PREVALENCE AND MOLECULAR ANALYSIS OF 2 HOT-SPOTS FOR ECTOPIC RECOMBINATION LEADING TO XX MALENESS

被引:15
作者
WANG, I
WEIL, D
LEVILLIERS, J
AFFARA, NA
DELACHAPELLE, A
PETIT, C
机构
[1] INST PASTEUR,UNITE GENET MOLEC HUMAINE,CNRS,URA 1968,F-75724 PARIS 15,FRANCE
[2] UNIV CAMBRIDGE,DIV GENET PATHOL,HUMAN MOLEC GENET RES GRP,CAMBRIDGE CB2 1QP,ENGLAND
[3] UNIV HELSINKI,DEPT MED GENET,SF-00290 HELSINKI,FINLAND
关键词
D O I
10.1006/geno.1995.1105
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Two hot spots of ectopic Xp-Yp recombination have previously been shown to be at the origin of XX maleness (Well et al., 1994, Nature Genet. 7:414-419). To get more insight into the molecular basis of the abnormal interchange, 25 Y(+) class 3 XX male patients were studied. The two hot spots were found to account for the aberrant exchange in more than 50% of the cases. In addition, there is a correlation between the prevalence of each hot spot and the degree of X-Y homology between the corresponding fragments, Sequencing of the X-Y junctions in six patients, who carried a breakpoint mapping in either of these two hot spot fragments, showed that their precise locations were different from one individual to the other. In particular, the results obtained here in four new patients exclude the possibility that the repeated elements, present in these X-Y homologous fragments, are responsible for the high incidence of X-Y interchanges observed. Moreover, the breakpoints of all 25 class 3 XX males were found to be arranged in the same order on the X and Y chromosomes. This suggests that most ectopic recombinations leading to class 3 XX maleness involve X-Y homologous sequences persisting from an ancestral larger block of homology on the short arms of both sex chromosomes. (C) 1995 Academic Press, Inc.
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页码:52 / 58
页数:7
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