<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Veloso A</submitter><funding>NIEHS NIH HHS</funding><funding>NHGRI NIH HHS</funding><funding>NCI NIH HHS</funding><funding>NIGMS NIH HHS</funding><pagination>896-905</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC4032854</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>24(6)</volume><pubmed_abstract>The rate of transcription elongation plays an important role in the timing of expression of full-length transcripts as well as in the regulation of alternative splicing. In this study, we coupled Bru-seq technology with 5,6-dichlorobenzimidazole 1-β-D-ribofuranoside (DRB) to estimate the elongation rates of over 2000 individual genes in human cells. This technique, BruDRB-seq, revealed gene-specific differences in elongation rates with a median rate of around 1.5 kb/min. We found that genes with rapid elongation rates showed higher densities of H3K79me2 and H4K20me1 histone marks compared to slower elongating genes. Furthermore, high elongation rates had a positive correlation with gene length, low complexity DNA sequence, and distance from the nearest active transcription unit. Features t</pubmed_abstract><journal>Genome research</journal><pubmed_title>Rate of elongation by RNA polymerase II is associated with specific gene features and epigenetic modifications.</pubmed_title><pmcid>PMC4032854</pmcid><funding_grant_id>P30 ES017885</funding_grant_id><funding_grant_id>R01 HG006786</funding_grant_id><funding_grant_id>1R21ES020946</funding_grant_id><funding_grant_id>1R01HG006786</funding_grant_id><funding_grant_id>P50CA130810</funding_grant_id><funding_grant_id>T32 GM007544</funding_grant_id><funding_grant_id>P50 CA130810</funding_grant_id><funding_grant_id>R21 ES020946</funding_grant_id><pubmed_authors>Magnuson B</pubmed_authors><pubmed_authors>Wilson TE</pubmed_authors><pubmed_authors>Biewen B</pubmed_authors><pubmed_authors>Veloso A</pubmed_authors><pubmed_authors>Paulsen MT</pubmed_authors><pubmed_authors>Ljungman M</pubmed_authors><pubmed_authors>Kirkconnell KS</pubmed_authors></additional><is_claimable>false</is_claimable><name>Rate of elongation by RNA polymerase II is associated with specific gene features and epigenetic modifications.</name><description>The rate of transcription elongation plays an important role in the timing of expression of full-length transcripts as well as in the regulation of alternative splicing. In this study, we coupled Bru-seq technology with 5,6-dichlorobenzimidazole 1-β-D-ribofuranoside (DRB) to estimate the elongation rates of over 2000 individual genes in human cells. This technique, BruDRB-seq, revealed gene-specific differences in elongation rates with a median rate of around 1.5 kb/min. We found that genes with rapid elongation rates showed higher densities of H3K79me2 and H4K20me1 histone marks compared to slower elongating genes. Furthermore, high elongation rates had a positive correlation with gene length, low complexity DNA sequence, and distance from the nearest active transcription unit. Features t</description><dates><release>2014-01-01T00:00:00Z</release><publication>2014 Jun</publication><modification>2025-04-03T22:06:37.755Z</modification><creation>2019-06-06T12:48:42Z</creation></dates><accession>S-EPMC4032854</accession><cross_references><pubmed>24714810</pubmed><doi>10.1101/gr.171405.113</doi></cross_references></HashMap>