NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Series GSE175491 Query DataSets for GSE175491
Status Public on May 26, 2021
Title Genetic compensation for cilia defects in cep290/NPHP6 mutants by upregulation of cilia-associated small GTPases
Organism Danio rerio
Experiment type Expression profiling by high throughput sequencing
Summary Mutations in CEP290, a large multidomain coiled coil protein, are associated with multiple cilia-associated syndromes. Over 130 CEP290 mutations have been linked to a wide spectrum of human ciliopathies, raising the question of how mutations in a single gene cause different disease syndromes. In zebrafish the expressivity of cep290 deficiencies were linked to the type of genetic ablation: acute cep290 morpholino knockdown caused severe cilia-related phenotypes while defects in a Crispr/Cas9 genetic mutant were restricted to photoreceptor defects. Here we show that milder phenotypes in genetic mutants were associated with upregulation of genes encoding the cilia-associated small GTPases arl3, arl13b, and unc119b. Upregulation of UNC119b was also observed in urine-derived renal epithelial cells from human JBTS CEP290 patients. Ectopic expression of arl3, arl13b and unc119b in cep290 morphant zebrafish embryos rescued Kupffer's vesicle cilia and partially rescued photoreceptor outer segment defects. The results suggest that genetic compensation by upregulation of genes involved in a common subcellular process, lipidated protein trafficking to cilia, may be a conserved mechanism contributing to genotype-phenotype variations observed in CEP290 deficiencies.
 
Overall design RNA from 72hpf zebrafish embryos was analyzed. Each sample consisted of pools of 30 embryos from cep290 morphants, maternal zygotic mutants or wildtype embryos. Biological triplicates were done.
 
Contributor(s) Cardenas-Rodriguez M, Austin-Tse C, Bergboer JG, Molinari E, Sugano Y, Bachmann-Gagescu R, Sayer JA, Drummond IA
Citation(s) 34155518
Submission date May 25, 2021
Last update date Aug 17, 2021
Contact name Iain A Drummond
E-mail(s) idrummond@mdibl.org
Phone 207 288 9880
Organization name Mount Desert Island Biological Laboratory
Department Davis Center for Regenerative Biology and Aging
Street address 159 Old Bar Harbor Road Bar Harbor
City Bar Harbor
State/province Maine
ZIP/Postal code 04609
Country USA
 
Platforms (1)
GPL14875 Illumina HiSeq 2000 (Danio rerio)
Samples (9)
GSM5335387 wildtype_TuAB_rep1
GSM5335388 wildtype_TuAB_rep2
GSM5335389 wildtype_TuAB_rep3
Relations
BioProject PRJNA732587

Download family Format
SOFT formatted family file(s) SOFTHelp
MINiML formatted family file(s) MINiMLHelp
Series Matrix File(s) TXTHelp

Supplementary file Size Download File type/resource
GSE175491_MCa1_complete_RPKM_table.txt.gz 2.1 Mb (ftp)(http) TXT
GSE175491_MZcep290Mutant_vs_cep290_Morpholino_DEG_genes_table.xlsx 246.6 Kb (ftp)(http) XLSX
GSE175491_WT_vs_MZcep290Mutant_DEG_genes_table.xlsx 690.2 Kb (ftp)(http) XLSX
GSE175491_WT_vs_cep290_Morpholino_DEG_genes_table.xlsx 694.9 Kb (ftp)(http) XLSX
Raw data are available in SRA
Processed data are available on Series record

| NLM | NIH | GEO Help | Disclaimer | Accessibility |
NCBI Home NCBI Search NCBI SiteMap