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胁迫条件下水稻(Oryza sativa L.)培养细胞的表达序列标签:参与ATP生成途径的基因转录本分析

Expressed sequence tags from cultured cells of rice (Oryza sativa L.) under stressed conditions: analysis of transcripts of genes engaged in ATP-generating pathways.

作者信息

Umeda M, Hara C, Matsubayashi Y, Li H H, Liu Q, Tadokoro F, Aotsuka S, Uchimiya H

机构信息

Institute of Molecular and Cellular Biosciences, University of Tokyo, Japan.

出版信息

Plant Mol Biol. 1994 Jun;25(3):469-78. doi: 10.1007/BF00043875.

Abstract

Large-scale sequencing of randomly selected cDNA clones was used to isolate numerous genes in rice (Oryza sativa L.). Total RNA used for cDNA synthesis was prepared from suspension-cultured cells of rice grown under stressed conditions, such as in saline or nitrogen-starvation conditions. A total of 780 cDNA clones were partially sequenced and about 15% could be identified as putative genes. In the library constructed under saline conditions, we identified several genes associated with signal transduction, such as protein kinase and small GTP-binding protein genes. Many stress-related genes were isolated from both the saline and nitrogen-starvation libraries. These results indicate that stress treatment of suspension-cultured cells makes it possible to efficiently isolate various types of plant genes. To examine the usefulness of such tagged cDNAs for the study of gene expression in a specific metabolic pathway, we analyzed mRNA levels of genes engaged in the ATP-generating pathways in cultured cells of rice under different stresses, such as 20% sucrose, salt stress, cold stress and nitrogen-starvation stress. The results suggest that the coordinated induction of several genes in key steps under stressed conditions may be essential for activation of the entire energy-producing pathway to maintain homeostasis in rice cells. Expressed sequence tags identified by random cDNA sequencing provide the opportunity to generate a transcript map of rice genes.

摘要

通过对随机选择的cDNA克隆进行大规模测序,从水稻(Oryza sativa L.)中分离出了许多基因。用于合成cDNA的总RNA是从在胁迫条件下生长的水稻悬浮培养细胞中制备的,这些胁迫条件诸如盐胁迫或氮饥饿条件。总共对780个cDNA克隆进行了部分测序,其中约15%可鉴定为推定基因。在盐胁迫条件下构建的文库中,我们鉴定出了几个与信号转导相关的基因,如蛋白激酶和小GTP结合蛋白基因。从盐胁迫文库和氮饥饿文库中都分离出了许多与胁迫相关的基因。这些结果表明,对悬浮培养细胞进行胁迫处理能够有效地分离出各种类型的植物基因。为了检验此类带标签的cDNA在研究特定代谢途径中基因表达方面的实用性,我们分析了水稻培养细胞在不同胁迫(如20%蔗糖、盐胁迫、冷胁迫和氮饥饿胁迫)下参与ATP生成途径的基因的mRNA水平。结果表明,在胁迫条件下关键步骤中几个基因的协同诱导对于激活整个能量产生途径以维持水稻细胞的稳态可能至关重要。通过随机cDNA测序鉴定出的表达序列标签为生成水稻基因转录图谱提供了机会。

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