DCP2
decapping mRNA 2
- Ensembl:
- ENSG00000172795
- UniProt:
- Q8IU60
- OMIM:
- 609844
- Synonyms:
- NUDT20
Cilia effects upon perturbation of DCP2
- Cilia number / % ciliated:
- No effect
- Loss-of-function effect:
- No effect
Ciliogenesis screen results (4 screens)
- Wheway et al. 2015 (siRNA) [siRNA]: No effect PMID:26167766
- Breslow et al. 2018 (CRISPR) [CRISPR]: Positive Regulator (Hh signaling, casTLE effect=-1.53) PMID:29459680
- Roosing et al. 2015 (siRNA) [siRNA]: No effect PMID:26595381
- Pusapati et al. 2018 (CRISPR) [CRISPR]: Positive Regulator (Hh signaling, neg_rank=749, lfc=-2.20) PMID:30270045
Phenotypes
- Mouse phenotype:
- abnormal coat/hair pigmentation; increased heart weight; preweaning lethality; complete penetrance
Subcellular localization
cell junctions, cilia associated gene, cytoplasmic bodies, nucleoplasm
Functional category
- Ciliary morphology regulation
- mRNA metabolism
Function
DCAP-1 and DCAP-2, which are the homologues of mammalian DCP1 and DCP2 mRNA decapping enzymes, respectively, are involved in formation of dual rod-type and wing-like shaped cilia in C. elegans. mRNA decapping enzyme catalyzeshydrolysis of 5′ cap structure of mRNA, which leads to degradation of mRNA. Rescue experiments showed that DCAP-2 acts not in glial cells surrounding cilia but in neurons. This is the first evidence to demonstrate that mRNA decapping is involved in ciliary shape formation(PMID: 28887031).
Model organism evidence
C. elegans (1 reference)
Cilia and flagella are evolutionarily conserved organelles that protrude from cell surfaces.
PMIDs: 28887031