A hexasome is the preferred substrate for the INO80 chromatin remodeling complex, allowing versatility of function

被引:24
作者
Hsieh, Laura J. [1 ]
Gourdet, Muryam A. [1 ,2 ]
Moore, Camille M. [1 ,2 ]
Munoz, Elise N. [1 ,2 ]
Gamarra, Nathan [1 ,2 ]
Ramani, Vijay [1 ]
Narlikar, Geeta J. [1 ]
机构
[1] Univ Calif San Francisco, Dept Biochem & Biophys, San Francisco, CA 94158 USA
[2] Univ Calif San Francisco, Tetrad Grad Program, San Francisco, CA 94158 USA
关键词
RNA-POLYMERASE-II; SWR-C; TRANSCRIPTION; YEAST; ENZYME; SWITCH; RSC;
D O I
10.1016/j.molcel.2022.04.026
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 critical role of the INO80 chromatin remodeling complex in transcription is commonly attributed to its nucleosome sliding activity. Here, we have found that INO80 prefers to mobilize hexasomes over nucleosomes. INO80's preference for hexasomes reaches up to similar to 60 fold when flanking DNA overhangs approach similar to 18-bp linkers in yeast gene bodies. Correspondingly, deletion of INO80 significantly affects the positions of hexasome-sized particles within yeast genes in vivo. Our results raise the possibility that INO80 promotes nucleosome sliding by dislodging an H2A-H2B dimer, thereby making a nucleosome transiently resemble a hexasome. We propose that this mechanism allows INO80 to rapidly mobilize nucleosomes at promoters and hexasomes within gene bodies. Rapid repositioning of hexasomes that are generated in the wake of transcription may mitigate spurious transcription. More generally, such versatility may explain how INO80 regulates chromatin architecture during the diverse processes of transcription, replication, and repair.
引用
收藏
页码:2098 / +
页数:20
相关论文
共 52 条
[1]   ATP-dependent chromatin remodeling shapes the long noncoding RNA landscape [J].
Alcid, Eric A. ;
Tsukiyama, Toshio .
GENES & DEVELOPMENT, 2014, 28 (21) :2348-2360
[2]   Structure and regulation of the human INO80-nucleosome complex [J].
Ayala, Rafael ;
Willhoft, Oliver ;
Aramayo, Ricardo J. ;
Wilkinson, Martin ;
McCormack, Elizabeth A. ;
Ocloo, Lorraine ;
Wigley, Dale B. ;
Zhang, Xiaodong .
NATURE, 2018, 556 (7701) :391-+
[3]   FACT facilitates transcription-dependent nucleosome alteration [J].
Belotserkovskaya, R ;
Oh, S ;
Bondarenko, VA ;
Orphanides, G ;
Studitsky, VM ;
Reinberg, D .
SCIENCE, 2003, 301 (5636) :1090-1093
[4]   The Arp8 and Arp4 module acts as a DNA sensor controlling INO80 chromatin remodeling [J].
Brahma, Sandipan ;
Ngubo, Mzwanele ;
Paul, Somnath ;
Udugama, Maheshi ;
Bartholomew, Blaine .
NATURE COMMUNICATIONS, 2018, 9
[5]   INO80 exchanges H2A.Z for H2A by translocating on DNA proximal to histone dimers [J].
Brahma, Sandipan ;
Udugama, Maheshi I. ;
Kim, Jongseong ;
Hada, Arjan ;
Bhardwaj, Saurabh K. ;
Hailu, Solomon G. ;
Lee, Tae-Hee ;
Bartholomew, Blaine .
NATURE COMMUNICATIONS, 2017, 8
[6]   A map of nucleosome positions in yeast at base-pair resolution [J].
Brogaard, Kristin ;
Xi, Liqun ;
Wang, Ji-Ping ;
Widom, Jonathan .
NATURE, 2012, 486 (7404) :496-501
[7]   A basic motif anchoring ISWI to nucleosome acidic patch regulates nucleosome spacing [J].
Dao, Hai T. ;
Dul, Barbara E. ;
Dann, Geoffrey P. ;
Liszczak, Glen P. ;
Muir, Tom W. .
NATURE CHEMICAL BIOLOGY, 2020, 16 (02) :134-+
[8]   Structural basis for ATP-dependent chromatin remodelling by the INO80 complex [J].
Eustermann, Sebastian ;
Schall, Kevin ;
Kostrewa, Dirk ;
Lakomek, Kristina ;
Strauss, Mike ;
Moldt, Manuela ;
Hopfner, Karl-Peter .
NATURE, 2018, 556 (7701) :386-+
[9]   The nucleosomal acidic patch relieves auto-inhibition by the ISWI remodeler SNF2h [J].
Gamarra, Nathan ;
Johnson, Stephanie L. ;
Trnka, Michael J. ;
Burlingame, Alma L. ;
Narlikar, Geeta .
ELIFE, 2018, 7
[10]   Genomic run-on evaluates transcription rates for all yeast genes and identifies gene regulatory mechanisms [J].
García-Martínez, J ;
Aranda, A ;
Pérez-Ortín, JE .
MOLECULAR CELL, 2004, 15 (02) :303-313