Cookies on this website

We use cookies to ensure that we give you the best experience on our website. If you click 'Accept all cookies' we'll assume that you are happy to receive all cookies and you won't see this message again. If you click 'Reject all non-essential cookies' only necessary cookies providing core functionality such as security, network management, and accessibility will be enabled. Click 'Find out more' for information on how to change your cookie settings.

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.

More information Original publication

DOI

10.1097/00001756-199710200-00013

Type

Journal article

Publication Date

1997-10-20T00:00:00+00:00

Volume

8

Pages

3251 - 3255

Total pages

4

Keywords

Animals, Blotting, Western, Brain Chemistry, Calcium-Calmodulin-Dependent Protein Kinases, Glycogen Synthase Kinase 3, Glycogen Synthase Kinases, Humans, Mice, Mice, Transgenic, Mutation, Phosphorylation, Polymerase Chain Reaction, Precipitin Tests, tau Proteins