Negative regulators of a growth factor-mediated signaling pathway in the nematode Caenorhabditis elegans
<p>Vulval differentiation in C. elegans is mediated by an Epidermal growth factor (EGF)- EGF receptor (EGFR) signaling pathway. I have cloned unc-101, a negative regulator of vulval differentiation of the nematode C. elegans. unc-101 encodes a homolog of AP47, the medium chain of the trans...
Summary: | <p>Vulval differentiation in C. elegans is mediated by an Epidermal
growth factor (EGF)- EGF receptor (EGFR) signaling pathway. I have
cloned unc-101, a negative regulator of vulval differentiation of the nematode
C. elegans. unc-101 encodes a homolog of AP47, the medium chain of the
trans-Golgi clathrin-associated protein complex. This identity was
confirmed by cloning and comparing sequence of a C. elegans homolog of
AP50, the medium chain of the plasma membrane clathrin-associated
protein complex. I provided the first genetic evidence that the trans-Golgi
clathrin-coated vesicles are involved in regulation of an EGF signaling
pathway. Most of the unc-101 alleles are deletions or nonsense mutations,
suggesting that these alleles severely reduce the unc-101 activity. A hybrid
gene that contains parts of unc-101 and mouse AP4 7 rescued at least two
phenotypes of unc-101 mutations, the Unc and the suppression of vulvaless
phenotype of let-23(sy1) mutation. Therefore, the functions of AP47 are
conserved between nematodes and mammals.</p>
<p>unc-101 mutations can cause a greater than wild-type vulval
differentiation in combination with certain mutations in sli-1, another
negative regulator of the vulval induction pathway. A mutation in a new
gene, rok-1, causes no defect by itself, but causes a greater than wild-type
vulval differentiation in the presence of a sli-1 mutation. The unc-101; rok-1;
sli-1 triple mutants display a greater extent of vulval differentiation than any
double mutant combinations of unc-101, rok-1 and sli-1. Therefore, rok-1
locus defines another negative regulator of the vulval induction pathway.</p>
<p>I analyzed a second gene encoding an AP47 homolog in C. elegans.
This gene, CEAP47, encodes a protein 72% identical to both unc-101 and
mammalian AP47. A hybrid gene containing parts of unc-101 and CEAP47
sequences can rescue phenotypes of unc-101 mutants, indicating that UNC-
101 and CEAP47 proteins can be redundant if expressed in the same set of
cells.</p> |
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