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CELL ADHESION AND ASSEMBLY: THE IRRE RECOGNITION MODULE Review

A Brief Overview on IRM Function Across Evolution

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Pages 264-269 | Received 16 Jan 2014, Accepted 24 Apr 2014, Published online: 08 Jul 2014

REFERENCES

  • Artero, R. D., Castanon, I., & Baylies, M. K. (2001). The immunoglobulin-like protein Hibris functions as a dose-dependent regulator of myoblast fusion and is differentially controlled by Ras and Notch signaling. Development, 128, 4251–4264.
  • Bao, S., & Cagan, R. (2005). Preferential adhesion mediated by Hibris and Roughest regulates morphogenesis and patterning in the Drosophila eye. Dev Cell, 8, 925–935.
  • Bao, S., Fischbach, K.-F., Corbin, V., & Cagan, R. L. (2010). Preferential adhesion maintains separation of ommatidia in the Drosophila eye. Dev Biol, 344, 948–956.
  • Bhalla, K., Luo, Y., Buchan, T., Beachem, M. A., Guzauskas, G. F., Ladd, S., et al. (2008). Alterations in CDH15 and KIRREL3 in patients with mild to severe intellectual disability. Am J Hum Genet, 83, 703–713.
  • Boschert, U., Ramos, R. G., Tix, S., Technau, G. M., & Fischbach, K. F. (1990). Genetic and developmental analysis of irreC, a genetic function required for optic chiasm formation in Drosophila. J Neurogenet, 6, 153–171.
  • Cagan, R. L. (2011). The Drosophila nephrocyte. Curr Opin Nephrol Hypertens, 20, 409–415.
  • Chao, D. L., & Shen, K. (2008). Functional dissection of SYG-1 and SYG-2, cell adhesion molecules required for selective synaptogenesis in C. elegans. Mol Cell Neurosci, 39, 248–257.
  • Christensen, E. I., Birn, H., Storm, T., Weyer, K., & Nielsen, R. (2012). Endocytic receptors in the renal proximal tubule Physiology (Bethesda), 27, 223–236.
  • Crossley, A. (1985). Nephrocytes and pericardial cells. In: Comprehensive insect physiology, biochemistry and Pharmacology (Vol. 3, pp. 487–516). Oxford: Pergamon Press.
  • Donoviel, D., Freed, D., Vogel, H., Potter, D.G., Hawkins, E., Barrish JP (2001). Proteinuria and perinatal lethality in mice lacking NEPH1, a novel protein with homology to NEPHRIN. Mol Cell Biol, 21, 4829–4836.
  • Dworak, H. A., Charles, M. A., Pellerano, L. B., & Sink, H. (2001). Characterization of Drosophila hibris, a gene related to human nephrin. Development, 128, 4265–4276.
  • Fischbach, K.-F., & Dittrich, A. P. M. (1989). The optic lobe of Drosophila melanogaster. I. A Golgi analysis of wild-type structure. Cell Tissue Res, 258, 441–475.
  • Fischbach, K.-F., Linneweber, G. A., Andlauer, T. F. M., Hertenstein, A., Bonengel, B., & Chaudhary, K. (2009). The irre cell recognition module (IRM) proteins. J Neurogenet, 23, 48–67.
  • Galletta, B. J., Chakravarti, M., Banerjee, R., & Abmayr, S. M. (2004). SNS: Adhesive properties, localization requirements and ectodomain dependence in S2 cells and embryonic myoblasts. Mech Dev, 121, 1455–1468.
  • Gerke, P., Benzing, T., & Höhne, M. (2006). Neuronal expression and interaction with the synaptic protein CASK suggest a role for Neph1 and Neph2 in synaptogenesis. J Comp Neurol, 478, 466–475.
  • Grahammer, F., Schell, C., & Huber, T. B. (2013). The podocyte slit diaphragm–from a thin grey line to a complex signalling hub. Nat Rev Nephrol, 9, 587–598.
  • Helmstädter, M., Lüthy, K., Gödel, M., Simons, M., Ashish, Nihalani, D., et al. (2012). Functional study of mammalian Neph proteins in Drosophila melanogaster. PloS one, 7, e40300.
  • Jäger, R., & Fischbach, K. (1989). Mass histology of adult heads. In M. Ashburner (Ed.), Drosophila: A Laboratory Manual (pp. 254–259). Cold Spring Harbor, NY: Cold Spring Harbor Laboratory Press.
  • Kestilä, M., Lenkkeri, U., Männikkö, M., Lamerdin, J., McCready, P., Putaala, H., et al. (1998). Positionally cloned gene for a novel glomerular protein–nephrin–is mutated in congenital nephrotic syndrome. Mol Cell, 1, 575–582.
  • Kim, J. M., Wu, H., Green, G., Winkler, C. A., Kopp, J. B., Miner, J. H., et al. (2003). CD2-associated protein haploinsufficiency is linked to glomerular disease susceptibility. Science, 300, 1298–1300.
  • Kramer-Zucker, A. G., Wiessner, S., Jensen, A. M., & Drummond, I.A. (2005). Organization of the pronephric filtration apparatus in zebrafish requires Nephrin, Podocin and the FERM domain protein Mosaic eyes. Dev Biol, 285, 316–329.
  • Meinertzhagen, I. A., Takemura, S., Lu, Z., Huang, S., Gao, S., Ting, C.-Y., & Lee, C.-H. (2009). From form to function: the ways to know a neuron. J Neurogenet, 23, 68–77.
  • Mills, R., & King, R. (1965). The pericardial cells of Drosophila melanogaster. Q J Microsc Sci, 106, 261–268.
  • Na, J., & Cagan, R. (2013). The Drosophila nephrocyte: back on stage. J Am Soc Nephrol, 24, 161–163.
  • Neumann-Haefelin, E., Kramer-Zucker, A., Slanchev, K., Hartleben, B., Noutsou, F., Martin, K., et al. (2010). A model organism approach: defining the role of Neph proteins as regulators of neuron and kidney morphogenesis. Hum Mol Genet, 19, 2347–2359.
  • Nishida, K., Hoshino, M., Kawaguchi, Y., & Murakami, F. (2010). Ptf1a directly controls expression of immunoglobulin superfamily molecules Nephrin and Neph3 in the developing central nervous system. J Biol Chem, 285, 373–380.
  • Nishida, K., Nakayama, K., Yoshimura, S., & Murakami, F. (2011). Role of Neph2 in pontine nuclei formation in the developing hindbrain. Mol Cell Neurosci, 46, 662–670.
  • Ramos, R. G., Igloi, G. L., Lichte, B., Baumann, U., Maier, D., Schneider, T., et al. (1993). The irregular chiasm C-roughest locus of Drosophila, which affects axonal projections and programmed cell death, encodes a novel immunoglobulin-like protein. Genes Dev, 7, 2533–2547.
  • Reiser, J., Polu, K. R., Möller, C. C., Kenlan, P., Altintas, M. M., Wei, C., et al. (2005). TRPC6 is a glomerular slit diaphragm-associated channel required for normal renal function. Nat Genet, 37, 739–744.
  • Reiter, C., Schimansky, T., Nie, Z., & Fischbach, K. F. (1996). Reorganization of membrane contacts prior to apoptosis in the Drosophila retina: the role of the IrreC-rst protein. Development, 122, 1931–1940.
  • Rochlin, K., Yu, S., Roy, S., & Baylies, M. K. (2010). Myoblast fusion: when it takes more to make one. Dev Biol, 341, 66–83.
  • Roselli, S., Gribouval, O., Boute, N., Sich, M., Benessy, F., Attié, T., et al. (2002). Podocin localizes in the kidney to the slit diaphragm area. Am J Pathol, 160, 131–139.
  • Ruiz-Gómez, M., Coutts, N., Price, A., Taylor, M. V., & Bate, M. (2000). Drosophila dumbfounded: a myoblast attractant essential for fusion. Cell, 102, 189–198.
  • Ruotsalainen, V., Ljungberg, P., Wartiovaara, J., Lenkkeri, U., Kestilä, M., Jalanko, H., et al. (1999). Nephrin is specifically located at the slit diaphragm of glomerular podocytes. Proc Natl Acad Sci U S A, 96, 7962–7967.
  • Schneider, T., Reiter, C., Eule, E., Bader, B., Lichte, B., Nie, Z., et al. (1995). Restricted expression of the irreC-rst protein is required for normal axonal projections of columnar visual neurons. Neuron, 15, 259–271.
  • Sellin, L., Huber, T., Gerke, P., & Quack, I. (2003). NEPH1 defines a novel family of podocin interacting proteins. FASEB J, 17, 115–117.
  • Shankland, S. J., Pippin, J. W., Reiser, J., & Mundel, P. (2007). Podocytes in culture: past, present, and future. Kidney Int, 72, 26–36.
  • Shen, K., & Bargmann, C. I. (2003). The immunoglobulin superfamily protein SYG-1 determines the location of specific synapses in C. elegans. Cell, 112, 619–630.
  • Shen, K., Fetter, R. D., & Bargmann, C. I. (2004). Synaptic specificity is generated by the synaptic guidepost protein SYG-2 and its receptor, SYG-1. Cell, 116, 869–881.
  • Simons, M., & Huber, T. B. (2009). Flying podocytes. Kidney Int, 75, 455–457.
  • Srinivas, B. P., Woo, J., Leong, W. Y., & Roy, S. (2007). A conserved molecular pathway mediates myoblast fusion in insects and vertebrates. Nat Genet, 39, 781–786.
  • Strünkelnberg, M., Bonengel, B., Moda, L. M., Hertenstein, A., de Couet, H. G., Ramos, R. G., & Fischbach, K. F. (2001). Rst and its paralogue kirre act redundantly during embryonic muscle development in Drosophila. Development, 128, 4229–4239.
  • Strünkelnberg, M., de Couet, H. G., Hertenstein, A., & Fischbach, K.-F. (2003). Interspecies comparison of a gene pair with partially redundant function: the rst and kirre genes in D. virilis and D. melanogaster. J Mol Evol, 56, 187–197.
  • Sugie, A., Umetsu, D., Yasugi, T., Fischbach, K.-F., & Tabata, T. (2010). Recognition of pre- and postsynaptic neurons via nephrin/NEPH1 homologs is a basis for the formation of the Drosophila retinotopic map. Development, 137, 3303–3313.
  • Surinder, K., & King, R. (1967). The ultrastructure of the wreath cells of Drosophila melanogaster larvae. Protoplasma, 63, 343–352.
  • Venugopala Reddy, G., Reiter, C., Shanbhag, S., Fischbach, K. F., & Rodrigues, V. (1999). Irregular chiasm-C-roughest, a member of the immunoglobulin superfamily, affects sense organ spacing on the Drosophila antenna by influencing the positioning of founder cells on the disc ectoderm. Dev Genes Evol, 209, 581–591.
  • Völker, L.A., Petry, M., Abdelsabour-Khalaf, M., Schweizer, H., Yusuf, F., Busch, T., et al. (2012). Comparative analysis of Neph gene expression in mouse and chicken development. Histochem Cell Biol, 137, 355–366.
  • Weavers, H., Pieto-Sánchez, S., Grawe, F., Garcia-López, A., Artero, R., Wilsch-Braeuninger, M., et al. (2009). The insect nephrocyte is a podocyte-like cell with a filtration slit diaphragm. Nature, 457, 322–326.
  • Winn, M. P., Conlon, P. J., Lynn, K. L., Farrington, M. K., Creazzo, T., Hawkins, A. F., et al. (2005). A mutation in the TRPC6 cation channel causes familial focal segmental glomerulosclerosis. Science, 308, 1801–1804.
  • Wolff, T., & Ready, D. F. (1991). Cell death in normal and rough eye mutants of Drosophila. Development, 113, 825–839.
  • Zhang, F., Zhao, Y., Chao, Y., Muir, K., & Han, Z. (2013a). Cubilin and amnionless mediate protein Reabsorption in Drosophila nephrocytes. J Am Soc Nephrol, 24, 209–216.
  • Zhang, F., Zhao, Y., & Han, Z. (2013b). An in vivo functional analysis system for renal gene discovery in Drosophila pericardial nephrocytes. J Am Soc Nephrol, 24, 191–197.
  • Zhuang, S., Shao, H., Guo, F., Trimble, R., Pearce, E., & Abmayr, S. M. (2009). Sns and Kirre, the Drosophila orthologs of Nephrin and Neph1, direct adhesion, fusion and formation of a slit diaphragm-like structure in insect nephrocytes. Development, 136, 2335–2344.

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