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Caenorhabditis elegans SUR-5 a Novel but Conserved Protein Negatively Regulates LET-60 Ras Activity during Vulval Induction

机译:秀丽隐杆线虫SUR-5一种新颖但保守的蛋白质在外阴诱导过程中负调控LET-60 Ras活性。

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摘要

The let-60 ras gene acts in a signal transduction pathway to control vulval differentiation in Caenorhabditis elegans. By screening suppressors of a dominant negative let-60 ras allele, we isolated three loss-of-function mutations in the sur-5 gene which appear to act as negative regulators of let-60 ras during vulval induction. sur-5 mutations do not cause an obvious mutant phenotype of their own, and they appear to specifically suppress only one of the two groups of let-60 ras dominant negative mutations, suggesting that the gene may be involved in a specific aspect of Ras activation. Consistent with its negative function, overexpressing sur-5 from an extragenic array partially suppresses the Multivulva phenotype of an activated let-60 ras mutation and causes synergistic phenotypes with a lin-45 raf mutation. We have cloned sur-5 and shown that it encodes a novel protein. We have also identified a potential mammalian SUR-5 homolog that is about 35% identical to the worm protein. SUR-5 also has some sequence similarity to acetyl coenzyme A synthetases and is predicted to contain ATP/GTP and AMP binding sites. Our results suggest that sur-5 gene function may be conserved through evolution.
机译:let-60 ras基因在信号转导通路中起作用,以控制秀丽隐杆线虫的外阴分化。通过筛选显性负性let-60 ras等位基因的抑制子,我们在sur-5基因中分离了三个功能丧失突变,这些突变似乎在外阴诱导期间充当let-60 ras的负调节剂。 sur-5突变不会引起其自身的明显突变表型,它们似乎仅特异性抑制两组let-60 ras显性负突变中的一种,这表明该基因可能与Ras激活的特定方面有关。 。与它的负功能一致,从外源阵列中过表达sur-5会部分抑制激活的let-60 ras突变的Multivulva表型,并导致与lin-45 raf突变的协同表型。我们已经克隆了sur-5,并表明它编码一种新蛋白。我们还确定了潜在的哺乳动物SUR-5同源物,与蠕虫蛋白约35%相同。 SUR-5也具有与乙酰辅酶A合成酶的序列相似性,并且预计包含ATP / GTP和AMP结合位点。我们的结果表明,sur-5基因功能可能通过进化得以保留。

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