The murine SNF5/INI1 chromatin remodeling factor is essential for embryonic development and tumor suppression

被引:0
|
作者
Klochendler-Yeivin, A
Fiette, L
Barra, J
Muchardt, C
Babinet, C
Yaniv, M
机构
[1] Inst Pasteur, CNRS, URA 1644, Unite Virus Oncogenes, F-75724 Paris 15, France
[2] Inst Pasteur, CNRS, URA 1960, Unite Histopathol, F-75724 Paris, France
[3] Inst Pasteur, CNRS, URA 1960, Unite Biol Dev, F-75724 Paris 15, France
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暂无
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
The assembly of eukaryotic DNA into nucleosomes and derived higher order structures constitutes a barrier for transcription, replication and repair. A number of chromatin remodeling complexes, as well as histone acetylation, were shown to facilitate gene activation. To investigate the function of two closely related mammalian SWI/SNF complexes in vivo, we inactivated the murine SNF5/INI1 gene, a common subunit of these two complexes. Mice lacking SNF5 protein stop developing at the peri-implantation stage, showing that the SWI/SNF complex is essential for early development and viability of early embryonic cells. Furthermore, heterozygous mice develop nervous system and soft tissue sarcomas. In these tumors the wild-type allele was lost, providing further evidence that SNF5 functions as a tumor suppressor gene in certain cell types.
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页码:500 / 506
页数:7
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