PAR3β, a novel homologue of the cell polarity protein PAR3, localizes to tight junctions

被引:54
作者
Kohjima, M
Noda, Y
Takeya, R
Saito, N
Takeuchi, K
Sumimoto, H
机构
[1] Kyushu Univ, Med Inst Bioregulat, Higashi Ku, Fukuoka 8128582, Japan
[2] Kyushu Univ, Grad Sch Med Sci, Dept Mol & Struct Biol, Fukuoka 8128582, Japan
[3] Kobe Univ, Biosignal Res Ctr, Mol Pharmacol Lab, Kobe, Hyogo 6578501, Japan
[4] Nagoya Univ, Dept Biol Sci, Nagoya, Aichi 4648602, Japan
关键词
PAR3; PAR6; atypical PKC; cell polarity; tight junction; epithelial cells;
D O I
10.1016/S0006-291X(02)02698-0
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
]The cell polarity protein PAR3, conserved from the nematode to the vertebrate, forms a complex with PAR6 and atypical protein kinase C (aPKC), and the protein complex occurs at the tight junctions in mammalian epithelial cells. Here we have cloned human cDNA for a novel PAR3 homologue, designated PAR3beta, whose messages are present in a variety of tissues and most abundantly expressed in the adult and fetal kidneys. The encoded protein of 1205 amino acids contains a region homologous to the aPKC-binding domain of PAR3alpha, another human homologue previously identified, and three PDZ domains; the first PDZ domain of PAR3alpha is considered to interact with PAR6. Unexpectedly, in contrast to other PAR3s found in various species, PAR3beta,is incapable of binding to any isotypes of PAR6 or aPKC. Nevertheless PAR3beta, expressed intrinsically or extrinsically, localizes to the tight junctions, indicating that the localization does not require the ternary complex formation. (C) 2002 Elsevier Science (USA). All rights reserved.
引用
收藏
页码:641 / 646
页数:6
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