A blooming resolvase at chromosomal fragile sites

被引:8
|
作者
Pellicioli, Achille [1 ]
Muzi-Falconi, Marco [1 ]
机构
[1] Univ Milan, Dipartimento Biosci, I-20133 Milan, Italy
关键词
REPLICATION STRESS; INSTABILITY; COMMON; STABILITY;
D O I
10.1038/ncb2812
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Common fragile sites (CFSs) are chromosomal regions that are prone to form breaks or gaps during mitosis, in particular following replication stress. The mechanisms modulating CFS expression and promoting safe chromatid transmission to daughter cells are not clear. Now CFS expression is shown to reflect the activity of the MUS81-EME1 resolvase complex which cooperates with the dissolving action of the BLM helicase to prevent uncontrolled chromosome breakage and to promote genome integrity.
引用
收藏
页码:883 / 885
页数:3
相关论文
共 50 条
  • [41] Cloning of genetically tagged chromosome break sequences reveals new fragile sites at 6p21 and 13q22
    Fechter, Anne
    Buettel, Isabel
    Kuehnel, Elisabeth
    Schwab, Manfred
    Savelyeva, Larissa
    INTERNATIONAL JOURNAL OF CANCER, 2007, 120 (11) : 2359 - 2367
  • [42] New Era of Mapping and Understanding Common Fragile Sites: An Updated Review on Origin of Chromosome Fragility
    Ji, Fang
    Zhu, Xinli
    Liao, Hongwei
    Ouyang, Liujian
    Huang, Yingfei
    Syeda, Madiha Zahra
    Ying, Songmin
    FRONTIERS IN GENETICS, 2022, 13
  • [43] Genome-wide high-resolution mapping of chromosome fragile sites in Saccharomyces cerevisiae
    Song, Wei
    Dominska, Margaret
    Greenwell, Patricia W.
    Petes, Thomas D.
    PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2014, 111 (21) : E2210 - E2218
  • [44] Perturbed replication induced genome wide or at common fragile sites is differently managed in the absence of WRN
    Murfuni, Ivana
    De Santis, Anita
    Federico, Maurizio
    Bignami, Margherita
    Pichierri, Pietro
    Franchitto, Annapaola
    CARCINOGENESIS, 2012, 33 (09) : 1655 - 1663
  • [45] DNA breaks at fragile sites generate oncogenic RET/PTC rearrangements in human thyroid cells
    Gandhi, M.
    Dillon, L. W.
    Pramanik, S.
    Nikiforov, Y. E.
    Wang, Y-H
    ONCOGENE, 2010, 29 (15) : 2272 - 2280
  • [46] Tumor Suppressor Genes within Common Fragile Sites Are Active Players in the DNA Damage Response
    Hazan, Idit
    Hofmann, Thomas G.
    Aqeilan, Rami I.
    PLOS GENETICS, 2016, 12 (12):
  • [47] First molecular-cytogenetic characterization of Fanconi anemia fragile sites in primary lymphocytes of FA-D2 patients in different stages of the disease
    Filipovic, Jelena
    Joksic, Gordana
    Vujic, Dragana
    Joksic, Ivana
    Mrasek, Kristin
    Weise, Anja
    Liehr, Thomas
    MOLECULAR CYTOGENETICS, 2016, 9
  • [48] CKAP2 Ensures Chromosomal Stability by Maintaining the Integrity of Microtubule Nucleation Sites
    Case, Chanelle M.
    Sackett, Dan L.
    Wangsa, Danny
    Karpova, Tatiana
    McNally, James G.
    Ried, Thomas
    Camps, Jordi
    PLOS ONE, 2013, 8 (05):
  • [49] Are common fragile sites merely structural domains or highly organized "functional'' units susceptible to oncogenic stress?
    Georgakilas, Alexandros G.
    Tsantoulis, Petros
    Kotsinas, Athanassios
    Michalopoulos, Ioannis
    Townsend, Paul
    Gorgoulis, Vassilis G.
    CELLULAR AND MOLECULAR LIFE SCIENCES, 2014, 71 (23) : 4519 - 4544
  • [50] FANCD2 binding identifies conserved fragile sites at large transcribed genes in avian cells
    Pentzold, Constanze
    Shah, Shiraz Ali
    Hansen, Niels Richard
    Le Tallec, Benoit
    Seguin-Orlando, Andaine
    Debatisse, Michelle
    Lisby, Michael
    Oestergaard, Vibe H.
    NUCLEIC ACIDS RESEARCH, 2018, 46 (03) : 1280 - 1294