Takeshita A, Nagayama Y, Fujiyama K, Yokoyama N, Namba H, Yamashita S, Izumi M, Nagataki S
First Department of Internal Medicine, Nagasaki University School of Medicine, Japan.
Biochem Biophys Res Commun. 1992 Nov 16;188(3):1214-9. doi: 10.1016/0006-291x(92)91360-3.
In the present study, we report the molecular cloning and sequencing of an alternatively spliced form of the human thyrotropin receptor (hTSHR) mRNA transcript, which has previously been detected on Northern blot analysis of human thyroid cells. The smaller hTSHR cDNA, designated hTSHR cDNA-I, is approximately 1 kb in size and encodes a protein of 253 amino acids. Comparison of the nucleotide sequence of hTSHR cDNA-I with available hTSHR genomic sequence data reveals that the cDNA-I contains exons 1-8 and unidentified DNA tract, presumably an intron. Thus, the hTSHR cDNA-I encodes for the N-terminal half of the extracellular domain of the hTSHR (approximately 60%). The truncated TSHR-I may be secreted and function as a TSH binding protein.
在本研究中,我们报告了人促甲状腺激素受体(hTSHR)mRNA转录本一种可变剪接形式的分子克隆和测序情况,此前在人甲状腺细胞的Northern印迹分析中已检测到该转录本。较小的hTSHR cDNA,命名为hTSHR cDNA-I,大小约为1 kb,编码一个含253个氨基酸的蛋白质。将hTSHR cDNA-I的核苷酸序列与现有的hTSHR基因组序列数据进行比较发现,cDNA-I包含外显子1-8和未知DNA片段,推测为一个内含子。因此,hTSHR cDNA-I编码hTSHR细胞外结构域的N端一半(约60%)。截短的TSHR-I可能会被分泌出来并作为一种促甲状腺激素结合蛋白发挥作用。