Literature DB >> 20807373

Supra-optimal expression of the cold-regulated OsMyb4 transcription factor in transgenic rice changes the complexity of transcriptional network with major effects on stress tolerance and panicle development.

Myoung-Ryoul Park1, Kil-Young Yun, Bijayalaxmi Mohanty, Venura Herath, Fuyu Xu, Edward Wijaya, Vladimir B Bajic, Song-Joong Yun, Benildo G De Los Reyes.   

Abstract

The R2R3-type OsMyb4 transcription factor of rice has been shown to play a role in the regulation of osmotic adjustment in heterologous overexpression studies. However, the exact composition and organization of its underlying transcriptional network has not been established to be a robust tool for stress tolerance enhancement by regulon engineering. OsMyb4 network was dissected based on commonalities between the global chilling stress transcriptome and the transcriptome configured by OsMyb4 overexpression. OsMyb4 controls a hierarchical network comprised of several regulatory sub-clusters associated with cellular defense and rescue, metabolism and development. It regulates target genes either directly or indirectly through intermediary MYB, ERF, bZIP, NAC, ARF and CCAAT-HAP transcription factors. Regulatory sub-clusters have different combinations of MYB-like, GCC-box-like, ERD1-box-like, ABRE-like, G-box-like, as1/ocs/TGA-like, AuxRE-like, gibberellic acid response element (GARE)-like and JAre-like cis-elements. Cold-dependent network activity enhanced cellular antioxidant capacity through radical scavenging mechanisms and increased activities of phenylpropanoid and isoprenoid metabolic processes involving various abscisic acid (ABA), jasmonic acid (JA), salicylic acid (SA), ethylene and reactive oxygen species (ROS) responsive genes. OsMyb4 network is independent of drought response element binding protein/C-repeat binding factor (DREB/CBF) and its sub-regulons operate with possible co-regulators including nuclear factor-Y. Because of its upstream position in the network hierarchy, OsMyb4 functions quantitatively and pleiotrophically. Supra-optimal expression causes misexpression of alternative targets with costly trade-offs to panicle development.
© 2010 Blackwell Publishing Ltd.

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Year:  2010        PMID: 20807373     DOI: 10.1111/j.1365-3040.2010.02221.x

Source DB:  PubMed          Journal:  Plant Cell Environ        ISSN: 0140-7791            Impact factor:   7.228


  36 in total

1.  The rice Osmyb4 gene enhances tolerance to frost and improves germination under unfavourable conditions in transgenic barley plants.

Authors:  Alexandra Soltész; Attila Vágújfalvi; Fulvia Rizza; Ildikó Kerepesi; Gábor Galiba; Luigi Cattivelli; Immacolata Coraggio; Cristina Crosatti
Journal:  J Appl Genet       Date:  2012-01-14       Impact factor: 3.240

Review 2.  Physiological and molecular changes in plants grown at low temperatures.

Authors:  Andreas Theocharis; Christophe Clément; Essaïd Ait Barka
Journal:  Planta       Date:  2012-04-20       Impact factor: 4.116

3.  Identification of transcriptome profiles and signaling pathways for the allelochemical juglone in rice roots.

Authors:  Wen-Chang Chi; Shih-Feng Fu; Tsai-Lien Huang; Yun-An Chen; Chi-Cien Chen; Hao-Jen Huang
Journal:  Plant Mol Biol       Date:  2011-11-05       Impact factor: 4.076

4.  Natural variation in the HAN1 gene confers chilling tolerance in rice and allowed adaptation to a temperate climate.

Authors:  Donghai Mao; Yeyun Xin; Yongjun Tan; Xiaojie Hu; Jiaojiao Bai; Zhao-Ying Liu; Yilan Yu; Lanying Li; Can Peng; Tony Fan; Yuxing Zhu; Ya-Long Guo; Songhu Wang; Dongping Lu; Yongzhong Xing; Longping Yuan; Caiyan Chen
Journal:  Proc Natl Acad Sci U S A       Date:  2019-02-11       Impact factor: 11.205

5.  The OsMYB30 Transcription Factor Suppresses Cold Tolerance by Interacting with a JAZ Protein and Suppressing β-Amylase Expression.

Authors:  Yan Lv; Mei Yang; Dan Hu; Zeyu Yang; Siqi Ma; Xianghua Li; Lizhong Xiong
Journal:  Plant Physiol       Date:  2017-01-06       Impact factor: 8.340

6.  Analysis of differential gene expression in cold-tolerant vs. cold-sensitive varieties of snap bean (Phaseolus vulgaris L.) in response to low temperature stress.

Authors:  Chang Liu; Xiaoxu Yang; Zhishan Yan; Youjun Fan; Guojun Feng; Dajun Liu
Journal:  Genes Genomics       Date:  2019-09-18       Impact factor: 1.839

7.  QTL mapping and development of candidate gene-derived DNA markers associated with seedling cold tolerance in rice (Oryza sativa L.).

Authors:  Suk-Man Kim; Jung-Pil Suh; Chung-Koon Lee; Jeong-Heui Lee; Yeong-Gyu Kim; Kshirod Kumar Jena
Journal:  Mol Genet Genomics       Date:  2014-01-24       Impact factor: 3.291

8.  Transcriptomic changes and signalling pathways induced by arsenic stress in rice roots.

Authors:  Tsai-Lien Huang; Quynh Thi Thuy Nguyen; Shih-Feng Fu; Chung-Yi Lin; Ying-Chih Chen; Hao-Jen Huang
Journal:  Plant Mol Biol       Date:  2012-09-18       Impact factor: 4.076

9.  OsbZIP71, a bZIP transcription factor, confers salinity and drought tolerance in rice.

Authors:  Citao Liu; Bigang Mao; Shujun Ou; Wei Wang; Linchuan Liu; Yanbin Wu; Chengcai Chu; Xiping Wang
Journal:  Plant Mol Biol       Date:  2013-08-06       Impact factor: 4.076

10.  A CCR4-associated factor 1, OsCAF1B, confers tolerance of low-temperature stress to rice seedlings.

Authors:  Jhen-Cheng Fang; Yin-Chuan Tsai; Wei-Lun Chou; Hsin-Yi Liu; Chun-Chen Chang; Shaw-Jye Wu; Chung-An Lu
Journal:  Plant Mol Biol       Date:  2020-10-06       Impact factor: 4.076

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