Cserjesi P, Fairley P, Brandhorst B P
Department of Biological Sciences, Simon Fraser University, Burnaby, B.C., Canada.
Biochem Cell Biol. 1992 Oct-Nov;70(10-11):1142-50. doi: 10.1139/o92-160.
The 5'-flanking region of the metallothionein (MT) gene LpMT1 of the sea urchin Lytechinus pictus includes three copies of a conserved sequence that includes the metal-responsive element (MRE) consensus core sequence required for heavy metal induction of other MT genes, a GC box, a G box of a putative basal level enhancer element which includes another MRE core element, and a poly(C) tract. A fragment of LpMT1 DNA from nucleotides +31 to -309 fused to a chloramphenicol acetyltransferase reporter gene was inducible with cadmium after injection into L. pictus embryos. This induced activity was greatly reduced in a deletion mutant which retained only 195 base pairs of 5'-flanking sequence, including the proximal pair of MREs and the G box, but excluding the poly(C) tract, GC box, and distal MRE. A potent human hMT-IIA gene promoter is marginally functional in L. pictus embryos. In contrast, the LpMT1 promoter is active in HeLa cells and in embryos of the sea urchin Strongylocentrotus purpuratus. The hMT-IIA gene may lack a cis-acting sequence element required for expression of MT genes in L. pictus embryos. The LpMT1 promoter is a powerful, inducible, promiscuous promoter useful for driving the expression of heterologous genes in sea urchin embryos.
海胆(Lytechinus pictus)金属硫蛋白(MT)基因LpMT1的5'侧翼区包含三个保守序列拷贝,其中包括其他MT基因重金属诱导所需的金属反应元件(MRE)共有核心序列、一个GC盒、一个假定的基础水平增强子元件的G盒(其中包括另一个MRE核心元件)以及一个聚(C)序列。从核苷酸+31至-309的LpMT1 DNA片段与氯霉素乙酰转移酶报告基因融合,注射到海胆胚胎后可被镉诱导。在一个缺失突变体中,这种诱导活性大大降低,该突变体仅保留了195个碱基对的5'侧翼序列,包括近端的一对MRE和G盒,但不包括聚(C)序列、GC盒和远端MRE。一个有效的人类hMT-IIA基因启动子在海胆胚胎中功能微弱。相比之下,LpMT1启动子在HeLa细胞和紫球海胆(Strongylocentrotus purpuratus)胚胎中具有活性。hMT-IIA基因可能缺乏在海胆胚胎中表达MT基因所需的顺式作用序列元件。LpMT1启动子是一个强大的、可诱导的、通用的启动子,可用于驱动海胆胚胎中异源基因的表达。