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Chlorosis seedling lethality 1 encoding a MAP3K protein is essential for chloroplast development in rice

BACKGROUND: Mitogen-activated protein kinase (MAPK) cascades are conserved signaling modules in eukaryotic organisms and play essential roles in immunity and stress responses. However, the role of MAPKs in chloroplast development remains to be evidently established. RESULTS: In this study, a rice ch...

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Autores principales: Liang, Jiayan, Zhang, Qiuxin, Liu, Yiran, Zhang, Jingjing, Wang, Wenyi, Zhang, Zemin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8734211/
https://www.ncbi.nlm.nih.gov/pubmed/34991480
http://dx.doi.org/10.1186/s12870-021-03404-9
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author Liang, Jiayan
Zhang, Qiuxin
Liu, Yiran
Zhang, Jingjing
Wang, Wenyi
Zhang, Zemin
author_facet Liang, Jiayan
Zhang, Qiuxin
Liu, Yiran
Zhang, Jingjing
Wang, Wenyi
Zhang, Zemin
author_sort Liang, Jiayan
collection PubMed
description BACKGROUND: Mitogen-activated protein kinase (MAPK) cascades are conserved signaling modules in eukaryotic organisms and play essential roles in immunity and stress responses. However, the role of MAPKs in chloroplast development remains to be evidently established. RESULTS: In this study, a rice chlorosis seedling lethality 1 (csl1) mutant with a Zhonghua11 (ZH11, japonica) background was isolated. Seedlings of the mutant were characterized by chlorotic leaves and death after the trefoil stage, and chloroplasts were observed to contain accumulated starch granules. Molecular cloning revealed that OsCSL1 encoded a MAPK kinase kinase22 (MKKK22) targeted to the endoplasmic reticulum (ER), and functional complementation of OsCSL1 was found to restore the normal phenotype in csl1 plants. The CRISPR/Cas9 technology was used for targeted disruption of OsCSL1, and the OsCSL1-Cas9 lines obtained therein exhibited yellow seedlings which phenocopied the csl1 mutant. CSL1/MKKK22 was observed to establish direct interaction with MKK4, and altered expression of MKK1 and MKK4 was detected in the csl1 mutant. Additionally, disruption of OsCSL1 led to reduced expression of chloroplast-associated genes, including chlorophyll biosynthetic genes, plastid-encoded RNA polymerases, nuclear-encoded RNA polymerase, and nuclear-encoded chloroplast genes. CONCLUSIONS: The findings of this study revealed that OsCSL1 played roles in regulating the expression of multiple chloroplast synthesis-related genes, thereby affecting their functions, and leading to wide-ranging defects, including chlorotic seedlings and severely disrupted chloroplasts containing accumulated starch granules. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12870-021-03404-9.
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spelling pubmed-87342112022-01-07 Chlorosis seedling lethality 1 encoding a MAP3K protein is essential for chloroplast development in rice Liang, Jiayan Zhang, Qiuxin Liu, Yiran Zhang, Jingjing Wang, Wenyi Zhang, Zemin BMC Plant Biol Research BACKGROUND: Mitogen-activated protein kinase (MAPK) cascades are conserved signaling modules in eukaryotic organisms and play essential roles in immunity and stress responses. However, the role of MAPKs in chloroplast development remains to be evidently established. RESULTS: In this study, a rice chlorosis seedling lethality 1 (csl1) mutant with a Zhonghua11 (ZH11, japonica) background was isolated. Seedlings of the mutant were characterized by chlorotic leaves and death after the trefoil stage, and chloroplasts were observed to contain accumulated starch granules. Molecular cloning revealed that OsCSL1 encoded a MAPK kinase kinase22 (MKKK22) targeted to the endoplasmic reticulum (ER), and functional complementation of OsCSL1 was found to restore the normal phenotype in csl1 plants. The CRISPR/Cas9 technology was used for targeted disruption of OsCSL1, and the OsCSL1-Cas9 lines obtained therein exhibited yellow seedlings which phenocopied the csl1 mutant. CSL1/MKKK22 was observed to establish direct interaction with MKK4, and altered expression of MKK1 and MKK4 was detected in the csl1 mutant. Additionally, disruption of OsCSL1 led to reduced expression of chloroplast-associated genes, including chlorophyll biosynthetic genes, plastid-encoded RNA polymerases, nuclear-encoded RNA polymerase, and nuclear-encoded chloroplast genes. CONCLUSIONS: The findings of this study revealed that OsCSL1 played roles in regulating the expression of multiple chloroplast synthesis-related genes, thereby affecting their functions, and leading to wide-ranging defects, including chlorotic seedlings and severely disrupted chloroplasts containing accumulated starch granules. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12870-021-03404-9. BioMed Central 2022-01-06 /pmc/articles/PMC8734211/ /pubmed/34991480 http://dx.doi.org/10.1186/s12870-021-03404-9 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Liang, Jiayan
Zhang, Qiuxin
Liu, Yiran
Zhang, Jingjing
Wang, Wenyi
Zhang, Zemin
Chlorosis seedling lethality 1 encoding a MAP3K protein is essential for chloroplast development in rice
title Chlorosis seedling lethality 1 encoding a MAP3K protein is essential for chloroplast development in rice
title_full Chlorosis seedling lethality 1 encoding a MAP3K protein is essential for chloroplast development in rice
title_fullStr Chlorosis seedling lethality 1 encoding a MAP3K protein is essential for chloroplast development in rice
title_full_unstemmed Chlorosis seedling lethality 1 encoding a MAP3K protein is essential for chloroplast development in rice
title_short Chlorosis seedling lethality 1 encoding a MAP3K protein is essential for chloroplast development in rice
title_sort chlorosis seedling lethality 1 encoding a map3k protein is essential for chloroplast development in rice
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8734211/
https://www.ncbi.nlm.nih.gov/pubmed/34991480
http://dx.doi.org/10.1186/s12870-021-03404-9
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