Leszyk J, Dumaswala R, Potter J D, Gusev N B, Verin A D, Tobacman L S, Collins J H
Department of Biology, Clarkson University, Potsdam, New York 13676.
Biochemistry. 1987 Nov 3;26(22):7035-42. doi: 10.1021/bi00396a027.
Troponin T (TnT) is the tropomyosin-binding subunit of troponin, the thin filament regulatory complex that confers calcium sensitivity to striated muscle contraction and actomyosin ATPase activity. Bovine cardiac muscle contains two isoforms (TnT-1 and TnT-2) of TnT that differ in sequence near their amino termini. Thin filaments containing TnT-2 require less calcium to activate the MgATPase rate of myosin than do thin filaments containing TnT-1. Using whole troponin T purified from adult bovine cardiac muscle, we have determined the complete amino acid sequence of the larger, more abundant isoform TnT-1. We confirmed that sequence differences between TnT-1 and TnT-2 are confined to the amino-terminal regions and found that TnT-1 makes up approximately 75% of the total troponin T isolated. Partial sequencing of the separated isoforms showed that the difference between them is due solely to residues 15-19 (Glu-Ala-Ala-Glu-Glu) of TnT-1 being absent from TnT-2. The deleted segment may correspond to the product of exon 4 of the chicken cardiac TnT gene [Cooper, T.A., & Ordahl, C.P. (1985) J. Biol. Chem. 260, 11140-11148]. Exon 5, which is developmentally regulated in the chicken, is not expressed in either TnT-1 or TnT-2. TnT-1 contains 284 amino acid residues and has a Mr of 33,808, while TnT-2 contains 279 amino acid residues and has a Mr of 33,279. Bovine cardiac TnT contains the only known thiol group in any isolated TnT (Cys-39 of TnT-1, Cys-34 of TnT-2). Comparison of bovine, rabbit, and chicken cardiac TnT sequences shows near identity of the amino-terminal 13 amino acid residues (exons 2 and 3 of the chicken cardiac gene), many differences in the following 60 residues (exons 4-8), and great similarity in the C-terminal 230 residues (exons 9-18).
肌钙蛋白T(TnT)是肌钙蛋白中与原肌球蛋白结合的亚基,原肌球蛋白是细肌丝调节复合物,可赋予横纹肌收缩和肌动球蛋白ATP酶活性钙敏感性。牛心肌含有两种TnT同工型(TnT-1和TnT-2),它们在氨基末端附近的序列不同。与含有TnT-1的细肌丝相比,含有TnT-2的细肌丝激活肌球蛋白MgATP酶活性所需的钙更少。我们使用从成年牛心肌中纯化的完整肌钙蛋白T,确定了较大且含量更丰富的同工型TnT-1的完整氨基酸序列。我们证实TnT-1和TnT-2之间的序列差异仅限于氨基末端区域,并且发现TnT-1约占分离出的总肌钙蛋白T的75%。对分离出的同工型进行部分测序表明,它们之间的差异仅在于TnT-2中不存在TnT-1的第15 - 19位残基(Glu-Ala-Ala-Glu-Glu)。缺失的片段可能对应于鸡心肌TnT基因外显子4的产物[库珀,T.A.,& 奥尔达尔,C.P.(1985年)《生物化学杂志》260,11140 - 11148]。在鸡中受发育调控的外显子5在TnT-1或TnT-2中均不表达。TnT-1包含284个氨基酸残基,Mr为33,808,而TnT-2包含279个氨基酸残基,Mr为33,279。牛心肌TnT在任何分离出的TnT中都含有唯一已知的巯基(TnT-1的Cys-39,TnT-2的Cys-34)。牛、兔和鸡心肌TnT序列的比较表明,氨基末端的13个氨基酸残基(鸡心肌基因的外显子2和3)几乎相同,接下来的60个残基(外显子4 - 8)有许多差异,而羧基末端的230个残基(外显子9 - 18)非常相似。