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Myostatin dominant negative allele products interact positively with wild type monomers

机译:肌生成抑制素占优势的负等位基因产物与野生型单体发生正相互作用

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摘要

Myostatin is an extracellular negative regulator of muscle growth with an important role in bovine muscular hypertrophy. It belongs to the transforming growth factor beta (TGFbeta) superfamily, and has structural and functional characteristics similar to those of its other members. Based on these characteristics, we designed three gene constructs in order to create a series of dominant negative (DN) alleles for murine myostatin. As a first requirement for any DN strategy, we first showed that each of the three mutant DN monomers were able to interact with wild type mature myostatin (wt-Mstn), both in a pull-down and a mammalian two-hybrid assay. In addition, the degree of DN-Mstn/wt-Mstn interaction was similar to that of wt-Mstn/wt-Mstn. These results suggest that the three designed alleles are good candidates for use in a DN-based strategy for generating muscular hypertrophy in cattle.
机译:肌生长抑制素是肌肉生长的细胞外负调节剂,在牛肌肉肥大中起重要作用。它属于转化生长因子β(TGFbeta)超家族,并且具有与其其他成员相似的结构和功能特征。基于这些特征,我们设计了三个基因构建体,以为鼠类肌肉生长抑制素创建一系列显性负(DN)等位基因。作为任何DN策略的第一个要求,我们首先证明了三种突变DN单体中的每一个都能够在下拉法和哺乳动物两杂交法中与野生型成熟肌生长抑制素(wt-Mstn)相互作用。另外,DN-Mstn / wt-Mstn的相互作用程度与wt-Mstn / wt-Mstn相似。这些结果表明,三个设计的等位基因是用于基于DN的牛肌肥大策略的良好候选者。

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