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 |
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Main Authors: | , , , , , |
Format: | Journal Article |
Language: | English |
Published: |
Hoboken
Wiley Subscription Services, Inc., A Wiley Company
01-10-2009
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Subjects: | |
Online Access: | Get full text |
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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. |
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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 |