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马铃薯中编码HMG-CoA还原酶的基因的hmg 1亚家族的特征。

Features of the hmg 1 subfamily of genes encoding HMG-CoA reductase in potato.

作者信息

Bhattacharyya M K, Paiva N L, Dixon R A, Korth K L, Stermer B A

机构信息

Samuel Roberts Noble Foundation, Plant Biology Division, Ardmore, OK 73402, USA.

出版信息

Plant Mol Biol. 1995 Apr;28(1):1-15. doi: 10.1007/BF00042033.

Abstract

3-Hydroxy-3-methylglutaryl coenzyme A reductase (HMGR) catalyzes a key step in isoprenoid metabolism leading to a range of compounds that are important for the growth, development and health of the plant. We have isolated 7 classes of genomic clones encoding HMGR from a potato genomic library. Comparison of nucleic acid sequences reveals a high degree of identity between all seven classes of clones and the potato hmg 1 gene described by Choi et al. (Plant Cell 4: 1333, 1992), indicating that all are members of the same subfamily in potato. A representative member (hmg 1.2) of the most abundant class of genomic clones was selected for further characterization. Transgenic tobacco and potato containing the beta-glucuronidase (GUS) reporter gene under the control of the hmg 1.2 promoter expressed GUS activity constitutively at a low level in many plant tissues. High levels of GUS activity were observed only in the pollen. GUS assays of isolated pollen, correlations of GUS activity with the HMGR activity of anthers, hmg 1.2 promoter deletion studies, and segregation analysis of the expression of hmg 1.2::GUS among the R2 pollen of R1 progeny plants demonstrated that the hmg 1.2 promoter controls pollen expression.

摘要

3-羟基-3-甲基戊二酰辅酶A还原酶(HMGR)催化类异戊二烯代谢中的关键步骤,该代谢过程会产生一系列对植物生长、发育和健康至关重要的化合物。我们从马铃薯基因组文库中分离出了7类编码HMGR的基因组克隆。核酸序列比较显示,所有7类克隆与Choi等人(《植物细胞》4: 1333, 1992)描述的马铃薯hmg 1基因高度同源,这表明它们都是马铃薯中同一亚家族的成员。从最丰富的一类基因组克隆中挑选了一个代表性成员(hmg 1.2)进行进一步研究。在hmg 1.2启动子控制下含有β-葡萄糖醛酸酶(GUS)报告基因的转基因烟草和马铃薯在许多植物组织中均组成性地低水平表达GUS活性。仅在花粉中观察到高水平的GUS活性。对分离出的花粉进行GUS检测、GUS活性与花药HMGR活性的相关性分析、hmg 1.2启动子缺失研究以及R1后代植株R2花粉中hmg 1.2::GUS表达的分离分析表明,hmg 1.2启动子控制花粉表达。

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