Correction of the spontaneous and DEB-induced chromosomal aberrations in Fanconi anemia cells of the FA(C) complementation group by the FACC gene

被引:2
|
作者
Stavropoulos, DJ
Sood, S
Tomkins, DJ
Buchwald, M
机构
[1] MCMASTER UNIV,DEPT PEDIAT,HAMILTON,ON L8N 3Z5,CANADA
[2] MCMASTER UNIV,DEPT BIOL,HAMILTON,ON L8N 3Z5,CANADA
[3] MCMASTER UNIV,DEPT PATHOL,HAMILTON,ON L8N 3Z5,CANADA
[4] HOSP SICK CHILDREN,RES INST,TORONTO,ON M5G 1X8,CANADA
[5] UNIV TORONTO,DEPT MOLEC & MED GENET,TORONTO,ON,CANADA
来源
CYTOGENETICS AND CELL GENETICS | 1996年 / 72卷 / 2-3期
关键词
D O I
10.1159/000134187
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Fanconi anemia (FA) cells are hypersensitive to the cytotoxic and clastogenic effects of DNA cross-linking agents. Four complementation groups have been identified to date. The gene (FACC) that corrects the hypersensitivity of one of them, FA(C), has been cloned. In the present study, both the increased spontaneous and diepoxybutane (DEB)-induced chromosomal instability in FA(C) lymphoblastoid cells were corrected by transfection of FACC.
引用
收藏
页码:194 / 196
页数:3
相关论文
共 50 条
  • [41] Inactivation of the Fanconi anemia group C gene augments interferon-gamma-induced apoptotic responses in hematopoietic cells
    Rathbun, RK
    Faulkner, GR
    Ostroski, MH
    Christianson, TA
    Hughes, G
    Jones, G
    Cahn, R
    Maziarz, R
    Royle, G
    Keeble, W
    Heinrich, MC
    Grompe, M
    Tower, TA
    Bagby, GC
    BLOOD, 1997, 90 (03) : 974 - 985
  • [42] The Fanconi anemia group C gene product is located in both the nucleus and cytoplasm of human cells
    Hoatlin, ME
    Christianson, TA
    Keeble, WW
    Hammond, AT
    Zhi, Y
    Heinrich, MC
    Tower, PA
    Bagby, GC
    BLOOD, 1998, 91 (04) : 1418 - 1425
  • [43] Functional correction of Fanconi anemia group C (FANCC) hematopoietic cells by the use of a novel lentiviral vector.
    Yamada, K
    Olsen, JC
    Walsh, CE
    BLOOD, 1999, 94 (10) : 176A - 176A
  • [44] Novel Lineage Depletion and Manufacturing Allows for Unprecedented Preservation of Autologous Blood Stem Cells for Gene Therapy of Fanconi Anemia Complementation Group.
    Adair, Jennifer
    Chandrasekaran, Devikha
    Schmuck, Stefanie
    Sghia-Hughes, Gabriella
    Choi, Grace
    Lee, Anne
    Haworth, Kevin G.
    Woolfrey, Ann
    Burroughs, Lauri S.
    Becker, Pamela S.
    Kiem, Hans-Peter
    BLOOD, 2017, 130
  • [46] Preclinical protocol for in vivo selection of hematopoietic stem cells corrected by gene therapy in Fanconi anemia group C
    Noll, M
    Bateman, RL
    D'Andrea, AD
    Grompe, M
    MOLECULAR THERAPY, 2001, 3 (01) : 14 - 23
  • [47] THE EFFECT OF THE FANCONI-ANEMIA COMPLEMENTATION GROUP-C (FACC) PROTEIN ON NITROGEN-MUSTARD (HN2)-INDUCED CYTOTOXICITY, APOPTOSIS G2/M ARREST AND DNA INTERSTRAND CROSS-LINKING
    MARATHI, UK
    REAGH, SH
    BRENT, TP
    JOURNAL OF CELLULAR BIOCHEMISTRY, 1995, : 326 - 326
  • [48] The Fanconi anemia complementation group C protein corrects DNA interstrand cross-link-specific apoptosis in HSC536N cells
    Marathi, UK
    Howell, SR
    Ashmun, RA
    Brent, TP
    BLOOD, 1996, 88 (06) : 2298 - 2305
  • [49] A NEW COMPLEMENTATION GROUP OF MITOMYCIN C-HYPERSENSITIVE CHINESE-HAMSTER CELL MUTANTS THAT CLOSELY RESEMBLES THE PHENOTYPE OF FANCONI-ANEMIA CELLS
    TELLEMAN, P
    OVERKAMP, WJI
    VANWESSEL, N
    STUDZIAN, K
    WETSELAAR, L
    NATARAJAN, AT
    ZDZIENICKA, MZ
    CANCER RESEARCH, 1995, 55 (15) : 3412 - 3416
  • [50] SPONTANEOUS AND INDUCED CHROMOSOMAL-ABERRATIONS AND GENE-MUTATIONS IN HUMAN-LYMPHOBLASTS - MITOMYCIN-C, METHYLNITROSOUREA, AND ETHYLNITROSOUREA
    JENSEN, JC
    THILLY, WG
    MUTATION RESEARCH, 1986, 160 (02): : 95 - 102