Yan Hai-Yan, Mita Kazuei, Zhao Xia, Tanaka Yoshikazu, Moriyama Minoru, Wang Huabin, Iwanaga Masashi, Kawasaki Hideki
Faculty of Agriculture, Utsunomiya University, 350 Mine, Utsunomiya, Tochigi 321-8505, Japan.
National Institute of Agrobiological Sciences, Owashi 1-2, Tsukuba 305-8643, Japan; State Key Laboratory of Silkworm Genome Biology, Southwest University, China.
Gene. 2017 Apr 15;608:58-65. doi: 10.1016/j.gene.2017.01.017. Epub 2017 Jan 23.
We previously reported regarding an ecdysone-inducible angiotensin-converting enzyme (ACE) gene. We found another four ACE genes in the Bombyx genome. The present study was undertaken to clarify the evolutionally changed function of the ACE of Bombyx mori. Core regions of deduced amino acid sequences of ACE genes were compared with those of other insect ACE genes. Five Bombyx genes have the conserved Zn-binding-site motif (HEXXH); however, BmAcer4 has only one and BmAcer3 has no catalytic ligand. BmAcer1 and BmAcer2 were expressed in several organs. BmAcer3 was expressed in testes, and BmAcer4 and BmAcer5 were expressed in compound eyes; however, the transcription levels of these three genes were very low. Quantitative RT-PCR and Western analysis were conducted to determine the tissue distribution and developmental expression of BmAcer1and BmAcer2. Transcripts of BmAcer1 and BmAcer2 were found in the reproductive organs during the larval and pupal stages. BmAcer1 was dominant in fat bodies during the feeding stage and showed high expression in the epidermis, wing discs, and pupal wing tissues after the wandering stage. Its expression patterns in epidermis, wing discs, and wing tissues resembled the hemolymph ecdysteroid titer in the larval and pupal stages. Acer1 was observed in the hemolymph at all stages, appearing to be the source of it are fat bodies, wings, and epidermis, and functioning after being secreted into the hemolymph. BmAcer2 was abundant in the midgut during the feeding stage and after the wandering stage and in silk glands after the pupal stage. We conclude that the evolution of BmAcer occurred through duplication, and, thereafter, functional diversification developed.
我们之前报道过一种蜕皮激素诱导型血管紧张素转换酶(ACE)基因。我们在家蚕基因组中又发现了另外四个ACE基因。本研究旨在阐明家蚕ACE进化过程中功能的变化。将ACE基因推导的氨基酸序列的核心区域与其他昆虫ACE基因的核心区域进行了比较。五个家蚕基因具有保守的锌结合位点基序(HEXXH);然而,BmAcer4只有一个,BmAcer3没有催化配体。BmAcer1和BmAcer2在多个器官中表达。BmAcer3在睾丸中表达,BmAcer4和BmAcer5在复眼中表达;然而,这三个基因的转录水平非常低。进行了定量RT-PCR和Western分析以确定BmAcer1和BmAcer2的组织分布和发育表达。在幼虫和蛹期的生殖器官中发现了BmAcer1和BmAcer2的转录本。BmAcer1在取食阶段的脂肪体中占主导地位,在化蛹阶段后的表皮、翅芽和蛹翅组织中高表达。它在表皮、翅芽和翅组织中的表达模式与幼虫和蛹期血淋巴中的蜕皮甾类滴度相似。在所有阶段的血淋巴中都观察到了Acer1,其来源似乎是脂肪体、翅膀和表皮,并在分泌到血淋巴后发挥作用。BmAcer2在取食阶段和化蛹阶段后在中肠中丰富,在蛹期后在丝腺中丰富。我们得出结论,BmAcer的进化是通过基因复制发生的,此后,功能多样化得以发展。