Regulation of septin organization and function in yeast

Trends in Cell Biology

Volumn 13, Issue 8, 2003, Pages 403-409

  Longtine, Mark S ^a   Bi, Erfei ^b  

^a OKLAHOMA STATE UNIVERSITY   (United States)

^b UNIVERSITY OF PENNSYLVANIA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

MYOSIN ADENOSINE TRIPHOSPHATASE; SEPTIN;

BUD; BUDDING; CELL CYCLE; CELL MEMBRANE; CELL STRUCTURE; CYTOKINESIS; DNA REPLICATION; MOLECULAR DYNAMICS; MORPHOGENESIS; NONHUMAN; PRIORITY JOURNAL; PROTEIN ANALYSIS; PROTEIN FUNCTION; PROTEIN LOCALIZATION; PROTEIN STRUCTURE; REVIEW; SACCHAROMYCES CEREVISIAE; TEMPERATURE SENSITIVITY; YEAST; YEAST CELL;

EUKARYOTA; SACCHAROMYCES; SACCHAROMYCES CEREVISIAE; SACCHAROMYCETALES;

EID: 0042848696     PISSN: 09628924     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0962-8924(03)00151-X     Document Type: Review

References (81)

1. Cooper J.A., Kiehart D.P. Septins may form a ubiquitous family of cytoskeletal filaments. J. Cell Biol. 134:1996;1345-1348.
2. Longtine M.S., et al. The septins: roles in cytokinesis and other processes. Curr. Opin. Cell Biol. 8:1996;106-119.
3. Field C.M., Kellogg D. Septins: cytoskeletal polymers or signalling GTPases? Trends Cell Biol. 9:1999;387-394.
4. Trimble W.S. Septins: a highly conserved family of membrane-associated GTPases with functions in cell division and beyond. J. Membr. Biol. 169:1999;75-81.
5. Kartmann B., Roth D. Novel roles for mammalian septins: from vesicle trafficking to oncogenesis. J. Cell Sci. 114:2001;839-844.
6. Nguyen T.Q., et al. The C. elegans septin genes, unc-59 and unc-61, are required for normal postembryonic cytokinesis and morphogenesis but have no essential function in embryogenesis. J. Cell Sci. 113:2000;3825-3837.
7. Momany M., et al. Characterization of the Aspergillus nidulans septin (asp) gene family. Genetics. 157:2001;969-977.
8. Gladfelter A.S., et al. The septin cortex at the yeast mother-bud neck. Curr. Opin. Microbiol. 4:2001;681-689.
9. Macara I.G., et al. Mammalian septins nomenclature. Mol. Biol. Cell. 13:2002;4111-4113.
10. Faty M., et al. Septins: a ring to part mother and daughter. Curr. Genet. 41:2002;123-131.
11. Field C.M., et al. A purified Drosophila septin complex forms filaments and exhibits GTPase activity. J. Cell Biol. 133:1996;605-616.
12. Hsu S.-C., et al. Subunit composition, protein interactions, and structures of the mammalian brain sec6/8 complex and septin filaments. Neuron. 20:1998;1111-1122.
13. Frazier J.A., et al. Polymerization of purified yeast septins: evidence that organized filament arrays may not be required for septin function. J. Cell Biol. 143:1998;737-749.
14. Mendoza M., et al. GTP binding induces filament assembly of a recombinant septin. Curr. Biol. 12:2002;1858-1863.
15. Sheffield P.J., et al. Borg/Septin interactions and the assembly of mammalian septin heterodimers, trimers and filaments. J. Biol. Chem. 278:2003;3483-3488.
16. Kinoshita M., et al. Self- and actin-templated assembly of mammalian septins. Dev. Cell. 3:2002;791-802.
17. Casamayor A., Snyder M. Molecular dissection of a yeast septin: distinct domains are required for septin interaction, localization, and function. Mol. Cell. Biol. 23:2003;2762-2777.
18. Mitchison T.J., Field C.M. Cytoskeleton: what does GTP do for septins? Curr. Biol. 12:2002;R788-R790.
19. Zhang J., et al. Phosphatidylinositol polyphosphate binding to the mammalian septin H5 is modulated by GTP. Curr. Biol. 9:1999;1458-1467.
20. Kim H.B., et al. Cellular morphogenesis in the Saccharomyces cerevisiae cell cycle: localization of the CDC3 gene product and the timing of events at the budding site. J. Cell Biol. 112:1991;535-544.
21. Ford S.K., Pringle J.R. Cellular morphogenesis in the Saccharomyces cerevisiae cell cycle: localization of the CDC11 gene product and the timing of events at the budding site. Dev. Genet. 12:1991;281-292.
22. Lippincott J., et al. The Tem1 small GTPase controls actomyosin and septin dynamics during cytokinesis. J. Cell Sci. 114:2001;1379-1386.
23. Fares H., et al. Identification of a developmentally regulated septin and involvement of the septins in spore formation in Saccharomyces cerevisiae. J. Cell Biol. 132:1996;399-411.
24. De Virgilio C., et al. SPR28, a sixth member of the septin gene family in Saccharomyces cerevisiae that is expressed specifically in sporulating cells. Microbiology. 142:1996;2897-2905.
25. Byers B., Goetsch L. A highly ordered ring of membrane-associated filaments in budding yeast. J. Cell Biol. 69:1976;717-721.
26. Byers B., Goetsch L. Loss of the filamentous ring in cytokinesis-defective mutants of budding yeast. J. Cell Biol. 70:1976;35.
27. Byers B. Cytology of the yeast life cycle. Strathern J.N., et al. The Molecular Biology of the Yeast Saccharomyces: Life Cycle and Inheritance. 1981;59-96 Cold Spring Harbor Laboratory Press.
28. Bi E. Cytokinesis in budding yeast: the relationship between actomyosin ring function and septum formation. Cell Struct. Funct. 26:2001;529-537.
29. Bi E., et al. Involvement of an actomyosin contractile ring in Saccharomyces cerevisiae cytokinesis. J. Cell Biol. 142:1998;1301-1312.
30. Tolliday N., et al. Direct evidence for a critical role of myosin II in budding yeast cytokinesis and the evolvability of new cytokinetic mechanisms in the absence of myosin II. Mol. Biol. Cell. 14:2003;798-809.
31. Lippincott J., Li R. Sequential assembly of myosin II, an IQGAP-like protein, and filamentous actin to a ring structure involved in budding yeast cytokinesis. J. Cell Biol. 140:1998;355-366.
32. Schmidt M., et al. In budding yeast, contraction of the actomyosin ring and formation of the primary septum at cytokinesis depend on each other. J. Cell Sci. 115:2002;293-302.
33. Neufeld T.P., Rubin G.M. The Drosophila peanut gene is required for cytokinesis and encodes a protein similar to yeast putative bud neck filament proteins. Cell. 77:1994;371-379.
34. Fares H., et al. Localization and possible functions of Drosophila septins. Mol. Biol. Cell. 6:1995;1843-1859.
35. Kinoshita M., et al. Nedd5, a mammalian septin, is a novel cytoskeletal component interacting with actin-based structures. Genes Dev. 11:1997;1535-1547.
36. Surka M.C., et al. The mammalian septin MSF localizes with microtubules and is required for the completion of cytokinesis. Mol. Biol. Cell. 13:2002;3532-3545.
37. Hales K.G., et al. Cytokinesis: an emerging unified theory for eukaryotes? Curr. Opin. Cell Biol. 11:1999;717-725.
38. Casamayor A., Snyder M. Bud-site selection and cell polarity in budding yeast. Curr. Opin. Microbiol. 5:2002;179-186.
39. Chant J., et al. Role of Bud3p in producing the axial budding pattern of yeast. J. Cell Biol. 129:1995;767-778.
40. Sanders S.L., Herskowitz I. The Bud4 protein of yeast, required for axial budding, is localized to the mother/bud neck in a cell cycle-dependent manner. J. Cell Biol. 134:1996;413-427.
41. Roemer T., et al. Selection of axial growth sites in yeast requires Axl2p, a novel plasma membrane glycoprotein. Genes Dev. 10:1996;777-793.
42. Schenkman L.R., et al. The role of cell cycle-regulated expression in the localization of spatial landmark proteins in yeast. J. Cell Biol. 156:2002;829-841.
43. DeMarini D.J., et al. A septin-based hierarchy of proteins required for localized deposition of chitin in the Saccharomyces cerevisiae cell wall. J. Cell Biol. 139:1997;75-93.
44. Takizawa P.A., et al. Plasma membrane compartmentalization in yeast by messenger RNA transport and a septin diffusion barrier. Science. 290:2000;341-344.
45. Barral Y., et al. Compartmentalization of the cell cortex by septins is required for maintenance of cell polarity in yeast. Mol. Cell. 5:2000;841-851.
46. Jensen S., et al. Spatial regulation of the guanine nucleotide exchange factor Lte1 in Saccharomyces cerevisiae. J. Cell Sci. 115:2002;4977-4991.
47. Seshan A., et al. Control of Lte1 localization by cell polarity determinants and Cdc14. Curr. Biol. 12:2002;2098-2110.
48. Segal M., Bloom K. Control of spindle polarity and orientation in Saccharomyces cerevisiae. Trends Cell Biol. 11:2001;160-166.
49. Kusch J., et al. Microtubule capture by the cleavage apparatus is required for proper spindle positioning in yeast. Genes Dev. 16:2002;1627-1639.
50. McMillan J.N., et al. A morphogenesis checkpoint monitors the actin cytoskeleton in yeast. J. Cell Biol. 142:1998;1487-1499.
51. Barral Y., et al. Nim1-related kinases coordinate cell cycle progression with the organization of the peripheral cytoskeleton in yeast. Genes Dev. 13:1999;176-187.
52. Longtine M.S., et al. Septin-dependent assembly of a cell cycle-regulatory module in Saccharomyces cerevisiae. Mol. Cell. Biol. 20:2000;4049-4061.
53. Bardin A.J., et al. A mechanism for coupling exit from mitosis to partitioning of the nucleus. Cell. 102:2000;21-31.
54. Castillon G.A., et al. Septins have a dual role in controlling mitotic exit in budding yeast. Curr. Biol. 13:2003;654-658.
55. Lipschutz J.H., Mostov K.E. Exocytosis: the many masters of the exocyst. Curr. Biol. 12:2002;R212-R214.
56. Beites C.L., et al. The septin CDCrel-1 binds syntaxin and inhibits exocytosis. Nat. Neurosci. 2:1999;434-439.
57. Jantti J., et al. Characterization of temperature-sensitive mutations in the yeast syntaxin 1 homologues Sso1p and Sso2p, and evidence of a distinct function for Sso1p in sporulation. J. Cell Sci. 115:2002;409-420.
58. Finger F.P., et al. Sec3p is a spatial landmark for polarized secretion in budding yeast. Cell. 92:1998;559-571.
59. Jeong J.W., et al. Characterization of the CDC10 product and the timing of events of the budding site of Saccharomyces cerevisiae. Mol. Cell. 12:2001;77-83.
60. Dobbelaere J., et al. Phosphorylation-dependent regulation of septin dynamics during the cell cycle. Dev. Cell. 4:2003;345-357.
61. Caviston, J.P. et al. The role of Cdc42p GTPase-activating proteins (GAPs) in assembly of the septin ring in yeast. Mol. Biol. Cell (in press).
62. Cid V.J., et al. Cell cycle control of septin ring dynamics in the budding yeast. Microbiology. 147:2001;1437-1450.
63. Johnson D.I. Cdc42: an essential Rho-type GTPase controlling eukaryotic cell polarity. Microbiol. Mol. Biol. Rev. 63:1999;54-105.
64. Pringle J.R., et al. Establishment of cell polarity in yeast. Cold Spring Harb. Symp. Quant. Biol. 60:1995;729-744.
65. Gladfelter A.S., et al. Isolation and characterization of effector-loop mutants of CDC42 in yeast. Mol. Biol. Cell. 12:2001;1239-1255.
66. Ayscough K.R., et al. High rates of actin filament turnover in budding yeast and roles for actin in establishment and maintenance of cell polarity revealed using the actin inhibitor Latrunculin-A. J. Cell Biol. 137:1997;399-416.
67. Bishop A.L., Hall A. Rho GTPases and their effector proteins. Biochem. J. 348:2000;241-255.
68. Joberty G., et al. Borg proteins control septin organization and are negatively regulated by Cdc42. Nat. Cell Biol. 3:2001;861-866.
69. Nern A., Arkowitz R.A. G proteins mediate changes in cell shape by stabilizing the axis of polarity. Mol. Cell. 5:2000;853-864.
70. Warenda A.J., Konopka J.B. Septin function in Candida albicans morphogenesis. Mol. Biol. Cell. 13:2002;2732-2746.
71. Gladfelter A.S., et al. Septin ring assembly involves cycles of GTP loading and hydrolysis by Cdc42p. J. Cell Biol. 156:2002;315-326.
72. Smith G.R., et al. GTPase-activating proteins for Cdc42. Eukaryot. Cell. 1:2002;469-480.
73. Kozubowski L., et al. A Bni4-Glc7 phosphatase complex that recruits chitin synthase to the site of bud emergence. Mol. Biol. Cell. 14:2003;26-39.
74. Lee P.R., et al. Bni5p, a septin-interacting protein, is required for normal septin function and cytokinesis in Saccharomyces cerevisiae. Mol. Cell. Biol. 22:2002;6906-6920.
75. Cvrckova F., et al. Ste20-like protein kinases are required for normal localization of cell growth and for cytokinesis in budding yeast. Genes Dev. 9:1995;1817-1830.
76. Longtine M.S., et al. Role of the yeast Gin4p protein kinase in septin assembly and the relationship between septin assembly and septin function. J. Cell Biol. 143:1998;719-736.
77. Bouquin N., et al. Regulation of cytokinesis by the Elm1 protein kinase in Saccharomyces cerevisiae. J. Cell Sci. 113:2000;1435-1445.
78. Weiss E.L., et al. Chemical genetic analysis of the budding-yeast p21-activated kinase Cla4p. Nat. Cell Biol. 2:2000;677-685.
79. Mortensen E.M., et al. Cell cycle-dependent assembly of a Gin4-septin complex. Mol. Biol. Cell. 13:2002;2091-2105.
80. Cid V.J., et al. Orchestrating the cell cycle in yeast: sequential localization of key mitotic regulators at the spindle pole and the bud neck. Microbiology. 148:2002;2647-2659.
81. Tang C.S., Reed S.I. Phosphorylation of the septin Cdc3 in G1 by the Cdc28 kinase is essential for efficient septin ring disassembly. Cell Cycle. 1:2002;42-49.