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成肌分化过程中RAP1蛋白的表达与定位

Expression and localization of RAP1 proteins during myogenic differentiation.

作者信息

Pizon V, Cifuentes-Diaz C, Mège R M, Baldacci G, Rieger F

机构信息

Laboratoire de Génétique et Biologie Moléculaire de la Réplication, CNRS-UPR 9044, Villejuif/France.

出版信息

Eur J Cell Biol. 1996 Mar;69(3):224-35.

PMID:8900487
Abstract

The RAP1 subfamily of small GTPases has been involved in various differentiation programs. In skeletal muscle, several lines of evidence suggest that various small GTPases could be implicated in muscle development. This raised the question of whether the RAP1 proteins (RAP1A and/or RAP1B) could be involved in myogenesis. In the present study, we report on the regulation of RAP1 transcripts and proteins during myogenic differentiation. Northern blot analysis performed with differentiated and undifferentiated C2 myogenic cells pointed out that both genes undergo specific regulation during myogenesis in vitro since differentiation of C2 cells was accompanied by a down-regulation of RAP1B gene transcription and continuous expression of the RAP1A mRNA. In addition, immunofluorescence experiments revealed the accumulation of the RAP1 proteins in differentiated C2 cells and in primary culture of mouse myotubes. Investigation of the intracellular location of RAP1 proteins in undifferentiated and differentiated C2 cells showed that the proteins were associated with the late endocytic compartments. To verify that the build-up of RAP1 proteins had a relevance for developmental mechanisms in vivo, we studied their expression and localization at different stages of skeletal muscle development. We found that RAP1 proteins accumulated in specialized muscle cell domains undergoing important modifications during early and late myogenesis: these were the neuromuscular and myotendinous junctions, respectively. Altogether, our data indicate that RAP1 proteins are regulated during myogenic differentiation.

摘要

小GTP酶的RAP1亚家族参与了各种分化程序。在骨骼肌中,有几条证据表明各种小GTP酶可能与肌肉发育有关。这就提出了一个问题,即RAP1蛋白(RAP1A和/或RAP1B)是否可能参与肌生成。在本研究中,我们报告了肌生成分化过程中RAP1转录本和蛋白的调控情况。对分化和未分化的C2肌源性细胞进行的Northern印迹分析指出,这两个基因在体外肌生成过程中都经历了特定的调控,因为C2细胞的分化伴随着RAP1B基因转录的下调和RAP1A mRNA的持续表达。此外,免疫荧光实验显示RAP1蛋白在分化的C2细胞和小鼠肌管的原代培养物中积累。对未分化和分化的C2细胞中RAP1蛋白的细胞内定位进行研究表明,这些蛋白与晚期内吞区室相关。为了验证RAP1蛋白的积累与体内发育机制相关,我们研究了它们在骨骼肌发育不同阶段的表达和定位。我们发现RAP1蛋白在早期和晚期肌生成过程中经历重要修饰的特殊肌肉细胞区域积累:这些区域分别是神经肌肉接头和肌腱连接点。总之,我们的数据表明RAP1蛋白在肌生成分化过程中受到调控。

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