1. SchekmanR, OrciL (1996) Coat proteins and vesicle budding. Science 271: 1526–1533.
2. RothmanJE (1994) Mechanisms of intracellular protein transport. Nature 372: 55–63.
3. GoldsteinJL, AndersonRG, BrownMS (1979) Coated pits, coated vesicles, and receptor-mediated endocytosis. Nature 279: 679–685.
4. RothTF, PorterKR (1964) Yolk Protein Uptake in the Oocyte of the Mosquito Aedes Aegypti. L. J Cell Biol 20: 313–332.
5. BalklavaZ, PantS, FaresH, GrantBD (2007) Genome-wide analysis identifies a general requirement for polarity proteins in endocytic traffic. Nat Cell Biol 9: 1066–1073.
6. GrantB, ZhangY, PaupardMC, LinSX, HallDH, et al. (2001) Evidence that RME-1, a conserved C. elegans EH-domain protein, functions in endocytic recycling. Nat Cell Biol 3: 573–579.
7. GrantBD, DonaldsonJG (2009) Pathways and mechanisms of endocytic recycling. Nat Rev Mol Cell Biol 10: 597–608.
8. PantS, SharmaM, PatelK, CaplanS, CarrCM, et al. (2009) AMPH-1/Amphiphysin/Bin1 functions with RME-1/Ehd1 in endocytic recycling. Nat Cell Biol 11: 1399–1410.
9. SatoM, SatoK, FonarevP, HuangCJ, LiouW, et al. (2005) Caenorhabditis elegans RME-6 is a novel regulator of RAB-5 at the clathrin-coated pit. Nat Cell Biol 7: 559–569.
10. HisaokaKK, FirlitCF (1962) The localization of nucleic acids during oogenesis in the zebrafish. Am J Anat 110: 203–215.
11. SelmanK, WallaceRA, SarkaA, QiX (1993) Stages of oocyte development in the zebrafish, Brachydanio rerio. J Morphol 218: 203–224.
12. WangY, GeW (2004) Developmental profiles of activin betaA, betaB, and follistatin expression in the zebrafish ovary: evidence for their differential roles during sexual maturation and ovulatory cycle. Biol Reprod 71: 2056–2064.
13. Babin PJ, Carnevali O, Lubzens E, Schneider WJ (2007) Molecular Aspects of Oocyte Vitellogenesis in Fish. In: Babin PJ, Cerda J, Lubzens E, editors. The Fish Oocyte: From Basic Studies to Biotechnological Applications. Dordrecht, The Netherlands: Springer. 39–76 p.
14. De MatteisMA, LuiniA (2011) Mendelian disorders of membrane trafficking. N Engl J Med 365: 927–938.
15. DionPA, DaoudH, RouleauGA (2009) Genetics of motor neuron disorders: new insights into pathogenic mechanisms. Nat Rev Genet 10: 769–782.
16. NixonRA (2013) The role of autophagy in neurodegenerative disease. Nat Med 19: 983–997.
17. FinstererJ, LoscherW, QuasthoffS, WanschitzJ, Auer-GrumbachM, et al. (2012) Hereditary spastic paraplegias with autosomal dominant, recessive, X-linked, or maternal trait of inheritance. J Neurol Sci 318: 1–18.
18. BlackstoneC (2012) Cellular pathways of hereditary spastic paraplegia. Annu Rev Neurosci 35: 25–47.
19. SalinasS, ProukakisC, CrosbyA, WarnerTT (2008) Hereditary spastic paraplegia: clinical features and pathogenetic mechanisms. Lancet Neurol 7: 1127–1138.
20. HaneinS, MartinE, BoukhrisA, ByrneP, GoizetC, et al. (2008) Identification of the SPG15 gene, encoding spastizin, as a frequent cause of complicated autosomal-recessive spastic paraplegia, including Kjellin syndrome. Am J Hum Genet 82: 992–1002.
21. SagonaAP, NezisIP, PedersenNM, LiestolK, PoultonJ, et al. (2010) PtdIns(3)P controls cytokinesis through KIF13A-mediated recruitment of FYVE-CENT to the midbody. Nat Cell Biol 12: 362–371.
22. KhundadzeM, KollmannK, KochN, BiskupC, NietzscheS, et al. (2013) A Hereditary Spastic Paraplegia Mouse Model Supports a Role of ZFYVE26/SPASTIZIN for the Endolysosomal System. PLoS Genet 9: e1003988.
23. MurmuRP, MartinE, RastetterA, EstevesT, MurielMP, et al. (2011) Cellular distribution and subcellular localization of spatacsin and spastizin, two proteins involved in hereditary spastic paraplegia. Mol Cell Neurosci 47: 191–202.
24. SlabickiM, TheisM, KrastevDB, SamsonovS, MundwillerE, et al. (2010) A genome-scale DNA repair RNAi screen identifies SPG48 as a novel gene associated with hereditary spastic paraplegia. PLoS Biol 8: e1000408.
25. VantaggiatoC, CrimellaC, AiroldiG, PolishchukR, BonatoS, et al. (2013) Defective autophagy in spastizin mutated patients with hereditary spastic paraparesis type 15. Brain 136: 3119–3139.
26. HirstJ, BarlowLD, FranciscoGC, SahlenderDA, SeamanMN, et al. (2011) The fifth adaptor protein complex. PLoS Biol 9: e1001170.
27. HirstJ, BornerGH, EdgarJ, HeinMY, MannM, et al. (2013) Interaction between AP-5 and the hereditary spastic paraplegia proteins SPG11 and SPG15. Mol Biol Cell 24: 2558–2569.
28. DoschR, WagnerDS, MintzerKA, RunkeG, WiemeltAP, et al. (2004) Maternal control of vertebrate development before the midblastula transition: mutants from the zebrafish I. Dev Cell 6: 771–780.
29. SigristCJ, CeruttiL, de CastroE, Langendijk-GenevauxPS, BulliardV, et al. (2010) PROSITE, a protein domain database for functional characterization and annotation. Nucleic Acids Res 38: D161–166.
30. PagniM, IoannidisV, CeruttiL, Zahn-ZabalM, JongeneelCV, et al. (2007) MyHits: improvements to an interactive resource for analyzing protein sequences. Nucleic Acids Res 35: W433–437.
31. StenmarkH, AaslandR, TohBH, D'ArrigoA (1996) Endosomal localization of the autoantigen EEA1 is mediated by a zinc-binding FYVE finger. J Biol Chem 271: 24048–24054.
32. PatkiV, LaweDC, CorveraS, VirbasiusJV, ChawlaA (1998) A functional PtdIns(3)P-binding motif. Nature 394: 433–434.
33. BurdCG, EmrSD (1998) Phosphatidylinositol(3)-phosphate signaling mediated by specific binding to RING FYVE domains. Mol Cell 2: 157–162.
34. GaullierJM, SimonsenA, D'ArrigoA, BremnesB, StenmarkH, et al. (1998) FYVE fingers bind PtdIns(3)P. Nature 394: 432–433.
35. PostlethwaitJH (2007) The zebrafish genome in context: ohnologs gone missing. J Exp Zool B Mol Dev Evol 308: 563–577.
36. SagonaAP, NezisIP, BacheKG, HaglundK, BakkenAC, et al. (2011) A tumor-associated mutation of FYVE-CENT prevents its interaction with Beclin 1 and interferes with cytokinesis. PLoS One 6: e17086.
37. MartinE, YanicostasC, RastetterA, NainiSM, MaouedjA, et al. (2012) Spatacsin and spastizin act in the same pathway required for proper spinal motor neuron axon outgrowth in zebrafish. Neurobiol Dis 48: 299–308.
38. GrohKJ, SchonenbergerR, EggenRI, SegnerH, SuterMJ (2013) Analysis of protein expression in zebrafish during gonad differentiation by targeted proteomics. Gen Comp Endocrinol 193: 210–220.
39. von HofstenJ, OlssonPE (2005) Zebrafish sex determination and differentiation: involvement of FTZ-F1 genes. Reprod Biol Endocrinol 3: 63.
40. HirstJ, IrvingC, BornerGH (2013) Adaptor protein complexes AP-4 and AP-5: new players in endosomal trafficking and progressive spastic paraplegia. Traffic 14: 153–164.
41. ChavrierP, PartonRG, HauriHP, SimonsK, ZerialM (1990) Localization of low molecular weight GTP binding proteins to exocytic and endocytic compartments. Cell 62: 317–329.
42. FassierC, HuttJA, ScholppS, LumsdenA, GirosB, et al. (2010) Zebrafish atlastin controls motility and spinal motor axon architecture via inhibition of the BMP pathway. Nat Neurosci 13: 1380–1387.
43. UllrichO, ReinschS, UrbeS, ZerialM, PartonRG (1996) Rab11 regulates recycling through the pericentriolar recycling endosome. J Cell Biol 135: 913–924.
44. GoldsteinJL, BrownMS, AndersonRG, RussellDW, SchneiderWJ (1985) Receptor-mediated endocytosis: concepts emerging from the LDL receptor system. Annu Rev Cell Biol 1: 1–39.
45. SchneiderWJ (1996) Vitellogenin receptors: oocyte-specific members of the low-density lipoprotein receptor supergene family. Int Rev Cytol 166: 103–137.
46. SireMF, BabinPJ, VernierJM (1994) Involvement of the Lysosomal System in Yolk Protein Deposit and Degradation during Vitellogenesis and Embryonic-Development in Trout. Journal of Experimental Zoology 269: 69–83.
47. KarinM, MintzB (1981) Receptor-mediated endocytosis of transferrin in developmentally totipotent mouse teratocarcinoma stem cells. J Biol Chem 256: 3245–3252.
48. YamashiroDJ, TyckoB, FlussSR, MaxfieldFR (1984) Segregation of transferrin to a mildly acidic (pH 6.5) para-Golgi compartment in the recycling pathway. Cell 37: 789–800.
49. WillinghamMC, HanoverJA, DicksonRB, PastanI (1984) Morphologic characterization of the pathway of transferrin endocytosis and recycling in human KB cells. Proc Natl Acad Sci U S A 81: 175–179.
50. El-JouniW, HaunS, HodeifyR, WalkerAH, MachacaK (2007) Vesicular traffic at the cell membrane regulates oocyte meiotic arrest. Development 134: 3307–3315.
51. ChenC, Garcia-SantosD, IshikawaY, SeguinA, LiL, et al. (2013) Snx3 regulates recycling of the transferrin receptor and iron assimilation. Cell Metab 17: 343–352.
52. ChengH, GovindanJA, GreensteinD (2008) Regulated trafficking of the MSP/Eph receptor during oocyte meiotic maturation in C. elegans. Curr Biol 18: 705–714.
53. JalabertB, TheronM-C, HeydorffM (1978) Production of fertilizable oocytes from follicles of rainbow trout (Salmo gairdnerii) following in vitro maturation and ovulation. Ann Biol anim Bioch Biophys 18: 461–470.
54. SelmanK, PetrinoTR, WallaceRA (1994) Experimental conditions for oocyte maturation in the zebrafish, Brachydanio rerio. The Journal of Experimental Zoology 269: 538–550.
55. NagahamaY (1985) Stimulation of 17 alpha,20 beta-dihydroxy-4-pregnen-3-one production in the granulosa cells of Amago salmon, Oncorhynchus rhodurus, by cyclic nucleotides. The Journal of Experimental Zoology 236: 371–375.
56. PaulsS, Geldmacher-VossB, Campos-OrtegaJA (2001) A zebrafish histone variant H2A.F/Z and a transgenic H2A.F/Z:GFP fusion protein for in vivo studies of embryonic development. Dev Genes Evol 211: 603–610.
57. SchielJA, ChildsC, PrekerisR (2013) Endocytic transport and cytokinesis: from regulation of the cytoskeleton to midbody inheritance. Trends Cell Biol 23: 319–327.
58. SimonGC, PrekerisR (2008) Mechanisms regulating targeting of recycling endosomes to the cleavage furrow during cytokinesis. Biochem Soc Trans 36: 391–394.
59. BarrFA, GrunebergU (2007) Cytokinesis: placing and making the final cut. Cell 131: 847–860.
60. HehnlyH, DoxseyS (2014) Rab11 endosomes contribute to mitotic spindle organization and orientation. Dev Cell 28: 497–507.
61. TaguchiT (2013) Emerging roles of recycling endosomes. J Biochem 153: 505–510.
62. UrbeS, HuberLA, ZerialM, ToozeSA, PartonRG (1993) Rab11, a small GTPase associated with both constitutive and regulated secretory pathways in PC12 cells. FEBS Lett 334: 175–182.
63. SatoM, GrantBD, HaradaA, SatoK (2008) Rab11 is required for synchronous secretion of chondroitin proteoglycans after fertilization in Caenorhabditis elegans. J Cell Sci 121: 3177–3186.
64. KhvotchevMV, RenM, TakamoriS, JahnR, SudhofTC (2003) Divergent functions of neuronal Rab11b in Ca2+-regulated versus constitutive exocytosis. J Neurosci 23: 10531–10539.
65. ChenW, FengY, ChenD, Wandinger-NessA (1998) Rab11 is required for trans-golgi network-to-plasma membrane transport and a preferential target for GDP dissociation inhibitor. Mol Biol Cell 9: 3241–3257.
66. BenliM, DoringF, RobinsonDG, YangX, GallwitzD (1996) Two GTPase isoforms, Ypt31p and Ypt32p, are essential for Golgi function in yeast. EMBO J 15: 6460–6475.
67. JeddG, MulhollandJ, SegevN (1997) Two new Ypt GTPases are required for exit from the yeast trans-Golgi compartment. J Cell Biol 137: 563–580.
68. LapierreLA, DornMC, ZimmermanCF, NavarreJ, BurnetteJO, et al. (2003) Rab11b resides in a vesicular compartment distinct from Rab11a in parietal cells and other epithelial cells. Exp Cell Res 290: 322–331.
69. LiuM (2011) The biology and dynamics of mammalian cortical granules. Reprod Biol Endocrinol 9: 149.
70. WesselGM, BrooksJM, GreenE, HaleyS, VoroninaE, et al. (2001) The biology of cortical granules. Int Rev Cytol 209: 117–206.
71. ToozeSA, MartensGJ, HuttnerWB (2001) Secretory granule biogenesis: rafting to the SNARE. Trends Cell Biol 11: 116–122.
72. MeldolesiJ, ChieregattiE, Luisa MalosioM (2004) Requirements for the identification of dense-core granules. Trends Cell Biol 14: 13–19.
73. KimT, Gondre-LewisMC, ArnaoutovaI, LohYP (2006) Dense-core secretory granule biogenesis. Physiology (Bethesda) 21: 124–133.
74. BeckerKA, HartNH (1999) Reorganization of filamentous actin and myosin-II in zebrafish eggs correlates temporally and spatially with cortical granule exocytosis. J Cell Sci 112(Pt 1): 97–110.
75. AsensioCS, SirkisDW, MaasJWJr, EgamiK, ToTL, et al. (2013) Self-assembly of VPS41 promotes sorting required for biogenesis of the regulated secretory pathway. Dev Cell 27: 425–437.
76. HartNH (1990) Fertilization in teleost fishes: mechanisms of sperm-egg interactions. Int Rev Cytol 121: 1–66.
77. HartNH, YuSF (1980) Cortical granule exocytosis and cell surface reorganization in eggs of Brachydanio. J Exp Zool 213: 137–159.
78. SteegmaierM, KlumpermanJ, FolettiDL, YooJS, SchellerRH (1999) Vesicle-associated membrane protein 4 is implicated in trans-Golgi network vesicle trafficking. Mol Biol Cell 10: 1957–1972.
79. EatonBA, HaugwitzM, LauD, MooreHP (2000) Biogenesis of regulated exocytotic carriers in neuroendocrine cells. J Neurosci 20: 7334–7344.
80. AhnHJ, ParkY, KimS, ParkHC, SeoSK, et al. (2010) The expression profile and function of Satb2 in zebrafish embryonic development. Mol Cells 30: 377–382.
81. KakhlonO, SakyaP, LarijaniB, WatsonR, ToozeSA (2006) GGA function is required for maturation of neuroendocrine secretory granules. EMBO J 25: 1590–1602.
82. NairS, LindemanRE, PelegriF (2013) In vitro oocyte culture-based manipulation of zebrafish maternal genes. Dev Dyn 242: 44–52.
83. BontemsF, SteinA, MarlowF, LyauteyJ, GuptaT, et al. (2009) Bucky ball organizes germ plasm assembly in zebrafish. Curr Biol 19: 414–422.
84. ClellandES, TanQ, BalofskyA, LacivitaR, PengC (2007) Inhibition of premature oocyte maturation: a role for bone morphogenetic protein 15 in zebrafish ovarian follicles. Endocrinology 148: 5451–5458.
85. OrciL, RavazzolaM, AmherdtM, LouvardD, PerreletA (1985) Clathrin-immunoreactive sites in the Golgi apparatus are concentrated at the trans pole in polypeptide hormone-secreting cells. Proc Natl Acad Sci U S A 82: 5385–5389.
86. ToozeJ, ToozeSA (1986) Clathrin-coated vesicular transport of secretory proteins during the formation of ACTH-containing secretory granules in AtT20 cells. J Cell Biol 103: 839–850.
87. PelissierA, ChauvinJP, LecuitT (2003) Trafficking through Rab11 endosomes is required for cellularization during Drosophila embryogenesis. Curr Biol 13: 1848–1857.
88. FergusonSM, De CamilliP (2012) Dynamin, a membrane-remodelling GTPase. Nat Rev Mol Cell Biol 13: 75–88.
89. SchmidSL, FrolovVA (2011) Dynamin: functional design of a membrane fission catalyst. Annu Rev Cell Dev Biol 27: 79–105.
90. PraefckeGJ, McMahonHT (2004) The dynamin superfamily: universal membrane tubulation and fission molecules? Nat Rev Mol Cell Biol 5: 133–147.
91. MaciaE, EhrlichM, MassolR, BoucrotE, BrunnerC, et al. (2006) Dynasore, a cell-permeable inhibitor of dynamin. Dev Cell 10: 839–850.
92. YamamotoK, OotaI (1967) An electron microscopic study of the formation of the yolk globule in the oocyte of zebrafish, Brachydanio rerio. Bull Fac Fish, Hokkaido Univ 17: 165–174.
93. WallaceRA, SelmanK (1990) Ultrastructural aspects of oogenesis and oocyte growth in fish and amphibians. J Electron Microsc Tech 16: 175–201.
94. Le Menn F, Cerda J, Babin PJ (2007) Ultrastructural aspects of the ontogeny and differentiation of ray-finned fish ovarian follicles. In: Babin PJ, Cerda J, Lubzens E, editors. The Fish Oocyte: From Basic Studies to Biotechnological Applications. Dordrecht, The Netherlands: Springer. 1–37 p.
95. WangX, KumarR, NavarreJ, CasanovaJE, GoldenringJR (2000) Regulation of vesicle trafficking in madin-darby canine kidney cells by Rab11a and Rab25. J Biol Chem 275: 29138–29146.
96. HoekstraD, TytecaD, van IJzendoornSC (2004) The subapical compartment: a traffic center in membrane polarity development. J Cell Sci 117: 2183–2192.
97. NakagawaT, SetouM, SeogD, OgasawaraK, DohmaeN, et al. (2000) A novel motor, KIF13A, transports mannose-6-phosphate receptor to plasma membrane through direct interaction with AP-1 complex. Cell 103: 569–581.
98. BonifacinoJS, RojasR (2006) Retrograde transport from endosomes to the trans-Golgi network. Nat Rev Mol Cell Biol 7: 568–579.
99. MorvanJ, ToozeSA (2008) Discovery and progress in our understanding of the regulated secretory pathway in neuroendocrine cells. Histochem Cell Biol 129: 243–252.
100. AsensioCS, SirkisDW, EdwardsRH (2010) RNAi screen identifies a role for adaptor protein AP-3 in sorting to the regulated secretory pathway. J Cell Biol 191: 1173–1187.
101. Dell'AngelicaEC (2009) AP-3-dependent trafficking and disease: the first decade. Curr Opin Cell Biol 21: 552–559.
102. PillayCS, ElliottE, DennisonC (2002) Endolysosomal proteolysis and its regulation. Biochem J 363: 417–429.
103. ArvanP, CastleD (1998) Sorting and storage during secretory granule biogenesis: looking backward and looking forward. Biochem J 332(Pt 3): 593–610.
104. PooMM (2001) Neurotrophins as synaptic modulators. Nat Rev Neurosci 2: 24–32.
105. CaroniP, DonatoF, MullerD (2012) Structural plasticity upon learning: regulation and functions. Nat Rev Neurosci 13: 478–490.
106. MinichielloL (2009) TrkB signalling pathways in LTP and learning. Nat Rev Neurosci 10: 850–860.
107. OrsoG, PendinD, LiuS, TosettoJ, MossTJ, et al. (2009) Homotypic fusion of ER membranes requires the dynamin-like GTPase atlastin. Nature 460: 978–983.
108. Westerfield M (2000) The zebrafish book: A guide for the laboratory use of zebrafish (Danio rerio). Eugene: University of Oregon Press.
109. SchindelinJ, Arganda-CarrerasI, FriseE, KaynigV, LongairM, et al. (2012) Fiji: an open-source platform for biological-image analysis. Nat Methods 9: 676–682.
110. StuderD, MichelM, MüllerM (1989) High pressure freezing comes of age. Scanning Microsc Suppl 3: 253–268 discussion 268–259.
111. LiuL, GeW (2007) Growth differentiation factor 9 and its spatiotemporal expression and regulation in the zebrafish ovary. Biol Reprod 76: 294–302.