Borden P, Song K, Heller R A
Institute for Biochemistry and Cell Biology, Syntex Research, Palo Alto, CA 94304.
Gene. 1994 Dec 30;151(1-2):315-20. doi: 10.1016/0378-1119(94)90677-7.
Cloning and characterization of the promoter region controlling the gene encoding human stromelysin (Str) has been previously reported [Quinones et al., J. Biol. Chem. 264 (1989) 8339-8344]. We have characterized independently isolated genomic clones of the STR promoter, designated pSKStrB and 682, that are considerably different from the published sequence. Although the sequences up to an XbaI site at -480 of the 5' regions are identical, a novel 1.0-kb segment exists upstream from -480. This sequence is absent from the published clone, but its presence in the genomic DNA from twelve individuals has been confirmed by both PCR analysis and restriction mapping. Upstream of the novel 1-kb segment, the sequence of the published clone reappears, but in pSKStrB exists in inverse orientation.
此前已有关于控制人基质溶解素(Str)编码基因的启动子区域的克隆及特性分析的报道[昆诺内斯等人,《生物化学杂志》264(1989)8339 - 8344]。我们对独立分离得到的STR启动子基因组克隆进行了特性分析,这些克隆命名为pSKStrB和682,与已发表序列有很大差异。尽管5'区域 - 480处直至XbaI位点的序列相同,但在 - 480上游存在一个新的1.0 kb片段。该序列在已发表的克隆中不存在,但通过PCR分析和限制性图谱分析已证实其存在于12个个体的基因组DNA中。在新的1 kb片段上游,已发表克隆的序列再次出现,但在pSKStrB中是以相反方向存在。