DNA-DEPENDENT KINASE (P350) AS A CANDIDATE GENE FOR THE MURINE SCID DEFECT

被引:578
作者
KIRCHGESSNER, CU
PATIL, CK
EVANS, JW
CUOMO, CA
FRIED, LM
CARTER, T
OETTINGER, MA
BROWN, JM
机构
[1] STANFORD UNIV,SCH MED,DEPT RADIAT ONCOL,STANFORD,CA 94305
[2] MASSACHUSETTS GEN HOSP,DEPT MOLEC BIOL,BOSTON,MA 02114
[3] ST JOHNS UNIV,DEPT BIOL SCI,JAMAICA,NY 11439
关键词
D O I
10.1126/science.7855601
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
Severe combined immunodeficient (SCID) mice are deficient in a recombination process utilized in both DNA double-strand break repair and in V(D)J recombination. The phenotype of these mice involves both cellular hypersensitivity to ionizing radiation and a lack of B and T cell immunity. The catalytic subunit of DNA-dependent protein kinase, p350, was identified as a strong candidate for the murine gene SCID. Both p350 and a gene complementing the SCID defect colocalize to human chromosome 8q11. Chromosomal fragments expressing p350 complement the SCID phenotype, and p350 protein levels are greatly reduced in cells derived from SCID mice compared to cells from wild-type mice.
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收藏
页码:1178 / 1183
页数:6
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