Department of Biological Sciences and Biotechnology, Tsinghua University, Beijing, PR China.
Comp Biochem Physiol B Biochem Mol Biol. 2010 Mar;155(3):331-9. doi: 10.1016/j.cbpb.2009.12.003. Epub 2010 Jan 1.
Prohormone convertases (PCs) are calcium-dependent serine endoproteases of the subtilisin family that play a key role in the posttranslational processing of precursors for bioactive peptides. In this study, the cDNA of PC1 from abalone (Haliotis diversicolor supertexta) was cloned and sequenced. The PC1 cDNA consisted of 2216 bp with an open reading frame of 2010 bp encoding a 670 amino acid peptide. Comparative structural analysis revealed that abalone PC1 shared high similarity and identity with most PC counterparts. The profile of deduced peptide of PC1 was composed of an N-terminal signal peptide, a prosegment domain, a catalytic domain and a P domain, which were common in many species. Sequence analysis indicated that the abalone PC1 was highly conserved in catalytic domain, including three conserved serine catalytic signatures that comprised a catalytic triad active center. Also conserved were the potential cleavage site for release of the mature peptide, a cognate integrin binding site RGD in P domain, and four cysteine residues involved in forming an intrachain disulfide bridge. To further investigate the functions of PC1 in abalone, real-time quantitative PCR was performed to determine the expression level of this gene at three different reproduction stages (i.e. pre-, during- and post-breeding). Results indicated that PC1 was expressed throughout the three stages but the expression levels varied with the timepoints and different tissues in abalone. The expression levels of PC1 in digestive gland were much higher than those of the gonad. In female abalone, the expression of PC1 was higher at pre-breeding and during-breeding stages (P<0.05), and the expression declined at the subsequent stage. Whereas, the level of PC1 in male individual did not exhibit a significant difference in various reproduction stages. Also, the natural enzyme activity of PC1 partially exhibited a similar tendency with the mRNA expression. According to the results, it can be concluded that PC1 gene is involved in the abalone reproduction process (e.g. spawning or sperming). PC1 is a potential prohormone processing enzyme and it may play a critical role in abalone physiological processes related to reproduction.
前激素转化酶(PCs)是枯草杆菌蛋白酶家族中的钙依赖性丝氨酸内肽酶,在生物活性肽前体的翻译后加工中发挥关键作用。本研究克隆并测序了鲍鱼(Haliotis diversicolor supertexta)PC1 的 cDNA。PC1 cDNA 由 2216bp 组成,开放阅读框为 2010bp,编码 670 个氨基酸的肽。比较结构分析表明,鲍鱼 PC1 与大多数 PC 同源物具有高度相似性和同一性。PC1 推导肽的图谱由 N 端信号肽、前导肽结构域、催化结构域和 P 结构域组成,这些结构域在许多物种中都很常见。序列分析表明,鲍鱼 PC1 在催化结构域高度保守,包括组成催化三联体活性中心的三个保守丝氨酸催化特征。P 结构域中成熟肽释放的潜在切割位点、同源整合素结合位点 RGD 以及参与形成链内二硫键的四个半胱氨酸残基也被保守。为了进一步研究 PC1 在鲍鱼中的功能,采用实时定量 PCR 法测定了该基因在三个不同繁殖阶段(即繁殖前、繁殖中和繁殖后)的表达水平。结果表明,PC1 在三个阶段均有表达,但表达水平随时间和鲍鱼不同组织而变化。在消化腺中,PC1 的表达水平明显高于性腺。在雌性鲍鱼中,繁殖前和繁殖期 PC1 的表达水平较高(P<0.05),随后阶段表达水平下降。而在雄性个体中,PC1 的水平在不同繁殖阶段没有显著差异。此外,PC1 的天然酶活性也表现出与 mRNA 表达相似的趋势。根据结果可以得出结论,PC1 基因参与了鲍鱼的繁殖过程(如产卵或排精)。PC1 是一种潜在的激素前体加工酶,可能在与繁殖相关的鲍鱼生理过程中发挥关键作用。