Cx40.8, a Cx43-like protein, forms gap junction channels inefficiently and may require Cx43 for its association at the plasma membrane

被引:9
作者
Gerhart, Sarah V. [1 ]
Jefferis, Rebecca [1 ]
Iovine, M. Kathryn [1 ]
机构
[1] Lehigh Univ, Dept Biol Sci, Bethlehem, PA 18015 USA
来源
FEBS LETTERS | 2009年 / 583卷 / 21期
关键词
Connexin; Cx40.8; Cx43; Gap junction; Zebrafish; Short fin; FIN REGENERATION; CONNEXIN43; GJA1; ZEBRAFISH FINS; PERMEABILITY; MUTATIONS; MECHANISMS; DISEASE; GROWTH; CELLS;
D O I
10.1016/j.febslet.2009.09.054
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
In addition to having a Cx43 ortholog, the zebra fish genome also contains a Cx43-like gene, Cx40.8. Here, we investigate the expression of cx40.8 in zebra fish fins and the function of Cx40.8 in HeLa cells. We find that cx40.8 is present in the same population of dividing cells as cx43. Unlike Cx43, dye coupling assays suggest that Cx40.8 only inefficiently forms functional gap junction channels. However, co-transfection reveals that Cx40.8 can co-localize with Cx43 in gap junction plaques, and that the resulting plaques contain functional gap junction channels. Together, these data suggest the possibility that Cx40.8 may functionally interact with Cx43 to regulate cell proliferation in vivo.
引用
收藏
页码:3419 / 3424
页数:6
相关论文
共 23 条
  • [11] Connexin43 (GJA1) is required in the population of dividing cells during fin regeneration
    Hoptak-Solga, Angela D.
    Nielsen, Sarah
    Jain, Isha
    Thummel, Ryan
    Hyde, David R.
    Iovine, M. Kathryn
    [J]. DEVELOPMENTAL BIOLOGY, 2008, 317 (02) : 541 - 548
  • [12] Zebrafish short fin mutations in connexin43 lead to aberrant gap junctional intercellular communication
    Hoptak-Solga, Angela D.
    Klein, Kathryn A.
    DeRosa, Adam M.
    White, Thomas W.
    Iovine, M. Kathryn
    [J]. FEBS LETTERS, 2007, 581 (17): : 3297 - 3302
  • [13] Mutations in connexin43 (GJA1) perturb bone growth in zebrafish fins
    Iovine, MK
    Higgins, EP
    Hindes, A
    Coblitz, B
    Johnson, SL
    [J]. DEVELOPMENTAL BIOLOGY, 2005, 278 (01) : 208 - 219
  • [14] Iovine MK, 2000, GENETICS, V155, P1321
  • [15] Closing the gap on autosomal dominant connexin-26 and connexin-43 mutants linked to human disease
    Laird, Dale W.
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2008, 283 (06) : 2997 - 3001
  • [16] Life cycle of connexins in health and disease
    Laird, DW
    [J]. BIOCHEMICAL JOURNAL, 2006, 394 : 527 - 543
  • [17] Biophysical properties of homomeric and heteromultimeric channels formed by cardiac connexins
    Moreno, AP
    [J]. CARDIOVASCULAR RESEARCH, 2004, 62 (02) : 276 - 286
  • [18] Connexin 43 (GJA1) mutations cause the pleiotropic phenotype of oculodentodigital dysplasia
    Paznekas, WA
    Boyadjiev, SA
    Shapiro, RE
    Daniels, O
    Wollnik, B
    Keegan, CE
    Innis, JW
    Dinulos, MB
    Christian, C
    Hannibal, MC
    Jabs, EW
    [J]. AMERICAN JOURNAL OF HUMAN GENETICS, 2003, 72 (02) : 408 - 418
  • [19] Tales of regeneration in zebrafish
    Poss, KD
    Keating, MT
    Nechiporuk, A
    [J]. DEVELOPMENTAL DYNAMICS, 2003, 226 (02) : 202 - 210
  • [20] Connexin43 regulates joint location in zebrafish fins
    Sims, Kenneth, Jr.
    Eble, Diane M.
    Iovine, M. Kathryn
    [J]. DEVELOPMENTAL BIOLOGY, 2009, 327 (02) : 410 - 418