Hirayama Y, Watabe S
Laboratory of Aquatic Molecular Biology and Biotechnology, Graduate School of Agricultural and Life Sciences, The University of Tokyo, Bunkyo, Japan.
Eur J Biochem. 1997 Jun 1;246(2):380-7. doi: 10.1111/j.1432-1033.1997.t01-2-00380.x.
We determined the primary structures of the three acclimation-temperature-associated isoforms of myosin subfragment-1 heavy chain from fast skeletal muscle of thermally acclimated carp. These isoforms were cloned by extending 5'-regions of cDNAs that encode the rod part of myosin heavy chain specifically expressed in 10 degrees C- and 30 degrees C-acclimated carp, together with the region that encodes an intermediate structure [Imai, J., Hirayama, Y., Kikuchi, K., Kakinuma, M. & Watabe, S. (1997) J. Exp. Biol. 200, 27-34]. These three isoforms generally resembled each other in primary structure, showing 94.8, 90.9, and 92% similarity between the 10 degrees C- and intermediate-type, between the 10 degrees C- and 30 degrees C-type, and between the intermediate- and 30 degrees C-type myosin heavy chains, respectively. However, isoform-specific differences were clearly observed between the 10 degrees C- and 30 degrees C-type heavy chains in the first 60 amino acid residues from the N-terminus, where the intermediate-type showed an intermediate feature in its sequence compared to the 10 degrees C- and 30 degrees C-type isoforms. Other striking differences were observed in two surface loops between the 10 degrees C- and 30 degrees C-type isoform. Five amino acid residues out of sixteen were different in loop 1 near the ATP-binding pocket, and six out of twenty were different in loop 2 on the actin-binding site. The loops connecting beta-sheets that are known to surround the ATP-binding pocket were highly conserved in primary structure for the three types. In northern blot analysis, the accumulated mRNA levels of the 10 degrees C- and intermediate-type isoforms were significantly higher in carp acclimated to 10 degrees C and 20 degrees C than carp acclimated to 30 degrees C, whereas the level of the 30 degrees C-type isoform was significantly higher in carp acclimated to 30 degrees C than those acclimated to 10 degrees C and 20 degrees C.
我们确定了热适应鲤鱼快速骨骼肌中肌球蛋白亚片段-1重链的三种与适应温度相关的同工型的一级结构。通过延伸编码在10℃和30℃适应鲤鱼中特异性表达的肌球蛋白重链杆状部分的cDNA的5'区域,以及编码中间结构的区域,克隆了这些同工型[今井,J.,平山,Y.,菊池,K.,鹿沼,M.和渡边,S.(1997年)《实验生物学杂志》200,27 - 34]。这三种同工型在一级结构上总体相似,10℃型与中间型、10℃型与30℃型、中间型与30℃型肌球蛋白重链之间的相似性分别为94.8%、90.9%和92%。然而,在N端的前60个氨基酸残基中,10℃型和30℃型重链之间明显观察到同工型特异性差异,其中中间型在序列上表现出介于10℃型和30℃型同工型之间的特征。在10℃型和30℃型同工型之间的两个表面环中也观察到了其他显著差异。在靠近ATP结合口袋的环1中,16个氨基酸残基中有5个不同,在肌动蛋白结合位点的环2中,20个氨基酸残基中有6个不同。已知围绕ATP结合口袋的连接β折叠的环在这三种类型的一级结构中高度保守。在Northern印迹分析中,适应10℃和20℃的鲤鱼中10℃型和中间型同工型的累积mRNA水平显著高于适应30℃的鲤鱼,而适应30℃的鲤鱼中30℃型同工型的水平显著高于适应于10℃和20℃的鲤鱼。