Chang K C
Veterinary Molecular Medicine Laboratory, Department of Veterinary Pathology, University of Glasgow.
J Muscle Res Cell Motil. 2000;21(5):451-61. doi: 10.1023/a:1005625302409.
The porcine sarcomeric fast 2a myosin heavy chain (MyHC) gene was previously found to require a region extending 3' from the transcriptional start site for high levels of expression. Here we established the existence of two novel opposing regulatory domains in intron 2. A positive regulatory element, defined to a 75bp region, resembles a TATA-less intronic promoter, with a consensus transcription initiation element. It can up-regulate its endogenous or a heterologous muscle promoter in a position specific manner, and on its own drive a reporter gene. In tandem with it is a dominant negative regulatory element, localised to a 81bp region, which can down-regulate its native gene and a heterologous muscle promoter. Bandshift and DNase I footprinting assays demonstrated that specific nuclear factors bound to both regulatory elements are distinctly different. Both elements appear to have no counterpart in intron 2 of the porcine fast 2x and 2b MyHC genes. Taken together, we demonstrate for the first time that a 5'-end terminal intron of a sarcomeric MyHC gene contains two critical regulatory domains, which may be involved in the complexity of temporo-spatial expression.
先前发现猪肌节快速2a肌球蛋白重链(MyHC)基因需要一个从转录起始位点向3'端延伸的区域才能实现高水平表达。在此,我们确定了内含子2中存在两个新的反向调控结构域。一个正向调控元件,限定在一个75bp的区域内,类似于一个无TATA框的内含子启动子,具有共有转录起始元件。它能够以位置特异性方式上调其内源或异源肌肉启动子,并自身驱动一个报告基因。与之串联的是一个显性负调控元件,定位于一个81bp的区域,它能够下调其天然基因和异源肌肉启动子。凝胶迁移和DNase I足迹分析表明,与这两个调控元件结合的特异性核因子明显不同。这两个元件在猪快速2x和2b MyHC基因的内含子2中似乎没有对应物。综上所述,我们首次证明肌节MyHC基因的5'端末端内含子包含两个关键调控结构域,这可能与时空表达的复杂性有关。