Acetylation Mimics Within a Single Nucleosome Alter Local DNA Accessibility In Compacted Nucleosome Arrays

被引:27
作者
Mishra, Laxmi N. [1 ]
Pepenella, Sharon [1 ]
Rogge, Ryan [2 ]
Hansen, Jeffrey C. [2 ]
Hayes, Jeffrey J. [1 ]
机构
[1] Univ Rochester, Med Ctr, Dept Biochem & Biophys, Rochester, NY 14642 USA
[2] Colorado State Univ, Dept Biochem & Mol Biol, Ft Collins, CO 80523 USA
基金
美国国家卫生研究院;
关键词
HISTONE TAIL DOMAINS; PIONEER TRANSCRIPTION FACTORS; CHROMATIN FIBER; H4-K16; ACETYLATION; SELF-ASSOCIATION; GENE-REGULATION; DYNAMICS; PROTEIN; ORGANIZATION; MODEL;
D O I
10.1038/srep34808
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
The activation of a silent gene locus is thought to involve pioneering transcription factors that initiate changes in the local chromatin structure to increase promoter accessibility and binding of downstream effectors. To better understand the molecular requirements for the first steps of locus activation, we investigated whether acetylation of a single nucleosome is sufficient to alter DNA accessibility within a condensed 25-nucleosome array. We found that acetylation mimics within the histone H4 tail domain increased accessibility of the surrounding linker DNA, with the increased accessibility localized to the immediate vicinity of the modified nucleosome. In contrast, acetylation mimics within the H3 tail had little effect, but were able to synergize with H4 tail acetylation mimics to further increase accessibility. Moreover, replacement of the central nucleosome with a nucleosome free region also resulted in increased local, but not global DNA accessibility. Our results indicate that modification or disruption of only a single target nucleosome results in significant changes in local chromatin architecture and suggest that very localized chromatin modifications imparted by pioneer transcription factors are sufficient to initiate a cascade of events leading to promoter activation.
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页数:11
相关论文
共 61 条
[1]   The effects of histone H4 tail acetylations on cation-induced chromatin folding and self-association [J].
Allahverdi, Abdollah ;
Yang, Renliang ;
Korolev, Nikolay ;
Fan, Yanping ;
Davey, Curt A. ;
Liu, Chuan-Fa ;
Nordenskioeld, Lars .
NUCLEIC ACIDS RESEARCH, 2011, 39 (05) :1680-1691
[2]   PARTICIPATION OF CORE HISTONE TAILS IN THE STABILIZATION OF THE CHROMATIN SOLENOID [J].
ALLAN, J ;
HARBORNE, N ;
RAU, DC ;
GOULD, H .
JOURNAL OF CELL BIOLOGY, 1982, 93 (02) :285-297
[3]   Effects of histone acetylation on the equilibrium accessibility of nucleosomal DNA target sites [J].
Anderson, JD ;
Lowary, PT ;
Widom, J .
JOURNAL OF MOLECULAR BIOLOGY, 2001, 307 (04) :977-985
[4]  
Annunziato AT, 2000, GENE EXPRESSION, V9, P37
[5]   Dynamics of coactivator recruitment and chromatin modifications during nuclear receptor mediated transcription [J].
Aoyagi, Sayura ;
Archer, Trevor K. .
MOLECULAR AND CELLULAR ENDOCRINOLOGY, 2008, 280 (1-2) :1-5
[6]   HISTONE HYPERACETYLATION - ITS EFFECTS ON NUCLEOSOME CONFORMATION AND STABILITY [J].
AUSIO, J ;
VANHOLDE, KE .
BIOCHEMISTRY, 1986, 25 (06) :1421-1428
[7]   Large-scale chromatin organization: the good, the surprising, and the still perplexing [J].
Belmont, Andrew S. .
CURRENT OPINION IN CELL BIOLOGY, 2014, 26 :69-78
[8]   Nucleosome arrays reveal the two-start organization of the chromatin fiber [J].
Dorigo, B ;
Schalch, T ;
Kulangara, A ;
Duda, S ;
Schroeder, RR ;
Richmond, TJ .
SCIENCE, 2004, 306 (5701) :1571-1573
[9]   Chromatin fiber folding: Requirement for the histone H4N-terminal tail [J].
Dorigo, B ;
Schalch, T ;
Bystricky, K ;
Richmond, TJ .
JOURNAL OF MOLECULAR BIOLOGY, 2003, 327 (01) :85-96
[10]   The core histone n-terminal tail domains function independently and additively during salt-dependent oligomerization of nucleosomal arrays [J].
Faye, G ;
Luger, K ;
Hansen, JC .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2005, 280 (40) :33701-33706