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通过分析合成序列鉴定小鼠金属硫蛋白-I启动子中的多个金属调控元件。

Identification of multiple metal regulatory elements in mouse metallothionein-I promoter by assaying synthetic sequences.

作者信息

Stuart G W, Searle P F, Palmiter R D

出版信息

Nature. 1985;317(6040):828-31. doi: 10.1038/317828a0.

Abstract

Metallothionein genes are transcriptionally regulated by a number of inducers including heavy metals. Previous mutational analyses of the mouse metallothionein-I gene (mMTI) promoter have delineated a heavy-metal regulatory region between -60 and -42 relative to the transcription start site. A synthetic copy of a 12-base-pair (bp) conserved sequence located within this region was subsequently shown to confer heavy-metal regulation on a heterologous gene. However, specific disruption of this metal regulatory element (MRE) within a wild-type mMTI promoter reduced but did not eliminate the heavy-metal response. The additional metal regulatory activity was localized to an upstream region containing four sequences homologous to the identified MRE. Similar sequences were also found in multiple copies in metallothionein genes from other species. Here we test synthetic copies of all five mMTI MRE homologues for metal regulatory activity. At least four of these sequences are able to confer heavy-metal regulation on a heterologous promoter.

摘要

金属硫蛋白基因受包括重金属在内的多种诱导剂的转录调控。先前对小鼠金属硫蛋白-I基因(mMTI)启动子的突变分析确定了相对于转录起始位点在-60至-42之间的重金属调控区域。随后发现位于该区域内的一个12碱基对(bp)保守序列的合成拷贝可赋予异源基因重金属调控能力。然而,野生型mMTI启动子内该金属调控元件(MRE)的特异性破坏会降低但不会消除重金属反应。额外的金属调控活性定位于一个上游区域,该区域包含四个与已鉴定的MRE同源的序列。在其他物种的金属硫蛋白基因中也发现了多个类似序列的拷贝。在这里,我们测试了所有五个mMTI MRE同源物的合成拷贝的金属调控活性。这些序列中至少有四个能够赋予异源启动子重金属调控能力。

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