DNA ligase IV is essential for V(D)J recombination and DNA double-strand break repair in human precursor lymphocytes

被引:282
作者
Grawunder, U
Zimmer, D
Fugmann, S
Schwarz, K
Lieber, MR [1 ]
机构
[1] Univ So Calif, Sch Med, Norris Comprehens Canc Ctr, Dept Pathol, Los Angeles, CA 90033 USA
[2] Univ Ulm, Dept Transfus Med, D-89081 Ulm, Germany
基金
美国国家卫生研究院;
关键词
D O I
10.1016/S1097-2765(00)80147-1
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Nonhomologous DNA end joining (NHEJ) is the major pathway for repairing double-strand DNA breaks. V(D)J recombination is a double-strand DNA breakage and rejoining process that relies on NHEJ for the joining steps. Here we show that the targeted disruption of both DNA ligase IV alleles in a human pre-B cell line renders the cells sensitive to ionizing radiation and ablates V(D)J recombination. This phenotype can only be reversed by complementation with DNA ligase IV but not by expression of either of the remaining two ligases, DNA ligase I or III. Hence, DNA ligase IV is the activity responsible for the ligation step in NHEJ and in V(D)J recombination.
引用
收藏
页码:477 / 484
页数:8
相关论文
共 43 条
  • [1] Reduced X-ray resistance and homologous recombination frequencies in a RAD54(-/-) mutant of the chicken DT40 cell line
    Bezzubova, O
    Silbergleit, A
    YamaguchiIwai, Y
    Takeda, S
    Buerstedde, JM
    [J]. CELL, 1997, 89 (02) : 185 - 193
  • [2] DEFECTIVE DNA-DEPENDENT PROTEIN-KINASE ACTIVITY IS LINKED TO V(D)J RECOMBINATION AND DNA-REPAIR DEFECTS ASSOCIATED WITH THE MURINE SCID MUTATION
    BLUNT, T
    FINNIE, NJ
    TACCIOLI, GE
    SMITH, GCM
    DEMENGEOT, J
    GOTTLIEB, TM
    MIZUTA, R
    VARGHESE, AJ
    ALT, FW
    JEGGO, PA
    JACKSON, SP
    [J]. CELL, 1995, 80 (05) : 813 - 823
  • [3] BOSMA M, 1988, CURR TOP MICROBIOL, V137, P197
  • [4] From BRCA1 to RAP1: A widespread BRCT module closely associated with DNA repair
    Callebaut, I
    Mornon, JP
    [J]. FEBS LETTERS, 1997, 400 (01): : 25 - 30
  • [5] Mammalian DNA double-strand break repair protein XRCC4 interacts with DNA ligase IV
    Critchlow, SE
    Bowater, RP
    Jackson, SP
    [J]. CURRENT BIOLOGY, 1997, 7 (08) : 588 - 598
  • [6] TARGETED DISRUPTION OF THE OCT-2 LOCUS IN A B-CELL PROVIDES GENETIC-EVIDENCE FOR 2-DISTINCT CELL-TYPE-SPECIFIC PATHWAYS OF OCTAMER ELEMENT-MEDIATED GENE ACTIVATION
    FELDHAUS, AL
    KLUG, CA
    ARVIN, KL
    SINGH, H
    [J]. EMBO JOURNAL, 1993, 12 (07) : 2763 - 2772
  • [7] UNEQUAL SIGNAL AND CODING JOINT FORMATION IN HUMAN V(D)J RECOMBINATION
    GAUSS, GH
    LIEBER, MR
    [J]. MOLECULAR AND CELLULAR BIOLOGY, 1993, 13 (07) : 3900 - 3906
  • [8] Gauss GH, 1996, MOL CELL BIOL, V16, P258
  • [9] DEAE-DEXTRAN ENHANCES ELECTROPORATION OF MAMMALIAN-CELLS
    GAUSS, GH
    LIEBER, MR
    [J]. NUCLEIC ACIDS RESEARCH, 1992, 20 (24) : 6739 - 6740
  • [10] Gauss GH, 1998, EUR J IMMUNOL, V28, P351, DOI 10.1002/(SICI)1521-4141(199801)28:01<351::AID-IMMU351>3.0.CO