Interspecies diversity of the occludin sequence: cDNA cloning of human, mouse, dog, and rat-kangaroo homologues

被引:268
作者
AndoAkatsuka, Y
Saitou, M
Hirase, T
Kishi, M
Sakakibara, A
Itoh, M
Yonemura, S
Furuse, M
Tsukita, S
机构
[1] KYOTO UNIV,FAC MED,DEPT CELL BIOL,SAKYO KU,KYOTO 606,JAPAN
[2] KYOTO UNIV,FAC MED,DEPT ANAT & DEV BIOL,SAKYO KU,KYOTO 606,JAPAN
[3] GRAD UNIV ADV STUDIES,SCH LIFE SCI,DEPT PHYSIOL SCI,OKAZAKI,AICHI 444,JAPAN
关键词
D O I
10.1083/jcb.133.1.43
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Occludin has been identified from chick liver as a novel integral membrane protein localizing at tight junctions (Furuse, M., T. Hirase, M. Itoh, A. Nagafuchi, S. Yonemura, Sa. Tsukita, and Sh. Tsukita. 1993. J. Cell Biol. 123:1777-1788). To analyze and modulate the functions of tight junctions, it would be advantageous to know the mammalian homologues of occludin and their genes. Here we describe the nucleotide sequences of full length cDNAs encoding occludin of rat-kangaroo (potoroo), human, mouse, and dog. Rat-kangaroo occludin cDNA was prepared from RNA isolated from PtK2 cell culture, using a mAb against chicken occludin, whereas the others were amplified by polymerase chain reaction based on the sequence found around the human neuronal apoptosis inhibitory protein gene. The amino acid sequences of the three mammalian (human, murine, and canine) occludins were very closely related to each other (similar to 90% identity), whereas they diverged considerably from those of chicken and rat-kangaroo (similar to 50% identity). Implications of these data and novel experimental options in cell biological research are discussed.
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页码:43 / 47
页数:5
相关论文
共 14 条
  • [1] FUJIMOTO K, 1995, J CELL SCI, V108, P3443
  • [2] OCCLUDIN - A NOVEL INTEGRAL MEMBRANE-PROTEIN LOCALIZING AT TIGHT JUNCTIONS
    FURUSE, M
    HIRASE, T
    ITOH, M
    NAGAFUCHI, A
    YONEMURA, S
    TSUKITA, S
    TSUKITA, S
    [J]. JOURNAL OF CELL BIOLOGY, 1993, 123 (06) : 1777 - 1788
  • [3] Furuse M, 1996, J CELL SCI, V109, P429
  • [4] DIRECT ASSOCIATION OF OCCLUDIN WITH ZO-1 AND ITS POSSIBLE INVOLVEMENT IN THE LOCALIZATION OF OCCLUDIN AT TIGHT JUNCTIONS
    FURUSE, M
    ITOH, M
    HIRASE, T
    NAGAFUCHI, A
    YONEMURA, S
    TSUKITA, S
    TSUKITA, S
    [J]. JOURNAL OF CELL BIOLOGY, 1994, 127 (06) : 1617 - 1626
  • [5] STRUCTURE, BIOCHEMISTRY, AND ASSEMBLY OF EPITHELIAL TIGHT JUNCTIONS
    GUMBINER, B
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY, 1987, 253 (06): : C749 - C758
  • [6] BREAKING THROUGH THE TIGHT JUNCTION BARRIER
    GUMBINER, BM
    [J]. JOURNAL OF CELL BIOLOGY, 1993, 123 (06) : 1631 - 1633
  • [7] Huynh TV, 1985, DNA CLONING TECHNIQU, V1, P49
  • [8] A 220-KD UNDERCOAT-CONSTITUTIVE PROTEIN - ITS SPECIFIC LOCALIZATION AT CADHERIN-BASED CELL CELL-ADHESION SITES
    ITOH, M
    YONEMURA, S
    NAGAFUCHI, A
    TSUKITA, S
    TSUKITA, S
    [J]. JOURNAL OF CELL BIOLOGY, 1991, 115 (05) : 1449 - 1462
  • [9] THE GENE FOR NEURONAL APOPTOSIS INHIBITORY PROTEIN IS PARTIALLY DELETED IN INDIVIDUALS WITH SPINAL MUSCULAR-ATROPHY
    ROY, N
    MAHADEVAN, MS
    MCLEAN, M
    SHUTLER, G
    YARAGHI, Z
    FARAHANI, R
    BAIRD, S
    BESNERJOHNSTON, A
    LEFEBVRE, C
    KANG, XL
    SALIH, M
    AUBRY, H
    TAMAI, K
    GUAN, XP
    IOANNOU, P
    CRAWFORD, TO
    DEJONG, PJ
    SURH, L
    IKEDA, JE
    KORNELUK, RG
    MACKENZIE, A
    [J]. CELL, 1995, 80 (01) : 167 - 178
  • [10] STRUCTURE, FUNCTION, AND REGULATION OF CELLULAR TIGHT JUNCTIONS
    SCHNEEBERGER, EE
    LYNCH, RD
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY, 1992, 262 (06): : L647 - L661