Dong Zhangji, Ge Jiachun, Xu Zhiqiang, Dong Xiaohua, Cao Shasha, Pan Jianlin, Zhao Qingshun
1 MOE Key Laboratory of Model Animal for Disease Study, Model Animal Research Center, Nanjing University , Nanjing, China .
Zebrafish. 2014 Jun;11(3):265-74. doi: 10.1089/zeb.2014.0974. Epub 2014 May 9.
Myostatin (Mstn), a member of the transforming growth factor β superfamily, plays an inhibiting role in mammalian muscle growth. Mammals like human, cattle, mouse, sheep, and dog carrying null alleles of Mstn display a double-muscle phenotype. Mstn is conserved in fish; however, little is known whether the fish with mutated mstn display a similar phenotype to mammals because of the lack of mutant fish with mstn null alleles. Previously, we knocked out one of the duplicated copies of myostatin gene (mstna) in yellow catfish using zinc-finger nucleases. In this study, we report the identification of the second myostatin gene (mstnb) and knockout of mstnb in yellow catfish. The gene comprises three exons. It is predicted to encode 373 amino acid residues. The predicted protein exhibits 59.3% identity with yellow catfish Mstna and 57.3% identity with human MSTN. Employing TALEN (transcription activator-like effector nucleases) technology, we obtained two founders (from four randomly selected founders) of yellow catfish carrying the mutated mstnb gene in their germ cells. Totally, six mutated alleles of mstnb were obtained from the founders. Among the six alleles, four are nonframeshift and two are frameshift mutation. The frameshift mutated alleles include mstnb(nju22), an 8 bp deletion, and mstnb(nju24), a complex type of mutation comprising a 7 bp deletion and a 12 bp insertion. They are predicted to encode function null Mstnb. Our results will help to understand the roles of mstn genes in fish growth.
肌肉生长抑制素(Mstn)是转化生长因子β超家族的成员之一,在哺乳动物肌肉生长中起抑制作用。携带Mstn无效等位基因的人类、牛、小鼠、绵羊和狗等哺乳动物表现出双肌表型。Mstn在鱼类中是保守的;然而,由于缺乏具有mstn无效等位基因的突变鱼,尚不清楚mstn突变的鱼是否表现出与哺乳动物相似的表型。此前,我们使用锌指核酸酶敲除了黄颡鱼中肌肉生长抑制素基因(mstna)的一个重复拷贝。在本研究中,我们报告了黄颡鱼中第二个肌肉生长抑制素基因(mstnb)的鉴定以及mstnb的敲除。该基因由三个外显子组成。预计它编码373个氨基酸残基。预测的蛋白质与黄颡鱼Mstna的同一性为59.3%,与人类MSTN的同一性为57.3%。利用转录激活样效应核酸酶(TALEN)技术,我们获得了两条在生殖细胞中携带突变mstnb基因的黄颡鱼奠基鱼(从随机选择的四条奠基鱼中获得)。总共从这些奠基鱼中获得了六个mstnb的突变等位基因。在这六个等位基因中,四个是非移码突变,两个是移码突变。移码突变等位基因包括mstnb(nju22),一个8 bp的缺失,以及mstnb(nju24),一种复杂类型的突变,包括一个7 bp的缺失和一个12 bp的插入。预计它们编码无功能的Mstnb。我们的结果将有助于了解mstn基因在鱼类生长中的作用。