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nebulin重复结构域对于原肌球蛋白与心肌肌节的正常维持是必需的。

The nebulette repeat domain is necessary for proper maintenance of tropomyosin with the cardiac sarcomere.

作者信息

Bonzo Jeremy R, Norris Andrea A, Esham Michael, Moncman Carole L

机构信息

Department of Molecular and Cellular Biochemistry, University of Kentucky, 741 S. Limestone, Lexington, KY 40536, USA.

出版信息

Exp Cell Res. 2008 Nov 15;314(19):3519-30. doi: 10.1016/j.yexcr.2008.09.001. Epub 2008 Sep 16.

Abstract

Nebulette is a cardiac-specific isoform of the giant actin-binding protein nebulin. Nebulette, having a mass of approximately 100 kDa, is only predicted to extend 150 nm from the edge of the Z-lines. Overexpression of the nebulette C-terminal linker and/or SH3 domains in chicken cardiomyocytes results in a loss of endogenous nebulette with a concomitant loss of tropomyosin (TPM) and troponin, as well as a shortening of the thin filaments. These data suggest that nebulette's position in the sarcomere is important for the maintenance of TPM, troponin and thin filament length. To evaluate this hypothesis, N-terminal nested truncations tagged with GFP were expressed in chicken cardiomyocytes and the cells were analyzed for the distribution of myofilament proteins. Minimal effects on the myofilaments were observed with N-terminal deletions of up to 10 modules; however, deletion of 15 modules replicated the phenotype observed with expression of the C-terminal fragments. Expression of internal deletions of nebulette verifies that a site between module 10 and 15 is important for TPM maintenance within the sarcomeric lattice. We have additionally isolated TPM cDNAs from a yeast two hybrid (Y2H) analysis. These data indicate the importance of the nebulette-TPM interactions in the maintenance and stability of the thin filaments.

摘要

细肌丝结合蛋白(nebulin)的心脏特异性同工型是细肌丝结合蛋白(nebulin)。细肌丝结合蛋白(nebulin)质量约为100 kDa,预计仅从Z线边缘延伸150 nm。在鸡心肌细胞中过表达细肌丝结合蛋白(nebulin)的C末端连接子和/或SH3结构域会导致内源性细肌丝结合蛋白(nebulin)丢失,同时原肌球蛋白(TPM)和肌钙蛋白也会丢失,以及细肌丝缩短。这些数据表明,细肌丝结合蛋白(nebulin)在肌节中的位置对于维持原肌球蛋白(TPM)、肌钙蛋白和细肌丝长度很重要。为了评估这一假设,在鸡心肌细胞中表达了用绿色荧光蛋白(GFP)标记的N末端嵌套截短体,并分析了细胞中肌丝蛋白的分布。N末端缺失多达10个模块时,对肌丝的影响最小;然而,缺失15个模块则重现了用C末端片段表达时观察到的表型。细肌丝结合蛋白(nebulin)内部缺失的表达证实,模块10和15之间的位点对于肌节晶格中原肌球蛋白(TPM)的维持很重要。我们还通过酵母双杂交(Y2H)分析分离出了原肌球蛋白(TPM)的cDNA。这些数据表明细肌丝结合蛋白(nebulin)与原肌球蛋白(TPM)的相互作用在细肌丝的维持和稳定性中的重要性。

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