Cargando…

A non-canonical promoter element drives spurious transcription of horizontally acquired bacterial genes

RNA polymerases initiate transcription at DNA sequences called promoters. In bacteria, the best conserved promoter feature is the AT-rich -10 element; a sequence essential for DNA unwinding. Further elements, and gene regulatory proteins, are needed to recruit RNA polymerase to the -10 sequence. Hen...

Descripción completa

Detalles Bibliográficos
Autores principales: Warman, Emily A, Singh, Shivani S, Gubieda, Alicia G, Grainger, David C
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7229825/
https://www.ncbi.nlm.nih.gov/pubmed/32297955
http://dx.doi.org/10.1093/nar/gkaa244
_version_ 1783534830601895936
author Warman, Emily A
Singh, Shivani S
Gubieda, Alicia G
Grainger, David C
author_facet Warman, Emily A
Singh, Shivani S
Gubieda, Alicia G
Grainger, David C
author_sort Warman, Emily A
collection PubMed
description RNA polymerases initiate transcription at DNA sequences called promoters. In bacteria, the best conserved promoter feature is the AT-rich -10 element; a sequence essential for DNA unwinding. Further elements, and gene regulatory proteins, are needed to recruit RNA polymerase to the -10 sequence. Hence, -10 elements cannot function in isolation. Many horizontally acquired genes also have a high AT-content. Consequently, sequences that resemble the -10 element occur frequently. As a result, foreign genes are predisposed to spurious transcription. However, it is not clear how RNA polymerase initially recognizes such sequences. Here, we identify a non-canonical promoter element that plays a key role. The sequence, itself a short AT-tract, resides 5 base pairs upstream of otherwise cryptic -10 elements. The AT-tract alters DNA conformation and enhances contacts between the DNA backbone and RNA polymerase.
format Online
Article
Text
id pubmed-7229825
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher Oxford University Press
record_format MEDLINE/PubMed
spelling pubmed-72298252020-05-21 A non-canonical promoter element drives spurious transcription of horizontally acquired bacterial genes Warman, Emily A Singh, Shivani S Gubieda, Alicia G Grainger, David C Nucleic Acids Res Gene regulation, Chromatin and Epigenetics RNA polymerases initiate transcription at DNA sequences called promoters. In bacteria, the best conserved promoter feature is the AT-rich -10 element; a sequence essential for DNA unwinding. Further elements, and gene regulatory proteins, are needed to recruit RNA polymerase to the -10 sequence. Hence, -10 elements cannot function in isolation. Many horizontally acquired genes also have a high AT-content. Consequently, sequences that resemble the -10 element occur frequently. As a result, foreign genes are predisposed to spurious transcription. However, it is not clear how RNA polymerase initially recognizes such sequences. Here, we identify a non-canonical promoter element that plays a key role. The sequence, itself a short AT-tract, resides 5 base pairs upstream of otherwise cryptic -10 elements. The AT-tract alters DNA conformation and enhances contacts between the DNA backbone and RNA polymerase. Oxford University Press 2020-05-21 2020-04-16 /pmc/articles/PMC7229825/ /pubmed/32297955 http://dx.doi.org/10.1093/nar/gkaa244 Text en © The Author(s) 2020. Published by Oxford University Press on behalf of Nucleic Acids Research. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Gene regulation, Chromatin and Epigenetics
Warman, Emily A
Singh, Shivani S
Gubieda, Alicia G
Grainger, David C
A non-canonical promoter element drives spurious transcription of horizontally acquired bacterial genes
title A non-canonical promoter element drives spurious transcription of horizontally acquired bacterial genes
title_full A non-canonical promoter element drives spurious transcription of horizontally acquired bacterial genes
title_fullStr A non-canonical promoter element drives spurious transcription of horizontally acquired bacterial genes
title_full_unstemmed A non-canonical promoter element drives spurious transcription of horizontally acquired bacterial genes
title_short A non-canonical promoter element drives spurious transcription of horizontally acquired bacterial genes
title_sort non-canonical promoter element drives spurious transcription of horizontally acquired bacterial genes
topic Gene regulation, Chromatin and Epigenetics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7229825/
https://www.ncbi.nlm.nih.gov/pubmed/32297955
http://dx.doi.org/10.1093/nar/gkaa244
work_keys_str_mv AT warmanemilya anoncanonicalpromoterelementdrivesspurioustranscriptionofhorizontallyacquiredbacterialgenes
AT singhshivanis anoncanonicalpromoterelementdrivesspurioustranscriptionofhorizontallyacquiredbacterialgenes
AT gubiedaaliciag anoncanonicalpromoterelementdrivesspurioustranscriptionofhorizontallyacquiredbacterialgenes
AT graingerdavidc anoncanonicalpromoterelementdrivesspurioustranscriptionofhorizontallyacquiredbacterialgenes
AT warmanemilya noncanonicalpromoterelementdrivesspurioustranscriptionofhorizontallyacquiredbacterialgenes
AT singhshivanis noncanonicalpromoterelementdrivesspurioustranscriptionofhorizontallyacquiredbacterialgenes
AT gubiedaaliciag noncanonicalpromoterelementdrivesspurioustranscriptionofhorizontallyacquiredbacterialgenes
AT graingerdavidc noncanonicalpromoterelementdrivesspurioustranscriptionofhorizontallyacquiredbacterialgenes