Role of Histone Tails and Single Strand DNA Breaks in Nucleosomal Arrest of RNA Polymerase

被引:3
|
作者
Gerasimova, Nadezhda S. [1 ,2 ]
Pestov, Nikolay A. [3 ]
Studitsky, Vasily M. [2 ,4 ]
机构
[1] Russian Acad Sci, Inst Gene Biol, Moscow 119334, Russia
[2] Lomonosov Moscow State Univ, Fac Biol, Moscow 119234, Russia
[3] Rutgers Robert Wood Johnson Med Sch, Dept Pharmacol, Piscataway, NJ 08854 USA
[4] Fox Chase Canc Ctr, Philadelphia, PA 19111 USA
基金
俄罗斯科学基金会;
关键词
DNA damage; DNA loop; chromatin structure; nucleosome; single-strand DNA breaks; transcription-coupled DNA repair; N-TERMINAL TAILS; TRANSCRIPTION BLOCKAGE; NONTRANSCRIBED STRAND; REPAIR; ELONGATION; BINDING; MECHANISMS; CHROMATIN; BARRIER; DAMAGE;
D O I
10.3390/ijms24032295
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
Transcription through nucleosomes by RNA polymerases (RNAP) is accompanied by formation of small intranucleosomal DNA loops (i-loops). The i-loops form more efficiently in the presence of single-strand breaks or gaps in a non-template DNA strand (NT-SSBs) and induce arrest of transcribing RNAP, thus allowing detection of NT-SSBs by the enzyme. Here we examined the role of histone tails and extranucleosomal NT-SSBs in i-loop formation and arrest of RNAP during transcription of promoter-proximal region of nucleosomal DNA. NT-SSBs present in linker DNA induce arrest of RNAP +1 to +15 bp in the nucleosome, suggesting formation of the i-loops; the arrest is more efficient in the presence of the histone tails. Consistently, DNA footprinting reveals formation of an i-loop after stalling RNAP at the position +2 and backtracking to position +1. The data suggest that histone tails and NT-SSBs present in linker DNA strongly facilitate formation of the i-loops during transcription through the promoter-proximal region of nucleosomal DNA.
引用
收藏
页数:16
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