Generation of a conditional CREB Ser133Ala knockin mouse

Phosphorylation of Ser133 in the transcription factor CREB is an important mechanism for regulating its transcriptional activity, however recent work has suggested significant roles for other regulatory inputs into CREB. To allow study of this in vivo, we have generated a Ser133 to alanine knockin m...

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Published in:Genesis (New York, N.Y. : 2000) Vol. 47; no. 10; pp. 688 - 696
Main Authors: Wingate, Andrew D., Martin, Kirsty J., Hunter, Chris, Carr, Julia M., Clacher, Carol, Arthur, J. Simon C.
Format: Journal Article
Language:English
Published: Hoboken Wiley Subscription Services, Inc., A Wiley Company 01-10-2009
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Summary:Phosphorylation of Ser133 in the transcription factor CREB is an important mechanism for regulating its transcriptional activity, however recent work has suggested significant roles for other regulatory inputs into CREB. To allow study of this in vivo, we have generated a Ser133 to alanine knockin mutation in the mouse CREB locus. As CREB knockout is perinatal lethal, a minigene strategy was used to allow conditional knockin of the Ser133Ala mutation in adult mice using Cre recombinase. While some expression of the mutated protein was observed prior to Cre expression, following Cre expression in either T cells or neurons only the mutated CREB protein was detected. genesis 47:688–696, 2009. © 2009 Wiley‐Liss, Inc.
Bibliography:Merck-Serono and Pfizer
GlaxoSmithKline
ArticleID:DVG20548
Boehringer Ingelheim
ark:/67375/WNG-Z6WFDZQV-X
AstraZeneca
istex:4AEB4CFB29962F687DAB9231326599CFC384A0E4
UK Medical Research Council and Wellcome Trust
ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:1526-954X
1526-968X
DOI:10.1002/dvg.20548