| Literature DB >> 9351652 |
J Brownlees1, N G Irving, J P Brion, B J Gibb, U Wagner, J Woodgett, C C Miller.
Abstract
In order to investigate the effect on tau of manipulating glycogen synthase kinase (GSK)-3beta activity in the brain, we created transgenic mice harbouring wild-type GSK-3beta genes or a mutant GSK-3beta that is predicted to be more active. Transgene-derived mRNAs were detected in the brains of a number of the transgenic mouse lines and several of these transgenic lines displayed transgenic GSK-3beta activity. Western blot analyses of the two lines with the highest levels of transgenic GSK-3beta activity revealed that the phosphorylation status of tau was elevated at the AT8 epitope. These observations strongly suggest that GSK-3beta is an in vivo tau kinase in the brain. Only low levels of expression of GSK-3beta were obtained and it is possible that high levels of GSK-3beta activity are lethal.Entities:
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Year: 1997 PMID: 9351652 DOI: 10.1097/00001756-199710200-00013
Source DB: PubMed Journal: Neuroreport ISSN: 0959-4965 Impact factor: 1.837