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Isolation and chromosomal mapping of human glycogen synthase kinase-3 alpha and -3 beta encoding genes.

作者信息

Shaw P C, Davies A F, Lau K F, Garcia-Barcelo M, Waye M M, Lovestone S, Miller C C, Anderton B H

机构信息

Department of Biochemistry, Chinese University of Hong Kong, Shatin, NT, Hong Kong.

出版信息

Genome. 1998 Oct;41(5):720-7.

PMID:9809441
Abstract

Glycogen synthase kinase-3 (GSK-3) is a serine-threonine kinase that exists as two isoforms, alpha and beta, encoded by separate genes. Phosphorylation targets include a variety of cytoplasmic and nuclear proteins. Recent studies found that neurofilaments, amyloid precursor protein, and tau proteins are substrates of GSK-3 and that aberrant phosphorylation of these proteins is implicated in pathologies of the nervous system. To analyse the organisation of these two genes, a YAC library was screened by polymerase chain reaction, using primers specific for human GSK-3 alpha and GSK-3 beta cDNA. Two clones, 220 and 285 kb in size, containing the complete GSK-3 alpha coding sequence, and two clones, 365 and 285 kb in size, containing the 5' coding sequence of GSK-3 beta, were isolated. By somatic cell hybrid panel DNA amplification and radiation hybrid mapping, GSK-3 alpha was found to be located at 19q13.2. On the other hand, by somatic cell hybrid panel DNA amplification and fluorescence in situ hybridisation using the 285-kb YAC clone, GSK-3 beta was mapped to 3q13.3.

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