3.8 Article

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

期刊

CELL MOTILITY AND THE CYTOSKELETON
卷 65, 期 1, 页码 59-72

出版社

WILEY-LISS
DOI: 10.1002/cm.20244

关键词

sarcomere; nebulin; alpha-actinin; thin filaments

资金

  1. NHLBI NIH HHS [R01 HL57461, R01 HL083146] Funding Source: Medline
  2. NATIONAL HEART, LUNG, AND BLOOD INSTITUTE [R01HL057461, R01HL083146] Funding Source: NIH RePORTER

向作者/读者索取更多资源

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.

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