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核光合基因ST-LS1上游区域增强子元件的鉴定

Identification of enhancer elements in the upstream region of the nuclear photosynthetic gene ST-LS1.

作者信息

Stockhaus J, Schell J, Willmitzer L

机构信息

Institut für Genbiologische Forschung Berlin GmbH, Federal Republic of Germany.

出版信息

Plant Cell. 1989 Aug;1(8):805-13. doi: 10.1105/tpc.1.8.805.

Abstract

The nuclear gene ST-LS1 from potato encodes a 10-kilodalton protein that is a component of the oxygen-evolving complex of photosystem II. Analysis of the expression of a reporter gene driven by chimeric promoters, consisting of ST-LS1 upstream sequences and a truncated cauliflower mosaic virus 35S promoter, suggests that a strong positive regulatory element is located between position -345 and -261, whereas both the region -261 to +11 and the more upstream region -1600 to -530 are devoid of autonomous strong positive elements detectable by this approach. The ST-LS1 upstream region contains redundant elements conferring light-regulated and organ-specific expression, one of them being located between position -130 and +11. In addition, enhancer-like sequences conferring light-regulated as well as organ-specific expression to heterologous promoters were identified. These sequences are functional not only when located 5'-upstream of the coding region but also when placed 3'-downstream of the polyadenylation signal, thus representing one of the first examples of a plant gene-derived enhancer being able to induce a truncated heterologous promoter from a position 3'-downstream of the transcription unit.

摘要

马铃薯的核基因ST-LS1编码一种10千道尔顿的蛋白质,该蛋白质是光系统II放氧复合体的一个组成部分。对由嵌合启动子驱动的报告基因表达进行分析,该嵌合启动子由ST-LS1上游序列和截短的花椰菜花叶病毒35S启动子组成,结果表明在-345至-261位之间存在一个强阳性调控元件,而-261至+11区域以及更上游的-1600至-530区域均没有通过这种方法可检测到的自主强阳性元件。ST-LS1上游区域包含赋予光调控和器官特异性表达的冗余元件,其中一个位于-130至+11位之间。此外,还鉴定出了赋予异源启动子光调控以及器官特异性表达的增强子样序列。这些序列不仅在位于编码区5'上游时起作用,而且在置于多聚腺苷酸化信号3'下游时也起作用,因此代表了植物基因来源的增强子能够从转录单元3'下游的位置诱导截短的异源启动子的首批实例之一。

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