4.6 Article

Identification of a Z-band associated protein complex involving KY, FLNC and IGFN1

期刊

EXPERIMENTAL CELL RESEARCH
卷 316, 期 11, 页码 1856-1870

出版社

ELSEVIER INC
DOI: 10.1016/j.yexcr.2010.02.027

关键词

Muscular dystrophy; Cytoskeleton; Z-disc; Sarcomere; Filamin C

资金

  1. UK Medical Research Council
  2. British Heart Foundation [FS/06/60]
  3. Medical Research Council [MC_U142684171, MC_U142684168, MC_U142684172, MC_U142684175] Funding Source: researchfish
  4. MRC [MC_U142684172, MC_U142684168, MC_U142684171, MC_U142684175] Funding Source: UKRI

向作者/读者索取更多资源

The KY protein underlies a form of muscular dystrophy in the mouse but its role in muscle remains elusive. Immunodetection of endogenous KY protein in C2C12-derived myotubes and expression of a recombinant form in neonatal cardiomyocytes indicated that KY is a Z-band associated protein. Moreover, characterization of a KY interacting protein fragment led to the identification of kin1 (Immunoglobulin-like and fibronectin type 3 domain containing 1). Igfn1 is a transcriptionally complex locus encoding many protein variants. A yeast two-hybrid screen identified the Z-band protein filamin C (FLNC) as an interacting partner. Consistent with this, expression of an IGFN1 recombinant fragment showed that the three N-terminal globular domains, common to at least five IGFN1 variants, are sufficient to provide Z-band targeting. Taken together, the yeast two-hybrid, biochemical and immunofluorescence data support the notion that KY, IGFN1 and FLNC are part of a Z-band associated protein complex likely to provide structural support to the skeletal muscle sarcomere. (C) 2010 Elsevier Inc. All rights reserved.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.6
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据