Khan H, Yarney T A, Sairam M R
Reproduction Research Laboratory, Clinical Research Institute of Montreal, Quebec, Canada.
Biochem Biophys Res Commun. 1993 Feb 15;190(3):888-94. doi: 10.1006/bbrc.1993.1132.
We report the cloning and characterization of two alternately spliced forms of ovine testicular follitropin receptor mRNA. A smaller receptor cDNA (151 A1) of 727 bp codes for a possible soluble receptor protein of 134 amino acids arising from exons 1-4 of the full length receptor. The 1.1 Kb cDNA clone (HK 18) extending up to the 8th exon codes for a mature protein of 259 amino acids with a single membrane spanning domain predicted by hydropathy analysis. As these structures account for 34% and 61% respectively of the extracellular domain of the full length receptor, we suggest that their putative protein products are likely to possess moderate or high affinity binding sites of physiological significance.
我们报道了绵羊睾丸促卵泡激素受体mRNA两种交替剪接形式的克隆及特性分析。一个较小的727 bp受体cDNA(151 A1)编码一种可能的可溶性受体蛋白,该蛋白由全长受体的外显子1 - 4产生,含134个氨基酸。1.1 Kb的cDNA克隆(HK 18)延伸至第8外显子,编码一个含259个氨基酸的成熟蛋白,通过亲水性分析预测其具有单个跨膜结构域。由于这些结构分别占全长受体细胞外结构域的34%和61%,我们认为它们的推定蛋白产物可能具有生理意义的中等或高亲和力结合位点。