Reaves B, Wilde A, Banting G
Department of Biochemistry, School of Medical Sciences, University of Bristol, U.K.
Biochem J. 1992 Apr 15;283 ( Pt 2)(Pt 2):313-6. doi: 10.1042/bj2830313.
TGN38 is an integral membrane protein previously shown to be predominantly localized to the trans-Golgi network (TGN) of cells by virtue of a signal contained within its cytoplasmic 'tail' [Luzio, Brake, Banting, Howell, Braghetta & Stanley (1990) Biochem. J. 270, 97-102]. We now (i) describe the isolation of cDNA clones encoding an isoform of TGN38, (ii) present the sequence of that isoform and (iii) describe the production and use of antibodies which specifically recognize the new isoform. This isoform, designated TGN41, is also predominantly localized to the TGN. The only sequence differences between the protein coding regions of cDNA clones encoding TGN38 and those encoding TGN41 occur within the region specifying the cytoplasmic tails of the two proteins. The TGN localization signal is shown to be within the sequence common to both proteins.
TGN38是一种整合膜蛋白,先前研究表明,由于其细胞质“尾部”包含的信号,它主要定位于细胞的反式高尔基体网络(TGN)[卢齐奥、布雷克、班廷、豪厄尔、布拉盖塔和斯坦利(1990年)《生物化学杂志》270卷,97 - 102页]。我们现在:(i)描述编码TGN38一种同工型的cDNA克隆的分离;(ii)给出该同工型的序列;(iii)描述特异性识别新同工型的抗体的制备及应用。这种同工型命名为TGN41,也主要定位于TGN。编码TGN38的cDNA克隆与编码TGN41的cDNA克隆在蛋白质编码区的唯一序列差异,出现在指定这两种蛋白质细胞质尾部的区域内。TGN定位信号显示在两种蛋白质共有的序列中。