Targeted disruption of CRE-binding factor TREE5 gene leads to cellular necrosis in cardiac myocytes at the embryonic stage

被引:52
作者
Masaki, T
Yoshida, M
Noguchi, S
机构
[1] Kanagawa Acad Sci & Technol, Meiji Inst Hlth Sci, Biosignal Pathway Project, Meiji Milk Prod Co Ltd, Kanagawa 2500862, Japan
[2] Univ Tokyo, Inst Med Sci, Dept Cellular & Mol Biol, Minato Ku, Tokyo 1088639, Japan
关键词
D O I
10.1006/bbrc.1999.0972
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
TREB5 (hXBP-1) is a basic region leucine zipper protein which binds to a CRE-like element in both human T-cell leukemia virus type 1 and MHC class II genes. To study the function(s) of TREB5 in normal development, we have generated TREB5 deficient mice by gene targeting. Heterozygous mutant mice have not exhibited any obvious abnormalities; however, homozygous mutant embryos die between embryonic days 10.5 and 14.5. The major defect responsible for lethality is cellular necrosis of cardiac myocytes located at the atrium and the truncus arteriosus with its following ventricle. Necrotic alteration was not observed in either the endocardial cushion or the conotruncal ridge. These results indicate that TREB5 plays an essential role in maintenance and/or growth of cardiac myocytes during cardiogenesis. (C) 1999 Academic Press.
引用
收藏
页码:350 / 356
页数:7
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