a result, 1.3 million nuclear CLIP tags and 0.2 million cytoplasmic CLIP tags were unique and used for further analysis (Table 2).
To generate a reliable definition of CLIP clusters, we used a cohort of ∼20 independent NOVA CLIP experiments. CLIP clusters were identified by a Hidden Markov Model (HMM), which will be described in detail elsewhere. For each of the clusters, the number of CLIP tags for each nuclear and cytoplasmic CLIP experiment was counted. Only clusters with ≥2 tags in the nuclear/cytoplasmic tags were kept for this study (81,162 clusters). To measure the robustness of each cluster, biological complexity (BC) was defined as the number of samples with at least 1 tag in the cluster. BC was calculated for nuclear and cytoplasmic CLIP experiments, respectively. For each cluster, we also count the number of tags overlapping with each position and define peak height by the maximum number of overlapping tags.
GO analysis was performed by using DAVID (http://david.abcc.ncifcrf.gov/).
Human sera from POMA patients was used to detect NOVA proteins in mixed cultured neurons. HSP-90 antibody (BD biosciences, CA), γ-tubulin (GTU88) antibody (Sigma, MO), hnRNP-C1/C2 antibody (Abcam, MA), NOVA2 antibody (Santa Cruz, CA) DLG3 (SAP102) and SCN9a antibodies (neuro-Mab, CA), STX2 antibody (Synaptic Systems, Germany), Neurofilament M antibody (Millipore, MA), UPF1 antibody (Dr Lykke-Andersen) and SYNGR3 antibody (Dr Janz) were used. All secondary antibodies mouse, rabbit, goat and human HRP- and Cy2/Cy3/Cy5-conjugated antibodies are from Jackson Immuno Research Laboratories, PA.
Primary mouse neuronal cultures were generated from E18.5 cortical neurons prepared as previously described (Eom et al., 2003). In brief, forebrain from embryonic 18.5 days mouse brain (WT and DKO) was dissected, trypsinized, and plated on poly-l-lysine coated coverslips and dishes (BD biosciences, CA) in neurobasal medium (Invitrogen, NY) for immunofluorescence and cultured for 10 days at 37°C in 5% CO2 and transfection with nucleofection was performed before plating. Emetine (100 μg/ml; Sigma, MO) was added to cells grown for 6 days in vitro (DIV) WT/DKO cultures for 10 hr.
Primary mouse neuronal cultures and N2a cells were transfected with siRNA ON-TARGETplus SMARTpool (Dharmacon, PA) and DY547 conjugated siRNAs by nucleofection (Lonza, NJ) as described by manufacturers. 48 hr after transfection with a SMARTpool of four siRNAs to Upf1 or an equimolar amount of non-targeting control siRNAs (Dharmacon, PA), the cells were fixed in paraformaldehyde (4% in PBS) at room temperature for 15 min for immunofluorescence and RNA was extracted for RT-PCR.
Immunofluorescence was performed as described (Racca et al., 2010) with the following modifications. After fixation, coverslips were incubated for 1 hr at room temperature in Tri Buffered Saline (TBS) with BSA (2%), FBS (2%) and Triton X-100 (0.1%). Primary antibody incubations were for another 1 hr at the same condition with BSA (1%) and Triton X-100 (0.1%). All secondary antibodies were affinity-purified donkey antibodies to mouse, rabbit or human IgG conjugated to a Cy2/Cy3/Cy5 (Jackson Immuno Research Laboratories, PA). Coverslips were mounted with prolong gold antifade reagent (Invitrogen, NY) after DAPI (4,6-diamidino-2-phenylindole dihydrochloride) staining the cells.
Seizures were induced as follows: 8-week old mice were given subcutaneous injection of methyl scopolamine nitrate (1 mg/kg). After 30 min, mice were given subcutaneous injection of pilocarpine (320–340 mg/kg). After 2 hr, RNA was extracted from brain (pilo vs sham) and RT-PCR was performed.
Adult Nova2 (-/+) and wild-type (+/+) mice (aged 6–9 months) were implanted for chronic EEG recordings. Mice were anesthetized with Avertin (1.25% tribromoethanol/amyl alcohol solution, i.p.) using a dose of 0.02 ml/g. Teflon-coated silver wire electrodes (0.005 inch diameter) soldered to a microminiature connector were implanted bilaterally into the subdural space over frontal, temporal, parietal, and occipital cortices. Digital EEG activity was monitored daily for up to 2 weeks during prolonged overnight and random 2 hr sample recordings (Stellate Systems, CA, Harmonie software version 6.0b). A digital video camera was used to simultaneously monitor behavior during the EEG recording periods. All recordings were carried out at least 24 hr after surgery on mice freely moving in the test cage.
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Benjamin BlencoweReviewing Editor; University of Toronto, Canada
eLife posts the editorial decision letter and author response on a selection of the published articles (subject to the approval of the authors). An edited version of the letter sent to the authors after peer review is shown, indicating the substantive concerns or comments; minor concerns are not usually shown. Reviewers have the opportunity to discuss the decision before the letter is sent (see review process). Similarly, the author response typicalsly shows only responses to the major concerns raised by the reviewers.
Thank you for choosing to send your work entitled “NOVA-dependent regulation of occult NMD exons controls synaptic protein levels after seizure” for consideration at eLife. Your article has been evaluated by a Senior Editor and 3 reviewers, one of whom is a member of eLife's Board of Reviewing Editors. The following individuals responsible for the peer review of your submission want to reveal their identity: Ben Blencowe and Doug Black.
The Reviewing Editor and the other reviewers discussed their comments before we reached this decision, and the Reviewing Editor has assembled the following comments based on the reviewers' reports.
In this manuscript, Eom and colleagues investigate the molecular basis by which the neural-specific splicing regulator Nova controls the levels of transcripts and corresponding proteins with important functions in the synapse. Using microarray profiling they detect ∼200 genes with increased transcript levels in the brains of wild-type mice compared to brains of Nova1/Nova2 double knockout (DKO) mice. A much smaller number of genes show the opposite behavior. Using HITS-CLIP data, the authors examine the nuclear-cytoplasmic distribution of Nova binding sites in transcripts with differences in steady-state levels. While Nova binding to 3′UTR sequences appears to control the levels of some transcripts, a more widespread mechanism involves Nova binding within intronic sequences adjacent to previously unannotated exons, referred to as “occult exons” by the authors. Nova-dependent suppression or activation of the PTC-introducing exons promotes increased or decreased transcript/protein levels, respectively. The authors further use pilocarpine-induced seizures to investigate how changes in electrical activity might impact Nova-dependent regulation of transcript levels.
The results described are interesting and will appeal to researchers in the fields of gene regulation and neurobiology. Although regulation of transcript levels via alternative splicing coupled to NMD has already been described in several biological contexts, the identification of a coherent network of splicing events subject to this mode of regulation, with potentially important roles in the synapse, is a significant advance. Moreover, the use of HITS-CLIP to identify novel exons that function in regulating transcript levels is a clever application of an already powerful genome-wide approach. The reviewers have several concerns that they would like to see addressed in a revised manuscript.
1. The authors conclude from their experiments involving pilocarpine-induced seizures that the “clear increases in utilization of the NMD exon suggest that the levels of these transcripts can be dynamically tuned by electrical activity”. However, pilocarpine-induced seizures are known to cause oxidative damage and neuronal loss (e.g., Turski et al. 1986, which the authors cite). The authors should attempt to address whether this treatment directly impacts Nova-dependent splicing activity. At the very least, they should mention the caveats of this experiment, soften their conclusions, and modify the manuscript title.
2. A possible alternative model for the physiological relevance of the authors' findings is that the Nova-dependent suppression of cryptic exons serves as a mechanism to ensure that specific neuronal transcripts are not spuriously expressed in non-neuronal cells. The authors could readily test this by performing RT-PCR assays on the Nova-regulated transcripts, +/- Upf1 knockdown, in non-neural cells. In this context, it is worth noting related work of Makeyev and co-workers (G&D 26, 1209; 2012), who have identified a class of Ptbp1-dependent retained introns that suppress expression of neural transcripts in non-neural cells.
3. The authors utilize a liberal cutoff in their identification of differentially expressed genes from their microarray analysis. A magnitude log2 change of 0.3 corresponds to slightly less than a 1.25 fold ratio change, and given the noise inherent in microarray measurements, it is unlikely that estimated changes in this range will validate at the same rate as those changes estimated to be >1.5 fold. Accordingly, the authors are requested to use qRT-PCR assays over the range of 229 genes predicted to show expression differences to assess false-positive rates. In this context, the descriptor “widespread” may be overstated.https://doi.org/10.7554/eLife.00178.030
- Robert B Darnell
- Taesun Eom
- Chaolin Zhang
- Kenneth Lay
- John Fak
- Robert B Darnell
- Jeffrey L Noebels
- Jeffrey L Noebels
- Robert B Darnell
- Robert B Darnell
- Huidong Wang
The funders had no role in study design, data collection and interpretation, or the decision to submit the work for publication.
Animal experimentation: This study was performed in strict accordance with the recommendations in the Guide for the Care and Use of Laboratory Animals of the National Institutes of Health. All of the animals were handled according to approved institutional animal care and use committee (IACUC) protocols of the Institutional Animal Care and Use Committee of Rockefeller University (protocol numbers 10064 and 10097).
- Benjamin Blencowe, Reviewing Editor, University of Toronto, Canada
- Received: August 22, 2012
- Accepted: November 29, 2012
- Version of Record published: January 22, 2013 (version 1)
© 2013, Eom et al.
This article is distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use and redistribution provided that the original author and source are credited.