Mundhenk Lars, Erickson Nancy A, Klymiuk Nikolai, Gruber Achim D
Department of Veterinary Pathology, Faculty of Veterinary Medicine, Freie Universität Berlin, Berlin, Germany.
Institute of Molecular Animal Breeding and Biotechnology, Ludwig-Maximilians-Universität, Oberschleissheim, Germany.
PLoS One. 2018 Jan 18;13(1):e0191512. doi: 10.1371/journal.pone.0191512. eCollection 2018.
Members of the chloride channel regulators, calcium-activated (CLCA) family, have been implicated in diverse biomedical conditions, including chronic inflammatory airway diseases such as asthma, chronic obstructive pulmonary disease, and cystic fibrosis, the activation of macrophages, and the growth and metastatic spread of tumor cells. Several observations, however, could not be repeated across species boundaries and increasing evidence suggests that select CLCA genes are particularly prone to dynamic species-specific evolvements. Here, we systematically characterized structural and expressional differences of the CLCA3 gene across mammalian species, revealing a spectrum of gene duplications, e.g., in mice and cows, and of gene silencing via diverse chromosomal modifications in pigs and many primates, including humans. In contrast, expression of a canonical CLCA3 protein from a single functional gene seems to be evolutionarily retained in carnivores, rabbits, guinea pigs, and horses. As an accepted asthma model, we chose the cat to establish the tissue and cellular expression pattern of the CLCA3 protein which was primarily found in mucin-producing cells of the respiratory tract and in stratified epithelia of the esophagus. Our results suggest that, among developmental differences in other CLCA genes, the CLCA3 gene possesses a particularly high dynamic evolutionary diversity with pivotal consequences for humans and other primates that seem to lack a CLCA3 protein. Our data also help to explain previous contradictory results on CLCA3 obtained from different species and warrant caution in extrapolating data from animal models in conditions where CLCA3 may be involved.
氯离子通道调节剂家族(CLCA)的成员与多种生物医学状况有关,包括哮喘、慢性阻塞性肺疾病和囊性纤维化等慢性炎症性气道疾病、巨噬细胞的激活以及肿瘤细胞的生长和转移扩散。然而,一些观察结果无法在不同物种间重复,越来越多的证据表明,某些CLCA基因特别容易发生动态的物种特异性进化。在这里,我们系统地描述了CLCA3基因在哺乳动物物种间的结构和表达差异,揭示了一系列基因重复现象,例如在小鼠和牛中,以及在猪和包括人类在内的许多灵长类动物中通过多种染色体修饰导致的基因沉默。相比之下,单一功能基因的典型CLCA3蛋白的表达似乎在食肉动物、兔子、豚鼠和马中得以进化保留。作为公认的哮喘模型,我们选择猫来建立CLCA3蛋白的组织和细胞表达模式,该蛋白主要存在于呼吸道的黏液分泌细胞和食管的复层上皮中。我们的结果表明,在其他CLCA基因的发育差异中,CLCA3基因具有特别高的动态进化多样性,这对似乎缺乏CLCA3蛋白的人类和其他灵长类动物具有关键影响。我们的数据也有助于解释先前从不同物种获得的关于CLCA3的相互矛盾的结果,并提醒在CLCA3可能涉及的情况下从动物模型推断数据时要谨慎。