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RAS1 AND A PUTATIVE GUANINE-NUCLEOTIDE EXCHANGE FACTOR PERFORM CRUCIAL STEPS IN SIGNALING BY THE SEVENLESS PROTEIN TYROSINE KINASE
Author(s): SIMON MA, BOWTELL DDL, DODSON GS, LAVERTY TR, RUBIN GM
Source: CELL    Volume: 67    Issue: 4    Pages: 701-716    Published: NOV 15 1991  
Times Cited: 624     References: 57     
Abstract: We have conducted a genetic screen for mutations that decrease the effectiveness of signaling by a protein tyrosine kinase, the product of the Drosophila melanogaster sevenless gene. These mutations define seven genes whose wild-type products may be required for signaling by sevenless. Four of the seven genes also appear to be essential for signaling by a second protein tyrosine kinase, the product of the Ellipse gene. The putative products of two of these seven genes have been identified. One encodes a ras protein. The other locus encodes a protein that is homologous to the S. cerevisiae CDC25 protein, an activator of guanine nucleotide exchange by ras proteins. These results suggest that the stimulation of ras protein activity is a key element in the signaling by sevenless and Ellipse and that this stimulation may be achieved by activating the exchange of GTP for bound GDP by the ras protein.
Document Type: Article
Language: English
Reprint Address: SIMON, MA (reprint author), UNIV CALIF BERKELEY, HOWARD HUGHES MED INST, BERKELEY, CA 94720 USA
Addresses:
1. UNIV CALIF BERKELEY, DEPT MOLEC & CELL BIOL, BERKELEY, CA 94720 USA
Publisher: CELL PRESS, 1050 MASSACHUSETTES AVE, CIRCULATION DEPT, CAMBRIDGE, MA 02138
Subject Category: Biochemistry & Molecular Biology; Cell Biology
IDS Number: GQ407
ISSN: 0092-8674
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