Cargando…
A comprehensive map of preferentially located motifs reveals distinct proximal cis-regulatory sequences in plants
Identification of cis-regulatory sequences controlling gene expression is an arduous challenge that is being actively explored to discover key genetic factors responsible for traits of agronomic interest. Here, we used a genome-wide de novo approach to investigate preferentially located motifs (PLMs...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9597372/ https://www.ncbi.nlm.nih.gov/pubmed/36311095 http://dx.doi.org/10.3389/fpls.2022.976371 |
_version_ | 1784816077360857088 |
---|---|
author | Rozière, Julien Guichard, Cécile Brunaud, Véronique Martin, Marie-Laure Coursol, Sylvie |
author_facet | Rozière, Julien Guichard, Cécile Brunaud, Véronique Martin, Marie-Laure Coursol, Sylvie |
author_sort | Rozière, Julien |
collection | PubMed |
description | Identification of cis-regulatory sequences controlling gene expression is an arduous challenge that is being actively explored to discover key genetic factors responsible for traits of agronomic interest. Here, we used a genome-wide de novo approach to investigate preferentially located motifs (PLMs) in the proximal cis-regulatory landscape of Arabidopsis thaliana and Zea mays. We report three groups of PLMs in both the 5’- and 3’-gene-proximal regions and emphasize conserved PLMs in both species, particularly in the 3’-gene-proximal region. Comparison with resources from transcription factor and microRNA binding sites shows that 79% of the identified PLMs are unassigned, although some are supported by MNase-defined cistrome occupancy analysis. Enrichment analyses further reveal that unassigned PLMs provide functional predictions that differ from those derived from transcription factor and microRNA binding sites. Our study provides a comprehensive map of PLMs and demonstrates their potential utility for future characterization of orphan genes in plants. |
format | Online Article Text |
id | pubmed-9597372 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-95973722022-10-27 A comprehensive map of preferentially located motifs reveals distinct proximal cis-regulatory sequences in plants Rozière, Julien Guichard, Cécile Brunaud, Véronique Martin, Marie-Laure Coursol, Sylvie Front Plant Sci Plant Science Identification of cis-regulatory sequences controlling gene expression is an arduous challenge that is being actively explored to discover key genetic factors responsible for traits of agronomic interest. Here, we used a genome-wide de novo approach to investigate preferentially located motifs (PLMs) in the proximal cis-regulatory landscape of Arabidopsis thaliana and Zea mays. We report three groups of PLMs in both the 5’- and 3’-gene-proximal regions and emphasize conserved PLMs in both species, particularly in the 3’-gene-proximal region. Comparison with resources from transcription factor and microRNA binding sites shows that 79% of the identified PLMs are unassigned, although some are supported by MNase-defined cistrome occupancy analysis. Enrichment analyses further reveal that unassigned PLMs provide functional predictions that differ from those derived from transcription factor and microRNA binding sites. Our study provides a comprehensive map of PLMs and demonstrates their potential utility for future characterization of orphan genes in plants. Frontiers Media S.A. 2022-10-12 /pmc/articles/PMC9597372/ /pubmed/36311095 http://dx.doi.org/10.3389/fpls.2022.976371 Text en Copyright © 2022 Rozière, Guichard, Brunaud, Martin and Coursol https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Plant Science Rozière, Julien Guichard, Cécile Brunaud, Véronique Martin, Marie-Laure Coursol, Sylvie A comprehensive map of preferentially located motifs reveals distinct proximal cis-regulatory sequences in plants |
title | A comprehensive map of preferentially located motifs reveals distinct proximal cis-regulatory sequences in plants |
title_full | A comprehensive map of preferentially located motifs reveals distinct proximal cis-regulatory sequences in plants |
title_fullStr | A comprehensive map of preferentially located motifs reveals distinct proximal cis-regulatory sequences in plants |
title_full_unstemmed | A comprehensive map of preferentially located motifs reveals distinct proximal cis-regulatory sequences in plants |
title_short | A comprehensive map of preferentially located motifs reveals distinct proximal cis-regulatory sequences in plants |
title_sort | comprehensive map of preferentially located motifs reveals distinct proximal cis-regulatory sequences in plants |
topic | Plant Science |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9597372/ https://www.ncbi.nlm.nih.gov/pubmed/36311095 http://dx.doi.org/10.3389/fpls.2022.976371 |
work_keys_str_mv | AT rozierejulien acomprehensivemapofpreferentiallylocatedmotifsrevealsdistinctproximalcisregulatorysequencesinplants AT guichardcecile acomprehensivemapofpreferentiallylocatedmotifsrevealsdistinctproximalcisregulatorysequencesinplants AT brunaudveronique acomprehensivemapofpreferentiallylocatedmotifsrevealsdistinctproximalcisregulatorysequencesinplants AT martinmarielaure acomprehensivemapofpreferentiallylocatedmotifsrevealsdistinctproximalcisregulatorysequencesinplants AT coursolsylvie acomprehensivemapofpreferentiallylocatedmotifsrevealsdistinctproximalcisregulatorysequencesinplants AT rozierejulien comprehensivemapofpreferentiallylocatedmotifsrevealsdistinctproximalcisregulatorysequencesinplants AT guichardcecile comprehensivemapofpreferentiallylocatedmotifsrevealsdistinctproximalcisregulatorysequencesinplants AT brunaudveronique comprehensivemapofpreferentiallylocatedmotifsrevealsdistinctproximalcisregulatorysequencesinplants AT martinmarielaure comprehensivemapofpreferentiallylocatedmotifsrevealsdistinctproximalcisregulatorysequencesinplants AT coursolsylvie comprehensivemapofpreferentiallylocatedmotifsrevealsdistinctproximalcisregulatorysequencesinplants |