| Literature DB >> 2447651 |
R Azarnia1, S Reddy, T E Kmiecik, D Shalloway, W R Loewenstein.
Abstract
Overexpression of the cellular src gene in NIH 3T3 cells causes reduction of cell-to-cell transmission of molecules in the 400- to 700-dalton range. This down-regulation of gap junctional communication correlates with the activity of the gene product, the protein tyrosine kinase pp60c-src. The down-regulation was enhanced by point mutation of Tyr527 (a site that is phosphorylated in pp60c-src and that inhibits kinase activity) or by substitution of the viral-src for the cellular-src carboxyl-terminal coding region. Mutation of Tyr416 (a site phosphorylated upon Tyr527 mutation) suppresses both the down-regulation of communication by Tyr527 mutation and that by gene overexpression. The regulation of communication by src may be important in the control of embryonic development and cellular growth.Entities:
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Year: 1988 PMID: 2447651 DOI: 10.1126/science.2447651
Source DB: PubMed Journal: Science ISSN: 0036-8075 Impact factor: 47.728