The high-mobility-group box protein SSRP1/T160 is essential for cell viability in day 3.5 mouse embryos

被引:57
作者
Cao, S
Bendall, H
Hicks, GG
Nashabi, A
Sakano, H
Shinkai, Y
Gariglio, M
Oltz, EA
Ruley, HE
机构
[1] Vanderbilt Univ, Sch Med, Dept Immunol & Microbiol, Nashville, TN 37232 USA
[2] New Biot, San Diego, CA 92121 USA
[3] Univ Manitoba, Winnipeg, MB R3E 0V9, Canada
[4] Manitoba Inst Cell Biol, Winnipeg, MB R3E 0V9, Canada
[5] Univ Tokyo, Grad Sch Sci, Dept Biophys & Biochem, Bunkyo Ku, Tokyo 1130032, Japan
[6] Kyoto Univ, Inst Virus Res, Kyoto 6068507, Japan
[7] Med Sch Novara, Dept Med Sci, I-28100 Novara, Italy
关键词
D O I
10.1128/MCB.23.15.5301-5307.2003
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 high-mobility-group (HMG) SSRP1 protein is a member of a conserved chromatin-remodeling complex (FACT/DUF/CP) implicated in DNA replication, basal and regulated transcription, and DNA repair. To assist in the functional analysis of SSRP1, the Ssrp1 gene was targeted in murine embryonic stem cells, and the mutation was introduced into the germ line. Embryos homozygous for the targeted allele die soon after implantation, and preimplantation blastocysts are defective for cell outgrowth and/or survival in vitro. The Ssrp1 mutation was also crossed into a p53 null background without affecting growth and/or survival defects caused by loss of Ssrp1 function. Thus, Ssrp1 appears to encode nonredundant and p53-independent functions that are essential for cell viability.
引用
收藏
页码:5301 / 5307
页数:7
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