CDC-25.1 stability is regulated by distinct domains to restrict cell division during embryogenesis in C. elegans. Export

@article{citeulike:3336996, abstract = {Cdc25 phosphatases are key positive cell cycle regulators that coordinate cell divisions with growth and morphogenesis in many organisms. Intriguingly in C. elegans, two cdc-25.1(gf) mutations induce tissue-specific and temporally restricted hyperplasia in the embryonic intestinal lineage, despite stabilization of the mutant CDC-25.1 protein in every blastomere. We investigated the molecular basis underlying the CDC-25.1(gf) stabilization and its associated tissue-specific phenotype. We found that both mutations affect a canonical beta-TrCP phosphodegron motif, while the F-box protein LIN-23, the beta-TrCP orthologue, is required for the timely degradation of CDC-25.1. Accordingly, depletion of lin-23 in wild-type embryos stabilizes CDC-25.1 and triggers intestinal hyperplasia, which is, at least in part, cdc-25.1 dependent. lin-23(RNAi) causes embryonic lethality owing to cell fate transformations that convert blastomeres to an intestinal fate, sensitizing them to increased levels of CDC-25.1. Our characterization of a novel destabilizing cdc-25.1(lf) intragenic suppressor that acts independently of lin-23 indicates that additional cues impinge on different motifs of the CDC-25.1 phosphatase during early embryogenesis to control its stability and turnover, in order to ensure the timely divisions of intestinal cells and coordinate them with the formation of the developing gut.}, author = {Hebeisen, M. and Roy, R.}, citeulike-article-id = {3336996}, citeulike-linkout-0 = {http://view.ncbi.nlm.nih.gov/pubmed/18287204}, citeulike-linkout-1 = {http://www.hubmed.org/display.cgi?uids=18287204}, citeulike-linkout-2 = {http://www.wormbase.org/db/misc/paper?name=WBPaper00031534}, journal = {Development}, keywords = {c\_elegans, caenorhabditis\_elegans, cdc-251, celegans, elegans, k06a57, k10b21, lin-23, nematode, other, wormbase}, posted-at = {2008-09-25 16:17:45}, priority = {3}, title = {CDC-25.1 stability is regulated by distinct domains to restrict cell division during embryogenesis in C. elegans.}, url = {http://view.ncbi.nlm.nih.gov/pubmed/18287204}, year = {2008} }

TY - JOUR ID - citeulike:3336996 L3 - citeulike-article-id:3336996 N2 - Cdc25 phosphatases are key positive cell cycle regulators that coordinate cell divisions with growth and morphogenesis in many organisms. Intriguingly in C. elegans, two cdc-25.1(gf) mutations induce tissue-specific and temporally restricted hyperplasia in the embryonic intestinal lineage, despite stabilization of the mutant CDC-25.1 protein in every blastomere. We investigated the molecular basis underlying the CDC-25.1(gf) stabilization and its associated tissue-specific phenotype. We found that both mutations affect a canonical beta-TrCP phosphodegron motif, while the F-box protein LIN-23, the beta-TrCP orthologue, is required for the timely degradation of CDC-25.1. Accordingly, depletion of lin-23 in wild-type embryos stabilizes CDC-25.1 and triggers intestinal hyperplasia, which is, at least in part, cdc-25.1 dependent. lin-23(RNAi) causes embryonic lethality owing to cell fate transformations that convert blastomeres to an intestinal fate, sensitizing them to increased levels of CDC-25.1. Our characterization of a novel destabilizing cdc-25.1(lf) intragenic suppressor that acts independently of lin-23 indicates that additional cues impinge on different motifs of the CDC-25.1 phosphatase during early embryogenesis to control its stability and turnover, in order to ensure the timely divisions of intestinal cells and coordinate them with the formation of the developing gut. JF - Development TI - CDC-25.1 stability is regulated by distinct domains to restrict cell division during embryogenesis in C. elegans. KW - c_elegans KW - caenorhabditis_elegans KW - cdc-251 KW - celegans KW - elegans KW - k06a57 KW - k10b21 KW - lin-23 KW - nematode KW - other KW - wormbase AU - Hebeisen, M AU - Roy, R PY - 2008/// UR - http://view.ncbi.nlm.nih.gov/pubmed/18287204 ER -