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马铃薯组织蛋白酶D抑制剂基因的克隆与特性分析

Cloning and characterization of a cathepsin D inhibitor gene from Solanum tuberosum L.

作者信息

Herbers K, Prat S, Willmitzer L

机构信息

Institut für Genbiologische Forschung GmbH, Berlin, Germany.

出版信息

Plant Mol Biol. 1994 Oct;26(1):73-83. doi: 10.1007/BF00039521.

Abstract

A DNA clone encoding a cathepsin D inhibitor CathInh was isolated from a potato genomic library using a CathInh cDNA as hybridization probe. The amino acid sequence of the coding region is nearly identical with a CathInh cDNA and CathInh proteins previously isolated from a tuber-specific cDNA library and from tubers, respectively. Analysis of GUS activity resulting from expression of chimeric CathInh promoter-GUS genes in transgenic potato plants revealed expression exclusively confined to potato tubers. No GUS activity could be detected in any other organ of the transgenic plants either constitutively or after wounding or treatment with abscisic and jasmonic acid (JA). Interestingly, part of the promoter region of the CathInh gene, essential for GUS activity in tubers, shows striking similarity to promoter regions of tuber-specific class I patatin genes.

摘要

以组织蛋白酶D抑制剂CathInh的cDNA作为杂交探针,从马铃薯基因组文库中分离出一个编码CathInh的DNA克隆。编码区的氨基酸序列与先前分别从块茎特异性cDNA文库和块茎中分离得到的CathInh cDNA及CathInh蛋白几乎完全相同。对嵌合CathInh启动子 - GUS基因在转基因马铃薯植株中表达所产生的GUS活性进行分析,结果表明其表达仅局限于马铃薯块茎。在转基因植株的任何其他器官中,无论是组成型表达、受伤后还是用脱落酸和茉莉酸(JA)处理后,均未检测到GUS活性。有趣的是,CathInh基因启动子区域中对块茎中GUS活性至关重要的部分,与I类块茎特异性Patatin基因的启动子区域具有显著相似性。

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