LOCALIZATION OF A GAMMA-GLUTAMYL-TRANSFERASE-RELATED GENE FAMILY ON CHROMOSOME-22

被引:43
作者
MORRIS, C
COURTAY, C
VANKESSEL, AG
TENHOEVE, J
HEISTERKAMP, N
GROFFEN, J
机构
[1] CHILDRENS HOSP LOS ANGELES,DEPT PATHOL,MOLEC DIAGNOSIS SECT,4650 SUNSET BLVD,LOS ANGELES,CA 90027
[2] CHRISTCHURCH HOSP,CYTOGENET & MOLEC ONCOL UNIT,CHRISTCHURCH,NEW ZEALAND
[3] CNRS,UNITE 597,F-54000 NANCY,FRANCE
[4] UNIV HOSP NIJMEGEN,DEPT HUMAN GENET,6500 HB NIJMEGEN,NETHERLANDS
关键词
D O I
10.1007/BF00230218
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
A gene family encompassing a minimum of four genes or pseudogenes for gamma-glutamyl transferase (GGT; EC 2.3.2.2) is present on chromosome 22q11. We have previously isolated a cDNA related to GGT but clearly not belonging to its gene family. The chromosomal location of this related gene, GGTLA1, has been determined by both isotopic and fluorescence in situ hybridization to metaphase cells and by Southern blot analysis of somatic cell hybrid DNAs. We show that GGTLA1 is part of a distinct gene family, which has at least four members (GGTLA1, GGTLA2, GGTLA3, GGTLA4). At least two loci are located on chromosome 22 within band q11 and proximal to the chronic myelogenous leukemia (CML) breakpoint in BCR (breakpoint cluster region gene). At least one other member is located more distally between the breakpoints found in Ewings sarcoma and CML. Some of the GGT and GGTLA family members are located on NotI restriction enzyme fragments of a similar size. Combined results indicate that a segment of human chromosome 22q11 has undergone large-scale amplification events relatively recently in evolution.
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页码:31 / 36
页数:6
相关论文
共 19 条
  • [1] ADHAM IM, 1989, HUM GENET, V88, P59
  • [2] BULLE F, 1987, HUM GENET, V76, P283
  • [3] AN IMPROVED METHOD FOR G-BANDING CHROMOSOMES AFTER INSITU HYBRIDIZATION
    CANNIZZARO, LA
    EMANUEL, BS
    [J]. CYTOGENETICS AND CELL GENETICS, 1984, 38 (04): : 308 - 309
  • [4] MAPPING OF 4 DISTINCT BCR-RELATED LOCI TO CHROMOSOME REGION 22Q11 - ORDER OF BCR LOCI RELATIVE TO CHRONIC MYELOGENOUS LEUKEMIA AND ACUTE LYMPHOBLASTIC-LEUKEMIA BREAKPOINTS
    CROCE, CM
    HUEBNER, K
    ISOBE, M
    FAINSTAIN, E
    LIFSHITZ, B
    SHTIVELMAN, E
    CANAANI, E
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1987, 84 (20) : 7174 - 7178
  • [5] ISOLATION OF ANONYMOUS, POLYMORPHIC DNA FRAGMENTS FROM HUMAN-CHROMOSOME 22Q12-QTER
    DUMANSKI, JP
    VANKESSEL, AHMG
    RUTTLEDGE, M
    WLADIS, A
    SUGAWA, N
    COLLINS, VP
    NORDENSKJOLD, M
    [J]. HUMAN GENETICS, 1990, 84 (03) : 219 - 222
  • [6] FEINBERG AP, 1984, ANAL BIOCHEM, V137, P266
  • [7] Geurts van Kessel A. H., 1980, CYTOGENET CELL GENET, V28, P169
  • [8] PHILADELPHIA CHROMOSOMAL BREAKPOINTS ARE CLUSTERED WITHIN A LIMITED REGION, BCR, ON CHROMOSOME-22
    GROFFEN, J
    STEPHENSON, JR
    HEISTERKAMP, N
    DEKLEIN, A
    BARTRAM, CR
    GROSVELD, G
    [J]. CELL, 1984, 36 (01) : 93 - 99
  • [9] IDENTIFICATION OF A HUMAN GAMMA-GLUTAMYL CLEAVING ENZYME RELATED TO, BUT DISTINCT FROM, GAMMA-GLUTAMYL TRANSPEPTIDASE
    HEISTERKAMP, N
    RAJPERTDEMEYTS, E
    URIBE, L
    FORMAN, HJ
    GROFFEN, J
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (14) : 6303 - 6307
  • [10] HEISTERKAMP N, 1983, Journal of Molecular and Applied Genetics, V2, P57