Molecular basis of chromatin remodeling by Rhp26, a yeast CSB ortholog

被引:10
作者
Wang, Wei [1 ,2 ,3 ]
Xu, Jun [1 ,2 ]
Limbo, Oliver [4 ]
Fei, Jia [5 ]
Kassavetis, George A. [5 ]
Chong, Jenny [1 ,2 ]
Kadonaga, James T. [5 ]
Russell, Paul [4 ]
Li, Bing [6 ]
Wang, Dong [1 ,2 ]
机构
[1] Univ Calif San Diego, Skaggs Sch Pharm & Pharmaceut Sci, Div Pharmaceut Sci, La Jolla, CA 92093 USA
[2] Univ Calif San Diego, Sch Med, Dept Cellular & Mol Med, La Jolla, CA 92093 USA
[3] Shandong Univ, Adv Med Res Inst, Jinan 250012, Shandong, Peoples R China
[4] Scripps Res Inst, Dept Mol Med, La Jolla, CA 92037 USA
[5] Univ Calif San Diego, Sect Mol Biol, La Jolla, CA 92093 USA
[6] Shanghai Jiao Tong Univ, Shanghai Key Lab Tumor Microenvironm & Inflammat, Dept Biochem & Mol Cell Biol, Sch Med, Shanghai 200025, Peoples R China
基金
国家重点研发计划; 中国国家自然科学基金; 美国国家卫生研究院;
关键词
chromatin remodeling; histone tail; SNF2-like family ATPase; Cockayne syndrome B; nucleosome sliding and eviction; TRANSCRIPTION-COUPLED REPAIR; GROUP-B PROTEIN; HISTONE H2A-H2B DIMER; NUCLEOSOME MOBILIZATION; EXTRANUCLEOSOMAL DNA; CONCERTED ACTION; EXCISION-REPAIR; BINDING DOMAIN; DAMAGE; MECHANISMS;
D O I
10.1073/pnas.1818163116
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
CSB/ERCC6 belongs to an orphan subfamily of SWI2/SNF2-related chromatin remodelers and plays crucial roles in gene expression, DNA damage repair, and the maintenance of genome integrity. The molecular basis of chromatin remodeling by Cockayne syndrome B protein (CSB) is not well understood. Here we investigate the molecular mechanism of chromatin remodeling by Rhp26, a Schizosaccharomyces pombe CSB ortholog. The molecular basis of chromatin remodeling and nucleosomal epitope recognition by Rhp26 is distinct from that of canonical chromatin remodelers, such as imitation switch protein (ISWI). We reveal that the remodeling activities are bidirectionally regulated by CSB-specific motifs: the N-terminal leucine-latch motif and the C-terminal coupling motif. Rhp26 remodeling activities depend mainly on H4 tails and to a lesser extent on H3 tails, but not on H2A and H2B tails. Rhp26 promotes the disruption of histone cores and the release of free DNA. Finally, we dissected the distinct contributions of two Rhp26 C-terminal regions to chromatin remodeling and DNA damage repair.
引用
收藏
页码:6120 / 6129
页数:10
相关论文
共 56 条
  • [1] A conserved N-terminal motif in Rad54 is important for chromatin remodeling and homologous strand pairing
    Alexiadis, V
    Lusser, A
    Kadonaga, JT
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (26) : 27824 - 27829
  • [2] A Ubiquitin-Binding Domain in Cockayne Syndrome B Required for Transcription-Coupled Nucleotide Excision Repair
    Anindya, Roy
    Mari, Pierre-Olivier
    Kristensen, Ulrik
    Kool, Hanneke
    Giglia-Mari, Giuseppina
    Mullenders, Leon H.
    Fousteri, Maria
    Vermeulen, Wim
    Egly, Jean-Marc
    Svejstrup, Jesper Q.
    [J]. MOLECULAR CELL, 2010, 38 (05) : 637 - 648
  • [3] Multiomic Analysis of the UV-Induced DNA Damage Response
    Boeing, Stefan
    Williamson, Laura
    Encheva, Vesela
    Gori, Ilaria
    Saunders, Rebecca E.
    Instrell, Rachael
    Aygun, Ozan
    Rodriguez-Martinez, Marta
    Weems, Juston C.
    Kelly, Gavin P.
    Conaway, Joan W.
    Conaway, Ronald C.
    Stewart, Aengus
    Howell, Michael
    Snijders, Ambrosius P.
    Svejstrup, Jesper Q.
    [J]. CELL REPORTS, 2016, 15 (07): : 1597 - 1610
  • [4] Functional delineation of three groups of the ATP-dependent family of chromatin remodeling enzymes
    Boyer, LA
    Logie, C
    Bonte, E
    Becker, PB
    Wade, PA
    Wolffe, AP
    Wu, C
    Imbalzano, AN
    Peterson, CL
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (25) : 18864 - 18870
  • [5] CHEN J, 1994, J BIOL CHEM, V269, P12482
  • [6] ATP-Dependent Chromatin Remodeling by Cockayne Syndrome Protein B and NAP1-Like Histone Chaperones Is Required for Efficient Transcription-Coupled DNA Repair
    Cho, Iltaeg
    Tsai, Pei-Fang
    Lake, Robert J.
    Basheer, Asjad
    Fan, Hua-Ying
    [J]. PLOS GENETICS, 2013, 9 (04):
  • [7] Mechanisms of action and regulation of ATP-dependent chromatin-remodelling complexes
    Clapier, Cedric R.
    Iwasa, Janet
    Cairns, Bradley R.
    Peterson, Craig L.
    [J]. NATURE REVIEWS MOLECULAR CELL BIOLOGY, 2017, 18 (07) : 407 - 422
  • [8] Regulation of DNA Translocation Efficiency within the Chromatin Remodeler RSC/Sth1 Potentiates Nucleosome Sliding and Ejection
    Clapier, Cedric R.
    Kasten, Margaret M.
    Parnell, Timothy J.
    Viswanathan, Ramya
    Szerlong, Heather
    Sirinakis, George
    Zhang, Yongli
    Cairns, Bradley R.
    [J]. MOLECULAR CELL, 2016, 62 (03) : 453 - 461
  • [9] Regulation of ISWI involves inhibitory modules antagonized by nucleosomal epitopes
    Clapier, Cedric R.
    Cairns, Bradley R.
    [J]. NATURE, 2012, 492 (7428) : 280 - +
  • [10] Regulation of ISW2 by concerted action of histone H4 tail and extranucleosomal DNA
    Dang, Weiwei
    Kagalwala, Mohamedi N.
    Bartholomew, Blaine
    [J]. MOLECULAR AND CELLULAR BIOLOGY, 2006, 26 (20) : 7388 - 7396