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1.
BMC Genomics ; 17(1): 870, 2016 11 04.
Article in English | MEDLINE | ID: mdl-27814694

ABSTRACT

BACKGROUND: Elymus nutans Griseb., is an important alpine perennial forage of Pooideae subfamily with strong inherited cold tolerance. To get a deeper insight into its molecular mechanisms of cold tolerance, we compared the transcriptome profiling by RNA-Seq in two genotypes of Elymus nutans Griseb. the tolerant Damxung (DX) and the sensitive Gannan (GN) under cold stress. RESULTS: The new E. nutans transcriptomes were assembled and comprised 200,520 and 181,331 transcripts in DX and GN, respectively. Among them, 5436 and 4323 genes were differentially expressed in DX and GN, with 170 genes commonly expressed over time. Early cold responses involved numerous genes encoding transcription factors and signal transduction in both genotypes. The AP2/EREBP famliy of transcription factors was predominantly expressed in both genotypes. The most significant transcriptomic changes in the later phases of cold stress are associated with oxidative stress, primary and secondary metabolism, and photosynthesis. Higher fold expressions of fructan, trehalose, and alpha-linolenic acid metabolism-related genes were detected in DX. The DX-specific dehydrins may be promising candidates to improve cold tolerance. Twenty-six hub genes played a central role in both genotypes under cold stress. qRT-PCR analysis of 26 genes confirmed the RNA-Seq results. CONCLUSIONS: The stronger transcriptional differentiation during cold stress in DX explains its better cold tolerance compared to GN. The identified fructan biosynthesis, alpha-linolenic acid metabolism, and DX-specific dehydrin-related genes may provide genetic resources for the improvement of cold-tolerant characters in DX. Our findings provide important clues for further studies of the molecular mechanisms underlying cold stress responses in plants.


Subject(s)
Cold-Shock Response/genetics , Elymus/genetics , Gene Expression Profiling , Transcriptome , Adaptation, Biological/genetics , Cluster Analysis , Computational Biology/methods , Gene Expression Regulation, Plant , Gene Regulatory Networks , Genotype , Molecular Sequence Annotation , Plant Growth Regulators/metabolism , Reproducibility of Results , Signal Transduction
2.
J Plant Res ; 129(5): 935-944, 2016 Sep.
Article in English | MEDLINE | ID: mdl-27216422

ABSTRACT

Gibberellins (GAs) affect forage growth and development; however, it is largely unknown how GAs regulate the metabolism of fructan (an important polysaccharide reserve in many cereals) and the regrowth of forage plants after defoliation. To explore the mechanism of the responses of defoliated sheepgrass [Leymus chinensis (Trin.) Tzvel] to GA, we sprayed defoliated sheepgrass with GA3 and/or paclobutrazol (PAC; an inhibitor of GA biosynthesis) and analyzed the growth characteristics, carbohydrate contents, and transcript levels of genes related to GA metabolism, GA signal transduction, and fructan metabolism. The results showed that spraying exogenous GA3 onto defoliated sheepgrass promoted leaf and internode elongation, while spraying with PAC inhibited leaf and internode elongation, compared with the control. Spraying GA3 onto defoliated sheepgrass also altered the fructan content by extending the period of fructan utilization. At the transcriptional level, exogenous GA3 increased the transcript levels of genes related to GA metabolism in the sheath. Taken together, our results suggest that exogenous GA3 stimulates the regrowth of defoliated sheepgrass regrowth by regulating GA and fructan-related genes, and by promoting endogenous GA synthesis, fructan metabolism, and signaling.


Subject(s)
Fructans/genetics , Gene Expression Regulation, Plant/drug effects , Genes, Plant , Gibberellins/pharmacology , Plant Leaves/physiology , Poaceae/growth & development , Poaceae/genetics , Biological Transport/drug effects , Carbohydrate Metabolism/drug effects , Carbohydrate Metabolism/genetics , Fructans/metabolism , Gibberellins/metabolism , Plant Leaves/drug effects , Poaceae/drug effects , RNA, Messenger/genetics , RNA, Messenger/metabolism , Signal Transduction/drug effects , Signal Transduction/genetics , Sucrose/metabolism , Transcription, Genetic/drug effects , Triazoles/pharmacology
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