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与I类马铃薯块茎蛋白启动子区域结合的核蛋白因子具有块茎特异性且受蔗糖诱导。

Nuclear protein factors binding to a class I patatin promoter region are tuber-specific and sucrose-inducible.

作者信息

Kim S Y, May G D, Park W D

机构信息

Department of Biochemistry and Biophysics, Texas A&M University, College Station 77843.

出版信息

Plant Mol Biol. 1994 Oct;26(2):603-15. doi: 10.1007/BF00013747.

Abstract

Genes encoding patatin, the major storage protein of the potato tuber, are generally divided into two classes, class I and class II. The expression of the class I patatin genes is normally tuber-specific, but can be induced in leaves by high concentrations of sucrose. By employing electrophoretic mobility shift assays (EMSA), we have identified nuclear protein factors that interact specifically with the proximal portion of the class I patatin promoter that is required for tuber-specific and sucrose-inducible expression. The factors were detected in nuclear extracts prepared from potato tubers and sucrose-induced leaves, but not in extracts from leaves of normal potato plants. Four putative transcription factor-binding sites were localized using DNase I footprinting. Competitive EMSA was employed to show that the same protein factor binds to at least two of the sites (boxes D and M). Interestingly, these two binding sites are highly homologous to light-responsive elements present in genes for the ribulose-1,5-bisphosphate carboxylase small subunit.

摘要

编码马铃薯块茎主要贮藏蛋白马铃薯Patatin的基因通常分为两类,即I类和II类。I类Patatin基因的表达通常具有块茎特异性,但高浓度蔗糖可诱导其在叶片中表达。通过电泳迁移率变动分析(EMSA),我们鉴定出了与I类Patatin启动子近端区域特异性相互作用的核蛋白因子,该区域是块茎特异性和蔗糖诱导表达所必需的。在从马铃薯块茎和蔗糖诱导的叶片中制备的核提取物中检测到了这些因子,但在正常马铃薯植株的叶片提取物中未检测到。使用DNase I足迹法定位了四个假定的转录因子结合位点。采用竞争性EMSA表明,同一蛋白因子与至少两个位点(D盒和M盒)结合。有趣的是,这两个结合位点与1,5-二磷酸核酮糖羧化酶小亚基基因中存在的光响应元件高度同源。

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