Control of Transcription Initiation by Biased Thermal Fluctuations on Repetitive Genomic Sequences

In the process of transcription initiation by RNA polymerase, promoter DNA sequences affect multiple reaction pathways determining the productivity of transcription. However, the question of how the molecular mechanism of transcription initiation depends on the sequence properties of promoter DNA re...

Full description

Bibliographic Details
Main Authors: Masahiko Imashimizu, Yuji Tokunaga, Ariel Afek, Hiroki Takahashi, Nobuo Shimamoto, David B. Lukatsky
Format: Article
Language:English
Published: MDPI AG 2020-09-01
Series:Biomolecules
Subjects:
Online Access:https://www.mdpi.com/2218-273X/10/9/1299
id doaj-3c0b6fc2bb6046b39b93029889027212
record_format Article
spelling doaj-3c0b6fc2bb6046b39b930298890272122020-11-25T03:47:22ZengMDPI AGBiomolecules2218-273X2020-09-01101299129910.3390/biom10091299Control of Transcription Initiation by Biased Thermal Fluctuations on Repetitive Genomic SequencesMasahiko Imashimizu0Yuji Tokunaga1Ariel Afek2Hiroki Takahashi3Nobuo Shimamoto4David B. Lukatsky5Cellular and Molecular Biotechnology Research Institute, National Institute of Advanced Industrial Science and Technology, Tokyo 135-0064, JapanCellular and Molecular Biotechnology Research Institute, National Institute of Advanced Industrial Science and Technology, Tokyo 135-0064, JapanCenter for Genomic and Computational Biology, Department of Biostatistics and Bioinformatics, Duke University, Durham, NC 27708, USAMedical Mycology Research Center, Chiba University, Chiba 260-8673, JapanNational Institute of Genetics, Mishima, Shizuoka 411-8540, JapanDepartment of Chemistry, Ben-Gurion University of the Negev, Beer-Sheva 8410501, IsraelIn the process of transcription initiation by RNA polymerase, promoter DNA sequences affect multiple reaction pathways determining the productivity of transcription. However, the question of how the molecular mechanism of transcription initiation depends on the sequence properties of promoter DNA remains poorly understood. Here, combining the statistical mechanical approach with high-throughput sequencing results, we characterize abortive transcription and pausing during transcription initiation by <i>Escherichia coli</i> RNA polymerase at a genome-wide level. Our results suggest that initially transcribed sequences, when enriched with thymine bases, contain the signal for inducing abortive transcription, whereas certain repetitive sequence elements embedded in promoter regions constitute the signal for inducing pausing. Both signals decrease the productivity of transcription initiation. Based on solution NMR and in vitro transcription measurements, we suggest that repetitive sequence elements within the promoter DNA modulate the nonlocal base pair stability of its double-stranded form. This stability profoundly influences the reaction coordinates of the productive initiation via pausing.https://www.mdpi.com/2218-273X/10/9/1299promoter sequencesrepetitive sequencespausingabortive initiationRNA polymerasenonlocal base pair stability
collection DOAJ
language English
format Article
sources DOAJ
author Masahiko Imashimizu
Yuji Tokunaga
Ariel Afek
Hiroki Takahashi
Nobuo Shimamoto
David B. Lukatsky
spellingShingle Masahiko Imashimizu
Yuji Tokunaga
Ariel Afek
Hiroki Takahashi
Nobuo Shimamoto
David B. Lukatsky
Control of Transcription Initiation by Biased Thermal Fluctuations on Repetitive Genomic Sequences
Biomolecules
promoter sequences
repetitive sequences
pausing
abortive initiation
RNA polymerase
nonlocal base pair stability
author_facet Masahiko Imashimizu
Yuji Tokunaga
Ariel Afek
Hiroki Takahashi
Nobuo Shimamoto
David B. Lukatsky
author_sort Masahiko Imashimizu
title Control of Transcription Initiation by Biased Thermal Fluctuations on Repetitive Genomic Sequences
title_short Control of Transcription Initiation by Biased Thermal Fluctuations on Repetitive Genomic Sequences
title_full Control of Transcription Initiation by Biased Thermal Fluctuations on Repetitive Genomic Sequences
title_fullStr Control of Transcription Initiation by Biased Thermal Fluctuations on Repetitive Genomic Sequences
title_full_unstemmed Control of Transcription Initiation by Biased Thermal Fluctuations on Repetitive Genomic Sequences
title_sort control of transcription initiation by biased thermal fluctuations on repetitive genomic sequences
publisher MDPI AG
series Biomolecules
issn 2218-273X
publishDate 2020-09-01
description In the process of transcription initiation by RNA polymerase, promoter DNA sequences affect multiple reaction pathways determining the productivity of transcription. However, the question of how the molecular mechanism of transcription initiation depends on the sequence properties of promoter DNA remains poorly understood. Here, combining the statistical mechanical approach with high-throughput sequencing results, we characterize abortive transcription and pausing during transcription initiation by <i>Escherichia coli</i> RNA polymerase at a genome-wide level. Our results suggest that initially transcribed sequences, when enriched with thymine bases, contain the signal for inducing abortive transcription, whereas certain repetitive sequence elements embedded in promoter regions constitute the signal for inducing pausing. Both signals decrease the productivity of transcription initiation. Based on solution NMR and in vitro transcription measurements, we suggest that repetitive sequence elements within the promoter DNA modulate the nonlocal base pair stability of its double-stranded form. This stability profoundly influences the reaction coordinates of the productive initiation via pausing.
topic promoter sequences
repetitive sequences
pausing
abortive initiation
RNA polymerase
nonlocal base pair stability
url https://www.mdpi.com/2218-273X/10/9/1299
work_keys_str_mv AT masahikoimashimizu controloftranscriptioninitiationbybiasedthermalfluctuationsonrepetitivegenomicsequences
AT yujitokunaga controloftranscriptioninitiationbybiasedthermalfluctuationsonrepetitivegenomicsequences
AT arielafek controloftranscriptioninitiationbybiasedthermalfluctuationsonrepetitivegenomicsequences
AT hirokitakahashi controloftranscriptioninitiationbybiasedthermalfluctuationsonrepetitivegenomicsequences
AT nobuoshimamoto controloftranscriptioninitiationbybiasedthermalfluctuationsonrepetitivegenomicsequences
AT davidblukatsky controloftranscriptioninitiationbybiasedthermalfluctuationsonrepetitivegenomicsequences
_version_ 1724502286993981440