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发动蛋白异构体在哺乳动物细胞中的差异分布。

Differential distribution of dynamin isoforms in mammalian cells.

作者信息

Cao H, Garcia F, McNiven M A

机构信息

Department of Biochemistry and Molecular Biology and Center for Basic Research in Digestive Diseases, Mayo Clinic and Foundation, Rochester, Minnesota 55905, USA.

出版信息

Mol Biol Cell. 1998 Sep;9(9):2595-609. doi: 10.1091/mbc.9.9.2595.

Abstract

Dynamins are 100-kDa GTPases that are essential for clathrin-coated vesicle formation during receptor-mediated endocytosis. To date, three different dynamin genes have been identified, with each gene expressing at least four different alternatively spliced forms. Currently, it is unclear whether these different dynamin gene products perform distinct or redundant cellular functions. Therefore, the focus of this study was to identify additional spliced variants of dynamin from rat tissues and to define the distribution of the dynamin family members in a cultured rat epithelial cell model (Clone 9 cells). After long-distance reverse transcription (RT)-PCR of mRNA from different rat tissues, the full-length cDNAs encoding the different dynamin isoforms were sequenced and revealed four additional spliced variants for dynamin I and nine for dynamin III. Thus, in rat tissues there are a total of at least 25 different mRNAs produced from the three dynamin genes. Subsequently, we generated stably transfected Clone 9 cells expressing full-length cDNAs of six different spliced forms tagged with green fluorescent protein. Confocal or fluorescence microscopy of these transfected cells revealed that many of the dynamin proteins associate with distinct membrane compartments, which include clathrin-coated pits at the plasma membrane and the Golgi apparatus, and several undefined vesicle populations. These results indicate that the dynamin family is more extensive than was originally predicted and suggest that the different dynamin proteins are localized to distinct cytoplasmic or membrane compartments.

摘要

发动蛋白是一类分子量为100 kDa的GTP酶,在受体介导的内吞作用过程中,对网格蛋白包被小泡的形成至关重要。迄今为止,已鉴定出三种不同的发动蛋白基因,每个基因至少表达四种不同的可变剪接形式。目前尚不清楚这些不同的发动蛋白基因产物是否执行不同的或冗余的细胞功能。因此,本研究的重点是从大鼠组织中鉴定发动蛋白的其他剪接变体,并在培养的大鼠上皮细胞模型(克隆9细胞)中确定发动蛋白家族成员的分布。对来自不同大鼠组织的mRNA进行长距离逆转录(RT)-PCR后,对编码不同发动蛋白异构体的全长cDNA进行测序,结果显示发动蛋白I有另外四种剪接变体,发动蛋白III有九种。因此,在大鼠组织中,这三种发动蛋白基因总共产生至少25种不同的mRNA。随后,我们构建了稳定转染的克隆9细胞,这些细胞表达六种不同剪接形式的、带有绿色荧光蛋白标签的全长cDNA。对这些转染细胞进行共聚焦或荧光显微镜观察发现,许多发动蛋白与不同的膜区室相关联,这些膜区室包括质膜上的网格蛋白包被小窝和高尔基体,以及几个未明确的小泡群体。这些结果表明,发动蛋白家族比最初预测的更为广泛,提示不同的发动蛋白定位于不同的细胞质或膜区室。

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