Takata K, Watanabe S, Hirono M, Tamaki M, Teraoka H, Hayashizaki Y
Institute for Molecular and Cellular Biology, Osaka University, Japan.
Biochem Biophys Res Commun. 1989 Dec 29;165(3):1035-42. doi: 10.1016/0006-291x(89)92706-x.
The nucleotide sequence of human thyroid stimulating hormone (hTSH) gene can encode a protein of 138 amino acids. However, the mature polypeptide is lacking 6 amino acids of the carboxyl-terminus (C-terminus), suggesting posttranslational cleavage of these residues. To analyze a possible function of these 6 amino acids, we expressed two hTSH beta cDNAs with or without the 6 codons for C-terminal extension, together with alpha subunit cDNA in CHO cells, and determined the amino acid sequence of C-terminus of hTSH beta. hTSH beta propeptides without C-terminal extension were glycosylated, associated with alpha subunit and secreted, as normal propeptides were, and its heterodimer with alpha subunit showed normal TSH bioactivity in FRTL-5 bioassay. These data indicate that the 6 amino acid C-terminal extension is not necessary for the hTSH maturation in the process of the biosynthesis and for its bioactivity.
人促甲状腺激素(hTSH)基因的核苷酸序列可编码一种由138个氨基酸组成的蛋白质。然而,成熟多肽在羧基末端(C末端)缺少6个氨基酸,这表明这些残基存在翻译后切割。为了分析这6个氨基酸的可能功能,我们在CHO细胞中共同表达了两个带有或不带有C末端延伸的6个密码子的hTSHβ cDNA以及α亚基cDNA,并确定了hTSHβ C末端的氨基酸序列。没有C末端延伸的hTSHβ前体肽会像正常前体肽一样进行糖基化、与α亚基结合并分泌,并且其与α亚基的异二聚体在FRTL-5生物测定中显示出正常的TSH生物活性。这些数据表明,这6个氨基酸的C末端延伸在生物合成过程中对于hTSH的成熟及其生物活性并非必需。