GENE COMPLEMENTING XERODERMA-PIGMENTOSUM GROUP A CELLS MAPS TO DISTAL HUMAN CHROMOSOME-9Q

被引:13
作者
HENNING, KA
SCHULTZ, RA
SEKHON, GS
FRIEDBERG, EC
机构
[1] STANFORD UNIV,MED CTR,SCH MED,DEPT GENET,STANFORD,CA 94305
[2] STANFORD UNIV,MED CTR,SCH MED,DEPT PATHOL,STANFORD,CA 94305
[3] UNIV MARYLAND,DIV HUMAN GENET,BALTIMORE,MD 21201
[4] UNIV WISCONSIN,DIV CLIN GENET,MADISON,WI 53705
关键词
D O I
10.1007/BF01232467
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
Phenotypic complementation of xeroderma pigmentosum group A (XP-A) cells by microcell-mediated transfer of a single rearranged neo-tagged human chromosome from a human-mouse somatic cell hybrid designated K3SUB1A9-3 was reported previously. Extended growth of this human-mouse hybrid in culture led to deletion of the small arm of the human chromosome, with concomitant loss of complementing ability when introduced into XP-A cells by microcell-mediated chromosome transfer. Cytogenetic analysis of both hybrids suggests that the complementing locus is on chromosome 9q22.2-q34.3, and Southern blot analysis confirms the presence of distal chromosome 9q sequences. © 1990 Plenum Publishing Corporation.
引用
收藏
页码:395 / 400
页数:6
相关论文
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