MOLECULAR-CLONING, PRIMARY STRUCTURE AND EXPRESSION OF THE HUMAN-X LINKED A1S9 GENE CDNA WHICH COMPLEMENTS THE TS A1S9 MOUSE L-CELL DEFECT IN DNA-REPLICATION

被引:59
作者
ZACKSENHAUS, E
SHEININ, R
机构
[1] Department of Microbiology, Faculty of Medicine, University of Toronto, Toronto, Ont. M5S 1A8
关键词
cDNA; cell cycle; DNA replication; temperature-sensitive mutants; X chromosome inactivation;
D O I
10.1002/j.1460-2075.1990.tb07483.x
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 temperature-sensitive ts A1S9 mutation of mouse L cells was previously shown to affect nuclear DNA replication and to be complemented by active and inactive human X chromosomes in human-ts A1S9 somatic cell hybrids. We report the isolation of cDNA clones which correct the ts A1S9 lesion, using as a probe a genomic fragment derived from the human A1S9 locus. The nucleotide sequence of the A1S9 cDNA encompasses a single open reading frame of 2409 bp which could encode a heretofore unreported protein of 90393 daltons. Southern blot hybridization of the A1S9 cDNA probe with DNA from various species revealed homologous sequences in vertebrates but not in yeast. Northern blot analysis of serum-starved, synchronized cells demonstrated that the A1S9 gene was expressed at a relatively low level in quiescent cells and at a higher and constant level throughout the cell cycle. Human cell lines harbouring increasing numbers of inactive X chromosomes (47, XXX, 49, XXXXX) were found to express the A1S9 gene at the same level as control cells (45, X), suggesting that the gene does not escape X chromosome inactivation.
引用
收藏
页码:2923 / 2929
页数:7
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