INTRAGENIC DOMINANT SUPPRESSORS OF GLP-1, A GENE ESSENTIAL FOR CELL-SIGNALING IN CAENORHABDITIS-ELEGANS, SUPPORT A ROLE FOR CDC1O/SWI6/ANKYRIN MOTIFS IN GLP-1 FUNCTION

被引:0
作者
LISSEMORE, JL [1 ]
CURRIE, PD [1 ]
TURK, CM [1 ]
MAINE, EM [1 ]
机构
[1] SYRACUSE UNIV,DEPT BIOL,SYRACUSE,NY 13244
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Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The glp-1 gene product mediates cell-cell interactions required for cell fate specification during development in Caenorhabditis elegans. To identify genes that interact with glp-1, we screened for dominant suppressors of two temperature-sensitive glp-1 alleles and recovered 18 mutations that suppress both germline and embryonic glp-1 phenotypes. These dominant suppressors are tightly linked to glp-1 and do not bypass the requirement for a distal tip cell, which is thought to be the source of a signal that is received and transduced by the GLP-1 protein. Using single-strand conformation polymorphism (SSCP) analysis and DNA sequencing, we found that at least 17 suppressors are second-site intragenic revertants. The suppressors, like the original glp-1(ts) mutations, are all located in the cdc10/SWI6/ankyrin domain of GLP-1. cdc10/SWI6/ankyrin motifs have been shown to mediate specific protein-protein interactions in other polypeptides. We propose that the glp-1(ts) mutations disrupt contact between GLP-1 and an as yet unidentified target protein(s) and that the dominant suppressor mutations restore appropriate protein-protein interactions.
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页码:1023 / 1034
页数:12
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