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残余样蛋白 2 有助于维持小鼠正常的肌纤维类型分布。

Vestigial-like 2 contributes to normal muscle fiber type distribution in mice.

机构信息

Department of Bioscience and Genetics, National Cerebral and Cardiovascular Center Research Institute, 5-7-1 Fujishirodai, Suita, Osaka, 565-8565, Japan.

Center for Fundamental Education, The University of Kitakyushu, 4-2-1 Kitagata, Kokura Minami-ku, Kitakyushu, Fukuoka, 802-8577, Japan.

出版信息

Sci Rep. 2017 Aug 2;7(1):7168. doi: 10.1038/s41598-017-07149-0.

Abstract

Skeletal muscle is composed of heterogeneous populations of myofibers that are classified as slow- and fast-twitch fibers. The muscle fiber-type is regulated in a coordinated fashion by multiple genes, including transcriptional factors and microRNAs (miRNAs). However, players involved in this regulation are not fully elucidated. One of the members of the Vestigial-like factors, Vgll2, is thought to play a pivotal role in TEA domain (TEAD) transcription factor-mediated muscle-specific gene expression because of its restricted expression in skeletal muscles of adult mice. Here, we generated Vgll2 null mice and investigated Vgll2 function in adult skeletal muscles. These mice presented an increased number of fast-twitch type IIb fibers and exhibited a down-regulation of slow type I myosin heavy chain (MyHC) gene, Myh7, which resulted in exercise intolerance. In accordance with the decrease in Myh7, down-regulation of miR-208b, encoded within Myh7 gene and up-regulation of targets of miR-208b, Sox6, Sp3, and Purβ, were observed in Vgll2 deficient mice. Moreover, we detected the physical interaction between Vgll2 and TEAD1/4 in neonatal skeletal muscles. These results suggest that Vgll2 may be both directly and indirectly involved in the programing of slow muscle fibers through the formation of the Vgll2-TEAD complex.

摘要

骨骼肌由多种肌纤维组成,这些肌纤维可分为慢肌纤维和快肌纤维。肌纤维类型通过多种基因(包括转录因子和 microRNAs(miRNAs))协调调控。然而,这种调控的参与者尚未完全阐明。Vestigial-like 因子家族的成员之一 Vgll2 因其在成年小鼠骨骼肌中的特异性表达而被认为在 TEA 结构域(TEAD)转录因子介导的肌肉特异性基因表达中发挥关键作用。在这里,我们生成了 Vgll2 敲除小鼠,并研究了 Vgll2 在成年骨骼肌中的功能。这些小鼠表现出 IIb 型快肌纤维数量增加,并出现 Myh7 基因(编码慢型 I 肌球蛋白重链(MyHC))表达下调,导致运动不耐受。与 Myh7 减少一致,Vgll2 缺陷小鼠中观察到 miR-208b 的下调,miR-208b 编码在 Myh7 基因内,以及 miR-208b 的靶基因 Sox6、Sp3 和 Purβ 的上调。此外,我们在新生骨骼肌中检测到 Vgll2 和 TEAD1/4 之间的物理相互作用。这些结果表明,Vgll2 可能通过形成 Vgll2-TEAD 复合物直接和间接参与慢肌纤维的编程。

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