The unnamed complex: what do we know about Smc5-Smc6?

被引:92
作者
De Piccoli, Giacomo [1 ]
Torres-Rosell, Jordi [1 ]
Aragon, Luis [1 ]
机构
[1] Univ London Imperial Coll Sci Technol & Med, MRC Clin Sci Ctr, Cell Cycle Grp, London W12 0NN, England
关键词
Smc5-Smc6; recombination; replication forks; rDNA; DOUBLE-STRAND BREAKS; STALLED REPLICATION FORKS; SISTER-CHROMATID EXCHANGE; DNA-DAMAGE RESPONSE; SACCHAROMYCES-CEREVISIAE; SCHIZOSACCHAROMYCES-POMBE; SUMO LIGASE; HOMOLOGOUS RECOMBINATION; CHECKPOINT RESPONSES; PROTEIN COMPLEX;
D O I
10.1007/s10577-008-9016-8
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 structural maintenance of chromosome (SMC) proteins constitute the cores of three protein complexes involved in chromosome metabolism; cohesin, condensin and the Smc5-Smc6 complex. While the roles of cohesin and condensin in sister chromatid cohesion and chromosome condensation respectively have been described, the cellular function of Smc5-Smc6 is as yet not understood, consequently the less descriptive name. The complex is involved in a variety of DNA repair pathways. It contains activities reminiscent of those described for cohesin and condensin, as well as several DNA helicases and endonucleases. It is required for sister chromatid recombination, and smc5-smc6 mutants suffer from the accumulation of unscheduled recombination intermediates. The complex contains a SUMO-ligase and potentially an ubiquitin-ligase; thus Smc5-Smc6 might presently have a dull name, but it seems destined to be recognized as a key player in the maintenance of chromosome stability. In this review we summarize our present understanding of this enigmatic protein complex.
引用
收藏
页码:251 / 263
页数:13
相关论文
共 70 条
  • [1] Smc5/6 is required for repair at collapsed replication forks
    Ampatzidou, Eleni
    Irmisch, Anja
    O'Connell, Matthew J.
    Murray, Johanne M.
    [J]. MOLECULAR AND CELLULAR BIOLOGY, 2006, 26 (24) : 9387 - 9401
  • [2] Nse2, a component of the Smc5-6 complex, is a SUMO ligase required for the response to DNA damage
    Andrews, EA
    Palecek, J
    Sergeant, J
    Taylor, E
    Lehmann, AR
    Watts, FZ
    [J]. MOLECULAR AND CELLULAR BIOLOGY, 2005, 25 (01) : 185 - 196
  • [3] DSB repair: the yeast paradigm
    Aylon, Y
    Kupiec, M
    [J]. DNA REPAIR, 2004, 3 (8-9) : 797 - 815
  • [4] The MAGE proteins: Emerging roles in cell cycle progression, apoptosis, and neurogenetic disease
    Barker, PA
    Salehi, A
    [J]. JOURNAL OF NEUROSCIENCE RESEARCH, 2002, 67 (06) : 705 - 712
  • [5] DNA replication-dependent formation of joint DNA molecules in Physarum polycephalum
    Bénard, M
    Maric, C
    Pierron, G
    [J]. MOLECULAR CELL, 2001, 7 (05) : 971 - 980
  • [6] LETHALITY INDUCED BY A SINGLE SITE-SPECIFIC DOUBLE-STRAND BREAK IN A DISPENSABLE YEAST PLASMID
    BENNETT, CB
    LEWIS, AL
    BALDWIN, KK
    RESNICK, MA
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (12) : 5613 - 5617
  • [7] Ubc9-and mms21-mediated sumoylation counteracts recombinogenic events at damaged replication forks
    Branzei, Dana
    Sollier, Julie
    Liberi, Giordano
    Zhao, Xiaolan
    Maeda, Daisuke
    Seki, Masayuki
    Enomoto, Takemi
    Ohta, Kunihiro
    Foiani, Marco
    [J]. CELL, 2006, 127 (03) : 509 - 522
  • [8] Cdc2-cyclin B kinase activity links Crb2 and Rqh1-topoisomerase III
    Caspari, T
    Murray, JM
    Carr, AM
    [J]. GENES & DEVELOPMENT, 2002, 16 (10) : 1195 - 1208
  • [9] Cohesin's binding to chromosomes depends on a separate complex consisting of Scc2 and Scc4 proteins
    Ciosk, R
    Shirayama, M
    Shevchenko, A
    Tanaka, TU
    Toth, A
    Shevchenko, A
    Nasmyth, K
    [J]. MOLECULAR CELL, 2000, 5 (02) : 243 - 254
  • [10] The evolution of SMC proteins: Phylogenetic analysis and structural implications
    Cobbe, N
    Heck, MMS
    [J]. MOLECULAR BIOLOGY AND EVOLUTION, 2004, 21 (02) : 332 - 347