Structure and nucleosome interaction of the yeast NuA4 and Piccolo-NuA4 histone acetyltransferase complexes

被引:68
作者
Chittuluru, Johnathan R. [1 ]
Chaban, Yuriy [1 ]
Monnet-Saksouk, Julie [2 ]
Carrozza, Michael J. [3 ]
Sapountzi, Vasileia [2 ]
Selleck, William [4 ]
Huang, Jiehuan [4 ]
Utley, Rhea T. [2 ]
Cramet, Myriam [2 ]
Allard, Stephane [2 ]
Cai, Gang [1 ]
Workman, Jerry L. [5 ]
Fried, Michael G. [6 ]
Tan, Song [4 ]
Cote, Jacques [2 ]
Asturias, Francisco J. [1 ]
机构
[1] Scripps Res Inst, Dept Cell Biol, La Jolla, CA 92037 USA
[2] Univ Laval, Canc Res Ctr, Hotel Dieu Quebec CHUQ, Quebec City, PQ, Canada
[3] Natl Inst Environm Hlth Sci, Lab Struct Biol, Res Triangle Pk, NC USA
[4] Penn State Univ, Ctr Eukaryot Gene Regulat, Dept Biochem & Mol Biol, University Pk, PA 16802 USA
[5] Stowers Inst Med Res, Kansas City, MO USA
[6] Univ Kentucky, Ctr Struct Biol, Dept Mol & Cellular Biochem, Lexington, KY USA
基金
美国国家卫生研究院;
关键词
CODING REGIONS; PROMOTER NUCLEOSOMES; ELECTRON-MICROSCOPY; EMBRYONIC STEM; H2A VARIANTS; CHROMATIN; TRANSCRIPTION; ACETYLATION; BINDING; ENHANCER;
D O I
10.1038/nsmb.2128
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
We have used EM and biochemistry to characterize the structure of NuA4, an essential yeast histone acetyltransferase (HAT) complex conserved throughout eukaryotes, and we have determined the interaction of NuA4 with the nucleosome core particle (NCP). The ATM-related Tra1 subunit, which is shared with the SAGA coactivator complex, forms a large domain joined to a second region that accommodates the catalytic subcomplex Piccolo and other NuA4 subunits. EM analysis of a NuA4-NCP complex shows the NCP bound at the periphery of NuA4. EM characterization of Piccolo and Piccolo-NCP provided further information about subunit organization and confirmed that histone acetylation requires minimal contact with the NCP. A small conserved region at the N terminus of Piccolo subunit enhancer of Polycomb-like 1 (Epl1) is essential for NCP interaction, whereas the subunit yeast homolog of mammalian Ing1 2 (Yng2) apparently positions Piccolo for efficient acetylation of histone H4 or histone H2A tails. Taken together, these results provide an understanding of the NuA4 subunit organization and the NuA4-NCP interactions.
引用
收藏
页码:1196 / U148
页数:9
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[31]   A Myc Network Accounts for Similarities between Embryonic Stem and Cancer Cell Transcription Programs [J].
Kim, Jonghwan ;
Woo, Andrew J. ;
Chu, Jianlin ;
Snow, Jonathan W. ;
Fujiwara, Yuko ;
Kim, Chul Geun ;
Cantor, Alan B. ;
Orkin, Stuart H. .
CELL, 2010, 143 (02) :313-324
[32]   Domains of Tra1 Important for Activator Recruitment and Transcription Coactivator Functions of SAGA and NuA4 Complexes [J].
Knutson, Bruce A. ;
Hahn, Steven .
MOLECULAR AND CELLULAR BIOLOGY, 2011, 31 (04) :818-831
[33]  
Luger K, 1999, METH MOL B, V119, P1
[34]   Functional dissection of the NuA4 histone acetyltransferase reveals its role as a genetic hub and that Eaf1 is essential for complex integrity [J].
Mitchell, Leslie ;
Lambert, Jean-Philippe ;
Gerdes, Maria ;
Al-Madhoun, Ashraf S. ;
Skerjanc, Ilona S. ;
Figeys, Daniel ;
Baetz, Kristin .
MOLECULAR AND CELLULAR BIOLOGY, 2008, 28 (07) :2244-2256
[35]   Role of an ING1 growth regulator in transcriptional activation and targeted histone acetylation by the NuA4 complex [J].
Nourani, A ;
Doyon, Y ;
Utley, RT ;
Allard, S ;
Lane, WS ;
Côté, J .
MOLECULAR AND CELLULAR BIOLOGY, 2001, 21 (22) :7629-7640
[36]   Sus1 is recruited to coding regions and functions during transcription elongation in association with SAGA and TREX2 [J].
Pascual-Garcia, Pau ;
Govind, Chhabi K. ;
Queralt, Ethel ;
Cuenca-Bono, Bernardo ;
Llopis, Ana ;
Chavez, Sebastian ;
Hinnebusch, Alan G. ;
Rodriguez-Navarro, Susana .
GENES & DEVELOPMENT, 2008, 22 (20) :2811-2822
[37]   UCSF chimera - A visualization system for exploratory research and analysis [J].
Pettersen, EF ;
Goddard, TD ;
Huang, CC ;
Couch, GS ;
Greenblatt, DM ;
Meng, EC ;
Ferrin, TE .
JOURNAL OF COMPUTATIONAL CHEMISTRY, 2004, 25 (13) :1605-1612
[38]   The tandem affinity purification (TAP) method:: A general procedure of protein complex purification [J].
Puig, O ;
Caspary, F ;
Rigaut, G ;
Rutz, B ;
Bouveret, E ;
Bragado-Nilsson, E ;
Wilm, M ;
Séraphin, B .
METHODS, 2001, 24 (03) :218-229
[39]   3-DIMENSIONAL RECONSTRUCTION FROM A SINGLE-EXPOSURE, RANDOM CONICAL TILT SERIES APPLIED TO THE 50S-RIBOSOMAL SUBUNIT OF ESCHERICHIA-COLI [J].
RADERMACHER, M ;
WAGENKNECHT, T ;
VERSCHOOR, A ;
FRANK, J .
JOURNAL OF MICROSCOPY, 1987, 146 :113-136
[40]   Global position and recruitment of HATs and HDACs in the yeast genome [J].
Robert, F ;
Pokholok, DK ;
Hannett, NM ;
Rinaldi, NJ ;
Chandy, M ;
Rolfe, A ;
Workman, JL ;
Gifford, DK ;
Young, RA .
MOLECULAR CELL, 2004, 16 (02) :199-209