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      C2H2 Zinc Finger Proteins: Master Regulators of Abiotic Stress Responses in Plants

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          Abstract

          Abiotic stresses such as drought and salinity are major environmental factors that limit crop yields. Unraveling the molecular mechanisms underlying abiotic stress resistance is crucial for improving crop performance and increasing productivity under adverse environmental conditions. Zinc finger proteins, comprising one of the largest transcription factor families, are known for their finger-like structure and their ability to bind Zn 2+. Zinc finger proteins are categorized into nine subfamilies based on their conserved Cys and His motifs, including the Cys2/His2-type (C2H2), C3H, C3HC4, C2HC5, C4HC3, C2HC, C4, C6, and C8 subfamilies. Over the past two decades, much progress has been made in understanding the roles of C2H2 zinc finger proteins in plant growth, development, and stress signal transduction. In this review, we focus on recent progress in elucidating the structures, functions, and classifications of plant C2H2 zinc finger proteins and their roles in abiotic stress responses.

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          Most cited references140

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          Drought and Salt Tolerance in Plants

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            Organization of cis-acting regulatory elements in osmotic- and cold-stress-responsive promoters.

            cis-Acting regulatory elements are important molecular switches involved in the transcriptional regulation of a dynamic network of gene activities controlling various biological processes, including abiotic stress responses, hormone responses and developmental processes. In particular, understanding regulatory gene networks in stress response cascades depends on successful functional analyses of cis-acting elements. The ever-improving accuracy of transcriptome expression profiling has led to the identification of various combinations of cis-acting elements in the promoter regions of stress-inducible genes involved in stress and hormone responses. Here we discuss major cis-acting elements, such as the ABA-responsive element (ABRE) and the dehydration-responsive element/C-repeat (DRE/CRT), that are a vital part of ABA-dependent and ABA-independent gene expression in osmotic and cold stress responses.
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              COLD1 confers chilling tolerance in rice.

              Rice is sensitive to cold and can be grown only in certain climate zones. Human selection of japonica rice has extended its growth zone to regions with lower temperature, while the molecular basis of this adaptation remains unknown. Here, we identify the quantitative trait locus COLD1 that confers chilling tolerance in japonica rice. Overexpression of COLD1(jap) significantly enhances chilling tolerance, whereas rice lines with deficiency or downregulation of COLD1(jap) are sensitive to cold. COLD1 encodes a regulator of G-protein signaling that localizes on plasma membrane and endoplasmic reticulum (ER). It interacts with the G-protein α subunit to activate the Ca(2+) channel for sensing low temperature and to accelerate G-protein GTPase activity. We further identify that a SNP in COLD1, SNP2, originated from Chinese Oryza rufipogon, is responsible for the ability of COLD(jap/ind) to confer chilling tolerance, supporting the importance of COLD1 in plant adaptation.
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                Author and article information

                Contributors
                Journal
                Front Plant Sci
                Front Plant Sci
                Front. Plant Sci.
                Frontiers in Plant Science
                Frontiers Media S.A.
                1664-462X
                20 February 2020
                2020
                : 11
                : 115
                Affiliations
                [1] 1Shandong Provincial Key Laboratory of Plant Stress, College of Life Sciences, Shandong Normal University , Jinan, China
                [2] 2College of Life Sciences, Qufu Normal University , Qufu, China
                Author notes

                Edited by: Vicent Arbona, University of Jaume I, Spain

                Reviewed by: Yong Hwa Cheong, Sunchon National University, South Korea; Arafat Abdel Hamed Abdel Latef, South Valley University, Egypt

                *Correspondence: Baoshan Wang, bswang@ 123456sdnu.edu.cn

                This article was submitted to Plant Abiotic Stress, a section of the journal Frontiers in Plant Science

                Article
                10.3389/fpls.2020.00115
                7044346
                32153617
                2f892b7c-18eb-4111-a434-6166efff1200
                Copyright © 2020 Han, Lu, Guo, Qiao, Sui, Qiu and Wang

                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.

                History
                : 03 October 2019
                : 24 January 2020
                Page count
                Figures: 2, Tables: 0, Equations: 0, References: 171, Pages: 13, Words: 6358
                Categories
                Plant Science
                Review

                Plant science & Botany
                abiotic stress,adaptation mechanism,c2h2 zinc finger proteins,plant,signaling pathways,stress response networks

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