Quantifying RNA synthesis at rate-limiting steps of transcription using nascent RNA-sequencing data
2022 (English)In: STAR Protocols, ISSN 2666-1667, Vol. 3, no 1, p. 101036-, article id 101036Article in journal (Refereed) Published
Abstract [en]
Nascent RNA-sequencing tracks transcription at nucleotide resolution. The genomic distribution of engaged transcription complexes, in turn, uncovers functional genomic regions. Here, we provide analytical steps to (1) identify transcribed regulatory elements de novo genome-wide, (2) quantify engaged transcription complexes at enhancers, promoter-proximal regions, divergent transcripts, gene bodies, and termination windows, and (3) measure distribution of transcription machineries and regulatory proteins across functional genomic regions. This protocol tracks engaged transcription complexes across functional genomic regions demonstrated in human K562 erythroleukemia cells. For complete details on the use and execution of this protocol, please refer to Vihervaara et al. (2021).
Place, publisher, year, edition, pages
Elsevier BV , 2022. Vol. 3, no 1, p. 101036-, article id 101036
Keywords [en]
Bioinformatics, Chromatin immunoprecipitation (ChIP), Gene Expression, Genetics, Genomics, RNAseq, Systems biology, RNA, human, nucleotide sequence, procedures, promoter region, regulatory sequence, sequence analysis, Base Sequence, Humans, Promoter Regions, Genetic, Regulatory Sequences, Nucleic Acid, Sequence Analysis, RNA
National Category
Developmental Biology
Identifiers
URN: urn:nbn:se:kth:diva-319158DOI: 10.1016/j.xpro.2021.101036ISI: 001055809900006PubMedID: 35036951Scopus ID: 2-s2.0-85122788986OAI: oai:DiVA.org:kth-319158DiVA, id: diva2:1700365
Note
QC 20220930
2022-09-302022-09-302023-09-21Bibliographically approved