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小鼠中两种TGN38同工型的菌株特异性存在以及TGN41的缺失。

Strain-specific presence of two TGN38 isoforms and absence of TGN41 in mouse.

作者信息

Kasai K, Takahashi S, Murakami K, Nakayama K

机构信息

Institute of Applied Biochemistry, University of Tsukuba, Ibaraki, Japan.

出版信息

J Biol Chem. 1995 Jun 16;270(24):14471-6. doi: 10.1074/jbc.270.24.14471.

Abstract

TGN38 and TGN41 are isoforms of an integral membrane protein that is predominantly localized to the trans-Golgi network (TGN) in rat cells. They have been proposed to form a heterodimer and to be involved in the budding of exocytic transport vesicles from the TGN. By cDNA cloning and analysis using polymerase chain reaction, we found that there were two TGN38 isoforms in a strain of mouse (ICR), whereas other strains examined (BALB/c, DBA/2, and C57BL/6) had only one TGN38. The major difference between the two isoforms was in the number of characteristic octapeptide repeats. Apart from this, there were several nucleotide substitutions between them. The two isoforms appeared to be derived from two distinct genes but not from one gene via alternative splicing. Furthermore, we failed to show the presence of TGN41 in all the strains examined. This result suggests that TGN38 may function as a monomer or a homodimer in mouse cells.

摘要

TGN38和TGN41是一种整合膜蛋白的异构体,该蛋白主要定位于大鼠细胞的反式高尔基体网络(TGN)。有人提出它们会形成异二聚体,并参与从TGN出芽的胞吐运输小泡的形成。通过使用聚合酶链反应进行cDNA克隆和分析,我们发现在一种小鼠品系(ICR)中有两种TGN38异构体,而所检测的其他品系(BALB/c、DBA/2和C57BL/6)只有一种TGN38。这两种异构体之间的主要差异在于特征性八肽重复序列的数量。除此之外,它们之间还有几个核苷酸替换。这两种异构体似乎源自两个不同的基因,而不是通过可变剪接源自一个基因。此外,我们未能在所检测的所有品系中显示出TGN41的存在。这一结果表明,TGN38在小鼠细胞中可能作为单体或同二聚体发挥作用。

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