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Rice H2A.Z negatively regulates genes responsive to nutrient starvation but promotes expression of key housekeeping genes

The H2A.Z histone variant plays a role in the modulation of environmental responses, but the nature of the associated mechanisms remains enigmatic. We investigated global H2A.Z deposition and transcriptomic changes in rice (Oryza sativa) upon exposure to phosphate (Pi) deficiency and in response to...

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Autores principales: Zahraeifard, Sara, Foroozani, Maryam, Sepehri, Aliasghar, Oh, Dong-Ha, Wang, Guannan, Mangu, Venkata, Chen, Bin, Baisakh, Niranjan, Dassanayake, Maheshi, Smith, Aaron P
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6137989/
https://www.ncbi.nlm.nih.gov/pubmed/29955860
http://dx.doi.org/10.1093/jxb/ery244
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author Zahraeifard, Sara
Foroozani, Maryam
Sepehri, Aliasghar
Oh, Dong-Ha
Wang, Guannan
Mangu, Venkata
Chen, Bin
Baisakh, Niranjan
Dassanayake, Maheshi
Smith, Aaron P
author_facet Zahraeifard, Sara
Foroozani, Maryam
Sepehri, Aliasghar
Oh, Dong-Ha
Wang, Guannan
Mangu, Venkata
Chen, Bin
Baisakh, Niranjan
Dassanayake, Maheshi
Smith, Aaron P
author_sort Zahraeifard, Sara
collection PubMed
description The H2A.Z histone variant plays a role in the modulation of environmental responses, but the nature of the associated mechanisms remains enigmatic. We investigated global H2A.Z deposition and transcriptomic changes in rice (Oryza sativa) upon exposure to phosphate (Pi) deficiency and in response to RNAi knockdown of OsARP6, which encodes a key component of the H2A.Z exchange complex. Both Pi deficiency and OsARP6-knockdown resulted in similar, profound effects on global H2A.Z distribution. H2A.Z in the gene body of stress-responsive genes was negatively correlated with gene expression, and this was more apparent in response to Pi deficiency. In contrast, the role of H2A.Z at the transcription start site (TSS) was more context dependent, acting as a repressor of some stress-responsive genes, but an activator of some genes with housekeeping functions. This was especially evident upon OsARP6-knockdown, which resulted in down-regulation of a number of genes linked to chloroplast function that contained decreases in H2A.Z at the TSS. Consistently, OsARP6-RNAi plants exhibited lower chlorophyll content relative to the wild-type. Our results demonstrate that gene body-localized H2A.Z plays a prominent role in repressing stress-responsive genes under non-inductive conditions, whereas H2A.Z at the TSS functions as a positive or negative regulator of transcription.
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spelling pubmed-61379892018-09-24 Rice H2A.Z negatively regulates genes responsive to nutrient starvation but promotes expression of key housekeeping genes Zahraeifard, Sara Foroozani, Maryam Sepehri, Aliasghar Oh, Dong-Ha Wang, Guannan Mangu, Venkata Chen, Bin Baisakh, Niranjan Dassanayake, Maheshi Smith, Aaron P J Exp Bot Research Papers The H2A.Z histone variant plays a role in the modulation of environmental responses, but the nature of the associated mechanisms remains enigmatic. We investigated global H2A.Z deposition and transcriptomic changes in rice (Oryza sativa) upon exposure to phosphate (Pi) deficiency and in response to RNAi knockdown of OsARP6, which encodes a key component of the H2A.Z exchange complex. Both Pi deficiency and OsARP6-knockdown resulted in similar, profound effects on global H2A.Z distribution. H2A.Z in the gene body of stress-responsive genes was negatively correlated with gene expression, and this was more apparent in response to Pi deficiency. In contrast, the role of H2A.Z at the transcription start site (TSS) was more context dependent, acting as a repressor of some stress-responsive genes, but an activator of some genes with housekeeping functions. This was especially evident upon OsARP6-knockdown, which resulted in down-regulation of a number of genes linked to chloroplast function that contained decreases in H2A.Z at the TSS. Consistently, OsARP6-RNAi plants exhibited lower chlorophyll content relative to the wild-type. Our results demonstrate that gene body-localized H2A.Z plays a prominent role in repressing stress-responsive genes under non-inductive conditions, whereas H2A.Z at the TSS functions as a positive or negative regulator of transcription. Oxford University Press 2018-09-14 2018-06-28 /pmc/articles/PMC6137989/ /pubmed/29955860 http://dx.doi.org/10.1093/jxb/ery244 Text en © The Author(s) 2018. Published by Oxford University Press on behalf of the Society for Experimental Biology. 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 Research Papers
Zahraeifard, Sara
Foroozani, Maryam
Sepehri, Aliasghar
Oh, Dong-Ha
Wang, Guannan
Mangu, Venkata
Chen, Bin
Baisakh, Niranjan
Dassanayake, Maheshi
Smith, Aaron P
Rice H2A.Z negatively regulates genes responsive to nutrient starvation but promotes expression of key housekeeping genes
title Rice H2A.Z negatively regulates genes responsive to nutrient starvation but promotes expression of key housekeeping genes
title_full Rice H2A.Z negatively regulates genes responsive to nutrient starvation but promotes expression of key housekeeping genes
title_fullStr Rice H2A.Z negatively regulates genes responsive to nutrient starvation but promotes expression of key housekeeping genes
title_full_unstemmed Rice H2A.Z negatively regulates genes responsive to nutrient starvation but promotes expression of key housekeeping genes
title_short Rice H2A.Z negatively regulates genes responsive to nutrient starvation but promotes expression of key housekeeping genes
title_sort rice h2a.z negatively regulates genes responsive to nutrient starvation but promotes expression of key housekeeping genes
topic Research Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6137989/
https://www.ncbi.nlm.nih.gov/pubmed/29955860
http://dx.doi.org/10.1093/jxb/ery244
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