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The histidine phosphotransfer AHP4 plays a negative role in Arabidopsis plant response to drought.
Ha, Chien Van; Mostofa, Mohammad Golam; Nguyen, Kien Huu; Tran, Cuong Duy; Watanabe, Yasuko; Li, Weiqiang; Osakabe, Yuriko; Sato, Mayuko; Toyooka, Kiminori; Tanaka, Maho; Seki, Motoaki; Burritt, David J; Anderson, Cheyenne Marie; Zhang, Ru; Nguyen, Huong Mai; Le, Vy Phuong; Bui, Hien Thuy; Mochida, Keiichi; Tran, Lam-Son Phan.
Afiliación
  • Ha CV; Stress Adaptation Research Unit, RIKEN Center for Sustainable Resource Science, Yokohama, 230-0045, Japan.
  • Mostofa MG; Donald Danforth Plant Science Center, 975 N Warson Rd, Saint Louis, Missouri, 63132, USA.
  • Nguyen KH; Institute of Genomics for Crop Abiotic Stress Tolerance, Department of Plant and Soil Science, Texas Tech University, 2500 Broadway, Lubbock, Texas, 79409, USA.
  • Tran CD; Stress Adaptation Research Unit, RIKEN Center for Sustainable Resource Science, Yokohama, 230-0045, Japan.
  • Watanabe Y; Institute of Genomics for Crop Abiotic Stress Tolerance, Department of Plant and Soil Science, Texas Tech University, 2500 Broadway, Lubbock, Texas, 79409, USA.
  • Li W; Stress Adaptation Research Unit, RIKEN Center for Sustainable Resource Science, Yokohama, 230-0045, Japan.
  • Osakabe Y; Agricultural Genetics Institute, Vietnam Academy of Agricultural Sciences, Hanoi, 100000, Vietnam.
  • Sato M; Stress Adaptation Research Unit, RIKEN Center for Sustainable Resource Science, Yokohama, 230-0045, Japan.
  • Toyooka K; Agricultural Genetics Institute, Vietnam Academy of Agricultural Sciences, Hanoi, 100000, Vietnam.
  • Tanaka M; Stress Adaptation Research Unit, RIKEN Center for Sustainable Resource Science, Yokohama, 230-0045, Japan.
  • Seki M; Stress Adaptation Research Unit, RIKEN Center for Sustainable Resource Science, Yokohama, 230-0045, Japan.
  • Burritt DJ; Jilin Da'an Agro-ecosystem National Observation Research Station, Changchun Jingyuetan Remote Sensing Experiment Station, Key Laboratory of Mollisols Agroecology, Northeast Institute of Geography and Agroecology, Chinese Academy of Sciences, Changchun, 130102, China.
  • Anderson CM; Institute of Plant Stress Biology, State Key Laboratory of Cotton Biology, Department of Biology, Henan University, 85 Minglun Street, Kaifeng, 475001, China.
  • Zhang R; School of Life Science and Technology, Tokyo Institute of Technology, J2-12, 4259 Nagatsuda-cho, Midori-ku, Yokohama, Kanagawa, 226-8502, Japan.
  • Nguyen HM; Mass Spectrometry and Microscopy Unit, RIKEN Center for Sustainable Resource Science, Yokohama, 230-0045, Japan.
  • Le VP; Mass Spectrometry and Microscopy Unit, RIKEN Center for Sustainable Resource Science, Yokohama, 230-0045, Japan.
  • Bui HT; Plant Genomic Network Research Team, RIKEN Center for Sustainable Resource Science, Yokohama, 230-0045, Japan.
  • Mochida K; Plant Epigenome Regulation Laboratory, RIKEN Cluster for Pioneering Research, Wako, Saitama, 351-0198, Japan.
  • Tran LP; Plant Genomic Network Research Team, RIKEN Center for Sustainable Resource Science, Yokohama, 230-0045, Japan.
Plant J ; 111(6): 1732-1752, 2022 09.
Article en En | MEDLINE | ID: mdl-35883014
ABSTRACT
Cytokinin plays an important role in plant stress responses via a multistep signaling pathway, involving the histidine phosphotransfer proteins (HPs). In Arabidopsis thaliana, the AHP2, AHP3 and AHP5 proteins are known to affect drought responses; however, the role of AHP4 in drought adaptation remains undetermined. In the present study, using a loss-of-function approach we showed that AHP4 possesses an important role in the response of Arabidopsis to drought. This is evidenced by the higher survival rates of ahp4 than wild-type (WT) plants under drought conditions, which is accompanied by the downregulated AHP4 expression in WT during periods of dehydration. Comparative transcriptome analysis of ahp4 and WT plants revealed AHP4-mediated expression of several dehydration- and/or abscisic acid-responsive genes involved in modulation of various physiological and biochemical processes important for plant drought acclimation. In comparison with WT, ahp4 plants showed increased wax crystal accumulation in stems, thicker cuticles in leaves, greater sensitivity to exogenous abscisic acid at germination, narrow stomatal apertures, heightened leaf temperatures during dehydration, and longer root length under osmotic stress. In addition, ahp4 plants showed greater photosynthetic efficiency, lower levels of reactive oxygen species, reduced electrolyte leakage and lipid peroxidation, and increased anthocyanin contents under drought, when compared with WT. These differences displayed in ahp4 plants are likely due to upregulation of genes that encode enzymes involved in reactive oxygen species scavenging and non-enzymatic antioxidant metabolism. Overall, our findings suggest that AHP4 plays a crucial role in plant drought adaptation.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Arabidopsis / Proteínas de Arabidopsis Idioma: En Revista: Plant J Asunto de la revista: BIOLOGIA MOLECULAR / BOTANICA Año: 2022 Tipo del documento: Article País de afiliación: Japón

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Arabidopsis / Proteínas de Arabidopsis Idioma: En Revista: Plant J Asunto de la revista: BIOLOGIA MOLECULAR / BOTANICA Año: 2022 Tipo del documento: Article País de afiliación: Japón