The FACT Histone Chaperone Guides Histone H4 Into Its Nucleosomal Conformation in Saccharomyces cerevisiae

被引:9
|
作者
McCullough, Laura [1 ]
Poe, Bryan [1 ]
Connell, Zaily [1 ]
Xin, Hua [1 ]
Formosa, Tim [1 ]
机构
[1] Univ Utah, Sch Med, Dept Biochem, Salt Lake City, UT 84112 USA
来源
GENETICS | 2013年 / 195卷 / 01期
基金
美国国家卫生研究院;
关键词
TRANSCRIPTION ELONGATION-FACTORS; RNA-POLYMERASE-II; STRUCTURAL BASIS; DNA-REPLICATION; CHROMATIN-STRUCTURE; CORE PARTICLE; YEAST FACT; IN-VIVO; BINDING; SPT16;
D O I
10.1534/genetics.113.153080
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The pob3-Q308K mutation alters the small subunit of the Saccharomyces cerevisiae histone/nucleosome chaperone Facilitates Chromatin Transactions (FACT), causing defects in both transcription and DNA replication. We describe histone mutations that suppress some of these defects, providing new insight into the mechanism of FACT activity in vivo. FACT is primarily known for its ability to promote reorganization of nucleosomes into a more open form, but neither the pob3-Q308K mutation nor the compensating histone mutations affect this activity. Instead, purified mutant FACT complexes fail to release from nucleosomes efficiently, and the histone mutations correct this flaw. We confirm that pob3-T252E also suppresses pob3-Q308K and show that combining two suppressor mutations can be detrimental, further demonstrating the importance of balance between association and dissociation for efficient FACT: nucleosome interactions. To explain our results, we propose that histone H4 can adopt multiple conformations, most of which are incompatible with nucleosome assembly. FACT guides H4 to adopt appropriate conformations, and this activity can be enhanced or diminished by mutations in Pob3 or histones. FACT can therefore destabilize nucleosomes by favoring the reorganized state, but it can also promote assembly by tethering histones and DNA together and maintaining them in conformations that promote canonical nucleosome formation.
引用
收藏
页码:101 / 113
页数:13
相关论文
共 50 条
  • [1] Insights into the role of histone H3 and histone H4 core modifiable residues in Saccharomyces cerevisiae
    Hyland, EA
    Cosgrove, MS
    Molina, H
    Wang, DX
    Pandey, A
    Cottee, RJ
    Boeke, JD
    MOLECULAR AND CELLULAR BIOLOGY, 2005, 25 (22) : 10060 - 10070
  • [2] Elucidating the function of histone H4 acetylation in RNA splicing in Saccharomyces cerevisiae
    Mendizabal, A. G.
    Kopew, J. S.
    Paripati, N.
    Kress, T. L.
    MOLECULAR BIOLOGY OF THE CELL, 2017, 28
  • [3] Investigating the Role of Histone H4 Acetylation in RNA Splicing in Saccharomyces cerevisiae
    Kopew, Jessica S.
    Mendizabal, Adriana G.
    Lin, Mengjia M.
    Kress, Tracy L.
    FASEB JOURNAL, 2019, 33
  • [4] Histone H4 Lysine 20 of Saccharomyces cerevisiae Is Monomethylated and Functions in Subtelomeric Silencing
    Edwards, Christopher R.
    Dang, Weiwei
    Berger, Shelley L.
    BIOCHEMISTRY, 2011, 50 (48) : 10473 - 10483
  • [5] The Histone H4 Acetyltransferase NuA4 is Required for Appropriate RNA Splicing in Saccharomyces Cerevisiae
    Palfini, Lawrence M.
    Maisner, Rose
    Gunning, Thomas
    Lin, Mengjia M.
    Kress, Tracy L.
    FASEB JOURNAL, 2019, 33
  • [6] A novel H2A/H4 nucleosomal histone acetyltransferase in Tetrahymena thermophila
    Ohba, R
    Steger, DJ
    Brownell, JE
    Mizzen, CA
    Cook, RG
    Côté, J
    Workman, JL
    Allis, CD
    MOLECULAR AND CELLULAR BIOLOGY, 1999, 19 (03) : 2061 - 2068
  • [7] Histone H4 Lysine 12 Acetylation Regulates Telomeric Heterochromatin Plasticity in Saccharomyces cerevisiae
    Zhou, Bo O.
    Wang, Shan-Shan
    Zhang, Yang
    Fu, Xiao-Hong
    Dang, Wei
    Lenzmeier, Brian A.
    Zhou, Jin-Qiu
    PLOS GENETICS, 2011, 7 (01):
  • [8] Structural basis for the recognition of histone H4 by the histone-chaperone RbAp46
    Murzina, Natalia V.
    Pei, Xue-Yuan
    Zhang, Wei
    Sparkes, Mike
    Vicente-Garcia, Jose
    Pratap, J. Venkatesh
    McLaughlin, Stephen H.
    Ben-Shahar, Tom Rolef
    Verreault, Alain
    Luisi, Ben F.
    Laue, Ernest D.
    STRUCTURE, 2008, 16 (07) : 1077 - 1085
  • [9] Histone H4 hyperacetylation precludes histone H4 lysine 20 trimethylation
    Sarg, B
    Helliger, W
    Talasz, H
    Koutzamani, E
    Lindner, HH
    JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (51) : 53458 - 53464
  • [10] The NuA4 Acetyltransferase, Acetylation of Histone H4 and the H2A.Z Variant Histone are Required for Appropriate RNA Splicing in Saccharomyces cerevisiae
    Bolle, Camila
    Snyder, Christopher
    Lin, Mengjia M.
    Kress, Tracy L.
    FASEB JOURNAL, 2022, 36