Institute of Gene Biology, Russian Academy of Sciences, 119334 Moscow, Russia.
Faculty of Biology, Lomonosov Moscow State University, 119234 Moscow, Russia.
Int J Mol Sci. 2023 Jan 24;24(3):2295. doi: 10.3390/ijms24032295.
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.
RNA 聚合酶(RNAP)在核小体上进行转录时会伴随形成小的核小体内部 DNA 环(i-环)。在非模板 DNA 链(NT-SSB)上存在单链断裂或缺口的情况下,i-环的形成效率更高,并诱导转录的 RNAP 停滞,从而使该酶能够检测到 NT-SSB。在这里,我们研究了组蛋白尾部和核小体外的 NT-SSB 在转录起始点附近核小体 DNA 转录过程中 i-环形成和 RNAP 停滞中的作用。连接 DNA 中存在的 NT-SSB 诱导 RNAP 在核小体中停滞在+1 到+15bp 处,表明 i-环的形成;在存在组蛋白尾部的情况下,停滞更为有效。一致地,DNA 足迹分析表明,在 RNAP 停滞在+2 位置并回溯到+1 位置后,形成了 i-环。数据表明,连接 DNA 中存在的组蛋白尾部和 NT-SSB 可强烈促进转录起始点附近核小体 DNA 区域中 i-环的形成。