Genetic analysis of specific and redundant roles for p38α and p38β MAPKs during mouse development

被引:47
|
作者
del Barco Barrantes, Ivan [1 ,2 ]
Manuel Coya, Juan [1 ]
Maina, Flavio [3 ]
Arthur, J. Simon C. [4 ]
Nebreda, Angel R. [1 ,2 ,5 ]
机构
[1] Ctr Nacl Invest Oncol, Madrid 28019, Spain
[2] Inst Res Biomed IRB Barcelona, Barcelona 08028, Spain
[3] Univ Aix Marseille 2, Dev Biol Inst Marseille Luminy, Ctr Natl Rech Sci, Unite Mixte Rech 6216, F-13288 Marseille 09, France
[4] Univ Dundee, MRC, Prot Phosphorylat Unit, Coll Life Sci, Dundee DD1 5EH, Scotland
[5] Inst Catalana Recerca & Estudis Avancats ICREA, Barcelona 08028, Spain
关键词
embryonic development; heart signaling; ACTIVATED PROTEIN-KINASE; CARDIOVASCULAR DEVELOPMENT; TRANSCRIPTION FACTOR; CARDIAC-HYPERTROPHY; CELL PROLIFERATION; SIGNALING PATHWAY; MICE LACKING; P38; MAPK; HEART; EXPRESSION;
D O I
10.1073/pnas.1015013108
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
p38 alpha MAPK is an important regulator of cellular responses induced by external cues, but the elucidation of physiological functions for p38 alpha has been complicated by the possible functional redundancy in vivo with the related family member p38 beta. We found that mice with combined deletion of p38 alpha and p38 beta display diverse developmental defects at midgestation, including major cardiovascular abnormalities, which are observed neither in single knockout nor in double heterozygous embryos. Expression analysis indicates specific functions of p38 alpha and p38 beta in the regulation of cardiac gene expression during development. By using knock-in animals that express p38 beta under control of the endogenous p38 alpha promoter, we also found that p38 beta cannot perform all of the functions of p38 alpha during embryogenesis. Our results identify essential roles for p38 alpha and p38 beta during development and suggest that some specific functions may be explained by differences in expression patterns.
引用
收藏
页码:12764 / 12769
页数:6
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