Eleven X chromosome breakpoints associated with premature ovarian failure (POF) map to a 15-Mb YAC contig spanning Xq21

被引:109
作者
Sala, C
Arrigo, G
Torri, G
Martinazzi, F
Riva, P
Larizza, L
Philippe, C
Jonveaux, P
Sloan, F
Labella, T
Toniolo, D
机构
[1] CNR, INST GENET BIOCHEM & EVOLUT, I-27100 PAVIA, ITALY
[2] DIBIT HSR, MILAN, ITALY
[3] UNIV MILAN, DEPT BIOL & MED GENET, I-20122 MILAN, ITALY
[4] CNR, INST PROT BIOCHEM & ENZYMOL, I-80125 NAPLES, ITALY
[5] UNIV HOSP NANCY, GENET LAB, NANCY, FRANCE
关键词
D O I
10.1006/geno.1996.4542
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
Eleven balanced X-autosome translocations associated with premature ovarian failure (POF) were mapped to a YAC contig spanning most of Xq21 and constructed between the DXS223 and DXS1171 loci. The contig corresponds to a genomic region of about 15 Mb and contains the whole X-Y homologous region. The most proximal and most distal breakpoints associated with POF were mapped 15 Mb apart. The remaining breakpoints were localized along this large region, in the X-specific and in the X-Y homologous region. Four of the YACs contained two breakpoints in the same or in flanking STS intervals, Our results confirm the cytological findings and suggest that a minimum number of eight different genes in Xq21 may be involved with ovary development. Interruption of such loci could be the cause of POF. (C) 1997 Academic Press.
引用
收藏
页码:123 / 131
页数:9
相关论文
共 35 条
  • [1] MAPPING THE TESTIS DETERMINANTS BY AN ANALYSIS OF Y-SPECIFIC SEQUENCES IN MALES WITH APPARENT XX AND XO KARYOTYPES AND FEMALES WITH XY KARYOTYPES
    AFFARA, NA
    FERGUSONSMITH, MA
    MAGENIS, RE
    TOLMIE, JL
    BOYD, E
    COOKE, A
    JAMIESON, D
    KWOK, K
    MITCHELL, M
    SNADDEN, L
    [J]. NUCLEIC ACIDS RESEARCH, 1987, 15 (18) : 7325 - 7342
  • [2] CONSTRUCTION AND CHARACTERIZATION OF A YEAST ARTIFICIAL CHROMOSOME LIBRARY CONTAINING 7 HAPLOID HUMAN GENOME EQUIVALENTS
    ALBERTSEN, HM
    ABDERRAHIM, H
    CANN, HM
    DAUSSET, J
    LEPASLIER, D
    COHEN, D
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (11) : 4256 - 4260
  • [3] A 3.5 GENOME EQUIVALENT MULTIACCESS YAC LIBRARY - CONSTRUCTION, CHARACTERIZATION, SCREENING AND STORAGE
    ANAND, R
    RILEY, JH
    BUTLER, R
    SMITH, JC
    MARKHAM, AF
    [J]. NUCLEIC ACIDS RESEARCH, 1990, 18 (08) : 1951 - 1956
  • [4] DEFINITION AND MAPPING OF STSS AT STR AND RFLP LOCI IN XP11-XQ22
    BARKER, DF
    FAIN, PR
    [J]. GENOMICS, 1993, 18 (03) : 712 - 716
  • [5] BROWNE DL, 1991, NUCLEIC ACIDS RES, V19, P1721, DOI 10.1093/nar/19.7.1721
  • [6] COULAM CB, 1986, OBSTET GYNECOL, V67, P604
  • [7] COULAM CB, 1982, FERTIL STERIL, V38, P645
  • [8] CREMERS FPM, 1990, AM J HUM GENET, V47, P622
  • [9] TELOMERE-ASSOCIATED CHROMOSOME FRAGMENTATION - APPLICATIONS IN GENOME MANIPULATION AND ANALYSIS
    FARR, CJ
    STEVANOVIC, M
    THOMSON, EJ
    GOODFELLOW, PN
    COOKE, HJ
    [J]. NATURE GENETICS, 1992, 2 (04) : 275 - 282
  • [10] Refined mapping and YAC contig construction of the X-linked cleft palate and ankyloglossia locus (CPX) including the proximal X-Y homology breakpoint within Xq21.3
    Forbes, SA
    Brennan, L
    Richardson, M
    Coffey, A
    Cole, CG
    Gregory, SG
    Bentley, DR
    Mumm, S
    Moore, GE
    Stanier, P
    [J]. GENOMICS, 1996, 31 (01) : 36 - 43