A genomic analysis of RNA polymerase II modification and chromatin architecture related to 3′ end RNA polyadenylation

作者: Z. Lian , A. Karpikov , J. Lian , M. C. Mahajan , S. Hartman

DOI: 10.1101/GR.075804.107

关键词: RNA polymerasePolymeraseMolecular biologyBiologyRNA polymerase IITranscription factor II FRNA polyadenylationRNA-dependent RNA polymeraseTermination factorTranscription (biology)

摘要: Genomic analyses have been applied extensively to analyze the process of transcription initiation in mammalian cells, but less transcript 3′ end formation and termination. We used a novel approach prepare fragments from polyadenylated RNA, mapped position poly(A) addition site using oligonucleotide arrays tiling 1% human genome. This revealed more ends than had annotated. The distribution these relative RNA polymerase II (PolII) di- trimethylated lysine 4 36 histone H3 was compared. A substantial fraction unannotated are intronic antisense embedding gene. Poly(A) annotated messages lie on average 2 kb upstream PolII binding (termination). Near termination sites, some internal unphosphorylated C-terminal domain (CTD) serine phosphorylated (POLR2A) accumulate, suggesting pausing perhaps dephosphorylation prior release. Lysine trimethylation occurs across transcribed genes, sometimes alternating with stretches DNA which dimethylation is prominent. methylation decreases at or near polyadenylation, disappearing before disappearance release DNA. Our results suggest that loss 3 later polymerase. latter often associated pausing. Overall, our study reveals extensive sites provides insights into events occur during formation.

参考文章(75)
Marco De Gobbi, Vip Viprakasit, Jim R Hughes, Chris Fisher, Veronica J Buckle, Helena Ayyub, Richard J Gibbons, Douglas Vernimmen, Yuko Yoshinaga, Pieter De Jong, Jan-Fang Cheng, Edward M Rubin, William G Wood, Don Bowden, Douglas R Higgs, None, A Regulatory SNP Causes a Human Genetic Disease by Creating a New Transcriptional Promoter Science. ,vol. 312, pp. 1215- 1217 ,(2006) , 10.1126/SCIENCE.1126431
M Lanotte, V Martin-Thouvenin, S Najman, P Balerini, F Valensi, R Berger, NB4, a maturation inducible cell line with t(15;17) marker isolated from a human acute promyelocytic leukemia (M3) Blood. ,vol. 77, pp. 1080- 1086 ,(1991) , 10.1182/BLOOD.V77.5.1080.1080
Vincent Le Texier, Jean-Jack Riethoven, Vasudev Kumanduri, Chellappa Gopalakrishnan, Fabrice Lopez, Daniel Gautheret, Thangavel Alphonse Thanaraj, AltTrans: transcript pattern variants annotated for both alternative splicing and alternative polyadenylation. BMC Bioinformatics. ,vol. 7, pp. 169- 169 ,(2006) , 10.1186/1471-2105-7-169
Rimantas Kodzius, Miki Kojima, Hiromi Nishiyori, Mari Nakamura, Shiro Fukuda, Michihira Tagami, Daisuke Sasaki, Kengo Imamura, Chikatoshi Kai, Matthias Harbers, Yoshihide Hayashizaki, Piero Carninci, CAGE: cap analysis of gene expression Nature Methods. ,vol. 3, pp. 211- 222 ,(2006) , 10.1038/NMETH0306-211
B. Li, M. Gogol, M. Carey, D. Lee, C. Seidel, J. L. Workman, Combined action of PHD and chromo domains directs the Rpd3S HDAC to transcribed chromatin. Science. ,vol. 316, pp. 1050- 1054 ,(2007) , 10.1126/SCIENCE.1139004
Y. H. Choi, C. H. Hagedorn, Purifying mRNAs with a high-affinity eIF4E mutant identifies the short 3′ poly(A) end phenotype Proceedings of the National Academy of Sciences of the United States of America. ,vol. 100, pp. 7033- 7038 ,(2003) , 10.1073/PNAS.1232347100
Stephen Buratowski, The CTD code. Nature Structural & Molecular Biology. ,vol. 10, pp. 679- 680 ,(2003) , 10.1038/NSB0903-679
Maarten Hoogenkamp, Hanna Krysinska, Richard Ingram, Gang Huang, Rachael Barlow, Deborah Clarke, Alexander Ebralidze, Pu Zhang, Hiromi Tagoh, Peter N. Cockerill, Daniel G. Tenen, Constanze Bonifer, The Pu.1 locus is differentially regulated at the level of chromatin structure and noncoding transcription by alternate mechanisms at distinct developmental stages of hematopoiesis. Molecular and Cellular Biology. ,vol. 27, pp. 7425- 7438 ,(2007) , 10.1128/MCB.00905-07