Department of Biochemistry and Molecular Biology, University of Athens, Athens, Greece.
PLoS One. 2013 Jul 10;8(7):e68074. doi: 10.1371/journal.pone.0068074. Print 2013.
Kallikreins are secreted serine proteases with important roles in human physiology. Human plasma kallikrein, encoded by the KLKB1 gene on locus 4q34-35, functions in the blood coagulation pathway, and in regulating blood pressure. The human tissue kallikrein and kallikrein-related peptidases (KLKs) have diverse expression patterns and physiological roles, including cancer-related processes such as cell growth regulation, angiogenesis, invasion, and metastasis. Prostate-specific antigen (PSA), the product of the KLK3 gene, is the most widely used biomarker in clinical practice today. A total of 15 KLKs are encoded by the largest contiguous cluster of protease genes in the human genome (19q13.3-13.4), which makes them ideal for evolutionary analysis of gene duplication events. Previous studies on the evolution of KLKs have traced mammalian homologs as well as a probable early origin of the family in aves, amphibia and reptilia. The aim of this study was to address the evolutionary and functional relationships between tissue KLKs and plasma kallikrein, and to examine the evolution of alternative splicing isoforms. Sequences of plasma and tissue kallikreins and their alternative transcripts were collected from the NCBI and Ensembl databases, and comprehensive phylogenetic analysis was performed by Bayesian as well as maximum likelihood methods. Plasma and tissue kallikreins exhibit high sequence similarity in the trypsin domain (>50%). Phylogenetic analysis indicates an early divergence of KLKB1, which groups closely with plasminogen, chymotrypsin, and complement factor D (CFD), in a monophyletic group distinct from trypsin and the tissue KLKs. Reconstruction of the earliest events leading to the diversification of the tissue KLKs is not well resolved, indicating rapid expansion in mammals. Alternative transcripts of each KLK gene show species-specific divergence, while examination of sequence conservation indicates that many annotated human KLK isoforms are missing the catalytic triad that is crucial for protease activity.
激肽释放酶是分泌的丝氨酸蛋白酶,在人体生理学中具有重要作用。人类血浆激肽释放酶由位于 4q34-35 基因座上的 KLKB1 基因编码,在血液凝固途径和调节血压中发挥作用。人类组织激肽释放酶和激肽释放酶相关肽酶(KLKs)具有不同的表达模式和生理作用,包括与癌症相关的过程,如细胞生长调节、血管生成、侵袭和转移。前列腺特异性抗原(PSA)是 KLK3 基因的产物,是当今临床实践中使用最广泛的生物标志物。KLK 基因家族是人类基因组中最大的连续蛋白酶基因簇(19q13.3-13.4)所编码的,共有 15 种 KLKs,这使得它们成为研究基因复制事件进化的理想选择。先前关于 KLK 进化的研究追踪了哺乳动物同源物以及该家族在鸟类、两栖动物和爬行动物中的早期起源。本研究旨在探讨组织激肽释放酶和血浆激肽释放酶之间的进化和功能关系,并研究其选择性剪接异构体的进化。从 NCBI 和 Ensembl 数据库中收集了血浆和组织激肽释放酶及其选择性转录本的序列,并通过贝叶斯和最大似然法进行了综合系统发育分析。血浆和组织激肽释放酶在胰蛋白酶结构域(>50%)中具有高度的序列相似性。系统发育分析表明,KLKB1 早期分化,与纤溶酶原、糜蛋白酶和补体因子 D(CFD)紧密聚为一组,与胰蛋白酶和组织激肽释放酶不同。导致组织激肽释放酶多样化的最早事件的重建还没有得到很好的解决,这表明在哺乳动物中迅速扩张。每个 KLK 基因的选择性转录本显示出物种特异性的分化,而对序列保守性的检查表明,许多注释的人类 KLK 同工型缺失了对蛋白酶活性至关重要的催化三联体。