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海胆胚胎中金属硫蛋白SpMTA基因启动子和内含子1区域的组合调控。

Combinatorial regulation by promoter and intron 1 regions of the metallothionein SpMTA gene in the sea urchin embryo.

作者信息

Bai G, Stuebing E W, Parker H R, Harlow P, Nemer M

机构信息

Institute for Cancer Research, Fox Chase Cancer Center, Philadelphia, Pennsylvania 19111.

出版信息

Mol Cell Biol. 1993 Feb;13(2):993-1001. doi: 10.1128/mcb.13.2.993-1001.1993.

Abstract

The SpMTA metallothionein gene of the sea urchin Strongylocentrotus purpuratus is regulated developmentally, histospecifically, and by heavy-metal induction. The sequenced 5' flank of the gene can be divided into proximal, middle, and distal regions, each containing a pair of metal response elements (MREs). Canonical 7-bp core sequences are present in all except the middle-region MREs c and d, which contain 1-bp mismatches. Metal-induced expression in transgenic blastulae was increased with each consecutive addition of the middle and distal regions to a chimeric reporter gene construct containing the proximal SpMTA promoter region. Reduced metal induction through point mutation of the distal MREs e and f indicated that the MREs themselves were largely responsible for the transcriptional increase. These activities were further enhanced by SpMTA intron 1, but not when a specific interior region of the intron had been deleted. The atypical MREs c and d did not support induction by themselves, i.e., when present alone with mutated proximal MREs a and b. However, in the presence of intron 1, they were able to substitute for the nullified MREs a and b in the promotion of metal-induced expression. This capability suggests, furthermore, that these atypical MREs, in addition to responding to an intron 1 region, participate cooperatively with the canonical proximal MREs.

摘要

紫海胆(Strongylocentrotus purpuratus)的SpMTA金属硫蛋白基因受到发育调控、组织特异性调控以及重金属诱导调控。该基因测序得到的5'侧翼可分为近端、中间和远端区域,每个区域都含有一对金属反应元件(MRE)。除了中间区域的MRE c和d含有1个碱基错配外,所有区域都存在典型的7个碱基核心序列。在含有近端SpMTA启动子区域的嵌合报告基因构建体中,随着中间和远端区域连续添加到构建体中,转基因囊胚中金属诱导的表达增加。通过对远端MRE e和f进行点突变降低金属诱导作用,表明MRE本身在很大程度上负责转录增加。SpMTA内含子1进一步增强了这些活性,但当内含子的特定内部区域被删除时则不然。非典型MRE c和d自身不支持诱导作用,即当与突变的近端MRE a和b单独存在时。然而,在内含子1存在的情况下,它们能够在促进金属诱导表达方面替代无效的MRE a和b。此外,这种能力表明,这些非典型MRE除了对内含子1区域做出反应外,还与典型的近端MRE协同参与作用。

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