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硫酸盐浓度对大豆种子贮藏蛋白基因表达及其在转基因拟南芥中的可逆性影响

Effects of sulfate concentrations on the expression of a soybean seed storage protein gene and its reversibility in transgenic Arabidopsis thaliana.

作者信息

Hirai M Y, Fujiwara T, Chino M, Naito S

机构信息

Department of Applied Biological Chemistry, University of Tokyo, Japan.

出版信息

Plant Cell Physiol. 1995 Oct;36(7):1331-9.

PMID:8564302
Abstract

Transgenic expression of genes encoding the alpha' and beta subunits of beta-conglycinin, one of the major seed storage proteins of soybean (Glycine max [L.] Merr.), was analyzed in Arabidopsis thaliana (L.) Heynh. under conditions of sulfate deficiency. Temporal patterns of expression of both the intact beta subunit gene and the beta subunit gene promoter fused to the beta-glucuronidase (GUS) gene are similar in soil-less cultures using rockwool, suggesting that the response to sulfate deficiency is regulated mainly at the level of transcription. In hydroponic cultures with various concentrations of sulfate, expression of both the intact beta subunit gene and the beta subunit gene promoter-GUS fusion gene were negatively correlated to increased sulfate concentrations in the culture medium. Transfer of transgenic A. thaliana plants carrying the beta subunit gene promoter-GUS fusion from sulfate-deficient to sulfate-sufficient control medium caused GUS activity in developing siliques to be repressed within two days. A reverse shift, where the plants were transferred from the control to sulfate-deficient medium, caused GUS activity to become higher than that in seeds of the control plants within two days. These results indicate that the expression of the beta subunit gene promoter responds rapidly to changes of sulfate availability.

摘要

在拟南芥中分析了编码大豆(Glycine max [L.] Merr.)主要种子贮藏蛋白之一β-伴大豆球蛋白α'和β亚基的基因的转基因表达情况。在以岩棉为基质的无土培养中,完整β亚基基因以及与β-葡萄糖醛酸酶(GUS)基因融合的β亚基基因启动子的表达时间模式相似,这表明对硫酸盐缺乏的响应主要在转录水平上受到调控。在含有不同浓度硫酸盐的水培中,完整β亚基基因以及β亚基基因启动子-GUS融合基因的表达与培养基中硫酸盐浓度的增加呈负相关。将携带β亚基基因启动子-GUS融合基因的转基因拟南芥植株从缺硫酸盐培养基转移到含充足硫酸盐的对照培养基中,导致发育中的角果中的GUS活性在两天内受到抑制。相反的转移,即从对照培养基转移到缺硫酸盐培养基中,导致GUS活性在两天内高于对照植株种子中的活性。这些结果表明,β亚基基因启动子的表达对硫酸盐可利用性的变化反应迅速。

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