Abstract
The septin family is a conserved GTP-binding protein family and was originally discovered through genetic screening for budding yeast mutants. Septins are implicated in many cellular processes in fungi and metazoa. The function of septins usually depends on septin assembling into oligomeric complexes and highly ordered polymers. The expansion of the septin gene number in vertebrates increased the complex diversity of septins. In this review, we first discuss the evolution, structures and assembly of septin proteins in yeast and metazoa. Then, we review the function of septin proteins in cytokinesis, membrane remodeling and compartmentalization.
Similar content being viewed by others
References
Hartwell LH (1971) Genetic control of cell division cycle in yeast. 4. Genes controlling bud emergence and cytokinesis. Exp Cell Res 69:265
Byers B, Goetsch L (1976) Highly ordered ring of membrane-associated filaments in budding yeast. J Cell Biol 69:717–721
Leipe DD, Wolf YI, Koonin EV, Aravind L (2002) Classification and evolution of P-loop GTPases and related ATPases. J Mol Biol 317:41–72
Kinoshita M (2003) The septins. Genome Biol 4
Field CM, Kellogg D (1999) Septins: cytoskeletal polymers or signalling GTPases? Trends Cell Biol 9:387–394
Longtine MS, Bi EF (2003) Regulation of septin organization and function in yeast. Trends Cell Biol 13:403–409
Versele M, Thorner J (2005) Some assembly required: yeast septins provide the instruction manual. Trends Cell Biol 15:414–424
Kinoshita M (2006) Diversity of septin scaffolds. Curr Opin Cell Biol 18:54–60
Spiliotis ET, Nelson WJ (2006) Here come the septins: novel polymers that coordinate intracellular functions and organization. J Cell Sci 119:4–10
Weirich CS, Erzberger JP, Barral Y (2008) The septin family of GTPases: architecture and dynamics. Nat Rev Mol Cell Biol 9:478–489
Barral Y, Kinoshita M (2008) Structural insights shed light onto septin assemblies and function. Curr Opin Cell Biol 20:12–18
Cao LH, Ding XM, Yu WB, Yang XM, Shen SQ, Yu L (2007) Phylogenetic and evolutionary analysis of the septin protein family in metazoan. FEBS Lett 581:5526–5532
Sanders SL, Herskowitz I (1996) 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 134:413–427
DeMarini DJ, Adams AEM, Fares H, DeVirgilio C, Valle G, Chuang JS, Pringle JR (1997) A septin-based hierarchy of proteins required for localized deposition of chitin in the Saccharomyces cerevisiae cell wall. J Cell Biol 139:75–93
Kusch J, Meyer A, Snyder MP, Barral Y (2002) Microtubule capture by the cleavage apparatus is required for proper spindle positioning in yeast. Genes Dev 16:1627–1639
Grava S, Schaerer F, Faty M, Philippsen P, Barral Y (2006) Asymmetric recruitment of dynein to spindle poles and microtubules promotes proper spindle orientation in yeast. Dev Cell 10:425–439
Barral Y, Parra M, Bidlingmaier S, Snyder M (1999) Nim1-related kinases coordinate cell cycle progression with the organization of the peripheral cytoskeleton in yeast. Genes Dev 13:176–187
Longtine MS, Theesfeld CL, McMillan JN, Weaver E, Pringle JR, Lew DJ (2000) Septin-dependent assembly of a cell cycle-regulatory module in Sacharomyces cerevisiae. Mol Cell Biol 20:4049–4061
Bi E, Maddox P, Lew DJ, Salmon ED, McMillan JN, Yeh E, Pringle JR (1998) Involvement of an actomyosin contractile ring in Saccharomyces cerevisiae cytokinesis. J Cell Biol 142:1301–1312
Shulewitz MJ, Inouye CJ, Thorner J (1999) Hsl7 localizes to a septin ring and serves as an adapter in a regulatory pathway that relieves tyrosine phosphorylation of Cdc28 protein kinase in Saccharomyces cerevisiae. Mol Cell Biol 19:7123–7137
Barral Y, Mermall V, Mooseker MS, Snyder M (2000) Compartmentalization of the cell cortex by septins is required for maintenance of cell polarity in yeast. Mol Cell 5:841–851
Dobbelaere J, Barral Y (2004) Spatial coordination of cytokinetic events by compartmentalization of the cell cortex. Science 305:393–396
Enserink JM, Smolka MB, Zhou HL, Kolodner RD (2006) Checkpoint proteins control morphogenetic events during DNA replication stress in Saccharomyces cerevisiae. J Cell Biol 175:729–741
Smolka MB, Chen SH, Maddox PS, Enserink JM, Albuquerque CP, Wei XX, Desai A, Kolodner RD, Zhou HL (2006) An FHA domain-mediated protein interaction network of Rad53 reveals its role in polarized cell growth. J Cell Biol 175:743–753
Nagata K, Kawajiri A, Matsui S, Takagishi M, Shiromizu T, Saitoh N, Izawa I, Kiyono T, Itoh TJ, Hotani H, Inagaki M (2003) Filament formation of MSF-A, a mammalian septin, in human mammary epithelial cells depends on interactions with microtubules. J Biol Chem 278:18538–18543
Kartmann B, Roth D (2001) Novel roles for mammalian septins: from vesicle trafficking to oncogenesis. J Cell Sci 114:839–844
Kremer BE, Adang LA, Macara IG (2007) Septins regulate actin organization and cell-cycle arrest through nuclear accumulation of NCK mediated by SOCS7. Cell 130:837–850
Kinoshita M, Kumar S, Mizoguchi A, Ide C, Kinoshita A, Haraguchi T, Hiraoka Y, Noda M (1997) Nedd5, a mammalian septin, is a novel cytoskeletal component interacting with actin-based structures. Genes Dev 11:1535–1547
Nguyen TQ, Sawa H, Okano H, White JG (2000) The C-elegans septin genes, unc-59 and unc-61, are required for normal postembryonic cytokineses and morphogenesis but have no essential function in embryogenesis. J Cell Sci 113:3825–3837
Spiliotis ET, Kinoshita M, Nelson WJ (2005) A mitotic septin scaffold required for mammalian chromosome congression and segregation. Science 307:1781–1785
Hsu SC, Hazuka CD, Roth R, Foletti DL, Heuser J, Scheller RH (1998) Subunit composition, protein interactions, and structures of the mammalian brain sec6/8 complex and septin filaments. Neuron 20:1111–1122
Finger FP, Kopish KR, White JG (2003) A role for septins in cellular and axonal migration in C-elegans. Dev Biol 261:220–234
Gonzalez ME, Makarova O, Peterson EA, Privette LM, Petty EM (2009) Up-regulation of SEPT9_v1 stabilizes c-Jun-N-Terminal kinase and contributes to its pro-proliferative activity in mammary epithelial cells. Cell Signal 21:477–487
Amir S, Wang R, Simons JW, Mabjeesh NJ (2009) SEPT9_v1 Up-regulates hypoxia-inducible factor 1 by preventing its RACK1-mediated degradation. J Biol Chem 284:11142–11151
Ihara M, Yamasaki N, Hagiwara A, Tanigaki A, Kitano A, Hikawa R, Tomimoto H, Noda M, Masashi T, Mori H, Hattori N, Miyakawa T, Kinoshita M (2007) Sept4, a component of presynaptic scaffold and Lewy bodies, is required for the suppression of alpha-synuclein neurotoxicity. Neuron 53:519–533
John CM, Hite RK, Weirich CS, Fitzgerald DJ, Jawhari H, Faty M, Schlapfer D, Kroschewski R, Winkler FK, Walz T, Barral Y, Steinmetz MO (2007) The Caenorhabditis elegans septin complex is nonpolar. EMBO J 26:3296–3307
Bertin A, McMurray MA, Grob P, Park SS, Garcia G, Patanwala I, Ng HL, Alber T, Thorner J, Nogales E (2008) Saccharomyces cerevisiae septins: supramolecular organization of heterooligomers and the mechanism of filament assembly. Proc Natl Acad Sci USA 105:8274–8279
Sirajuddin M, Farkasovsky M, Hauer F, Kuhlmann D, Macara IG, Weyand M, Stark H, Wittinghofer A (2007) Structural insight into filament formation by mammalian septins. Nature 449:311–315
Pan FF, Malmberg RL, Momany M (2007) Analysis of septins across kingdoms reveals orthology and new motifs. BMC Evol Biol 7:103
Zhang JS, Kong C, Xie H, McPherson PS, Grinstein S, Trimble WS (1999) Phosphatidyl inositol polyphosphate binding to the mammalian septin H5 is modulated by GTP. Curr Biol 9:1458–1467
Casamayor A, Snyder M (2003) Molecular dissection of a yeast septin: Distinct domains are required for septin interaction, localization, and function. Mol Cell Biol 23:2762–2777
Versele M, Gullbrand B, Shulewitz MJ, Cid VJ, Bahmanyar S, Chen RE, Barth P, Alber T, Thorner J (2004) Protein-protein interactions governing septin heteropentamer assembly and septin filament organization in Saccharomyces cerevisiae. Mol Biol Cell 15:4568–4583
Lukoyanova N, Baldwin SA, Trinick J (2008) 3D reconstruction of mammalian septin filaments. J Mol Biol 376:1–7
Kinoshita M, Field CM, Coughlin ML, Straight AF, Mitchison TJ (2002) Self- and actin-templated assembly of mammalian septins. Dev Cell 3:791–802
Field CM, AlAwar O, Rosenblatt J, Wong ML, Alberts B, Mitchison TJ (1996) A purified Drosophila septin complex forms filaments and exhibits GTPase activity. J Cell Biol 133:605–616
Frazier JA, Wong ML, Longtine MS, Pringle JR, Mann M, Mitchison TJ, Field C (1998) Polymerization of purified yeast septins: evidence that organized filament arrays may not be required for septin function. J Cell Biol 143:737–749
Mendoza M, Hyman AA, Glotzer M (2002) GTP binding induces filament assembly of a recombinant septin. Curr Biol 12:1858–1863
Versele M, Thorner J (2004) Septin collar formation in budding yeast requires GTP binding and direct phosphorylation by the PAK, Cla4. J Cell Biol 164:701–715
An HB, Morrell JL, Jennings JL, Link AJ, Gould KL (2004) Requirements of fission yeast septins for complex formation, localization, and function. Mol Biol Cell 15:5551–5564
Sheffield PJ, Oliver CJ, Kremer BE, Sheng ST, Shao ZF, Macara IG (2003) Borg/septin interactions and the assembly of mammalian septin heterodimers, trimers, and filaments. J Biol Chem 278:3483–3488
Nagata K, Asano T, Nozawa Y, Inagaki M (2004) Biochemical and cell biological analyses of a mammalian septin complex, Sept7/9b/11. J Biol Chem 279:55895–55904
Joberty G, Perlungher RR, Sheffield PJ, Kinoshita M, Noda M, Haystead T, Macara IG (2001) Borg proteins control septin organization and are negatively regulated by Cdc42. Nat Cell Biol 3:861–866
Kinoshita M (2003) Assembly of mammalian septins. J Biochem 134:491–496
Hall PA, Jung K, Hillan KJ, Russell SEH (2005) Expression profiling the human septin gene family. J Pathol 206:269–278
Rodal AA, Kozubowski L, Goode BL, Drubin DG, Hartwig JH (2005) Actin and septin ultrastructures at the budding yeast cell cortex. Mol Biol Cell 16:372–384
Gladfelter AS, Pringle JR, Lew DJ (2001) The septin cortex at the yeast mother–bud neck. Curr Opin Microbiol 4:681–689
Iwase M, Luo JY, Nagaraj S, Longtine M, Kim HB, Haarer BK, Caruso C, Tong ZT, Pringle JR, Bi EF (2006) Role of a Cdc42p effector pathway in recruitment of the yeast septins to the presumptive bud site. Mol Biol Cell 17:1110–1125
Lippincott J, Shannon KB, Shou WY, Deshaies J, Li R (2001) The Tem1 small GTPase controls actomyosin and septin dynamics during cytokinesis. J Cell Sci 114:1379–1386
Caviston JP, Longtine M, Pringle JR, Bi E (2003) The role of Cdc42p GTPase-activating proteins in assembly of the septin ring in yeast. Mol Biol Cell 14:4051–4066
Dobbelaere J, Gentry MS, Hallberg RL, Barral Y (2003) Phosphorylation-dependent regulation of septin dynamics during the cell cycle. Dev Cell 4:345–357
Vrabioiu AM, Mitchison TJ (2006) Structural insights into yeast septin organization from polarized fluorescence microscopy. Nature 443:466–469
Vrabioiu AM, Mitchison TJ (2007) Symmetry of septin hourglass and ring structures. J Mol Biol 372:37–49
McMurray MA, Thorner J (2008) Septin stability and recycling during dynamic structural transitions in cell division and development. Curr Biol 18:1203–1208
Berlin A, Paoletti A, Chang F (2003) Mid2p stabilizes septin rings during cytokinesis in fission yeast. J Cell Biol 160:1083–1092
Tasto JJ, Morrell JL, Gould KL (2003) An anillin homologue, Mid2p, acts during fission yeast cytokinesis to organize the septin ring and promote cell separation. J Cell Biol 160:1093–1103
Wu JQ, Kuhn JR, Kovar DR, Pollard TD (2003) Spatial and temporal pathway for assembly and constriction of the contractile ring in fission yeast cytokinesis. Dev Cell 5:723–734
Ihara M, Kinoshita A, Yamada S, Tanaka H, Tanigaki A, Kitano A, Goto M, Okubo K, Nishiyama H, Ogawa O, Takahashi C, Ogawa O, Takahashi C, Itohara S, Nishimune Y, Noda M, Kinoshita M (2005) Cortical organization by the septin cytoskeleton is essential for structural and mechanical integrity of mammalian spermatozoa. Dev Cell 8:343–352
Kissel H, Georgescu MM, Larisch S, Manova K, Hunnicutt GR, Steller H (2005) The Sept4 septin locus is required for sperm terminal differentiation in mice. Dev Cell 8:353–364
Oegema K, Savoian MS, Mitchison TJ, Field CM (2000) Functional analysis of a human homologue of the Drosophila actin binding protein anillin suggests a role in cytokinesis. J Cell Biol 150:539–551
Schmidt K, Nichols BJ (2004) Functional interdependence between septin and actin cytoskeleton. BMC Cell Biol 5:43
Nagaraj S, Rajendran A, Jackson CE, Longtine MS (2008) Role of nucleotide binding in septin-septin interactions and septin localization in Saccharomyces cerevisiae. Mol Cell Biol 28:5120–5137
Vega IE, Hsu SC (2003) The septin protein Nedd5 associates with both the exocyst complex and microtubules and disruption of its GTPase activity promotes aberrant neurite sprouting in PC12 cells. NeuroReport 14:31–37
Hanai N, Nagata K, Kawajiri A, Shiromizu T, Saitoh N, Hasegawa Y, Murakami S, Inagaki M (2004) Biochemical and cell biological characterization of a mammalian septin, Sept 11. FEBS Lett 568:83–88
Robertson C, Church SW, Nagar HA, Price J, Hall PA, Russell SEH (2004) Properties of SEPT9 isoforms and the requirement for GTP binding. J Pathol 203:519–527
Ding XM, Yu WB, Liu M, Shen SQ, Chen F, Cao LH, Wan B, Yu L (2008) GTP binding is required for SEPT12 to form filaments and to interact with SEPT11. Molecules and Cells 25:385–389
Vrabioiu AM, Gerber SA, Gygi SP, Field CM, Mitchison TJ (2004) The majority of the Saccharomyces cerevisiae septin complexes do not exchange guanine nucleotides. J Biol Chem 279:3111–3118
Huang Y, Surka MC, Reynaud D, Pace-Asciak C, Trimble WS (2006) GTP binding and hydrolysis kinetics of human septin 2. FEBS J 273:3248–3260
Gladfelter AS, Bose I, Zyla TR, Bardes ESG, Lew DJ (2002) Septin ring assembly involves cycles of GTP loading and hydrolysis by Cdc42p. J Cell Biol 156:315–326
Smith GR, Givan SA, Cullen P, Sprague GF (2002) GTPase-activating proteins for Cdc42. Eukaryotic Cell 1:469–480
Park HO, Bi EF (2007) Central roles of small GTPases in the development of cell polarity in yeast and beyond. Microbiol Mol Biol Rev 71:48–96
Jeong JW, Kim DH, Choi SY, Kim HB (2001) Characterization of the CDC10 product and the timing of events of the budding site of Saccharomyces cerevisiae. Molecules and Cells 12:77–83
Longtine MS, Fares H, Pringle JR (1998) Role of the yeast Gin4p protein kinase in septin assembly and the relationship between septin assembly and septin function. J Cell Biol 143:719–736
Bouquin N, Barral Y, Courbeyrette R, Blondel M, Snyder M, Mann C (2000) Regulation of cytokinesis by the Elm1 protein kinase in Saccharomyces cerevisiae. J Cell Sci 113:1435–1445
Lee PR, Song S, Ro HS, Park CJ, Lippincott J, Li R, Pringle JR, De Virgilio C, Longtine MS, Lee KS (2002) Bni5p, a septin-interacting protein, is required for normal septin function and cytokinesis in Saccharomyces cerevisiae. Mol Cell Biol 22:6906–6920
Gladfelter AS, Kozubowski L, Zyla TR, Lew DJ (2005) Interplay between septin organization, cell cycle and cell shape in yeast. J Cell Sci 118:1617–1628
Kadota J, Yamamoto T, Yoshiuchi S, Bi E, Tanaka K (2004) Regulation of the initial septin ring assembly by polarisome components, a PAK kinase Cla4p, and the actin cytoskeleton in budding yeast. Mol Biol Cell 15:45A–45A
Mortensen EM, McDonald H, Yates J, Kellogg DR (2002) Cell cycle-dependent assembly of a Gin4-septin complex. Mol Biol Cell 13:2091–2105
Asano S, Park JE, Yu LR, Zhou M, Sakchaisri K, Park CJ, Kang YH, Thorner J, Veenstra TD, Lee KS (2006) Direct phosphorylation and activation of a Nim1-related kinase Gin4 by Elm1 in budding yeast. J Biol Chem 281:27090–27098
Ito H, Iwamoto I, Morishita R, Nozawa Y, Narumiya S, Asano T, Nagata KI (2005) Possible role of Rho/Rhotekin signaling in mammalian septin organization. Oncogene 24:7064–7072
Nagata KI, Inagaki M (2005) Cytoskeletal modification of Rho guanine nucleotide exchange factor activity: identification of a Rho guanine nucleotide exchange factor as a binding partner for Sept9b, a mammalian septin. Oncogene 24:65–76
Becker W, Lutz B (2008) The down syndrome candidate dual-specificity tyrosine phosphorylation-regulated kinase 1a phosphorylates the neurodegeneration-related septin 4. Neuroscience 157:596–605
Xue J, Tsang CW, Gai WP, Malladi CS, Trimble WS, Rostas JAP, Robinson PJ (2004) Septin 3 (G-septin) is a developmentally regulated phosphoprotein enriched in presynaptic nerve terminals. J Neurochem 91:579–590
Xue J, Wang X, Malladi CS, Kinoshita M, Milburn PJ, Lengyel I, Rostas JAP, Robinson PJ (2000) Phosphorylation of a new brain-specific septin, G-septin, by cGMP-dependent protein kinase. J Biol Chem 275:10047–10056
Qi MY, Yu WB, Liu S, Jia HJ, Tang LS, Shen MJ, Yan XM, Saiyin H, Lang QY, Wan B, Zhao SY, Yu L (2005) Septin1, a new interaction partner for human serine/threonine kinase aurora-B. Biochem Biophys Res Commun 336:994–1000
She YM, Huang YW, Zhang L, Trimble WS (2004) Septin 2 phosphorylation: theoretical and mass spectrometric evidence for the existence of a single phosphorylation site in vivo. Rapid Commun Mass Spectrom 18:1123–1130
Amin ND, Zheng YL, Kesavapany S, Kanungo J, Guszczynski T, Sihag RK, Rudrabhatla P, Albers W, Grant P, Pant HC (2008) Cyclin-dependent kinase 5 phosphorylation of human septin SEPT5 (hCDCrel-1) modulates exocytosis. J Neurosci 28:3631–3643
Johnson ES, Blobel G (1999) Cell cycle-regulated attachment of the ubiquitin-related protein SUMO to the yeast septins. J Cell Biol 147:981–993
Johnson ES, Gupta AA (2001) An E3-like factor that promotes SUMO conjugation to the yeast septins. Cell 106:735–744
Takahashi Y, Iwase M, Konishi M, Tanaka M, Toh-e A, Kikuchi Y (1999) Smt3, a SUMO-1 homolog, is conjugated to Cdc3, a component of septin rings at the mother-bud neck in budding yeast. Biochem Biophys Res Commun 259:582–587
Takahashi Y, Kahyo T, Toh-e A, Yasuda H, Kikuchi Y (2001) Yeast Ull1/Siz1 is a novel SUM01/Smt3 ligase for septin components and functions as an adaptor between conjugating enzyme and substrates. J Biol Chem 276:48973–48977
Takahashi Y, Mizoi J, Toh-e A, Kikuchi Y (2000) Yeast Ulp1, an Smt3-specific protease, associates with nucleoporins. J Biochem 128:723–725
Makhnevych T, Ptak C, Lusk CP, Aitchison JD, Wozniak RW (2007) The role of karyopherins in the regulated sumoylation of septins. J Cell Biol 177:39–49
Shih HP, Hales KG, Pringle JR, Peifer M (2002) Identification of septin-interacting proteins and characterization of the Smt3/SUMO-conjugation system in Drosophila. J Cell Sci 115:1259–1271
Field CM, Coughlin M, Doberstein S, Marty T, Sullivan W (2005) Characterization of anillin mutants reveals essential roles in septin localization and plasma membrane integrity. Development 132:2849–2860
Silverman-Gavrila RV, Hales KG, Wilde A (2008) Anillin-mediated targeting of Peanut to pseudocleavage furrows is regulated by the GTPase Ran. Mol Biol Cell 19:3735–3744
Vallen EA, Caviston J, Bi E (2000) Roles of Hof1p, Bni1p, Bnr1p, and Myo1p in cytokinesis in Saccharomyces cerevisiae. Mol Biol Cell 11:593–611
Cid VJ, Adamikova L, Sanchez M, Molina M, Nombela C (2001) Cell cycle control of septin ring dynamics in the budding yeast. Microbiol Sgm 147:1437–1450
Bardin AJ, Visintin R, Amon A (2000) A mechanism for coupling exit from mitosis to partitioning of the nucleus. Cell 102:21–31
Pereira G, Schiebel E (2005) Kin4 kinase delays mitotic exit in response to spindle alignment defect. Mol Cell 19:209–221
Jensen S, Geymonat M, Johnson AL, Segal M, Johnston LH (2002) Spatial regulation of the guanine nucleotide exchange factor Lte1 in Saccharomyces cerevisiae. J Cell Sci 115:4977–4991
Seshan A, Bardin AJ, Amon A (2002) Control of Lte1 localization by cell polarity determinants and Cdc14. Curr Biol 12:2098–2110
Castillon GA, Adames NR, Rosello CH, Seidel HS, Longtine MS, Cooper JA, Heil-Chapdelaine RA (2003) Septins have a dual role in controlling mitotic exit in budding yeast. Curr Biol 13:654–658
D’Aquino KE, Monje-Casas F, Paulson J, Reiser V, Charles GM, Lai L, Shokat KM, Amon A (2005) The protein kinase Kin4 inhibits exit from mitosis in response to spindle position defects. Mol Cell 19:223–234
Hu FH, Wang YC, Liu D, Li YM, Qin J, Elledge SJ (2001) Regulation of the Bub2/Bfal GAP complex by Cdc5 and cell cycle checkpoints. Cell 107:655–665
Sakchaisri K, Asano S, Yu LR, Shulewitz MJ, Park CJ, Park JE, Cho YW, Veenstra TD, Thorner J, Lee KS (2004) Coupling morphogenesis to mitotic entry. Proc Natl Acad Sci USA 101:4124–4129
Hanrahan J, Snyder M (2003) Cytoskeletal activation of a checkpoint kinase. Mol Cell 12:663–673
Szkotnicki L, Crutchley JsM, Zyla TR, Bardes ESG, Lew DJ (2008) The checkpoint kinase Hsl1p is activated by Elm1p-dependent phosphorylation. Mol Biol Cell 19:4675–4686
Luedeke C, Frei SB, Sbalzarini I, Schwarz H, Spang A, Barral Y (2005) Septin-dependent compartmentalization of the endoplasmic reticulum during yeast polarized growth. J Cell Biol 169:897–908
Shcheprova Z, Baldi S, Frei SB, Gonnet G, Barral Y (2008) A mechanism for asymmetric segregation of age during yeast budding. Nature 454:U728–U764
Neufeld TP, Rubin GM (1994) The Drosophila Peanut gene is required for cytokinesis and encodes a protein similar to yeast putative bud neck filament proteins. Cell 77:37–371
Zhu M, Wang FS, Yan F, Yao PY, Du J, Gao XJ, Wang XW, Wu Q, Ward T, Li JJ, Kioko S, Hu RM, Xie W, Ding X, Yao XB (2008) Septin 7 interacts with centromere-associated protein E and is required for its kinetochore localization. J Biol Chem 283:18916–18925
Joo E, Surka MC, Trimble WS (2007) Mammalian SEPT2 is required for scaffolding nonmuscle myosin II and its kinases. Dev Cell 13:677–690
Kremer BE, Haystead T, Macara IG (2005) Mammalian septins regulate microtubule stability through interaction with the microtubule-binding protein MAPP-1. Mol Biol Cell 16:4648–4659
Sisson JC, Field C, Ventura R, Royou A, Sullivan W (2000) Lava lamp, a novel peripheral Golgi protein, is required for Drosophila melanogaster cellularization. J Cell Biol 151:905–917
Spiliotis ET, Hunt SJ, Hu Q, Kinoshita M, Nelson WJ (2008) Epithelial polarity requires septin coupling of vesicle transport to polyglutamylated microtubules. J Cell Biol 180:295–303
Huang YW, Yan M, Collins RF, DiCiccio JE, Grinstein S, Trimble WS (2008) Mammalian septins are required for phagosome formation. Mol Biol Cell 19:1717–1726
Xie YL, Vessey JP, Konecna A, Dahm R, Macchi P, Kiebler MA (2007) The GTP-binding protein septin 7 is critical for dendrite branching and dendritic-spine morphology. Curr Biol 17:1746–1751
Tada T, Simonetta A, Batterton M, Kinoshita M, Edbauer D, Sheng M (2007) Role of septin cytoskeleton in spine morphogenesis and dendrite development in neurons. Curr Biol 17:1752–1758
Schmidt K, Nichols BJ (2004) A barrier to lateral diffusion in the cleavage furrow of dividing mammalian cells. Curr Biol 14:1002–1006
Steels JD, Estey MR, Froese CD, Reynaud D, Pace-Asciak C, Trimble WS (2007) Sept12 is a component of the mammalian sperm tail annulus. Cell Motil Cytoskeleton 64:794–807
Beites CL, Xie H, Bowser R, Trimble WS (1999) The septin CDCrel-1 binds syntaxin and inhibits exocytosis. Nat Neurosci 2:434–439
Beites CL, Campbell KA, Trimble WS (2005) The septin Sept5/CDCrel-1 competes with alpha-SNAP for binding to the SNARE complex. Biochem J 385:347–353
Taniguchi M, Taoka M, Itakura M, Asada A, Saito T, Kinoshita M, Takahashi M, Isobe T, Hisanaga S (2007) Phosphorylation of adult type Sept5 (CDCrel-1) by cyclin-dependent kinase 5 inhibits interaction with syntaxin-1. J Biol Chem 282:7869–7876
Dent J, Kato K, Peng XR, Martinez C, Cattaneo M, Poujol C, Nurden P, Nurden A, Trimble WS, Ware J (2002) A prototypic platelet septin and its participation in secretion. Proc Natl Acad Sci USA 99:3064–3069
Tsang CW, Fedchyshyn M, Harrison J, Xie H, Xue J, Robinson PJ, Wang LY, Trimble WS (2008) Superfluous role of mammalian septins 3 and 5 in neuronal development and synaptic transmission. Mol Cell Biol 28:7012–7029
Rittmeyer EN, Daniel S, Hsu SC, Osman MA (2008) A dual role for IQGAP1 in regulating exocytosis. J Cell Sci 121:391–403
Tanaka-Takiguchi Y, Kinoshita M, Takiguchi K (2009) Septin-mediated uniform bracing of phospholipid membranes. Curr Biol 19:140–145
Acknowledgments
We apologize to our colleagues for having to omit many references in this review, owing to space limitations.
Author information
Authors and Affiliations
Corresponding author
Rights and permissions
About this article
Cite this article
Cao, L., Yu, W., Wu, Y. et al. The evolution, complex structures and function of septin proteins. Cell. Mol. Life Sci. 66, 3309–3323 (2009). https://doi.org/10.1007/s00018-009-0087-2
Received:
Revised:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1007/s00018-009-0087-2