Card
Series GSE278932 Query DataSets for GSE278932
Status Public on Mar 13, 2025
Title Direct targets of the transcription factor Six1 identify novel candidate deafness genes
Organism Homo sapiens
Experiment type Expression profiling by high throughput sequencing
Summary Branchio-otic (BOS) and Branchio-oto-renal (BOR) syndromes are autosomal dominant disorders featuring multiple birth defects including ear, renal and branchial malformations. Mutations in the homeodomain transcription factor SIX1 and its co-factor EYA1 have been identified in about 50% of BOS/BOR patients, while causative mutations are unknown in the other half. We hypothesise that SIX1 target genes represent new BOS/BOR candidates. Using published transcriptomic and epigenomic data from chick ear progenitors, we first identify putative Six1 targets. Next, we provide evidence that Six1 directly regulates these targets: Six1 binds to their enhancers and functional experiments in Xenopus and chick confirm that Six1 controls their expression. Finally, we show that most chick Six1 targets are also expressed in the human developing ear and are associated with known deafness loci. Together, our results not only characterise the molecular mechanisms that mediate Six1 function in the developing ear, but also provide new candidates for human congenital deafness.
 
Overall design Molecular characterisation of developing otic vesicle (OV) in humans is currently limited. We present the first transcriptome analysis of human embryonic OV from Carnegie stage (CS) 13 and CS14. OV (right and left), dorsal hind brain (DHB) and ventral hind brain (VHB) fresh tissues was dissected from a single embryo per replicate to perform bulk RNA seq. In total two bilogical replicated for each tissue was collected for both the stages respectively. To identify genes enriched in the OV at each of the developmnetal time points (CS13 &CS14) differential gene expression analysis using DESeq2 was performed comparing the bulk RNA seq data obtained from OV and DHB tissues from respective stages.
 
Contributor(s) Ranganathan R, Sari F, Wang S, Thiery A, Buzzi AL, Moody SA, Streit A
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Submission date Oct 07, 2024
Last update date Mar 13, 2025
Contact name Andrea Streit
Organization name King's college London
Department CCRB
Lab Andrea Streit
Street address Great Maze Pond
City London
ZIP/Postal code SE1 9RT
Country United Kingdom
 
Platforms (1)
GPL20301 Illumina HiSeq 4000 (Homo sapiens)