RFX3
regulatory factor X3
- Ensembl:
- ENSG00000080298
- UniProt:
- P48380
- OMIM:
- 601337
Cilia effects upon perturbation of RFX3
- Loss-of-function effect:
- Shorter cilia
Ciliogenesis screen results (4 screens)
- Kim2016: Not Reported
- Wheway et al. 2015 (siRNA) [siRNA]: No effect PMID:26167766
- Breslow et al. 2018 (CRISPR) [CRISPR]: No Significant Effect PMID:29459680
- Roosing et al. 2015 (siRNA) [siRNA]: No effect PMID:26595381
Subcellular localization
cilia associated gene, nucleus
Functional category
- Ciliary assembly/disassembly
- Actin & cytoskeleton regulation
- T cell biology
- Protein processing & maturation
- Cell migration & adhesion
- Transcription regulation
Function
Transcription factor regulating expression of ciliary assembly (like Dync2li1, Foxj1 and Bbs4) and axonemal dyneins involved in ciliary motility (D hc11, D hc9 and D hc5), by binding directly to the promoters of their genes. Regulates the orthologs of genes involved inhuman PCD. It may also cooperate with FOXJ1 to regulate the expression of cilia genes ( 19671664). Regulates the expression of D2lic in mouse, a gene implicated in intraflagellar transport, a proces required for the assembly and mainte nce of cilia. RFX3 is essential for the differentiation of nodal monocilia and for LR patterning ( 15121860). Together with FOXJ1, plays a role in modulating differentiation in multiciliated cells ( 23822649).
Model organism evidence
Foxn3 is part of a transcriptional network that regulates primary cilia in the developing retina.
Foxn3 is required to suppress aberrant ciliogenesis in nonphotoreceptor retinal neurons.
We demonstrate that the depletion of multiple components of the switch/sucrose non-fermentable (SWI/SNF) chromatin remodeling complex induces ciliopathy-like phenotypes in zebrafish embryos.
PMIDs: 41213452