CHROMOSOMAL LOCALIZATION OF THE HUMAN HISTONE H2A.X GENE TO 11Q23.2-Q23.3 BY FLUORESCENCE IN-SITU HYBRIDIZATION

被引:0
|
作者
IVANOVA, VS
ZIMONJIC, D
POPESCU, N
BONNER, WM
机构
[1] NCI,MOLEC PHARMACOL LAB,BETHESDA,MD 20892
[2] NCI,BIOL LAB,BETHESDA,MD 20892
关键词
D O I
暂无
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The human histone H2A.X gene is unusual in that its transcripts are alternatively processed to yield two species, one a 0.6-kb replication-linked histone mRNA and the other a 1.6-kb polyadenylated mRNA. The H2A.X gene has been localized by fluorescence in situ hybridization to chromosome 11q23.2-q23.3, away from the known clusters of human histone genes on chromosomes 1, 6, and 12. Assignment to chromosome 11 was substantiated by analysis of human-hamster somatic cell hybrid lines. As this work was being completed, an 89-bps sequence overlap was found between the downstream regions of the H2A.X gene and the recently sequenced hydroxymethylbilane (HMB)-synthase gene. The H2A.X and HMB-synthase genes have an unusual arrangement, being transcribed towards each other with their polyadenylation sites 330 bp apart. In addition the HMB-synthase gene contains constitutive and erythroid specific promoters. K562, an erythroid cell line, was found to contain a high concentration of the 1.6-kb polyadenylated H2A.X mRNA.
引用
收藏
页码:303 / 306
页数:4
相关论文
共 50 条
  • [1] CHROMOSOMAL MAPPING OF THE HUMAN HISTONE GENE-H2AZ TO 4Q24 BY FLUORESCENCE IN-SITU HYBRIDIZATION
    POPESCU, N
    ZIMONJIC, D
    HATCH, C
    BONNER, W
    GENOMICS, 1994, 20 (02) : 333 - 335
  • [2] LOCALIZATION OF THE HUMAN OB GENE (OBS) TO CHROMOSOME 7Q32 BY FLUORESCENCE IN-SITU HYBRIDIZATION
    GEFFROY, S
    DEVOS, P
    STAELS, B
    DUBAN, B
    AUWERX, J
    DEMARTINVILLE, B
    GENOMICS, 1995, 28 (03) : 603 - 604
  • [3] 11Q TRISOMY DETECTED BY FLUORESCENCE IN-SITU HYBRIDIZATION
    TAKANO, T
    YAMANOUCHI, Y
    KAWASHIMA, S
    DATE, M
    HASHIRA, S
    KIDA, M
    ABE, T
    NAKAHORI, Y
    NAKAGOME, Y
    CLINICAL GENETICS, 1993, 44 (06) : 324 - 328
  • [4] CHROMOSOMAL LOCALIZATION OF THE HUMAN CILIARY NEUROTROPHIC FACTOR GENE (CNTF) TO 11Q12 BY FLUORESCENCE INSITU HYBRIDIZATION
    GIOVANNINI, M
    ROMO, AJ
    EVANS, GA
    CYTOGENETICS AND CELL GENETICS, 1993, 63 (01): : 62 - &
  • [5] CHROMOSOME MAPPING OF 11 HUMAN PROBES IN THE REGION 5Q2-]Q3 BY FLUORESCENCE IN-SITU HYBRIDIZATION
    RICHARD, F
    MULERIS, M
    DUTRILLAUX, B
    CYTOGENETICS AND CELL GENETICS, 1995, 68 (3-4): : 207 - 210
  • [6] CHROMOSOMAL LOCALIZATION OF THE HUMAN ECT2 PROTOONCOGENE TO 3Q26.1-]Q26.2 BY SOMATIC-CELL ANALYSIS AND FLUORESCENCE IN-SITU HYBRIDIZATION
    TAKAI, S
    LONG, JE
    YAMADA, K
    MIKI, T
    GENOMICS, 1995, 27 (01) : 220 - 222
  • [7] CHROMOSOMAL LOCALIZATION OF THE RAT ERYTHROPOIETIN RECEPTOR GENE BY FLUORESCENCE IN-SITU HYBRIDIZATION
    LIANG, P
    KITADA, K
    OSAKA, M
    SERIKAWA, T
    TAKAHASHI, R
    YAMADA, Y
    HIAI, H
    SUGIYAMA, T
    JAPANESE JOURNAL OF GENETICS, 1995, 70 (04): : 525 - 531
  • [8] ASSIGNMENT OF THE HUMAN PYRUVATE-CARBOXYLASE GENE (PC) TO 11Q13.4 BY FLUORESCENCE IN-SITU HYBRIDIZATION
    WALKER, ME
    BAKER, E
    WALLACE, JC
    SUTHERLAND, GR
    CYTOGENETICS AND CELL GENETICS, 1995, 69 (3-4): : 187 - 189
  • [9] ASSIGNMENT OF THE HUMAN GLYPICAN GENE (GPC1) TO 2Q35-Q37 BY FLUORESCENCE IN-SITU HYBRIDIZATION
    VERMEESCH, JR
    MERTENS, G
    DAVID, G
    MARYNEN, P
    GENOMICS, 1995, 25 (01) : 327 - 329
  • [10] Localization of the gene encoding the Ran-binding protein RanBP2 to human chromosome 2q11-q13 by fluorescence in situ hybridization
    Krebber, H
    Bastians, H
    Hoheisel, J
    Lichter, P
    Ponstingl, H
    Joos, S
    GENOMICS, 1997, 43 (02) : 247 - 248