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Generation of a Conditional CREB Ser133Ala Knockin Mouse

期刊

GENESIS
卷 47, 期 10, 页码 688-696

出版社

WILEY
DOI: 10.1002/dvg.20548

关键词

CREB; phosphorylation; knockin; CreLoxP; transgenic mice

资金

  1. UK Medical Research Council and Wellcome Trust
  2. AstraZeneca
  3. Boehringer Ingelheim
  4. GlaxoSmithKline
  5. Merck-Serono
  6. Pfizer
  7. Medical Research Council [MC_U127081014] Funding Source: researchfish
  8. MRC [MC_U127081014] Funding Source: UKRI

向作者/读者索取更多资源

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. (C) 2009 Wiley-Liss, Inc.

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