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Genome-Wide Identification of Regulatory Elements and Reconstruction of Gene Regulatory Networks of the Green Alga Chlamydomonas reinhardtii under Carbon Deprivation

The unicellular green alga Chlamydomonas reinhardtii is a long-established model organism for studies on photosynthesis and carbon metabolism-related physiology. Under conditions of air-level carbon dioxide concentration [CO(2)], a carbon concentrating mechanism (CCM) is induced to facilitate cellul...

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Autores principales: Vischi Winck, Flavia, Arvidsson, Samuel, Riaño-Pachón, Diego Mauricio, Hempel, Sabrina, Koseska, Aneta, Nikoloski, Zoran, Urbina Gomez, David Alejandro, Rupprecht, Jens, Mueller-Roeber, Bernd
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3816576/
https://www.ncbi.nlm.nih.gov/pubmed/24224019
http://dx.doi.org/10.1371/journal.pone.0079909
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author Vischi Winck, Flavia
Arvidsson, Samuel
Riaño-Pachón, Diego Mauricio
Hempel, Sabrina
Koseska, Aneta
Nikoloski, Zoran
Urbina Gomez, David Alejandro
Rupprecht, Jens
Mueller-Roeber, Bernd
author_facet Vischi Winck, Flavia
Arvidsson, Samuel
Riaño-Pachón, Diego Mauricio
Hempel, Sabrina
Koseska, Aneta
Nikoloski, Zoran
Urbina Gomez, David Alejandro
Rupprecht, Jens
Mueller-Roeber, Bernd
author_sort Vischi Winck, Flavia
collection PubMed
description The unicellular green alga Chlamydomonas reinhardtii is a long-established model organism for studies on photosynthesis and carbon metabolism-related physiology. Under conditions of air-level carbon dioxide concentration [CO(2)], a carbon concentrating mechanism (CCM) is induced to facilitate cellular carbon uptake. CCM increases the availability of carbon dioxide at the site of cellular carbon fixation. To improve our understanding of the transcriptional control of the CCM, we employed FAIRE-seq (formaldehyde-assisted Isolation of Regulatory Elements, followed by deep sequencing) to determine nucleosome-depleted chromatin regions of algal cells subjected to carbon deprivation. Our FAIRE data recapitulated the positions of known regulatory elements in the promoter of the periplasmic carbonic anhydrase (Cah1) gene, which is upregulated during CCM induction, and revealed new candidate regulatory elements at a genome-wide scale. In addition, time series expression patterns of 130 transcription factor (TF) and transcription regulator (TR) genes were obtained for cells cultured under photoautotrophic condition and subjected to a shift from high to low [CO(2)]. Groups of co-expressed genes were identified and a putative directed gene-regulatory network underlying the CCM was reconstructed from the gene expression data using the recently developed IOTA (inner composition alignment) method. Among the candidate regulatory genes, two members of the MYB-related TF family, Lcr1 (Low-CO (2) response regulator 1) and Lcr2 (Low-CO (2) response regulator 2), may play an important role in down-regulating the expression of a particular set of TF and TR genes in response to low [CO(2)]. The results obtained provide new insights into the transcriptional control of the CCM and revealed more than 60 new candidate regulatory genes. Deep sequencing of nucleosome-depleted genomic regions indicated the presence of new, previously unknown regulatory elements in the C. reinhardtii genome. Our work can serve as a basis for future functional studies of transcriptional regulator genes and genomic regulatory elements in Chlamydomonas.
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spelling pubmed-38165762013-11-09 Genome-Wide Identification of Regulatory Elements and Reconstruction of Gene Regulatory Networks of the Green Alga Chlamydomonas reinhardtii under Carbon Deprivation Vischi Winck, Flavia Arvidsson, Samuel Riaño-Pachón, Diego Mauricio Hempel, Sabrina Koseska, Aneta Nikoloski, Zoran Urbina Gomez, David Alejandro Rupprecht, Jens Mueller-Roeber, Bernd PLoS One Research Article The unicellular green alga Chlamydomonas reinhardtii is a long-established model organism for studies on photosynthesis and carbon metabolism-related physiology. Under conditions of air-level carbon dioxide concentration [CO(2)], a carbon concentrating mechanism (CCM) is induced to facilitate cellular carbon uptake. CCM increases the availability of carbon dioxide at the site of cellular carbon fixation. To improve our understanding of the transcriptional control of the CCM, we employed FAIRE-seq (formaldehyde-assisted Isolation of Regulatory Elements, followed by deep sequencing) to determine nucleosome-depleted chromatin regions of algal cells subjected to carbon deprivation. Our FAIRE data recapitulated the positions of known regulatory elements in the promoter of the periplasmic carbonic anhydrase (Cah1) gene, which is upregulated during CCM induction, and revealed new candidate regulatory elements at a genome-wide scale. In addition, time series expression patterns of 130 transcription factor (TF) and transcription regulator (TR) genes were obtained for cells cultured under photoautotrophic condition and subjected to a shift from high to low [CO(2)]. Groups of co-expressed genes were identified and a putative directed gene-regulatory network underlying the CCM was reconstructed from the gene expression data using the recently developed IOTA (inner composition alignment) method. Among the candidate regulatory genes, two members of the MYB-related TF family, Lcr1 (Low-CO (2) response regulator 1) and Lcr2 (Low-CO (2) response regulator 2), may play an important role in down-regulating the expression of a particular set of TF and TR genes in response to low [CO(2)]. The results obtained provide new insights into the transcriptional control of the CCM and revealed more than 60 new candidate regulatory genes. Deep sequencing of nucleosome-depleted genomic regions indicated the presence of new, previously unknown regulatory elements in the C. reinhardtii genome. Our work can serve as a basis for future functional studies of transcriptional regulator genes and genomic regulatory elements in Chlamydomonas. Public Library of Science 2013-11-01 /pmc/articles/PMC3816576/ /pubmed/24224019 http://dx.doi.org/10.1371/journal.pone.0079909 Text en © 2013 Vischi Winck et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Vischi Winck, Flavia
Arvidsson, Samuel
Riaño-Pachón, Diego Mauricio
Hempel, Sabrina
Koseska, Aneta
Nikoloski, Zoran
Urbina Gomez, David Alejandro
Rupprecht, Jens
Mueller-Roeber, Bernd
Genome-Wide Identification of Regulatory Elements and Reconstruction of Gene Regulatory Networks of the Green Alga Chlamydomonas reinhardtii under Carbon Deprivation
title Genome-Wide Identification of Regulatory Elements and Reconstruction of Gene Regulatory Networks of the Green Alga Chlamydomonas reinhardtii under Carbon Deprivation
title_full Genome-Wide Identification of Regulatory Elements and Reconstruction of Gene Regulatory Networks of the Green Alga Chlamydomonas reinhardtii under Carbon Deprivation
title_fullStr Genome-Wide Identification of Regulatory Elements and Reconstruction of Gene Regulatory Networks of the Green Alga Chlamydomonas reinhardtii under Carbon Deprivation
title_full_unstemmed Genome-Wide Identification of Regulatory Elements and Reconstruction of Gene Regulatory Networks of the Green Alga Chlamydomonas reinhardtii under Carbon Deprivation
title_short Genome-Wide Identification of Regulatory Elements and Reconstruction of Gene Regulatory Networks of the Green Alga Chlamydomonas reinhardtii under Carbon Deprivation
title_sort genome-wide identification of regulatory elements and reconstruction of gene regulatory networks of the green alga chlamydomonas reinhardtii under carbon deprivation
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3816576/
https://www.ncbi.nlm.nih.gov/pubmed/24224019
http://dx.doi.org/10.1371/journal.pone.0079909
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