mLin-7 is localized to the basolateral surface of renal epithelia via its NH2 terminus

被引:41
作者
Straight, SW
Karnak, D
Borg, JP
Kamberov, E
Dare, H
Margolis, B
Wade, JB
机构
[1] Univ Michigan, Med Ctr,Sch Med, Howard Hughes Med Inst, Dept Internal Med, Ann Arbor, MI 48109 USA
[2] Univ Michigan, Sch Med, Howard Hughes Med Inst, Dept Biol Chem, Ann Arbor, MI 48109 USA
[3] Univ Maryland, Sch Med, Dept Physiol, Baltimore, MD 21201 USA
关键词
protein targeting; Madin-Darby canine kidney cells; kidney; protein interactions; epithelia;
D O I
10.1152/ajprenal.2000.278.3.F464
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
In Caenorhabditis elegans, the basolateral localization of the Let-23 growth factor receptor tyrosine kinase requires the expression of three genes: lin-2, lin-7, and lin-10. Mammalian homologs of these three genes have been identified, and a complex of their protein products exists in mammalian neurons. In this paper, we examine the interaction of these mammalian proteins in renal epithelia. Coprecipitation experiments demonstrated that mLin-2/CASK binds to mLin-7, and immunofluorescent labeling showed that these proteins colocalized at the basolateral surface of Madin-Darby canine kidney cells and renal epithelia. Although labeling intensity varied markedly among different renal epithelial cells, those cells strongly expressing mLin-7 also showed intense mLin-2/CASK labeling. We have also demonstrated that mLin-2/CASK binding requires amino acids 12-32 of mLin-7 and have shown that this region of mLin-7 is also necessary for the targeting of mLin-7 to the basolateral surface. Furthermore, the overexpression of mLin-2/CASK mutants in Madin-Darby canine kidney cells caused endogenous mLin-7 to mislocalize. In summary, the NH(2) terminus of mLin-7 is crucial for its basolateral localization, likely through its interaction with mLin-2/CASK.
引用
收藏
页码:F464 / F475
页数:12
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