The BRCA1 and 1A1.3B promoters are parallel elements of a genomic duplication at 17q21

被引:26
作者
Barker, DF
Liu, XD
Almeida, ERA
机构
[1] Department of Physiology, Univ. of Utah Hlth. Sciences Center, Salt Lake City, UT 84108
[2] Department of Physiology, Univ. of Utah Hlth. Sciences Center, University of Utah Research Park, Salt Lake City, UT 84108
关键词
D O I
10.1006/geno.1996.0618
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 results of experiments aimed at detecting polymorphisms and mutations in the BRCA1 promoter region as well as comparisons of two published DNA sequences indicated that two similar but distinct copies of this region exist in the human genome, PCR primers specific for amplification of each of the related sequences were developed and new genomic clones corresponding to each of the two promoter regions were isolated from rearrangement-resistant libraries. Sequence analysis of the clones and specific PCR products reveals two similar genomic arrangements of head-to-head genes, The BRCA1 gene is closely apposed to a gene structure that is similar but not identical to 1A1.3B, and the 1A1.3B gene is apposed to a gene structure that has strong similarity to BRCA1 but also significant differences, STS analysis of YAC and P1 clones located in the vicinity of BRCA1 indicates that these similar promoter regions are elements of a direct duplication, New hypotheses for genetic mechanisms that may be involved in breast and ovarian cancer etiology are raised by the identification of this duplicated genetic structure on chromosome 17q. (C) 1996 Academic Press, Inc.
引用
收藏
页码:215 / 222
页数:8
相关论文
共 37 条
[31]   COMMON ORIGINS OF BRCA1 MUTATIONS IN CANADIAN BREAST AND OVARIAN-CANCER FAMILIES [J].
SIMARD, J ;
TONIN, P ;
DUROCHER, F ;
MORGAN, K ;
ROMMENS, J ;
GINGRAS, S ;
SAMSON, C ;
LEBLANC, JF ;
BELANGER, C ;
DION, F ;
LIU, Q ;
SKOLNICK, M ;
GOLDGAR, D ;
SHATTUCKEIDENS, D ;
LABRIE, F ;
NAROD, SA .
NATURE GENETICS, 1994, 8 (04) :392-398
[32]  
STEICHENGERSDORF E, 1994, AM J HUM GENET, V55, P870
[33]   THE CARRIER FREQUENCY OF THE BRCA1 185DELAG MUTATION IS APPROXIMATELY 1 PERCENT IN ASHKENAZI-JEWISH INDIVIDUALS [J].
STRUEWING, JP ;
ABELIOVICH, D ;
PERETZ, T ;
AVISHAI, N ;
KABACK, MM ;
COLLINS, FS ;
BRODY, LC .
NATURE GENETICS, 1995, 11 (02) :198-200
[34]   INHERITED BREAST AND OVARIAN-CANCER [J].
SZABO, CI ;
KING, MC .
HUMAN MOLECULAR GENETICS, 1995, 4 :1811-1817
[35]  
van Tuinen P, 1987, Genomics, V1, P374, DOI 10.1016/0888-7543(87)90042-5
[36]   CHARACTERIZATION OF FREQUENT DELETIONS CAUSING STEROID 21-HYDROXYLASE DEFICIENCY [J].
WHITE, PC ;
VITEK, A ;
DUPONT, B ;
NEW, MI .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1988, 85 (12) :4436-4440
[37]   DISTINCT TRANSCRIPTION START SITES GENERATE 2 FORMS OF BRCA1 MESSENGER-RNA [J].
XU, CF ;
BROWN, MA ;
CHAMBERS, JA ;
GRIFFITHS, B ;
NICOLAI, H ;
SOLOMON, E .
HUMAN MOLECULAR GENETICS, 1995, 4 (12) :2259-2264