Nemer M, Stuebing E W, Bai G, Parker H R
Institute for Cancer Research, Fox Chase Cancer Center, Philadelphia, PA 19111, USA.
Mech Dev. 1995 Apr;50(2-3):131-7. doi: 10.1016/0925-4773(94)00330-p.
The SpMTA metallothionein (MT) gene of the sea urchin Strongylocentrotus purpuratus is restricted in its expression to the aboral ectoderm in gastrulae and pluteus larvae. The proximal 1.6 kb of the 5'-flanking region together with the 1.12-kb first intron of the SpMTA gene are sufficient for its correct cell-type specific expression in transgenic embryos. This restricted spatial expression is largely eliminated by deletion of an interior 405-bp region in the intron. Within this region is a 295-bp, genomically repetitive, transposon-like segment (Nemer et al., 1993), containing several sequence motifs highly homologous to posited regulatory elements in the promoters of other genes (Thiebaud et al., 1990). The P3A and P5 sites in this apparent regulatory cassette were shown through competition to bind with relatively high affinities the same nuclear factors, bound by their counterpart sites in the CyIIIa actin promoter.
紫海胆(Strongylocentrotus purpuratus)的SpMTA金属硫蛋白(MT)基因在原肠胚和长腕幼虫中仅在反口外胚层表达。SpMTA基因5'侧翼区近端的1.6 kb片段与1.12 kb的首个内含子足以使其在转基因胚胎中正确进行细胞类型特异性表达。通过缺失内含子内部一个405 bp的区域,这种受限的空间表达在很大程度上被消除。该区域内有一个295 bp的、基因组重复的、转座子样片段(Nemer等人,1993年),包含几个与其他基因启动子中假定调控元件高度同源的序列基序(Thiebaud等人,1990年)。通过竞争实验表明,这个明显的调控盒中的P3A和P5位点以相对较高的亲和力结合相同的核因子,这些核因子也结合在肌动蛋白CyIIIa启动子的对应位点上。