Biotechnology Research Division, National Fisheries Research and Development Institute, Busan 619-705, Korea.
Int J Mol Sci. 2013 Aug 13;14(8):16672-84. doi: 10.3390/ijms140816672.
We identified and characterized the primary structure of the Korean oily bitterling Acheilognathus koreensis fast skeletal myosin light chain 2 (Akmlc2f), gene. Encoded by seven exons spanning 3955 bp, the deduced 168-amino acid AkMLC2f polypeptide contained an EF-hand calcium-binding motif and showed strong homology (80%-98%) with the MLC2 proteins of Ictalurus punctatus and other species, including mammals. Akmlc2f mRNA was highly enriched in skeletal muscles, and was detectable in other tissues. The upstream regions of Akmlc2f included a TATA box, one copy of a putative MEF-2 binding site and several putative C/EBPβ binding sites. The functional activity of the promoter region of Akmlc2f was examined using luciferase and red fluorescent protein reporters. The Akmlc2f promoter-driven reporter expressions were detected and increased by the C/EBPβ transcription factor in HEK293T cells. The activity of the promoter of Akmlc2f was also confirmed in the developing zebrafish embryo. Although the detailed mechanism underlying the expression of Akmlc2f remains unknown, these results suggest the muscle-specific expression of Akmlc2f transcript and the functional activation of Akmlc2f promoter by C/EBPβ.
我们鉴定并描述了韩国油性苦鱼(Acheilognathus koreensis)快速骨骼肌肌球蛋白轻链 2(Akmlc2f)基因的一级结构。该基因由跨越 3955bp 的七个外显子编码,推测的 168 个氨基酸的 AkMLC2f 多肽含有一个 EF 手钙离子结合基序,与 Ictalurus punctatus 和其他物种(包括哺乳动物)的 MLC2 蛋白具有很强的同源性(80%-98%)。Akmlc2f mRNA 在骨骼肌中高度富集,在其他组织中也可检测到。Akmlc2f 的上游区域包括一个 TATA 盒、一个假定的 MEF-2 结合位点拷贝和几个假定的 C/EBPβ 结合位点。使用荧光素酶和红色荧光蛋白报告基因检测 Akmlc2f 启动子区域的功能活性。在 HEK293T 细胞中,C/EBPβ 转录因子可检测并增加 Akmlc2f 启动子驱动的报告基因表达。Akmlc2f 启动子在发育中的斑马鱼胚胎中的活性也得到了证实。虽然 Akmlc2f 表达的详细机制尚不清楚,但这些结果表明 Akmlc2f 转录物的肌肉特异性表达和 C/EBPβ 对 Akmlc2f 启动子的功能激活。