Claudins reign

References

• Furuse M, Fujita K, Hiiragi T, Fujimoto K, Tsukita S. Claudin-1 and -2: novel integral membrane proteins localizing at tight junctions with no sequence similarity to occludin. J Cell Biol 1998; 141:1539 - 50; http://dx.doi.org/10.1083/jcb.141.7.1539; PMID: 9647647
   PubMed Web of Science ®Google Scholar
• Furuse M, Sasaki H, Fujimoto K, Tsukita S. A single gene product, claudin-1 or -2, reconstitutes tight junction strands and recruits occludin in fibroblasts. J Cell Biol 1998; 143:391 - 401; http://dx.doi.org/10.1083/jcb.143.2.391; PMID: 9786950
   PubMed Web of Science ®Google Scholar
• Morita K, Sasaki H, Furuse M, Tsukita S. Endothelial claudin: claudin-5/TMVCF constitutes tight junction strands in endothelial cells. J Cell Biol 1999; 147:185 - 94; http://dx.doi.org/10.1083/jcb.147.1.185; PMID: 10508865
   PubMed Web of Science ®Google Scholar
• Nitta T, Hata M, Gotoh S, Seo Y, Sasaki H, Hashimoto N, et al. Size-selective loosening of the blood-brain barrier in claudin-5-deficient mice. J Cell Biol 2003; 161:653 - 60; http://dx.doi.org/10.1083/jcb.200302070; PMID: 12743111
   PubMed Web of Science ®Google Scholar
• Gow A, Davies C, Southwood CM, Frolenkov G, Chrustowski M, Ng L, et al. Deafness in Claudin 11-null mice reveals the critical contribution of basal cell tight junctions to stria vascularis function. J Neurosci 2004; 24:7051 - 62; http://dx.doi.org/10.1523/JNEUROSCI.1640-04.2004; PMID: 15306639
   PubMed Web of Science ®Google Scholar
• Furuse M, Hata M, Furuse K, Yoshida Y, Haratake A, Sugitani Y, et al. Claudin-based tight junctions are crucial for the mammalian epidermal barrier: a lesson from claudin-1-deficient mice. J Cell Biol 2002; 156:1099 - 111; http://dx.doi.org/10.1083/jcb.200110122; PMID: 11889141
   PubMed Web of Science ®Google Scholar
• Wilcox ER, Burton QL, Naz S, Riazuddin S, Smith TN, Ploplis B, et al. Mutations in the gene encoding tight junction claudin-14 cause autosomal recessive deafness DFNB29. Cell 2001; 104:165 - 72; http://dx.doi.org/10.1016/S0092-8674(01)00200-8; PMID: 11163249
   PubMed Web of Science ®Google Scholar
• Tatum R, Zhang Y, Lu Q, Kim K, Jeansonne BG, Chen YH. WNK4 phosphorylates ser(206) of claudin-7 and promotes paracellular Cl(-) permeability. FEBS Lett 2007; 581:3887 - 91; http://dx.doi.org/10.1016/j.febslet.2007.07.014; PMID: 17651736
   PubMed Web of Science ®Google Scholar
• Kollmar R, Nakamura SK, Kappler JA, Hudspeth AJ. Expression and phylogeny of claudins in vertebrate primordia. Proc Natl Acad Sci U S A 2001; 98:10196 - 201; http://dx.doi.org/10.1073/pnas.171325898; PMID: 11517306
   PubMed Web of Science ®Google Scholar
• Krause G, Winkler L, Mueller SL, Haseloff RF, Piontek J, Blasig IE. Structure and function of claudins. Biochim Biophys Acta 2008; 1778:631 - 45; http://dx.doi.org/10.1016/j.bbamem.2007.10.018; PMID: 18036336
   PubMed Web of Science ®Google Scholar
• Morita K, Furuse M, Fujimoto K, Tsukita S. Claudin multigene family encoding four-transmembrane domain protein components of tight junction strands. Proc Natl Acad Sci U S A 1999; 96:511 - 6; http://dx.doi.org/10.1073/pnas.96.2.511; PMID: 9892664
   PubMed Web of Science ®Google Scholar
• Turksen K, Troy TC. Junctions gone bad: claudins and loss of the barrier in cancer. Biochim Biophys Acta 2011; 1816:73 - 9; PMID: 21515339
   PubMed Web of Science ®Google Scholar
• Blasig IE, Winkler L, Lassowski B, Mueller SL, Zuleger N, Krause E, et al. On the self-association potential of transmembrane tight junction proteins. Cell Mol Life Sci 2006; 63:505 - 14; http://dx.doi.org/10.1007/s00018-005-5472-x; PMID: 16456617
   PubMed Web of Science ®Google Scholar
• Coyne CB, Gambling TM, Boucher RC, Carson JL, Johnson LG. Role of claudin interactions in airway tight junctional permeability. Am J Physiol Lung Cell Mol Physiol 2003; 285:L1166 - 78; PMID: 12909588
   PubMed Web of Science ®Google Scholar
• Mitic LL, Unger VM, Anderson JM. Expression, solubilization, and biochemical characterization of the tight junction transmembrane protein claudin-4. Protein Sci 2003; 12:218 - 27; http://dx.doi.org/10.1110/ps.0233903; PMID: 12538885
   PubMed Web of Science ®Google Scholar
• Van Itallie CM, Anderson JM. Claudins and epithelial paracellular transport. Annu Rev Physiol 2006; 68:403 - 29; http://dx.doi.org/10.1146/annurev.physiol.68.040104.131404; PMID: 16460278
   PubMed Web of Science ®Google Scholar
• Kiuchi-Saishin Y, Gotoh S, Furuse M, Takasuga A, Tano Y, Tsukita S. Differential expression patterns of claudins, tight junction membrane proteins, in mouse nephron segments. J Am Soc Nephrol 2002; 13:875 - 86; PMID: 11912246
   PubMed Web of Science ®Google Scholar
• Simon DB, Lu Y, Choate KA, Velazquez H, Al-Sabban E, Praga M, et al. Paracellin-1, a renal tight junction protein required for paracellular Mg2+ resorption. Science 1999; 285:103 - 6; http://dx.doi.org/10.1126/science.285.5424.103; PMID: 10390358
   PubMed Web of Science ®Google Scholar
• Holmes JL, Van Itallie CM, Rasmussen JE, Anderson JM. Claudin profiling in the mouse during postnatal intestinal development and along the gastrointestinal tract reveals complex expression patterns. Gene Expr Patterns 2006; 6:581 - 8; http://dx.doi.org/10.1016/j.modgep.2005.12.001; PMID: 16458081
   PubMed Web of Science ®Google Scholar
• Troy TC, Li Y, O’Malley L, Turksen K. The temporal and spatial expression of Claudins in epidermal development and the accelerated program of epidermal differentiation in K14-CaSR transgenic mice. Gene Expr Patterns 2007; 7:423 - 30; http://dx.doi.org/10.1016/j.modgep.2006.11.006; PMID: 17182288
   PubMed Web of Science ®Google Scholar
• Colegio OR, Van Itallie CM, McCrea HJ, Rahner C, Anderson JM. Claudins create charge-selective channels in the paracellular pathway between epithelial cells. Am J Physiol Cell Physiol 2002; 283:C142 - 7; http://dx.doi.org/10.1152/ajpcell.00038.2002; PMID: 12055082
   PubMed Web of Science ®Google Scholar
• Van Itallie CM, Rogan S, Yu A, Vidal LS, Holmes J, Anderson JM. Two splice variants of claudin-10 in the kidney create paracellular pores with different ion selectivities. Am J Physiol Renal Physiol 2006; 291:F1288 - 99; http://dx.doi.org/10.1152/ajprenal.00138.2006; PMID: 16804102
   PubMed Web of Science ®Google Scholar
• Evans MJ, von Hahn T, Tscherne DM, Syder AJ, Panis M, Wölk B, et al. Claudin-1 is a hepatitis C virus co-receptor required for a late step in entry. Nature 2007; 446:801 - 5; http://dx.doi.org/10.1038/nature05654; PMID: 17325668
   PubMed Web of Science ®Google Scholar
• Meertens L, Bertaux C, Cukierman L, Cormier E, Lavillette D, Cosset FL, et al. The tight junction proteins claudin-1, -6, and -9 are entry cofactors for hepatitis C virus. J Virol 2008; 82:3555 - 60; http://dx.doi.org/10.1128/JVI.01977-07; PMID: 18234789
   PubMed Web of Science ®Google Scholar
• Zheng A, Yuan F, Li Y, Zhu F, Hou P, Li J, et al. Claudin-6 and claudin-9 function as additional coreceptors for hepatitis C virus. J Virol 2007; 81:12465 - 71; http://dx.doi.org/10.1128/JVI.01457-07; PMID: 17804490
   PubMed Web of Science ®Google Scholar
• Hamazaki Y, Itoh M, Sasaki H, Furuse M, Tsukita S. Multi-PDZ domain protein 1 (MUPP1) is concentrated at tight junctions through its possible interaction with claudin-1 and junctional adhesion molecule. J Biol Chem 2002; 277:455 - 61; http://dx.doi.org/10.1074/jbc.M109005200; PMID: 11689568
   PubMed Web of Science ®Google Scholar
• Itoh M, Furuse M, Morita K, Kubota K, Saitou M, Tsukita S. Direct binding of three tight junction-associated MAGUKs, ZO-1, ZO-2, and ZO-3, with the COOH termini of claudins. J Cell Biol 1999; 147:1351 - 63; http://dx.doi.org/10.1083/jcb.147.6.1351; PMID: 10601346
   PubMed Web of Science ®Google Scholar
• Müller D, Kausalya PJ, Bockenhauer D, Thumfart J, Meij IC, Dillon MJ, et al. Unusual clinical presentation and possible rescue of a novel claudin-16 mutation. J Clin Endocrinol Metab 2006; 91:3076 - 9; http://dx.doi.org/10.1210/jc.2006-0200; PMID: 16705067
   PubMed Web of Science ®Google Scholar
• D’Souza T, Agarwal R, Morin PJ. Phosphorylation of claudin-3 at threonine 192 by cAMP-dependent protein kinase regulates tight junction barrier function in ovarian cancer cells. J Biol Chem 2005; 280:26233 - 40; http://dx.doi.org/10.1074/jbc.M502003200; PMID: 15905176
   PubMed Web of Science ®Google Scholar
• Tanaka M, Kamata R, Sakai R. EphA2 phosphorylates the cytoplasmic tail of Claudin-4 and mediates paracellular permeability. J Biol Chem 2005; 280:42375 - 82; http://dx.doi.org/10.1074/jbc.M503786200; PMID: 16236711
   PubMed Web of Science ®Google Scholar
• Lane NJ, Skaer HI. Intercellular junctions in insect tissues. Adv Insect Physiol 1980; 15:35 - 213; http://dx.doi.org/10.1016/S0065-2806(08)60141-1
   Google Scholar
• Hua VB, Chang AB, Tchieu JH, Kumar NM, Nielsen PA, Saier MH Jr.. Sequence and phylogenetic analyses of 4 TMS junctional proteins of animals: connexins, innexins, claudins and occludins. J Membr Biol 2003; 194:59 - 76; http://dx.doi.org/10.1007/s00232-003-2026-8; PMID: 14502443
   PubMed Web of Science ®Google Scholar
• Wu VM, Schulte J, Hirschi A, Tepass U, Beitel GJ. Sinuous is a Drosophila claudin required for septate junction organization and epithelial tube size control. J Cell Biol 2004; 164:313 - 23; http://dx.doi.org/10.1083/jcb.200309134; PMID: 14734539
   PubMed Web of Science ®Google Scholar
• Price MG, Davis CF, Deng F, Burgess DL. The alpha-amino-3-hydroxyl-5-methyl-4-isoxazolepropionate receptor trafficking regulator “stargazin” is related to the claudin family of proteins by Its ability to mediate cell-cell adhesion. J Biol Chem 2005; 280:19711 - 20; http://dx.doi.org/10.1074/jbc.M500623200; PMID: 15760900
   PubMed Web of Science ®Google Scholar
• Ihrie RA, Marques MR, Nguyen BT, Horner JS, Papazoglu C, Bronson RT, et al. Perp is a p63-regulated gene essential for epithelial integrity. Cell 2005; 120:843 - 56; http://dx.doi.org/10.1016/j.cell.2005.01.008; PMID: 15797384
   PubMed Web of Science ®Google Scholar
• Attardi LD, Reczek EE, Cosmas C, Demicco EG, McCurrach ME, Lowe SW, et al. PERP, an apoptosis-associated target of p53, is a novel member of the PMP-22/gas3 family. Genes Dev 2000; 14:704 - 18; PMID: 10733530
   PubMed Web of Science ®Google Scholar
• Bruggeman LA, Martinka S, Simske JS. Expression of TM4SF10, a Claudin/EMP/PMP22 family cell junction protein, during mouse kidney development and podocyte differentiation. Dev Dyn 2007; 236:596 - 605; http://dx.doi.org/10.1002/dvdy.21052; PMID: 17195181
   PubMed Web of Science ®Google Scholar
• Katoh M, Katoh M. CLDN23 gene, frequently down-regulated in intestinal-type gastric cancer, is a novel member of CLAUDIN gene family. Int J Mol Med 2003; 11:683 - 9; PMID: 12736707
   PubMed Web of Science ®Google Scholar
• Kim J, Kim I, Yang JS, Shin YE, Hwang J, Park S, et al. Rewiring of PDZ domain-ligand interaction network contributed to eukaryotic evolution. PLoS Genet 2012; 8:e1002510; http://dx.doi.org/10.1371/journal.pgen.1002510; PMID: 22346764
   PubMedGoogle Scholar
• Tonikian R, Zhang Y, Sazinsky SL, Currell B, Yeh JH, Reva B, et al. A specificity map for the PDZ domain family. PLoS Biol 2008; 6:e239; http://dx.doi.org/10.1371/journal.pbio.0060239; PMID: 18828675
   PubMedGoogle Scholar
• Lane NJ. Tight junctions in invertebrates. In: Cereijido MaA, J., ed. Tight Junctions. New York: CRC Press, 2001:39-59.
   Google Scholar
• Spiegel E, Howard L. Development of cell junctions in sea-urchin embryos. J Cell Sci 1983; 62:27 - 48; PMID: 6684666
   PubMed Web of Science ®Google Scholar
• Tepass U, Hartenstein V. The development of cellular junctions in the Drosophila embryo. Dev Biol 1994; 161:563 - 96; http://dx.doi.org/10.1006/dbio.1994.1054; PMID: 8314002
   PubMed Web of Science ®Google Scholar
• Noirot-Timothee C, Noirot C. Septate and scalariform junctions in arthropods. Int Rev Cytol 1980; 63:97 - 140; http://dx.doi.org/10.1016/S0074-7696(08)61758-1; PMID: 20795303
   PubMedGoogle Scholar
• Gilula NB, Branton D, Satir P. The septate junction: a structural basis for intercellular coupling. Proc Natl Acad Sci U S A 1970; 67:213 - 20; http://dx.doi.org/10.1073/pnas.67.1.213; PMID: 5272312
   PubMed Web of Science ®Google Scholar
• Satir P, Gilula NB. The fine structure of membranes and intercellular communication in insects. Annu Rev Entomol 1973; 18:143 - 66; http://dx.doi.org/10.1146/annurev.en.18.010173.001043; PMID: 4617557
   PubMed Web of Science ®Google Scholar
• Davidson LA. A freeze fracture and thin section study of intestinal cell membranes and intercellular junctions of a nematode, Ascaris. Tissue Cell 1983; 15:27 - 37; http://dx.doi.org/10.1016/0040-8166(83)90031-9; PMID: 6857633
   PubMed Web of Science ®Google Scholar
• Lane NJ, Swales LS. Stages in the assembly of pleated and smooth septate junctions in developing insect embryos. J Cell Sci 1982; 56:245 - 62; PMID: 7166566
   PubMed Web of Science ®Google Scholar
• Behr M, Riedel D, Schuh R. The claudin-like megatrachea is essential in septate junctions for the epithelial barrier function in Drosophila. Dev Cell 2003; 5:611 - 20; http://dx.doi.org/10.1016/S1534-5807(03)00275-2; PMID: 14536062
   PubMed Web of Science ®Google Scholar
• Genova JL, Fehon RG. Neuroglian, Gliotactin, and the Na+/K+ ATPase are essential for septate junction function in Drosophila. J Cell Biol 2003; 161:979 - 89; http://dx.doi.org/10.1083/jcb.200212054; PMID: 12782686
   PubMed Web of Science ®Google Scholar
• Wu VM, Yu MH, Paik R, Banerjee S, Liang Z, Paul SM, et al. Drosophila Varicose, a member of a new subgroup of basolateral MAGUKs, is required for septate junctions and tracheal morphogenesis. Development 2007; 134:999 - 1009; http://dx.doi.org/10.1242/dev.02785; PMID: 17267446
   PubMed Web of Science ®Google Scholar
• Nelson KS, Furuse M, Beitel GJ. The Drosophila Claudin Kune-kune is required for septate junction organization and tracheal tube size control. Genetics 2010; 185:831 - 9; http://dx.doi.org/10.1534/genetics.110.114959; PMID: 20407131
   PubMed Web of Science ®Google Scholar
• Suzuki A, Ohno S. The PAR-aPKC system: lessons in polarity. J Cell Sci 2006; 119:979 - 87; http://dx.doi.org/10.1242/jcs.02898; PMID: 16525119
   PubMed Web of Science ®Google Scholar
• Fehon RG, Dawson IA, Artavanis-Tsakonas S. A Drosophila homologue of membrane-skeleton protein 4.1 is associated with septate junctions and is encoded by the coracle gene. Development 1994; 120:545 - 57; PMID: 8162854
   PubMed Web of Science ®Google Scholar
• Baumgartner S, Littleton JT, Broadie K, Bhat MA, Harbecke R, Lengyel JA, et al. A Drosophila neurexin is required for septate junction and blood-nerve barrier formation and function. Cell 1996; 87:1059 - 68; http://dx.doi.org/10.1016/S0092-8674(00)81800-0; PMID: 8978610
   PubMed Web of Science ®Google Scholar
• Woods DF, Wu JW, Bryant PJ. Localization of proteins to the apico-lateral junctions of Drosophila epithelia. Dev Genet 1997; 20:111 - 8; http://dx.doi.org/10.1002/(SICI)1520-6408(1997)20:2<111::AID-DVG4>3.0.CO;2-A; PMID: 9144922
   PubMedGoogle Scholar
• Schulte J, Tepass U, Auld VJ. Gliotactin, a novel marker of tricellular junctions, is necessary for septate junction development in Drosophila. J Cell Biol 2003; 161:991 - 1000; http://dx.doi.org/10.1083/jcb.200303192; PMID: 12782681
   PubMed Web of Science ®Google Scholar
• Knust E, Bossinger O. Composition and formation of intercellular junctions in epithelial cells. Science 2002; 298:1955 - 9; http://dx.doi.org/10.1126/science.1072161; PMID: 12471248
   PubMed Web of Science ®Google Scholar
• Costa M, Raich W, Agbunag C, Leung B, Hardin J, Priess JR. A putative catenin-cadherin system mediates morphogenesis of the Caenorhabditis elegans embryo. J Cell Biol 1998; 141:297 - 308; http://dx.doi.org/10.1083/jcb.141.1.297; PMID: 9531567
   PubMed Web of Science ®Google Scholar
• Pettitt J, Cox EA, Broadbent ID, Flett A, Hardin J. The Caenorhabditis elegans p120 catenin homologue, JAC-1, modulates cadherin-catenin function during epidermal morphogenesis. J Cell Biol 2003; 162:15 - 22; http://dx.doi.org/10.1083/jcb.200212136; PMID: 12847081
   PubMed Web of Science ®Google Scholar
• Bossinger O, Klebes A, Segbert C, Theres C, Knust E. Zonula adherens formation in Caenorhabditis elegans requires dlg-1, the homologue of the Drosophila gene discs large. Dev Biol 2001; 230:29 - 42; http://dx.doi.org/10.1006/dbio.2000.0113; PMID: 11161560
   PubMed Web of Science ®Google Scholar
• Firestein BL, Rongo C. DLG-1 is a MAGUK similar to SAP97 and is required for adherens junction formation. Mol Biol Cell 2001; 12:3465 - 75; PMID: 11694581
   PubMed Web of Science ®Google Scholar
• Köppen M, Simske JS, Sims PA, Firestein BL, Hall DH, Radice AD, et al. Cooperative regulation of AJM-1 controls junctional integrity in Caenorhabditis elegans epithelia. Nat Cell Biol 2001; 3:983 - 91; http://dx.doi.org/10.1038/ncb1101-983; PMID: 11715019
   PubMed Web of Science ®Google Scholar
• McMahon L, Legouis R, Vonesch JL, Labouesse M. Assembly of C. elegans apical junctions involves positioning and compaction by LET-413 and protein aggregation by the MAGUK protein DLG-1. J Cell Sci 2001; 114:2265 - 77; PMID: 11493666
   PubMed Web of Science ®Google Scholar
• Simske JS, Köppen M, Sims P, Hodgkin J, Yonkof A, Hardin J. The cell junction protein VAB-9 regulates adhesion and epidermal morphology in C. elegans. Nat Cell Biol 2003; 5:619 - 25; http://dx.doi.org/10.1038/ncb1002; PMID: 12819787
   PubMed Web of Science ®Google Scholar
• Aono S, Legouis R, Hoose WA, Kemphues KJ. PAR-3 is required for epithelial cell polarity in the distal spermatheca of C. elegans. Development 2004; 131:2865 - 74; http://dx.doi.org/10.1242/dev.01146; PMID: 15151982
   PubMed Web of Science ®Google Scholar
• Michaux G, Gansmuller A, Hindelang C, Labouesse M. CHE-14, a protein with a sterol-sensing domain, is required for apical sorting in C. elegans ectodermal epithelial cells. Curr Biol 2000; 10:1098 - 107; http://dx.doi.org/10.1016/S0960-9822(00)00695-3; PMID: 10996790
   PubMed Web of Science ®Google Scholar
• Shibata Y, Fujii T, Dent JA, Fujisawa H, Takagi S. EAT-20, a novel transmembrane protein with EGF motifs, is required for efficient feeding in Caenorhabditis elegans. Genetics 2000; 154:635 - 46; PMID: 10655217
   PubMed Web of Science ®Google Scholar
• Bilder D, Perrimon N. Localization of apical epithelial determinants by the basolateral PDZ protein Scribble. Nature 2000; 403:676 - 80; http://dx.doi.org/10.1038/35001108; PMID: 10688207
   PubMed Web of Science ®Google Scholar
• Legouis R, Gansmuller A, Sookhareea S, Bosher JM, Baillie DL, Labouesse M. LET-413 is a basolateral protein required for the assembly of adherens junctions in Caenorhabditis elegans. Nat Cell Biol 2000; 2:415 - 22; http://dx.doi.org/10.1038/35017046; PMID: 10878806
   PubMed Web of Science ®Google Scholar
• Bossinger O, Fukushige T, Claeys M, Borgonie G, McGhee JD. The apical disposition of the Caenorhabditis elegans intestinal terminal web is maintained by LET-413. Dev Biol 2004; 268:448 - 56; http://dx.doi.org/10.1016/j.ydbio.2004.01.003; PMID: 15063180
   PubMed Web of Science ®Google Scholar
• McCarter J, Bartlett B, Dang T, Schedl T. Soma-germ cell interactions in Caenorhabditis elegans: multiple events of hermaphrodite germline development require the somatic sheath and spermathecal lineages. Dev Biol 1997; 181:121 - 43; http://dx.doi.org/10.1006/dbio.1996.8429; PMID: 9013925
   PubMed Web of Science ®Google Scholar
• Schedl T. Developmental genetics of the germ line In: D. Riddle TB, B. Meyer and J. Priess, ed. C elegans II. Cold Spring Harbor: Cold Spring Harbor Laboratory Press., 1997:241-70.
   Google Scholar
• Hall DH, Winfrey VP, Blaeuer G, Hoffman LH, Furuta T, Rose KL, et al. Ultrastructural features of the adult hermaphrodite gonad of Caenorhabditis elegans: relations between the germ line and soma. Dev Biol 1999; 212:101 - 23; http://dx.doi.org/10.1006/dbio.1999.9356; PMID: 10419689
   PubMed Web of Science ®Google Scholar
• Hall DH, Altun ZF. Reproductive System. In: Press CSHL, ed. C elegans Atlas. Cold Spring Harbor, 2008:243-91.
   Google Scholar
• Piekny AJ, Johnson JL, Cham GD, Mains PE. The Caenorhabditis elegans nonmuscle myosin genes nmy-1 and nmy-2 function as redundant components of the let-502/Rho-binding kinase and mel-11/myosin phosphatase pathway during embryonic morphogenesis. Development 2003; 130:5695 - 704; http://dx.doi.org/10.1242/dev.00807; PMID: 14522875
   PubMed Web of Science ®Google Scholar
• Piekny AJ, Mains PE. Rho-binding kinase (LET-502) and myosin phosphatase (MEL-11) regulate cytokinesis in the early Caenorhabditis elegans embryo. J Cell Sci 2002; 115:2271 - 82; PMID: 12006612
   PubMed Web of Science ®Google Scholar
• Wissmann A, Ingles J, Mains PE. The Caenorhabditis elegans mel-11 myosin phosphatase regulatory subunit affects tissue contraction in the somatic gonad and the embryonic epidermis and genetically interacts with the Rac signaling pathway. Dev Biol 1999; 209:111 - 27; http://dx.doi.org/10.1006/dbio.1999.9242; PMID: 10208747
   PubMed Web of Science ®Google Scholar
• Asano A, Asano K, Sasaki H, Furuse M, Tsukita S. Claudins in Caenorhabditis elegans: their distribution and barrier function in the epithelium. Curr Biol 2003; 13:1042 - 6; http://dx.doi.org/10.1016/S0960-9822(03)00395-6; PMID: 12814550
   PubMed Web of Science ®Google Scholar
• Christophe-Hobertus C, Kooy F, Gecz J, Abramowicz MJ, Holinski-Feder E, Schwartz C, et al. TM4SF10 gene sequencing in XLMR patients identifies common polymorphisms but no disease-associated mutation. BMC Med Genet 2004; 5:22; http://dx.doi.org/10.1186/1471-2350-5-22; PMID: 15345028
   PubMedGoogle Scholar
• Christophe-Hobertus C, Szpirer C, Guyon R, Christophe D. Identification of the gene encoding Brain Cell Membrane Protein 1 (BCMP1), a putative four-transmembrane protein distantly related to the Peripheral Myelin Protein 22 / Epithelial Membrane Proteins and the Claudins. BMC Genomics 2001; 2:3; http://dx.doi.org/10.1186/1471-2164-2-3; PMID: 11472633
   PubMedGoogle Scholar
• Holzman LB, St John PL, Kovari IA, Verma R, Holthofer H, Abrahamson DR. Nephrin localizes to the slit pore of the glomerular epithelial cell. Kidney Int 1999; 56:1481 - 91; http://dx.doi.org/10.1046/j.1523-1755.1999.00719.x; PMID: 10504499
   PubMed Web of Science ®Google Scholar
• Huber TB, Benzing T. The slit diaphragm: a signaling platform to regulate podocyte function. Curr Opin Nephrol Hypertens 2005; 14:211 - 6; http://dx.doi.org/10.1097/01.mnh.0000165885.85803.a8; PMID: 15821412
   PubMed Web of Science ®Google Scholar
• Barletta GM, Kovari IA, Verma RK, Kerjaschki D, Holzman LB. Nephrin and Neph1 co-localize at the podocyte foot process intercellular junction and form cis hetero-oligomers. J Biol Chem 2003; 278:19266 - 71; http://dx.doi.org/10.1074/jbc.M301279200; PMID: 12646566
   PubMed Web of Science ®Google Scholar
• Khoshnoodi J, Sigmundsson K, Ofverstedt LG, Skoglund U, Obrink B, Wartiovaara J, et al. Nephrin promotes cell-cell adhesion through homophilic interactions. Am J Pathol 2003; 163:2337 - 46; http://dx.doi.org/10.1016/S0002-9440(10)63590-0; PMID: 14633607
   PubMed Web of Science ®Google Scholar
• Verma R, Wharram B, Kovari I, Kunkel R, Nihalani D, Wary KK, et al. Fyn binds to and phosphorylates the kidney slit diaphragm component Nephrin. J Biol Chem 2003; 278:20716 - 23; http://dx.doi.org/10.1074/jbc.M301689200; PMID: 12668668
   PubMed Web of Science ®Google Scholar
• Verma R, Kovari I, Soofi A, Nihalani D, Patrie K, Holzman LB. Nephrin ectodomain engagement results in Src kinase activation, nephrin phosphorylation, Nck recruitment, and actin polymerization. J Clin Invest 2006; 116:1346 - 59; http://dx.doi.org/10.1172/JCI27414; PMID: 16543952
   PubMed Web of Science ®Google Scholar
• Garg P, Verma R, Nihalani D, Johnstone DB, Holzman LB. Neph1 cooperates with nephrin to transduce a signal that induces actin polymerization. Mol Cell Biol 2007; 27:8698 - 712; http://dx.doi.org/10.1128/MCB.00948-07; PMID: 17923684
   PubMed Web of Science ®Google Scholar
• Lahdenperä J, Kilpeläinen P, Liu XL, Pikkarainen T, Reponen P, Ruotsalainen V, et al. Clustering-induced tyrosine phosphorylation of nephrin by Src family kinases. Kidney Int 2003; 64:404 - 13; http://dx.doi.org/10.1046/j.1523-1755.2003.00097.x; PMID: 12846735
   PubMed Web of Science ®Google Scholar
• Li H, Lemay S, Aoudjit L, Kawachi H, Takano T. SRC-family kinase Fyn phosphorylates the cytoplasmic domain of nephrin and modulates its interaction with podocin. J Am Soc Nephrol 2004; 15:3006 - 15; http://dx.doi.org/10.1097/01.ASN.0000146689.88078.80; PMID: 15579503
   PubMed Web of Science ®Google Scholar
• Liu XL, Kilpeläinen P, Hellman U, Sun Y, Wartiovaara J, Morgunova E, et al. Characterization of the interactions of the nephrin intracellular domain. FEBS J 2005; 272:228 - 43; http://dx.doi.org/10.1111/j.1432-1033.2004.04408.x; PMID: 15634346
   PubMed Web of Science ®Google Scholar
• Harita Y, Kurihara H, Kosako H, Tezuka T, Sekine T, Igarashi T, et al. Neph1, a component of the kidney slit diaphragm, is tyrosine-phosphorylated by the Src family tyrosine kinase and modulates intracellular signaling by binding to Grb2. J Biol Chem 2008; 283:9177 - 86; http://dx.doi.org/10.1074/jbc.M707247200; PMID: 18258597
   PubMed Web of Science ®Google Scholar
• Zhu J, Sun N, Aoudjit L, Li H, Kawachi H, Lemay S, et al. Nephrin mediates actin reorganization via phosphoinositide 3-kinase in podocytes. Kidney Int 2008; 73:556 - 66; http://dx.doi.org/10.1038/sj.ki.5002691; PMID: 18033240
   PubMed Web of Science ®Google Scholar
• Azhibekov TA, Wu Z, Padiyar A, Bruggeman LA, Simske JS. TM4SF10 and ADAP interaction in podocytes: role in Fyn activity and nephrin phosphorylation. Am J Physiol Cell Physiol 2011; 301:C1351 - 9; http://dx.doi.org/10.1152/ajpcell.00166.2011; PMID: 21881001
   PubMedGoogle Scholar
• Laketa V, Simpson JC, Bechtel S, Wiemann S, Pepperkok R. High-content microscopy identifies new neurite outgrowth regulators. Mol Biol Cell 2007; 18:242 - 52; http://dx.doi.org/10.1091/mbc.E06-08-0666; PMID: 17093056
   PubMed Web of Science ®Google Scholar
• Shen K, Fetter RD, Bargmann CI. Synaptic specificity is generated by the synaptic guidepost protein SYG-2 and its receptor, SYG-1. Cell 2004; 116:869 - 81; http://dx.doi.org/10.1016/S0092-8674(04)00251-X; PMID: 15035988
   PubMed Web of Science ®Google Scholar
• Shen K, Bargmann CI. The immunoglobulin superfamily protein SYG-1 determines the location of specific synapses in C. elegans. Cell 2003; 112:619 - 30; http://dx.doi.org/10.1016/S0092-8674(03)00113-2; PMID: 12628183
   PubMed Web of Science ®Google Scholar
• Putzke AP, Hikita ST, Clegg DO, Rothman JH. Essential kinase-independent role of a Fer-like non-receptor tyrosine kinase in Caenorhabditis elegans morphogenesis. Development 2005; 132:3185 - 95; http://dx.doi.org/10.1242/dev.01900; PMID: 15958510
   PubMed Web of Science ®Google Scholar
• Lockwood C, Zaidel-Bar R, Hardin J. The C. elegans zonula occludens ortholog cooperates with the cadherin complex to recruit actin during morphogenesis. Curr Biol 2008; 18:1333 - 7; http://dx.doi.org/10.1016/j.cub.2008.07.086; PMID: 18718757
   PubMed Web of Science ®Google Scholar
• Fanning AS, Van Itallie CM, Anderson JM. Zonula occludens-1 and -2 regulate apical cell structure and the zonula adherens cytoskeleton in polarized epithelia. Mol Biol Cell 2012; 23:577 - 90; http://dx.doi.org/10.1091/mbc.E11-09-0791; PMID: 22190737
   PubMed Web of Science ®Google Scholar
• Vanhoven MK, Bauer Huang SL, Albin SD, Bargmann CI. The claudin superfamily protein nsy-4 biases lateral signaling to generate left-right asymmetry in C. elegans olfactory neurons. Neuron 2006; 51:291 - 302; http://dx.doi.org/10.1016/j.neuron.2006.06.029; PMID: 16880124
   PubMed Web of Science ®Google Scholar
• Lesch BJ, Gehrke AR, Bulyk ML, Bargmann CI. Transcriptional regulation and stabilization of left-right neuronal identity in C. elegans. Genes Dev 2009; 23:345 - 58; http://dx.doi.org/10.1101/gad.1763509; PMID: 19204119
   PubMed Web of Science ®Google Scholar
• Tanaka-Hino M, Sagasti A, Hisamoto N, Kawasaki M, Nakano S, Ninomiya-Tsuji J, et al. SEK-1 MAPKK mediates Ca2+ signaling to determine neuronal asymmetric development in Caenorhabditis elegans. EMBO Rep 2002; 3:56 - 62; http://dx.doi.org/10.1093/embo-reports/kvf001; PMID: 11751572
   PubMed Web of Science ®Google Scholar
• Wes PD, Bargmann CI. C. elegans odour discrimination requires asymmetric diversity in olfactory neurons. Nature 2001; 410:698 - 701; http://dx.doi.org/10.1038/35070581; PMID: 11287957
   PubMed Web of Science ®Google Scholar
• Chuang CF, Bargmann CIA. A Toll-interleukin 1 repeat protein at the synapse specifies asymmetric odorant receptor expression via ASK1 MAPKKK signaling. Genes Dev 2005; 19:270 - 81; http://dx.doi.org/10.1101/gad.1276505; PMID: 15625192
   PubMed Web of Science ®Google Scholar
• Chuang CF, Vanhoven MK, Fetter RD, Verselis VK, Bargmann CI. An innexin-dependent cell network establishes left-right neuronal asymmetry in C. elegans. Cell 2007; 129:787 - 99; http://dx.doi.org/10.1016/j.cell.2007.02.052; PMID: 17512411
   PubMed Web of Science ®Google Scholar
• Schumacher JA, Hsieh YW, Chen S, Pirri JK, Alkema MJ, Li WH, et al. Intercellular calcium signaling in a gap junction-coupled cell network establishes asymmetric neuronal fates in C. elegans. Development 2012; 139:4191 - 201; http://dx.doi.org/10.1242/dev.083428; PMID: 23093425
   PubMed Web of Science ®Google Scholar
• Tamura K, Dudley J, Nei M, Kumar S. MEGA4: Molecular Evolutionary Genetics Analysis (MEGA) software version 4.0. Mol Biol Evol 2007; 24:1596 - 9; http://dx.doi.org/10.1093/molbev/msm092; PMID: 17488738
   PubMed Web of Science ®Google Scholar
• Kunitomo H, Uesugi H, Kohara Y, Iino Y. Identification of ciliated sensory neuron-expressed genes in Caenorhabditis elegans using targeted pull-down of poly(A) tails. Genome Biol 2005; 6:R17; http://dx.doi.org/10.1186/gb-2005-6-2-r17; PMID: 15693946
   PubMedGoogle Scholar
• Hamamichi S, Rivas RN, Knight AL, Cao S, Caldwell KA, Caldwell GA. Hypothesis-based RNAi screening identifies neuroprotective genes in a Parkinson’s disease model. Proc Natl Acad Sci U S A 2008; 105:728 - 33; http://dx.doi.org/10.1073/pnas.0711018105; PMID: 18182484
   PubMed Web of Science ®Google Scholar
• Kao CY, Los FC, Huffman DL, Wachi S, Kloft N, Husmann M, et al. Global functional analyses of cellular responses to pore-forming toxins. PLoS Pathog 2011; 7:e1001314; http://dx.doi.org/10.1371/journal.ppat.1001314; PMID: 21408619
   PubMedGoogle Scholar
• Meissner B, Rogalski T, Viveiros R, Warner A, Plastino L, Lorch A, et al. Determining the sub-cellular localization of proteins within Caenorhabditis elegans body wall muscle. PLoS One 2011; 6:e19937; http://dx.doi.org/10.1371/journal.pone.0019937; PMID: 21611156
   PubMedGoogle Scholar
• Meissner B, Warner A, Wong K, Dube N, Lorch A, McKay SJ, et al. An integrated strategy to study muscle development and myofilament structure in Caenorhabditis elegans. PLoS Genet 2009; 5:e1000537; http://dx.doi.org/10.1371/journal.pgen.1000537; PMID: 19557190
   PubMedGoogle Scholar