Ishibashi Kenichi, Morishita Yoshiyuki, Tanaka Yasuko
Division of Pathophysiology, Meiji Pharmaceutical University, Kiyose, Tokyo, 204-8588, Japan.
Division of Nephrology, Saitama Medical Center, Jichi Medical University, 1-847 Ohmiya, Saitama-City, Saitama, 330-8503, Japan.
Adv Exp Med Biol. 2017;969:35-50. doi: 10.1007/978-94-024-1057-0_2.
Aquaporins (AQPs ) are a family of transmembrane proteins present in almost all species including virus. They are grossly divided into three subfamilies based on the sequence around a highly conserved pore-forming NPA motif: (1) classical water -selective AQP (CAQP), (2) glycerol -permeable aquaglyceroporin (AQGP) and (3) AQP super-gene channel, superaquaporin (SAQP). AQP is composed of two tandem repeats of conserved three transmembrane domains and a NPA motif. AQP ancestors probably started in prokaryotes by the duplication of half AQP genes to be diversified into CAQPs or AQGPs by evolving a subfamily-specific carboxyl-terminal NPA motif. Both AQP subfamilies may have been carried over to unicellular eukaryotic ancestors, protists and further to multicellular organisms. Although fungus lineage has kept both AQP subfamilies, the plant lineage has lost AQGP after algal ancestors with extensive diversifications of CAQPs into PIP, TIP, SIP, XIP, HIP and LIP with a possible horizontal transfer of NIP from bacteria. Interestingly, the animal lineage has obtained new SAQP subfamily with highly deviated NPA motifs, especially at the amino-terminal halves in both prostomial and deuterostomial animals. The prostomial lineage has lost AQGP after hymenoptera, while the deuterostomial lineage has kept all three subfamilies up to the vertebrate with diversified CAQPs (AQP0, 1, 2, 4, 5, 6, 8) and AQGPs (AQP3, 7, 9, 10) with limited SAQPs (AQP11, 12) in mammals. Whole-genome duplications, local gene duplications and horizontal gene transfers may have produced the AQP diversity with adaptive selections and functional alternations in response to environment changes. With the above evolutionary perspective in mind, the function of each AQP could be speculated by comparison among species to get new insights into physiological roles of AQPs . This evolutionary guidance in AQP research will lead to deeper understandings of water and solute homeostasis.
水通道蛋白(AQPs)是一类几乎存在于所有物种(包括病毒)中的跨膜蛋白家族。根据高度保守的成孔NPA基序周围的序列,它们大致分为三个亚家族:(1)经典水选择性水通道蛋白(CAQP),(2)甘油可渗透的水甘油通道蛋白(AQGP)和(3)水通道蛋白超基因通道,即超级水通道蛋白(SAQP)。水通道蛋白由两个保守的三个跨膜结构域和一个NPA基序的串联重复组成。水通道蛋白的祖先可能起源于原核生物,通过半水通道蛋白基因的复制,通过进化出亚家族特异性的羧基末端NPA基序,分化为CAQPs或AQGPs。两个水通道蛋白亚家族可能都遗传给了单细胞真核生物祖先、原生生物,并进一步遗传给了多细胞生物。虽然真菌谱系保留了两个水通道蛋白亚家族,但植物谱系在藻类祖先之后失去了AQGP,CAQPs广泛分化为PIP、TIP、SIP、XIP、HIP和LIP,并且可能从细菌水平转移了NIP。有趣的是,动物谱系获得了具有高度偏离的NPA基序的新SAQP亚家族,特别是在原口动物和后口动物的氨基末端一半。原口动物谱系在膜翅目之后失去了AQGP,而后口动物谱系在脊椎动物中保留了所有三个亚家族,CAQPs(AQP0、1、2、4、5、6、8)和AQGPs(AQP3、7、9、10)多样化,在哺乳动物中SAQPs有限(AQP11、12)。全基因组复制、局部基因复制和水平基因转移可能通过适应性选择和功能改变产生了水通道蛋白的多样性,以响应环境变化。基于上述进化观点,可以通过物种间比较推测每个水通道蛋白的功能,从而对水通道蛋白的生理作用有新的认识。水通道蛋白研究中的这种进化指导将有助于更深入地理解水和溶质的稳态。