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首页> 外文期刊>Asian-Australasian Journal of Animal Sciences >Cloning and prokaryotic expression of the mature fragment of the Chinese yellow bovine myostatin gene.
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Cloning and prokaryotic expression of the mature fragment of the Chinese yellow bovine myostatin gene.

机译:中国黄牛肌肉生长抑制素基因成熟片段的克隆及原核表达。

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摘要

Myostatin is a member of the transforming growth factor- beta (TGF- beta ) super-family. It acts as a negative regulator for skeletal muscle growth. Myostatin mutations are characterized by a visible, generalized increase in muscle mass in double muscled cattle breeds. To understand the biochemistry and physiology of the Chinese Yellow bovine myostatin gene, we report here for the first time expression of the gene in Escherichia coli (E. coli). Primers of the myostatin gene of Chinese Yellow Cattle were designed on the basis of the reported bovine myostatin mRNA sequence (Gen-Bank Accession No. NM005259) and optimized for E. coli codon usage. XhoI and EcoRI restriction enzyme sites were incorporated in the primers, and then cloning vector and expression vector were constructed in a different host bacterium. The expressed protein had a molecule mass of about 16 kDa as determined by SDS-PAGE under reducing conditions. The expressed protein reacted specifically with myostatin monoclonal antibody on immunoblots. Our studies should lead to the investigation of the differences in myostatin genes of various cattle and could benefit human health and food animal agriculture..
机译:肌生长抑制素是转化生长因子-β(TGF-β)超家族的成员。它充当骨骼肌生长的负调节剂。肌生长抑制素突变的特征是双肌肉牛品种的肌肉质量明显,普遍增加。为了了解中国黄牛肌肉生长抑制素基因的生物化学和生理学,我们在此首次报道该基因在大肠杆菌(E. coli)中的表达。根据报道的牛肌生长抑制素mRNA序列(Gen-Bank登录号NM005259)设计中国黄牛肌生长抑制素基因的引物,并针对大肠杆菌密码子进行了优化。将XhoI和EcoRI限制性酶切位点掺入引物中,然后在不同的宿主细菌中构建克隆载体和表达载体。通过还原条件下的SDS-PAGE测定,表达的蛋白质具有约16kDa的分子量。表达的蛋白质在免疫印迹上与肌生长抑制素单克隆抗体发生特异性反应。我们的研究应导致对各种牛肌肉生长抑制素基因差异的研究,并可能有益于人类健康和食用动物农业。

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