Requirement for Ku80 in growth and immunoglobulin V(D)J recombination

被引:556
作者
Nussenzweig, A
Chen, CH
Soares, VD
Sanchez, M
Sokol, K
Nussenzweig, MC
Li, GC
机构
[1] MEM SLOAN KETTERING CANC CTR,DEPT MED PHYS,NEW YORK,NY 10021
[2] MEM SLOAN KETTERING CANC CTR,DEPT RADIAT ONCOL,NEW YORK,NY 10021
[3] MEM SLOAN KETTERING CANC CTR,PROGRAM MOL BIOL,NEW YORK,NY 10021
[4] MEM SLOAN KETTERING CANC CTR,HOWARD HUGHES MED INST,LAB MOL IMMUNOL,NEW YORK,NY 10021
[5] MEM SLOAN KETTERING CANC CTR,LAB ANIM RES CTR,NEW YORK,NY 10021
关键词
D O I
10.1038/382551a0
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
THE DNA-dependent protein kinase (DNA-PK) is a mammalian serine/threonine kinase that is implicated in the repair of DNA double-strand breaks(1-4), DNA replication(1,5), transcription(6-8), and V(D)J recombination(9-12). To determine the role of the DNA-binding subunit of DNA-PK in vivo, we targeted Ku80 in mice. In mutant mice, T and B lymphocyte development is arrested at early progenitor stages and there is a profound deficiency in V(D)J rearrangement. Although Ku80(-/-) mice are viable and reproduce, they are 40-60% of the size of littermate controls. Consistent with this growth defect, fibroblasts derived from Ku80(-/-) embryos showed an early loss of proliferating cells, a prolonged doubling time, and intact cell-cycle checkpoints that prevented cells with damaged DNA from entering the cell-cycle. The unexpected growth phenotype suggests a new and important link between Ku80 and growth control.
引用
收藏
页码:551 / 555
页数:5
相关论文
共 29 条
[1]   DNA-DAMAGE AND THE DNA-ACTIVATED PROTEIN-KINASE [J].
ANDERSON, CW .
TRENDS IN BIOCHEMICAL SCIENCES, 1993, 18 (11) :433-437
[2]   DEFECTIVE DNA-DEPENDENT PROTEIN-KINASE ACTIVITY IS LINKED TO V(D)J RECOMBINATION AND DNA-REPAIR DEFECTS ASSOCIATED WITH THE MURINE SCID MUTATION [J].
BLUNT, T ;
FINNIE, NJ ;
TACCIOLI, GE ;
SMITH, GCM ;
DEMENGEOT, J ;
GOTTLIEB, TM ;
MIZUTA, R ;
VARGHESE, AJ ;
ALT, FW ;
JEGGO, PA ;
JACKSON, SP .
CELL, 1995, 80 (05) :813-823
[3]   COMPLEMENTATION OF THE IONIZING-RADIATION SENSITIVITY, DNA END BINDING, AND V(D)J RECOMBINATION DEFECTS OF DOUBLE-STRAND BREAK REPAIR MUTANTS BY THE P86 KU AUTOANTIGEN [J].
BOUBNOV, NV ;
HALL, KT ;
WILLS, Z ;
LEE, SE ;
HE, DM ;
BENJAMIN, DM ;
PULASKI, CR ;
BAND, H ;
REEVES, W ;
HENDRICKSON, EA ;
WEAVER, DT .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (03) :890-894
[4]   LYMPHOCYTE-T DEVELOPMENT IN SCID MICE IS ARRESTED SHORTLY AFTER THE INITIATION OF T-CELL RECEPTOR DELTA-GENE RECOMBINATION [J].
CARROLL, AM ;
BOSMA, MJ .
GENES & DEVELOPMENT, 1991, 5 (08) :1357-1366
[5]  
CARROLL AM, 1993, MOL CELL BIOL, V13, P3623
[6]   Disruption of DNA-PK in Ku80 mutant xrs-6 and the implications in DNA double-strand break repair [J].
Chen, FQ ;
Peterson, SR ;
Story, MD ;
Chen, DJ .
MUTATION RESEARCH-DNA REPAIR, 1996, 362 (01) :9-19
[7]   CHROMOSOMAL POSITION OF REARRANGING GENE SEGMENTS INFLUENCES ALLELIC EXCLUSION IN TRANSGENIC MICE [J].
COSTA, TEF ;
SUH, H ;
NUSSENZWEIG, MC .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (06) :2205-2208
[8]  
Errami A, 1996, MOL CELL BIOL, V16, P1519
[9]   DNA-DEPENDENT PROTEIN-KINASE ACTIVITY IS ABSENT IN XRS-6 CELLS - IMPLICATIONS FOR SITE-SPECIFIC RECOMBINATION AND DNA DOUBLE-STRAND BREAK REPAIR [J].
FINNIE, NJ ;
GOTTLIEB, TM ;
BLUNT, T ;
JEGGO, PA ;
JACKSON, SP .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (01) :320-324
[10]  
GETTS RC, 1994, J BIOL CHEM, V269, P15981