The BRCT regions of tumor suppressor BRCA1 and of XRCC1 show DNA end binding activity with a multimerizing feature

被引:51
作者
Yamane, K
Katayama, E
Tsuruo, T
机构
[1] Univ Tokyo, Inst Mol & Cellular Biosci, Biomed Res Lab, Bunkyo Ku, Tokyo 1130032, Japan
[2] Japanese Fdn Canc Res, Ctr Canc Chemotherapy, Toshima Ku, Tokyo 1708455, Japan
[3] Univ Tokyo, Inst Med Sci, Dept Fine Morphol, Minato Ku, Tokyo 1088639, Japan
关键词
BRCA1; BRCT; DNA damage binding; Cut5/Rad4; nijmegen breakage syndrome;
D O I
10.1006/bbrc.2000.3983
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
The BRCT regions are two repeating structures in BRCA1 at the carboxyl-terminus and are ubiquitous in some proteins involved in cell cycle checkpoint and in DNA repair. Here, using electron microscopy, we show direct evidence that the BRCT regions of BRCA1 bound double-strand breaks of DNA. The BRCT regions could multimerize thus forming large protein particles. Smeared patterns of DNA fragments were consistently shown in the gel retardation assay. A single BRCT was sufficient for DNA binding. The smeared patterns were also observed in BRCTs of TopBP1, suggesting: that multimerization may be an important feature of BRCTs. The recombinant second BRCT of XRCC1 (X-ray repair cross-complementing group 1), whose folding was determined by X-ray crystallography, also showed similar DNA end binding images. It is possible that some BRCTs are fundamental structures that detect DNA damages. (C) 2000 Academic Press.
引用
收藏
页码:678 / 684
页数:7
相关论文
共 28 条
  • [1] A superfamily of conserved domains in DNA damage responsive cell cycle checkpoint proteins
    Bork, P
    Hofmann, K
    Bucher, P
    Neuwald, AF
    Altschul, SF
    Koonin, EV
    [J]. FASEB JOURNAL, 1997, 11 (01) : 68 - 76
  • [2] 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
  • [3] The second BRCT domain of BRCA-1 proteins interacts with p53 and stimulates transcription from the p21WAF1/CIP1 promoter
    Chai, YL
    Cui, JQ
    Shao, NS
    Reddy, ESP
    Rao, VN
    [J]. ONCOGENE, 1999, 18 (01) : 263 - 268
  • [4] ASK1 mediates apoptotic cell death induced by genotoxic stress
    Chen, ZH
    Seimiya, H
    Naito, M
    Mashima, T
    Kizaki, A
    Dan, S
    Imaizumi, M
    Ichijo, H
    Miyazono, K
    Tsuruo, T
    [J]. ONCOGENE, 1999, 18 (01) : 173 - 180
  • [5] Female embryonic lethality in mice nullizygous for both Msh2 and p53
    Cranston, A
    Bocker, T
    Reitmair, A
    Palazzo, J
    Wilson, T
    Mak, T
    Fishel, R
    [J]. NATURE GENETICS, 1997, 17 (01) : 114 - 118
  • [6] Activation of c-Abl tyrosine kinase requires caspase activation and is not involved in JNK/SAPK activation during apoptosis of human monocytic leukemia U937 cells
    Dan, S
    Naito, M
    Seimiya, H
    Kizaki, A
    Mashima, T
    Tsuruo, T
    [J]. ONCOGENE, 1999, 18 (06) : 1277 - 1283
  • [7] HELA NUCLEAR-PROTEIN RECOGNIZING DNA TERMINI AND TRANSLOCATING ON DNA FORMING A REGULAR DNA MULTIMERIC PROTEIN COMPLEX
    DEVRIES, E
    VANDRIEL, W
    BERGSMA, WG
    ARNBERG, AC
    VANDERVLIET, PC
    [J]. JOURNAL OF MOLECULAR BIOLOGY, 1989, 208 (01) : 65 - 78
  • [8] RETRACTED: BRCA1 required for transcription-coupled repair of oxidative DNA damage (Retracted article. See vol 300, pg 1657, June 13 2003)
    Gowen, LC
    Avrutskaya, AV
    Latour, AM
    Koller, BH
    Leadon, SA
    [J]. SCIENCE, 1998, 281 (5379) : 1009 - 1012
  • [9] DNA ligase IV binds to XRCC4 via a motif located between rather than within its BRCT domains
    Grawunder, U
    Zimmer, D
    Lieber, MR
    [J]. CURRENT BIOLOGY, 1998, 8 (15) : 873 - 876
  • [10] KAUFMANN SH, 1989, CANCER RES, V49, P5870