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小鼠伴肌动蛋白的末端区域:序列分析及与N-RAP的互补定位

Terminal regions of mouse nebulin: sequence analysis and complementary localization with N-RAP.

作者信息

Herrera A H, Elzey B, Law D J, Horowits R

机构信息

Laboratory of Physical Biology, National Institute of Arthritis and Musculoskeletal and Skin Diseases, National Institutes of Health, Bethesda, Maryland 20892-2751, USA.

出版信息

Cell Motil Cytoskeleton. 2000 Mar;45(3):211-22. doi: 10.1002/(SICI)1097-0169(200003)45:3<211::AID-CM4>3.0.CO;2-Y.

Abstract

The regions of mouse nebulin extending from the ends of the super repeats to the C-terminus and N-terminus were cloned and sequenced. Comparison of the mouse sequence with the previously published human sequence shows that the terminal regions of nebulin are highly conserved. The four phosphorylation motifs and SH3 domain found at the C-terminus of mouse nebulin are identical to those found in human nebulin, with the exception of four conservative substitutions. The modules linking this C-terminal region to the super repeats have deletions relative to both fetal and adult human nebulins that correspond to integral numbers of modules, making the mouse C-terminal simple repeat region among the shortest observed to date. The N-terminal region and the C-terminal modules were expressed in Escherichia coli and used for antibody production. Immunofluorescent labeling of these regions of nebulin in isolated myofibrils demonstrates that they are located near the center of the sarcomere and near the Z-line, respectively. Immunogold labeling with antibodies raised against the N-terminal nebulin sequence localizes this region in the A-band near the tips of the thin filaments. Nebulin localization is complementary to that of N-RAP, another muscle-specific protein containing nebulin-like super repeats; nebulin is exclusively found in the sarcomeres, while N-RAP is confined to the terminal bundles of actin filaments at the myotendinous junction. Cell Motil. Cytoskeleton 3:211-222, 2000 Published 2000 Wiley-Liss, Inc.

摘要

对小鼠伴肌动蛋白从超级重复序列末端延伸至C端和N端的区域进行了克隆和测序。将小鼠序列与先前发表的人类序列进行比较,结果显示伴肌动蛋白的末端区域高度保守。在小鼠伴肌动蛋白C端发现的四个磷酸化基序和SH3结构域与人类伴肌动蛋白中的相同,只是有四个保守性替换。连接该C端区域与超级重复序列的模块相对于胎儿和成人的人类伴肌动蛋白都有缺失,这些缺失相当于整数个模块,使得小鼠C端的简单重复区域成为迄今为止所观察到的最短的区域之一。N端区域和C端模块在大肠杆菌中表达并用于抗体生产。对分离的肌原纤维中伴肌动蛋白的这些区域进行免疫荧光标记表明,它们分别位于肌节中心附近和Z线附近。用针对伴肌动蛋白N端序列产生的抗体进行免疫金标记,将该区域定位在细肌丝末端附近的A带中。伴肌动蛋白的定位与N-RAP互补,N-RAP是另一种含有伴肌动蛋白样超级重复序列的肌肉特异性蛋白;伴肌动蛋白仅存在于肌节中,而N-RAP局限于肌腱连接点处肌动蛋白丝的末端束中。《细胞运动与细胞骨架》3:211 - 222,2000年 2000年由威利 - 利斯公司出版

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