We therefore tested whether cdt 2 could interact with gap 1 to cause a Muv phenotype. We found selleck compound that cdt 2 in the gap 1 background causes 43% of animals to present a Muv phenotype. We also con firmed that cdt 2 only marginally interacts with lin 15A or lin 15B. In addition, RNAi of cdt 2 slightly increases penetrance of the Muv phenotype observed in a lin 15AB mutant, which is consistent with an atypical synMuv activity. CDT 2 prevents excessive LET 23 EGFR signalling during vulva development The genetic interaction observed with gap 1 suggested that cdt 2 could be involved in attenuation of LET 23 LET 60 MPK 1 signalling. Therefore, we addressed whether depletion of cdt 2 could cause excessive LET 23 LET 60 MPK 1 signalling in a non redundant fash ion as previously described for gap 1, other negative modulators of LET 60 signalling, and a subset of synMuv genes.
To this end, we used egl 17,cfp, a reporter for exces sive LET 23 LET 60 MPK 1 signalling during vulva development. In wild type animals, egl 17,cfp is only expressed in primary cells at the third larval stage. However, under conditions of excess LET 23 LET 60 MPK 1 sig nalling, egl 17,cfp expression persists in secondary cells. We found that depletion of cdt 2 by RNAi causes persistent expression of egl 17,cfp in P5. p and P7. p descendant cells of 50% of the animals analysed. Taken together, the genetic interaction with gap 1 and the persistent expres sion of egl 17,cfp, strongly suggest that CDT 2 is an attenuator of GSK-3 LET 23 LET 60 MPK 1 signalling during vulva development.
CUL 4 prevents excessive LET 23 EGFR signalling during vulva development Mammalian CDT2 has been found associated with the CUL4 DDB1 ubiquitin ligase complex, which prompted us to test whether the C. elegans homologues of the complex would possess an activity similar to CDT 2. RNAi of cul 4, ddb 1, or rbx 1 did not produce a Muv phenotype in the gap 1 background, but the rere plication phenotype could be detected in these experiments. Because RNAi knock down animals might retain residual activity, we also investigated the phenotype of a cul 4 deletion mutant. Using a cul 4 knock out strain and the egl 17,cfp assay, we assessed a possible role of cul 4 in attenuation of LET 23 signalling. Although cul 4 homozygotes arrest development as larvae and do not complete vulva devel opment, the vulval precursor cells can undergo one cell division, allowing assay of persistent egl 17,cfp expression in secondary P.
px cells. We found that egl 17,cfp expression persists in secondary cells after first EPZ-5676 mechanism division. At this stage, 75% of the cul 4 homozygotes had persistent expression compared to 10% of heterozygotes. We obtained similar results analysing P. p cells, 62. 5% of cul 4 cul 4 animals have persistent expression of egl 17,cfp compared to 18% of cul 4 animals.
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