Aphidicolin-induced FRA3B breakpoints cluster in two distinct regions

被引:44
作者
Wang, L
Paradee, W
Mullins, C
Shridhar, R
Rosati, R
Wilke, CM
Glover, TW
Smith, DI
机构
[1] MAYO CLIN & MAYO FDN,DEPT LAB MED & PATHOL,DIV EXPT PATHOL,ROCHESTER,MN 55905
[2] EMORY UNIV,SCH MED,HOWARD HUGHES MED INST,ATLANTA,GA
[3] WAYNE STATE UNIV,SCH MED,DEPT INTERNAL MED,KARMANOS CANC INST,DIV HEMATOL ONCOL,DETROIT,MI 48201
[4] UNIV MICHIGAN,SCH MED,DEPT PEDIAT,ANN ARBOR,MI
[5] UNIV MICHIGAN,SCH MED,DEPT HUMAN GENET,ANN ARBOR,MI
关键词
D O I
10.1006/geno.1997.4690
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
The common fragile site at chromosomal band 3p14.2 (FRA3B) is the most sensitive single site in the human genome to induced chromosomal lesions. This fragile site may predispose chromosome 3p to breakage that is commonly observed in lung, renal, and many other cancers, We previously used aphidicolin induction of FRA3B expression in a chromosome S-only somatic cell hybrid to generate a series of hybrids with breakpoints in the 3p14.2 region. These breakpoints were localized to two distinct clusters, separated by 200 kb, that lie on either side of a region of frequent breakage within FRA3B as observed by FISH analysis. Seven proximal aphidicolin-induced breakpoints were localized at or near the end of a THE element. The THE-1 element is flanked by LINE and Alu repetitive elements. The eight distal aphidicolin-induced breakpoints clustered in a region capable of forming multiple hairpin-like structures, Thus repetitive elements and hairpin-like structures may be responsible for chromosome fragility in this region. (C) 1997 Academic Press.
引用
收藏
页码:485 / 488
页数:4
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