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Tytuł:
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Comparative transcriptome profiling of chilling stress responsiveness in two contrasting rice genotypes.
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Autorzy:
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Zhang T; Engineering Research Center for Plant Biotechnology and Germplasm Utilization, Ministry of Education, State Key Laboratory of Hybrid Rice, College of Life Sciences, Wuhan University, Wuhan, China.
Zhao X
Wang W
Pan Y
Huang L
Liu X
Zong Y
Zhu L
Yang D
Fu B
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Źródło:
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PloS one [PLoS One] 2012; Vol. 7 (8), pp. e43274. Date of Electronic Publication: 2012 Aug 17.
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Typ publikacji:
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Comparative Study; Journal Article; Research Support, Non-U.S. Gov't
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Język:
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English
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Imprint Name(s):
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Original Publication: San Francisco, CA : Public Library of Science
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MeSH Terms:
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Cold Temperature*
Gene Expression Regulation, Plant/*genetics
Oryza/*genetics
Stress, Physiological/*genetics
Cluster Analysis ; Gene Expression Profiling ; Gene Expression Regulation, Plant/physiology ; Genotype ; Oligonucleotide Array Sequence Analysis ; Quantitative Trait Loci/genetics ; Real-Time Polymerase Chain Reaction ; Regulon/genetics ; Stress, Physiological/physiology ; Time Factors
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References:
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Molecular Sequence:
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GEO GSE38023
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Entry Date(s):
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Date Created: 20120823 Date Completed: 20130501 Latest Revision: 20220311
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Update Code:
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20240104
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PubMed Central ID:
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PMC3422246
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DOI:
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10.1371/journal.pone.0043274
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PMID:
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22912843
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Rice is sensitive to chilling stress, especially at the seedling stage. To elucidate the molecular genetic mechanisms of chilling tolerance in rice, comprehensive gene expressions of two rice genotypes (chilling-tolerant LTH and chilling-sensitive IR29) with contrasting responses to chilling stress were comparatively analyzed. Results revealed a differential constitutive gene expression prior to stress and distinct global transcription reprogramming between the two rice genotypes under time-series chilling stress and subsequent recovery conditions. A set of genes with higher basal expression were identified in chilling-tolerant LTH compared with chilling-sensitive IR29, indicating their possible role in intrinsic tolerance to chilling stress. Under chilling stress, the major effect on gene expression was up-regulation in the chilling- tolerant genotype and strong repression in chilling-sensitive genotype. Early responses to chilling stress in both genotypes featured commonly up-regulated genes related to transcription regulation and signal transduction, while functional categories for late phase chilling regulated genes were diverse with a wide range of functional adaptations to continuous stress. Following the cessation of chilling treatments, there was quick and efficient reversion of gene expression in the chilling-tolerant genotype, while the chilling-sensitive genotype displayed considerably slower recovering capacity at the transcriptional level. In addition, the detection of differentially-regulated TF genes and enriched cis-elements demonstrated that multiple regulatory pathways, including CBF and MYBS3 regulons, were involved in chilling stress tolerance. A number of the chilling-regulated genes identified in this study were co-localized onto previously fine-mapped cold-tolerance-related QTLs, providing candidates for gene cloning and elucidation of molecular mechanisms responsible for chilling tolerance in rice.