iPSC characterisation of pluripotency.
(A) Immunofluorescence staining at Day 16 of the Spontaneous in vitro differentiation protocol. SOX17 (SRY-BOX 17; endoderm-related), TUJ1 (Neuronal Class III β-Tubulin; ectoderm-related), and SMA (Alpha Smooth Muscle Actin; mesoderm-related) markers are shown. Nuclei were counterstained with DAPI. Scale bar, 500 µm. n=1 biological replicate per line.
(B) Immunofluorescence for pluripotency markers NANOG, OCT4, TRA-1-60, TRA-1-81 in iPSC lines. Nuclei were counterstained with DAPI. Scale bar, 200 µm. n=1 biological replicate per line.
(C) Epi-Pluri-Score testing for iPSC lines. DNA methylation profiles (β-values) in genes ANKRD46, C14orf115, and POU5F1 for all iPSC lines match profiles of pluripotent samples (red cloud). n=1 biological replicate per line.
(D) RT PCR in iPSC lines for expression of pluripotency markers SOX2, KLF4, NANOG, OCT4. H9 human embryonic stem cell (H9 hESC) line and human dermal fibroblasts were used as positive and negative controls, respectively. GAPDH was used as a housekeeping gene. n=1 biological replicate per line.
(E) RT PCR in iPSC lines for detection of Sendai virus genome and pluripotency transgenes. A positive (+ve) control (SeV DNA) and a negative control (cDNA from the H9 human embryonic stem cell line, H9 hESC) were also analysed. GAPDH was used as a housekeeping gene. n=1 biological replicate per line.
(F) Chromatograms from genomic DNA sequencing in BPAN iPSC lines. iPSC lines maintain disease-causing mutations. WDR45 disease-causing mutations are highlighted in the red rectangles. n=1 biological replicate per line.
(G) SNP array analysis of all iPSC lines used for downstream experiments, including the two isogenic controls. Representative images. All deletions/ gains in iPSCs used for downstream experiments were small (<5Mb) and deemed as non-pathogenic by BlueFuse Multi. n=1 biological replicate per line.
(H) Alignment of wild type, patient 02 (c.19C>T), patient 03 (c.700C>T) and CRISPR corrected WDR45 genomic DNA (above) and amino acid (below) sequences. Premature protein truncation results from both c.19C>T and c.700C>T mutations. For each CRISPR-corrected line, three nucleotide substitutions have occurred after HDR (red rectangles). For both corrections, the first two are silent/ synonymous changes and, overall, the sequence leads to translation of a full-length WDR45 protein.