Lasp-2 expression, localization, and ligand interactions: A new Z-disc scaffolding protein

被引:28
作者
Zieseniss, Anke [1 ]
Terasaki, Asako G. [2 ]
Gregorio, Carol C. [1 ]
机构
[1] Univ Arizona, Dept Cell Biol & Anat, Tucson, AZ 85724 USA
[2] Chiba Univ, Grad Sch Sci & Technol, Chiba 260, Japan
来源
CELL MOTILITY AND THE CYTOSKELETON | 2008年 / 65卷 / 01期
关键词
sarcomere; nebulin; alpha-actinin; thin filaments;
D O I
10.1002/cm.20244
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The nebulin family of actin-binding proteins plays an important role in actin filament dynamics in a variety of cells including striated muscle. We report here the identification of a new striated muscle Z-disc associated protein: lasp-2 (LIM and SH3 domain protein-2). Lasp-2 is the most recently identified member of the nebulin family. To evaluate the role of lasp-2 in striated muscle, lasp-2 gene expression and localization were studied in chick and mouse tissue, as well as in primary cultures of chick cardiac and skeletal myocytes. Lasp-2 mRNA was detected as early as chick embryonic stage 25 and lasp-2 protein was associated with developing pre-myofibril structures, Z-discs of mature myofibrils, focal adhesions, and intercalated discs of cultured cardiomyocytes. Expression of GFP-tagged lasp-2 deletion constructs showed that the C-terminal region of lasp-2 is important for its localization in striated muscle cells. Lasp-2 organizes actin filaments into bundles and interacts directly with the Z-disc protein alpha-actinin. These results are consistent with a function of lasp-2 as a scaffolding and actin filament organizing protein within striated muscle Z-discs.
引用
收藏
页码:59 / 72
页数:14
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