Jacob R, Preuss U, Panzer P, Alfalah M, Quack S, Roth M G, Naim H, Naim H Y
Department of Physiological Chemistry, School of Veterinary Medicine Hannover, D-30559 Hannover, Germany.
J Biol Chem. 1999 Mar 19;274(12):8061-7. doi: 10.1074/jbc.274.12.8061.
Lactase-phlorizin hydrolase (LPH) is an apical protein in intestinal cells. The location of sorting signals in LPH was investigated by preparing a series of mutants that lacked the LPH cytoplasmic domain or had the cytoplasmic domain of LPH replaced by sequences that comprised basolateral targeting signals and overlapping internalization signals of various potency. These signals are mutants of the cytoplasmic domain of the influenza hemagglutinin (HA), which have been shown to be dominant in targeting HA to the basolateral membrane. The LPH-HA chimeras were expressed in Madin-Darby canine kidney (MDCK) and colon carcinoma (Caco-2) cells, and their transport to the cell surface was analyzed. All of the LPH mutants were targeted correctly to the apical membrane. Furthermore, the LPH-HA chimeras were internalized, indicating that the HA tails were available to interact with the cytoplasmic components of clathrin-coated pits. The introduction of a strong basolateral sorting signal into LPH was not sufficient to override the strong apical signals of the LPH external domain or transmembrane domains. These results show that basolateral sorting signals are not always dominant over apical sorting signals in proteins that contain each and suggest that sorting of basolateral from apical proteins occurs within a common compartment where competition for sorting signals can occur.
乳糖酶-根皮苷水解酶(LPH)是肠细胞中的一种顶端蛋白。通过制备一系列突变体来研究LPH中分拣信号的位置,这些突变体要么缺少LPH的胞质结构域,要么LPH的胞质结构域被包含基底外侧靶向信号和不同强度重叠内化信号的序列所取代。这些信号是流感血凝素(HA)胞质结构域的突变体,已证明在将HA靶向基底外侧膜方面具有主导作用。LPH-HA嵌合体在犬肾上皮细胞(MDCK)和结肠癌细胞(Caco-2)中表达,并分析它们向细胞表面的转运。所有LPH突变体都正确靶向顶端膜。此外,LPH-HA嵌合体被内化,表明HA尾部可与网格蛋白包被小窝的胞质成分相互作用。将强基底外侧分拣信号引入LPH不足以克服LPH胞外结构域或跨膜结构域的强顶端信号。这些结果表明,在同时包含这两种信号的蛋白质中,基底外侧分拣信号并不总是比顶端分拣信号占主导地位,并表明基底外侧蛋白与顶端蛋白的分拣发生在一个共同的区室中,在那里可能会发生对分拣信号的竞争。