Diverse evolutionary paths to cell adhesion

Trends in Cell Biology

Volumn 20, Issue 12, 2010, Pages 734-742

  Abedin, Monika ^a   King, Nicole ^a  

^a UNIVERSITY OF CALIFORNIA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ALGA; CELL ADHESION; CELL JUNCTION; CELL MATURATION; CELL WALL; COMPARATIVE STUDY; CYTOLOGY; DICTYOSTELIUM; DROSOPHILA; EXTRACELLULAR MATRIX; MOLECULAR PHYLOGENY; NONHUMAN; PRIORITY JOURNAL; REVIEW;

ANIMALS; BIOLOGICAL EVOLUTION; CELL ADHESION; EUKARYOTA; EXTRACELLULAR MATRIX; FUNGI; PLANTS;

ALGAE; ANIMALIA; DICTYOSTELIUM; FUNGI; VOLVOX;

EID: 78650193431     PISSN: 09628924     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tcb.2010.08.002     Document Type: Review

References (74)

1. Jarvis M.C., et al. Intercellular adhesion and cell separation in plants. Plant Cell Environ. 2003, 26:977-989.
2. Gumbiner B.M. Cell adhesion: the molecular basis of tissue architecture and morphogenesis. Cell 1996, 84:345-357.
3. King N. The unicellular ancestry of animal development. Dev. Cell 2004, 7:313-325.
4. Baldauf S.L. The deep roots of eukaryotes. Science 2003, 300:1703-1706.
5. Carroll S.B. Chance and necessity: the evolution of morphological complexity and diversity. Nature 2001, 409:1102-1109.
6. King N., et al. The genome of the choanoflagellate Monosiga brevicollis and the origin of metazoans. Nature 2008, 451:783-788.
7. Prochnik S.E., et al. Genomic analysis of organismal complexity in the multicellular green alga Volvox carteri. Science 2010, 329:223-226.
8. Cock J.M., et al. The Ectocarpus genome and the independent evolution of multicellularity in brown algae. Nature 2010, 465:617-621.
9. Medina M., et al. Phylogeny of Opisthokonta and the evolution of multicellularity and complexity in Fungi and Metazoa. Int. J. Astrobiol. 2003, 2:203-211.
10. Nozaki H., et al. Origin and evolution of the colonial volvocales (Chlorophyceae) as inferred from multiple, chloroplast gene sequences. Mol. Phylogenet. Evol. 2000, 17:256-268.
11. Tyler S. Epithelium - the primary building block for metazoan complexity. Integr. Comp. Biol. 2003, 43:55-63.
12. Pokutta S., Weis W.I. Structure and mechanism of cadherins and catenins in cell-cell contacts. Annu. Rev. Cell Dev. Biol. 2007, 23:237-261.
13. Boury-Esnault N., et al. Larval development in the Homoscleromorpha (Porifera, Demospongiae). Invertebr. Biol. 2003, 122:187-202.
14. Sakarya O., et al. A post-synaptic scaffold at the origin of the animal kingdom. PLoS ONE 2007, 1-9.
15. Abedin M., King N. The premetazoan ancestry of cadherins. Science 2008, 319:946-948.
16. Spiegel I., Peles E. Cellular junctions of myelinated nerves (Review). Mol. Membr. Biol. 2002, 19:95-101.
17. Bing-Yu M., et al. Morphological and functional studies on the epidermal cells of amphioxus (Branchiostoma belcheri tsingtauense) at different developmental stages. Chin. J. Oceanol. Limnol. 1997, 15:236-241.
18. Banerjee S., et al. Organization and function of septate junctions: an evolutionary perspective. Cell. Biochem. Biophys. 2006, 46:65-77.
19. Nichols S.A., et al. Early evolution of animal cell signaling and adhesion genes. Proc. Natl. Acad. Sci. U. S. A. 2006, 103:12451-12456.
20. Ledger P.W. Septate junctions in the calcareous sponge Sycon ciliatum. Tissue Cell 1975, 7:13-18.
21. Leys S.P., et al. Epithelia and integration in sponges. Integr. Comp. Biol. 2009, 49:167-177.
22. Shestopalov V.I., Panchin Y. Pannexins and gap junction protein diversity. Cell. Mol. Life Sci. 2008, 65:376-394.
23. Chapman J.A., et al. The dynamic genome of Hydra. Nature 2010, 464:592-596.
24. Westfall J.A., et al. Neuro-epitheliomuscular cell and neuro-neuronal gap junctions in Hydra. J. Neurocytol. 1980, 9:725-732.
25. Litvin O., et al. What is hidden in the pannexin treasure trove: the sneak peek and the guesswork. J. Cell Mol. Med. 2006, 10:613-634.
26. Sasakura Y., et al. A genomewide survey of developmentally relevant genes in Ciona intestinalis. X. Genes for cell junctions and extracellular matrix. Dev. Genes Evol. 2003, 213:303-313.
27. Lane N.J., et al. Tight and gap junctions in the intestinal tract of tunicates (Urochordata): a freeze-fracture study. J. Cell Sci. 1986, 84:1-17.
28. Lane N.J., et al. Cell junctions in amphioxus (Cephalochordata): a thin section and freeze-fracture study. Tissue Cell 1987, 19:399-411.
29. Anderson J.M., et al. Setting up a selective barrier at the apical junction complex. Curr. Opin. Cell Biol. 2004, 16:140-145.
30. Wu V.M., et al. Sinuous is a Drosophila claudin required for septate junction organization and epithelial tube size control. J. Cell Biol. 2004, 164:313-323.
31. Behr M., et al. The claudin-like megatrachea is essential in septate junctions for the epithelial barrier function in Drosophila. Dev. Cell 2003, 5:611-620.
32. Yagi T. Clustered protocadherin family. Dev. Growth Differ. 2008, 50(Suppl. 1):S131-S140.
33. Halbleib J.M., Nelson W.J. Cadherins in development: cell adhesion, sorting, and tissue morphogenesis. Genes Dev. 2006, 20:3199-3214.
34. Boute N., et al. Type IV collagen in sponges, the missing link in basement membrane ubiquity. Biol. Cell 1996, 88:37-44.
35. Ereskovsky A.V., et al. The Homoscleromorph sponge Oscarella lobularis, a promising sponge model in evolutionary and developmental biology: model sponge Oscarella lobularis. Bioessays 2009, 31:89-97.
36. Aouacheria A., et al. Insights into early extracellular matrix evolution: spongin short chain collagen-related proteins are homologous to basement membrane type IV collagens and form a novel family widely distributed in invertebrates. Mol. Biol. Evol. 2006, 23:2288-2302.
37. Muller W.E., Muller I.M. Analysis of the sponge [Porifera] gene repertoire: implications for the evolution of the metazoan body plan. Prog. Mol. Subcell. Biol. 2003, 37:1-33.
38. Brower D.L., et al. Molecular evolution of integrins: genes encoding integrin beta subunits from a coral and a sponge. Proc. Natl. Acad. Sci. U. S. A. 1997, 94:9182-9187.
39. Sebe-Pedros A., et al. Ancient origin of the integrin-mediated adhesion and signaling machinery. Proc. Natl. Acad. Sci. U. S. A. 2010, 107:10142-10147.
40. King N., et al. Evolution of key cell signaling and adhesion protein families predates animal origins. Science 2003, 301:361-363.
41. Bonner J.T. The origins of multicellularity. Int. Biol. 1997, 1:27-36.
42. Nelson W.J. Regulation of cell-cell adhesion by the cadherin-catenin complex. Biochem. Soc. Trans. 2008, 36:149-155.
43. Brar S.K., Siu C.H. Characterization of the cell adhesion molecule gp24 in Dictyostelium discoideum. Mediation of cell-cell adhesion via a Ca(2+)-dependent mechanism. J. Biol. Chem. 1993, 268:24902-24909.
44. Sesaki H., Siu C.H. Novel redistribution of the Ca(2+)-dependent cell adhesion molecule DdCAD-1 during development of Dictyostelium discoideum. Dev. Biol. 1996, 177:504-516.
45. Lin Z., et al. Solution structures of the adhesion molecule DdCAD-1 reveal new insights into Ca(2+)-dependent cell-cell adhesion. Nat. Struct. Mol. Biol. 2006, 13:1016-1022.
46. Siu C.H., et al. Regulation of cell-cell adhesion during Dictyostelium development. Semin. Cell Dev. Biol. 2004, 15:633-641.
47. Wang J., et al. The membrane glycoprotein gp150 is encoded by the lagC gene and mediates cell-cell adhesion by heterophilic binding during Dictyostelium development. Dev. Biol. 2000, 227:734-745.
48. Wong E., et al. Disruption of the gene encoding the cell adhesion molecule DdCAD-1 leads to aberrant cell sorting and cell-type proportioning during Dictyostelium development. Development 2002, 129:3839-3850.
49. Nicol A., et al. Cell-sorting in aggregates of Dictyostelium discoideum. J. Cell Sci. 1999, 112:3923-3929.
50. Steinberg M.S. Differential adhesion in morphogenesis: a modern view. Curr. Opin. Genet. Dev. 2007, 17:281-286.
51. Sallee J.L., et al. Regulation of cell adhesion by protein-tyrosine phosphatases: II. Cell-cell adhesion. J. Biol. Chem. 2006, 281:16189-16192.
52. Secko D.M., et al. An activated Ras protein alters cell adhesion by dephosphorylating Dictyostelium DdCAD-1. Microbiology 2006, 152:1497-1505.
53. Grimson M.J., et al. Adherens junctions and beta-catenin-mediated cell signalling in a non-metazoan organism. Nature 2000, 408:727-731.
54. Nelson W.J., Nusse R. Convergence of Wnt, Beta-catenin and cadherin pathways. Science 2004, 303:1483-1487.
55. Nakada T., et al. Molecular systematics of Volvocales (Chlorophyceae, Chlorophyta) based on exhaustive 18S rRNA phylogenetic analyses. Mol. Phylogenet. Evol. 2008, 48:281-291.
56. Kirk D.L. A twelve-step program for evolving multicellularity and a division of labor. Bioessays 2005, 27:299-310.
57. Woessner J.P., Goodenough U.W. Volvocine cell walls and their constituent glycoproteins: an evolutionary perspective. Protoplasma 1994, 1-14.
58. Fulton A.B. Colonial development in Pandorina morum. II. Colony morphogenesis and formation of the extracellular matrix. Dev. Biol. 1978, 64:236-251.
59. Adair W.S., et al. Nucleated assembly of Chlamydomonas and Volvox cell walls. J. Cell Biol. 1987, 105:2373-2382.
60. Adair W.S., Appel H. Identification of a highly conserved hydroxyproline-rich glycoprotein in the cell wall of Chlamydomonas reinhardtii and two other Volvocales. Planta 1989, 179:381-386.
61. Hallmann A., Kirk D.L. The developmentally regulated ECM glycoprotein ISG plays an essential role in organizing the ECM and orienting the cells of Volvox. J. Cell Sci. 2000, 113:4605-4617.
62. Woessner J.P., et al. Domain conservation in several volvocalean cell wall proteins. Plant Mol. Biol. 1994, 26:947-960.
63. Hallmann A. Extracellular matrix and sex-inducing pheromone in Volvox. Int. Rev. Cytol. 2003, 227:131-182.
64. Hallmann A. The pherophorins: common, versatile building blocks in the evolution of extracellular matrix architecture in Volvocales. Plant. J. 2006, 45:292-307.
65. Willats W.G., et al. Modulation of the degree and pattern of methyl-esterification of pectic homogalacturonan in plant cell walls. Implications for pectin methyl esterase action, matrix properties, and cell adhesion. J. Biol. Chem. 2001, 276:19404-19413.
66. Sarkar P., et al. Plant cell walls throughout evolution: towards a molecular understanding of their design principles. J. Exp. Bot. 2009, 60:3615-3635.
67. Klis, F.M. et al. (2007) A molecular and genomic view of the fungal cell wall. In Biology of the Fungal Cell, The Mycota VIII (2nd edn) (Howard, R.J. and Gow, N.A.R., eds.) pp. 97-112, Springer.
68. Marshall C.R., Valentine J.W. The importance of preadapted genomes in the origin of the animal bodyplans and the Cambrian explosion. Evolution 2009, 64:1189-1201.
69. Monod J. Chance and Necessity 1971, Vintage Books.
70. Magie C.R., Martindale M.Q. Cell-cell adhesion in the cnidaria: insights into the evolution of tissue morphogenesis. Biol. Bull. 2008, 214:218-232.
71. Sabella C., et al. Cyclosporin A suspends transplantation reactions in the marine sponge Microciona prolifera. J. Immunol. 2007, 179:5927-5935.
72. Lane N.J., Chandler H.J. Definitive evidence for the existence of tight junctions in invertebrates. J. Cell Biol. 1980, 86:765-774.
73. Reber-Muller S., et al. Integrin and talin in the jellyfish Podocoryne carnea. Cell Biol. Int. 2001, 25:753-769.
74. Srivastava M., et al. The Amphimedon queenslandica genome and the evolution of animal complexity. Nature 2010, 446:720-726.