Abstract
Cell polarity and asymmetry play a fundamental role in embryo development. The unequal segregation of determinants, cues, and activities is the major event in the differentiation of cell fate and function in all multicellular organisms. In oocytes, polarity and asymmetry in the distribution of different molecules are prerequisites for the progression and proper outcome of embryonic development. The mouse oocyte, like the oocytes of other mammals, seems to apply a less stringent strategy of polarization than other vertebrates. The mouse embryo undergoes a regulative type of development, which permits the full rectification of development even if the embryo loses up to half of its cells or its size is experimentally doubled during the early stages of embryogenesis. Such pliability is strongly related to the proper oocyte polarization before fertilization. Thus, the molecular mechanisms leading to the development and maintenance of oocyte polarity must be included in any fundamental understanding of the principles of embryo development. In this chapter, we provide an overview of current knowledge regarding the development and maintenance of polarity and asymmetry in the distribution of organelles and molecules in the mouse oocyte. Curiously, the mouse oocyte becomes polarized at least twice during ontogenesis; the question of how this phenomenon is achieved and what role it might play is addressed in this chapter.
Access this chapter
Tax calculation will be finalised at checkout
Purchases are for personal use only
References
Albertini DF (2011) NOBOX does right for the follicle reserve: insights into premature ovarian failure. J Assist Reprod Genet 28:567–568
Albertini DF, Barrett SL (2004) The developmental origins of mammalian oocyte polarity. Semin Cell Dev Biol 15:599–606
Anifandis G, Dafopoulos K, Messini CI, Chalvatzas N, Messinis IE (2010) Effect of the position of the polar body during ICSI on fertilization rate and embryo development. Reprod Sci 17:849–853
Araki K, Naito K, Haraguchi S, Suzuki R, Yokoyama M, Inoue M, Aizawa S, Toyoda Y, Sato E (1996) Meiotic abnormalities of c-mos knockout mouse oocytes: activation after first meiosis or entrance into third meiotic metaphase. Biol Reprod 55:1315–1324
Arion D, Meijer L (1989) M-phase-specific protein kinase from mitotic sea urchin eggs: cyclic activation depends on protein synthesis and phosphorylation but does not require DNA or RNA synthesis. Exp Cell Res 183:361–375
Azoury J, Lee KW, Georget V, Rassinier P, Leader B, Verlhac MH (2008) Spindle positioning in mouse oocytes relies on a dynamic meshwork of actin filaments. Curr Biol 18:1514–1519
Azoury J, Verlhac MH, Dumont J (2009) Actin filaments: key players in the control of asymmetric divisions in mouse oocytes. Biol Cell 101:69–76
Azoury J, Lee KW, Georget V, Hikal P, Verlhac MH (2011) Symmetry breaking in mouse oocytes requires transient F-actin meshwork destabilization. Development 138:2903–2908
Bailly E, Dorée M, Nurse P, Bornens M (1989) p34cdc2 is located in both nucleus and cytoplasm; part is centrosomally associated at G2/M and enters vesicles at anaphase. EMBO J 8:3985–3995
Balakier H, Czolowska R (1977) Cytoplasmic control of nuclear maturation in mouse oocytes. Exp Cell Res 110:466–469
Barrett SL, Albertini DF (2007) Allocation of gamma-tubulin between oocyte cortex and meiotic spindle influences asymmetric cytokinesis in the mouse oocyte. Biol Reprod 6:949–957
Barrett SL, Albertini DF (2010) Cumulus cell contact during oocyte maturation in mice regulates meiotic spindle positioning and enhances developmental competence. J Assist Reprod Genet 27:29–39
Bashour AM, Fullerton AT, Hart MJ, Bloom GS (1997) IQGAP1, a Rca- and Cdc42-binding protein, directly binds and cross-links microfilaments. J Cell Biol 137:1555–1566
Bergstrom CT, Pritchard J (1998) Germline bottlenecks and the evolutionary maintenance of mitochondrial genomes. Genetics 149:2135–2146
Bielak-Zmijewska A, Kolano A, Szczepanska K, Maleszewski M, Borsuk E (2008) Cdc42 protein acts upstream of IQGAP1 and regulates cytokinesis in mouse oocytes and embryos. Dev Biol 322:21–32
Bouchet C, Steffann J, Corcos J, Monnot S, Paquis V, Rotig A, Lebon S, Levy P, Royer G, Giurgea I, Gigarel N, Benachi A, Dumez Y, Munnich A, Bonnefont JP (2006) Prenatal diagnosis of myopathy, encephalopathy, lactic acidosis, and stroke-like syndrome: contribution to understanding mitochondrial DNA segregation during human embryofetal development. J Med Genet 43:788–792
Brunet S, Maro B (2007) Germinal vesicle position and meiotic maturation in mouse oocyte. Reproduction 133:1069–1072
Brunet S, Verlhac MH (2011) Positioning to get out of meiosis: the asymmetry of division. Hum Reprod Update 17:68–75
Cao L, Shitara H, Horii T, Nagao Y, Imai H, Abe K, Hara T, Hayashi J, Yonekawa H (2007) The mitochondrial bottleneck occurs without reduction of mtDNA content in female mouse germ cells. Nat Genet 39:386–390
Cao L, Shitara H, Sugimoto M, Hayashi J, Abe K, Yonekawa H (2009) New evidence confirms that the mitochondrial bottleneck is generated without reduction of mitochondrial DNA content in early primordial germ cells of mice. PLoS Genet 5:e1000756
Capco DG, Gallicano GI, McGaughey RW, Downing KH, Larabell CA (1993) Cytoskeletal sheets of mammalian eggs and embryos: a lattice-like network of intermediate filaments. Cell Motil Cytoskeleton 24:85–99
Cau J, Hall A (2005) Cdc42 controls the polarity of the actin and microtubule cytoskeletons through two distinct signal transduction pathways. J Cell Sci 118:2579–2587
Chesnel F, Bazile F, Pascal A, Kubiak JZ (2006) Cyclin B dissociation from CDK1 precedes its degradation upon MPF inactivation in mitotic extracts of Xenopus laevis embryos. Cell Cycle 5:1687–1698
Ciemerych MA, Tarkowski AK, Kubiak JZ (1998) Autonomous activation of histone H1 kinase, cortical activity and microtubule organization in one- and two-cell mouse embryos. Biol Cell 90:557–564
Colledge WH, Carlton MB, Udy GB, Evans MJ (1994) Disruption of c-mos causes parthenogenetic development of unfertilized mouse eggs. Nature 370:65–68
Cox RT, Spradling AC (2003) A Balbiani body and the fusome mediate mitochondrial inheritance during Drosophila oogenesis. Development 130:1579–1590
Cox RT, Spradling AC (2006) Milton controls the early acquisition of mitochondria by Drosophila oocytes. Development 133:3371–3377
Cree LM, Samuels DC, de Sousa Lopes SC, Rajasimha HK, Wonnapinij P, Mann JR, Dahl HH, Chinnery PF (2008) A reduction of mitochondrial DNA molecules during embryogenesis explains the rapid segregation of genotypes. Nat Genet 40:249–254
Cui XS, Li XY, Kim NH (2007) Cdc42 is implicated in polarity during meiotic resumption and blastocyst formation in the mouse. Mol Reprod Dev 74:785–794
de Pennart H, Verlhac MH, Cibert C, Santa Maria A, Maro B (1993) Okadaic acid induces spindle lengthening and disrupts the interaction of microtubules with the kinetochores in metaphase II-arrested mouse oocytes. Dev Biol 157:170–181
De Smedt V, Szollosi D, Kloc M (2000) The Balbiani body: asymmetry in the mammalian oocyte. Genesis 26:208–212
Dean NL, Battersby BJ, Ao A, Gosden RG, Tan SL, Shoubridge EA, Molnar MJ (2003) Prospect of preimplantation genetic diagnosis for heritable mitochondrial DNA diseases. Mol Hum Reprod 9:631–638
Deng M, Kishikawa H, Yanagimachi R, Kopf GS, Schultz RM et al (2003) Chromatin-mediated cortical granule redistribution is responsible for the formation of the cortical granule-free domain in mouse eggs. Dev Biol 257:166–176
Deng M, Williams CJ, Schultz RM (2005) Role of MAP kinase and myosin light chain kinase in chromosome-induced development of mouse egg polarity. Dev Biol 278:358–366
Ducka AM, Joel P, Popwicz GM, Trybus KM, Schleicher M, Noegel AA, Huber R, Holak TA, Sitar T (2010) Structures of actin-bound Wiskott-Aldrich syndrome protein homology 2 (WH2) domains of Spire and the implication for filament nucleation. Proc Natl Acad Sci USA 107:11757–11762
Dumont J, Million K, Sunderland K, Rassinier P, Hyunjung L, Leader B, Verlhac M-H (2007) Formin-2 is required for spindle migration and for late steps of cytokinesis in mouse oocytes. Dev Biol 301:254–265
Duncan FE, Moss SB, Schultz RM, Williams CJ (2005) PAR-3 defines a central subdomain of the cortical actin cap in mouse eggs. Dev Biol 280:38–47
Edwards RG (2000) The role of embryonic polarities in preimplantation growth and implantation of mammalian embryos. Hum Reprod Suppl 6:1–8
Edwards RG (2001) Ovarian differentiation and human embryo quality. 1. Molecular and morphogenetic homologies between oocytes and embryos in Drosophila, C. elegans, Xenopus and mammals. Reprod Biomed Online 3:138–160
Edwards RG, Ludwig M (2003) Are major defects in children conceived in vitro due to innate problems in patients or to induced genetic damage? Reprod Biomed Online 7:131–138
Eichenlaub-Ritter U, Wieczorek M, Lüke S, Seidel T (2011) Age related changes in mitochondrial function and new approaches to study redox regulation in mammalian oocytes in response to age or maturation conditions. Mitochondrion 11(5):783–796
El-Mestrah M, Castle PE, Borossa G, Kan FW (2002) Subcellular distribution of ZP1, ZP2, and ZP3 glycoproteins during folliculogenesis and demonstration of their topographical disposition within the zona matrix of mouse ovarian oocytes. Biol Reprod 66:866–876
Esposito G, Vitale AM, Leijten FP, Strik AM, Koonen-Reemst AM, Yurttas P, Robben TJ, Coonrod S, Gossen JA (2007) Peptidylarginine deiminase (PAD) 6 is essential for oocyte cytoskeletal sheet formation and female fertility. Mol Cell Endocrinol 273:25–31
Etienne-Manneville S, Hall A (2002) Rho GTPases in cell biology. Nature 420:629–635
Evangelista M, Zigmond S, Boone C (2003) Formins: signaling effectors for assembly and polarization of actin filaments. J Cell Sci 116:2603–2611
Evans JP, Foster JA, McAvey BA, Gerton GL, Kopf GS, Schultz RM (2000) The effects of perturbation of cell polarity on molecular markers of sperm-egg binding sites on mouse eggs. Biol Reprod 62:76–84
Fukata M, Kuroda S, Fujii K, Nakamura T, Shoji I, Matsuura Y, Okawa K, Iwamatsu A, Kikuchi A, Kaibuchi K (1997) Regulation of cross-linking of actin filament by IQGAP1, a target for Cdc42. J Biol Chem 272:29579–29583
Fukata M, Kuroda S, Nakagawa M, Kawajiri A, Itoh N, Shoji I, Matsuura Y, Yonehara S, Fujisawa H, Kikuchi A, Kaibuchi K (1999) Cdc42 and Rac1 regulate the interaction of IQGAP1 with beta-catenin. J Biol Chem 274:26044–26050
Gallicano GI, Larabell CA, McGaughey RW, Capco DG (1994) Novel cytoskeletal elements in mammalian eggs are composed of a unique arrangement of intermediate filaments. Mech Dev 45:211–226
Gautier J, Norbury C, Lohka M, Nurse P, Maller J (1988) Purified maturation-promoting factor contains the product of a Xenopus homolog of the fission yeast cell cycle control gene cdc2+. Cell 54:433–439
Gautier J, Minshull J, Lohka M, Glotzer M, Hunt T, Maller JL (1990) Cyclin is a component of maturation-promoting factor from Xenopus. Cell 60:487–494
Glotzer M (2005) The molecular requirements for cytokinesis. Science 307:1735–1739
Glotzer M, Murray AW, Kirschner MW (1991) Cyclin is degraded by the ubiquitin pathway. Nature 349:132–138
Gönczy P (2002) Mechanisms of spindle positioning: focus on flies and worms. Trends Cell Biol 12:332–339
Guertin DA, Trautmann S, McCollum D (2002) Cytokinesis in eukaryotes. Microbiol Mol Biol Rev 66:155–178
Halet G, Carroll J (2007) Rac activity is polarized and regulates meiotic spindle stability and anchoring in mammalian oocytes. Dev Cell 12:309–317
Harris ES, Higgs HN (2004) Actin cytoskeleton: formins lead the way. Curr Biol 14:R520–R522
Hiiragi T, Alarcon VB, Fujimori T, Louvet-Vallee S, Maleszewski M, Marikawa Y, Maro B, Solter D (2006) Where do we stand now? Mouse early embryo patterning meeting in Freiburg, Germany (2005). Int J Dev Biol 50:581–586; discussion 586–587
Hoodbhoy T, Avilés M, Baibakov B, Epifano O, Jiménez-Movilla M, Gauthier L, Dean J (2006) ZP2 and ZP3 traffic independently within oocytes prior to assembly into the extracellular zona pellucida. Mol Cell Biol 26:7991–7998
Huo LJ, Fan HY, Zhong ZS, Chen DY, Schatten H, Sun QY (2004) Ubiquitin-proteasome pathway modulates mouse oocyte meiotic maturation and fertilization via regulation of MAPK cascade and cyclin B1 degradation. Mech Dev 121:1275–1287
Huo LJ, Yu LZ, Liang CG, Fan HY, Chen DY, Sun QY (2005) Cell-cycle-dependent subcellular localization of cyclin B1, phosphorylated cyclin B1 and p34cdc2 during oocyte meiotic maturation and fertilization in mouse. Zygote 13:45–53
Jenuth JP, Peterson AC, Fu K, Shoubridge EA (1996) Random genetic drift in the female germline explains the rapid segregation of mammalian mitochondrial DNA. Nat Genet 14:146–151
Johnson MH (2009) From mouse egg to mouse embryo: polarities, axes, and tissues. Annu Rev Cell Dev Biol 25:483–512
Kan R, Yurttas P, Kim B, Jin M, Wo L, Lee B, Gosden R, Coonrod SA (2011) Regulation of mouse oocyte microtubule and organelle dynamics by PADI6 and the cytoplasmic lattices. Dev Biol 350:311–322
Kloc M, Etkin LD (1995) Two distinct pathways for the localization of RNAs at the vegetal cortex in Xenopus oocytes. Development 121:287–297
Kloc M, Etkin LD (1998) Apparent continuity between the METRO and late RNA localization pathways during oogenesis in Xenopus. Mech Dev 73:95–106
Kloc M, Larabell C, Etkin LD (1996) Elaboration of the messenger transport organizer pathway (METRO) for localization of RNA to the vegetal cortex of Xenopus oocytes. Dev Biol 180:119–130
Kloc M, Larabell C, Chan P-YA, Etkin L (1998) Contribution of METRO pathway localized molecules to the organization of the germ cell lineage. Mech Dev 75:81–93
Kloc M, Bilinski S, Chan AP, Allen LH, Zearfoss NR, Etkin LD (2001) RNA localization and germ cell determination in Xenopus. Int Rev Cytol 203:63–91
Kloc M, Bilinski S, Dougherty MT, Brey EM, Etkin LD (2004a) Formation, architecture and polarity of female germline cyst in Xenopus. Dev Biol 266:43–61
Kloc M, Bilinski S, Etkin LD (2004b) The Balbiani body and germ cell determinants: 150 years later. Curr Top Dev Biol 59:1–36
Kloc M, Jaglarz M, Dougherty M, Stewart MD, Nel-Themaat L, Bilinski S (2008) Mouse early oocytes are transiently polar: three-dimensional and ultrastructural analysis. Exp Cell Res 314:3245–3254
Kozma R, Ahmed S, Best A, Lim L (1995) The Ras-related protein Cdc42Hs and bradykinine promote formation of peripheral actin microspikes and filopodia in Swiss 3T3 fibroblasts. Mol Cell Biol 15:1942–1952
Kubiak JZ (2012) Protein kinase assays for measuring MPF and MAPK activities in mouse and rat oocytes and early embryos. In: Homer H (ed) Methods in molecular biology. Springer, Heidelberg (in press)
Kubiak J, Paldi A, Weber M, Maro B (1991) Genetically identical parthenogenetic mouse embryos produced by inhibition of the first meiotic cleavage with cytochalasin D. Development 111:763–769
Kubiak JZ, Weber M, Géraud G, Maro B (1992) Cell cycle modification during the transitions between meiotic M-phases in mouse oocytes. J Cell Sci 102:457–467
Kubiak JZ, Weber M, de Pennart H, Winston NJ, Maro B (1994) The metaphase II arrest in mouse oocytes is controlled through microtubule-dependent destruction of cyclin B in the presence of CSF. EMBO J 12:3773–3778
Kuroda S, Fukata M, Nakagawa M, Fujii K, Nakamura T, Ookubo T, Izawa I, Nagase T, Nomura N, Tani H, Shoji I, Matsuura Y, Yonehara S, Kaibuchi K (1998) Role of IQGAP1, a target of the small GTPases Cdc42 and Rac1, in regulation of E-cadherin-mediated cell-cell adhesion. Science 281:832–835
Labbé JC, Picard A, Karsenti E, Dorée M (1988) An M-phase-specific protein kinase of Xenopus oocytes: partial purification and possible mechanism of its periodic activation. Dev Biol 127:157–169
Labbé JC, Picard A, Peaucellier G, Cavadore JC, Nurse P, Doree M (1989) Purification of MPF from starfish: identification as the H1 histone kinase p34cdc2 and a possible mechanism for its periodic activation. Cell 57:253–263
Laipis PJ, Van de Walle MJ, Hauswirth WW (1988) Unequal partitioning of bovine mitochondrial genotypes among siblings. Proc Natl Acad Sci USA 85:8107–8110
Larson SM, Lee HJ, Hung PH, Matthews LM, Robinson DN, Evans JP (2010) Cortical mechanics and meiosis II completion in mammalian oocytes are mediated by myosin-II and Ezrin-Radixin-Moesin (ERM) proteins. Mol Biol Cell 21:3182–3192
Leader B, Lim H, Carabatsos MJ, Harrington A, Ecsedy J, Pellman D, Maas R, Leder P (2002) Formin-2, polyploidy, hypofertility and positioning of the meiotic spindle in mouseoocytes. Nat Cell Biol 4:921–929
Lechowska A, Bilinski S, Choi Y, Shin Y, Kloc M, Rajkovic A (2011) Premature ovarian failure in nobox-deficient mice is caused by defects in somatic cell invasion and germ cell cyst breakdown. J Assist Reprod Genet 28:583–589
Ledan E, Polanski Z, Terret ME, Maro B (2001) Meiotic maturation of the mouse oocyte requires an equilibrium between cyclin B synthesis and degradation. Dev Biol 232:400–413
Lei Y, Warrior R (2000) The Drosophila Lissencephaly1 (DLis1) is required for nuclear migration. Dev Biol 226:57–72
Levi M, Ninio-Mani L, Shalgi R (2012). Src Protein Kinases in Mouse and Rat Oocytes and Embryos. Results Probl Cell Differ. 55., 93–106
Li S, Ou XH, Wang ZB et al (2010) ERK3 is required for metaphase-anaphase transition in mouse oocyte meiosis. PLoS One 5(9):pii: e13074
Longo FJ (1987) Actin-plasma membrane associations in mouse eggs and oocytes. J Exp Zool 243:299–309
Longo FJ, Chen DY (1985) Development of cortical polarity in mouse eggs: involvement of the meiotic apparatus. Dev Biol 107:382–394
Ma C, Benink HA, Cheng D, Montplaisir V, Wang L, Xi Y, Zheng PP, Bement WM, Liu XJ (2006) Cdc42 activation couples spindle positioning to first polar body formation in oocyte maturation. Curr Biol 16:214–220
Maciejewska Z, Pascal A, Kubiak JZ, Ciemerych MA (2011) Phosphorylated ERK5/BMK1 transiently accumulates within division spindles in mouse oocytes and preimplantation embryos. Folia Histochem Cytobiol 49(3):528–534
Maro B, Johnson MH, Webb M, Flach G (1986) Mechanism of polar body formation in the mouse oocyte: an interaction between the chromosomes, the cytoskeleton and the plasma membrane. J Embryol Exp Morphol 92:11–32
Masui Y, Markert CL (1971) Cytoplasmic control of nuclear behavior during meiotic maturation of frog oocytes. J Exp Zool 177:129–145
Mitra J, Schultz RM (1996) Regulation of the acquisition of meiotic competence in the mouse: changes in the subcellular localization of cdc2, cyclin B1, cdc25C and wee1, and in the concentration of these proteins and their transcripts. J Cell Sci 109:2407–2415
Miyazaki A, Kato KH, Nemoto S (2005) Role of microtubules and centrosomes in the eccentric relocation of the germinal vesicle upon meiosis reinitiation in sea-cucumber oocytes. Dev Biol 280:237–247
Monnot S, Gigarel N, Samuels DC, Burlet P, Hesters L, Frydman N, Frydman R, Kerbrat V, Funalot B, Martinovic J, Benachi A, Feingold J, Munnich A, Bonnefont JP, Steffann J (2011) Segregation of mtDNA throughout human embryofetal development: m.3243A > G as a model system. Hum Mutat 32:116–125
Mullins RD, Heuser JA, Pollard TD (1998) The interaction of Arp2/3 complex with actin: nucleation, high affinity pointed end capping, and formation of branching networks of filaments. Proc Natl Acad Sci USA 95:6181–6186
Na J, Zernicka-Goetz M (2006) Asymmetric positioning and organization of the meiotic spindle of mouse oocytes requires CDC42 function. Curr Biol 16:1249–1254
Nakagomi S, Barsoum MJ, Bossy-Wetzel E, Sütterlin C, Malhotra V, Lipton SA (2008) A golgi fragmentation pathway in neurodegeneration. Neurobiol Dis 29:221–231
Nishiyama A, Tachibana K, Igarashi Y, Yasuda H, Tanahashi N, Tanaka K, Ohsumi K, Kishimoto T (2000) A nonproteolytic function of the proteasome is required for the dissociation of Cdc2 and cyclin B at the end of M phase. Genes Dev 14:2344–2357
Nobes CD, Hall A (1995) Rho, Rac and Cdc42 GTPases: regulators of actin structures, cell adhesion and motility. Biochem Soc Trans 23:456–459
Noritake J, Watanabe T, Sato K, Wang S, Kaibuchi K (2005) IQGAP1: a key regulator of adhesion and migration. J Cell Sci 118:2085–2092
Ookata K, Hisanaga S, Bulinski JC, Murofushi H, Aizawa H, Itoh TJ, Hotani H, Okumura E, Tachibana K, Kishimoto T (1995) Cyclin B interaction with microtubule-associated protein 4 (MAP4) targets p34cdc2 kinase to microtubules and is a potential regulator of M-phase microtubule dynamics. J Cell Biol 128:849–862
Pepling ME, Spradling AC (1998) Female mouse germ cells form synchronously dividing cysts. Development 125:3323–3328
Pepling ME, Wilhelm JE, O’Hara AL, Gephardt GW, Spradling AC (2007) Mouse oocytes within germ cell cysts and primordial follicles contain a Balbiani body. Proc Natl Acad Sci USA 104:187–192
Pfender S, Kuznetsov V, Pleiser S, Kerkhoff E, Schuh M (2011) Spire-type actin nucleators cooperate with Formin-2 to drive asymmetric oocyte division. Curr Biol 21:955–960
Pines J, Hunter T (1991) Human cyclins A and B1 are differentially located in the cell and undergo cell cycle-dependent nuclear transport. J Cell Biol 115:1–17
Quinlan ME, Heuser JE, Kerkhoff E, Mullins RD (2005) Drosophila Spire is an actin nucleation factor. Nature 433:382–388
Rajkovic A, Pangas SA, Ballow D, Suzumori N, Matzuk MM (2004) NOBOX deficiency disrupts early folliculogenesis and oocytespecific gene expression. Science 305:1157–1159
Rime H, Ozon R (1990) Protein phosphatases are involved in the in vivo activation of histone H1 kinase in mouse oocyte. Dev Biol 141:115–122
Roze D, Rousset F, Michalakis Y (2005) Germline bottlenecks, biparental inheritance and selection on mitochondrial variants: a two-level selection model. Genetics 170:1385–1399
Sanfins A, Lee GY, Plancha CE, Overstrom EW, Albertini DF (2003) Distinctions in meiotic spindle structure and assembly during in vitro and in vivo maturation of mouse oocytes. Biol Reprod 69:2059–2067
Sanfins A, Plancha CE, Overstrom EW, Albertini DF (2004) Meiotic spindle morphogenesis in in vivo and in vitro matured mouse oocytes: insights into the relationship between nuclear and cytoplasmic quality. Hum Reprod 19:2889–2899
Sardet C, Prodon F, Dumollard R, Chang P, Chênevert J (2002) Structure and function of the egg cortex from oogenesis through fertilization. Dev Biol 241:1–23
Schindler K (2011) Protein kinases and protein phosphatases that regulate meiotic maturation in mouse oocytes. Results Probl Cell Differ 53:309–341
Schindler K, Schultz RM (2009) The CDC14A phosphatase regulates oocyte maturation in mouse. Cell Cycle 8:1090–1098
Schuh M, Ellenberg J (2008) A new model for asymmetric spindle positioning in mouse oocytes. Curr Biol 18:1986–1992
Shannon KB, Li R (1999) The multiple roles of Cyk1p in the assembly and function of the actomyosin ring in budding yeast. Mol Biol Cell 10:283–296
Simerly C, Nowak G, de Lanerolle P, Schatten G (1998) Differential expression and functions of cortical myosin IIA and IIB isotypes during meiotic maturation, fertilization and mitosis in mouse oocytes and embryos. Mol Biol Cell 9:2509–2525
Sun SC, Sun QY, Kim NH (2011a) JMY is required for asymmetric division and cytokinesis in mouse oocytes. Mol Hum Reprod 17:286–295
Sun SC, Wang ZB, Xu YN, Lee SE, Cui XS, Kim NH (2011b) Arp2/3 complex regulates asymmetric division and cytokinesis in mouse oocytes. PLoS One 6:e18392
Swan A, Nguyen T, Suter B (1999) Drosophila Lissencephaly-1 functions with Bic-D and dynein in oocyte determination and nuclear positioning. Nat Cell Biol 1:444–449
Szollosi D, Calarco P, Donahue RP (1972) Absence of centrioles in the first and second meiotic spindles of mouse oocytes. J Cell Sci 11:521–541
Tan X, Peng A, Wang Y, Tang Z (2005) The effects of proteasome inhibitor lactacystin on mouse oocyte meiosis and first cleavage. Sci China C Life Sci 48:287–294
Terada Y, Simerly C, Schatten G (2000) Microfilament stabilization by jasplakinolide arrests oocyte maturation, cortical granule exocytosis, sperm incorporation cone resorption, and cell-cycle progression, but not DNA replication, during fertilization in mice. Mol Reprod Dev 56:89–98
Van Blerkom J, Bell H (1986) Regulation of development in the fully grown mouse oocyte: chromosome-mediated temporal and spatial differentiation of the cytoplasm and plasma membrane. J Embryol Exp Morphol 93:213–238
Verlhac MH, de Pennart H, Maro B, Cobb MH, Clarke HJ (1993) MAP kinase becomes stably activated at metaphase and is associated with microtubule-organizing centers during meiotic maturation of mouse oocytes. Dev Biol 158, 330–340
Verlhac MH, Kubiak JZ, Weber M, Géraud G, Colledge WH, Evans MJ, Maro B (1996) Mos is required for MAP kinase activation and is involved in microtubule organization during meiotic maturation in the mouse. Development 122:815–822
Verlhac M-H, Lefebvre C, Guillaud P, Rassinier P, Maro B (2000) Asymmetric division in mouse oocytes: with or without Mos. Curr Biol 10:1303–1306
VerMilyea MD, Maneck M, Yoshida N, Blochberger I, Suzuki E, Suzuki T, Spang R, Klein CA, Perry AC (2011) Transcriptome asymmetry within mouse zygotes but not between early embryonic sister blastomeres. EMBO J 30:1841–1851
Vinot S, Le T, Maro B, Louvet-Vallee S (2004) Two Par6 proteins become asymmetrically localized during establishment of polarity in mouse oocytes. Curr Biol 14:520–525
Vinot S, Le T, Ohno S, Pawson T, Maro B, Louvet-Vallée S (2005) Asymmetric distribution of PAR proteins in the mouse embryo begins at the 8-cell stage during compaction. Dev Biol 282:307–319
Wai T, Teoli D, Shoubridge EA (2008) The mitochondrial DNA genetic bottleneck results from replication of a subpopulation of genomes. Nat Genet 40:1484–1488
Weber M, Kubiak JZ, Arlinghaus RB, Pines J, Maro B (1991) c-mos proto-oncogene product is partly degraded after release from meiotic arrest and persists during interphase in mouse zygotes. Dev Biol 148:393–397
Winston NJ (1997) Stability of cyclin B protein during meiotic maturation and the first mitotic cell division in mouse oocytes. Biol Cell 89:211–219
Wright PW, Bolling LC, Calvert ME, Sarmento OF, Berkeley EV, Shea MC, Hao Z, Jayes FC, Bush LA, Shetty J, Shore AN, Reddi PP, Tung KS, Samy E, Allietta MM, Sherman NE, Herr JC, Coonrod SA (2003) ePAD, an oocyte and early embryo-abundant peptidylarginine deiminase-like protein that localizes to egg cytoplasmic sheets. Dev Biol 256:73–88
Xiong B, Yu LZ, Wang Q, Ai JS, Yin S, Liu JH, OuYang YC, Hou Y, Chen DY, Zou H, Sun QY (2007) Regulation of intracellular MEK1/2 translocation in mouse oocytes: cytoplasmic dynein/dynactin-mediated poleward transport and cyclin B degradation-dependent release from spindle poles. Cell Cycle 6:1521–1527
Yang HY, McNally K, McNally FJ (2003) MEI-1/katanin is required for translocation of the meiosis I spindle to the oocyte cortex in C. elegans. Dev Biol 260:245–259
Yang HY, Mains PE, McNally FJ (2005) Kinesin-1 mediates translocation of the meiotic spindle to the oocyte cortex through KCA-1, a novel cargo adapter. J Cell Biol 169:447–457
Yasuda S, Taniguchi H, Oceguera-Yanez F, Ando Y, Watanabe S, Monypenny J, Narumiya S (2006) An essential role of Cdc42-like GTPases in mitosis of HeLa cells. FEBS Lett 580:3375–3380
Yi K, Unruh JR, Deng M, Slaughter BD, Rubinstein B, Li R (2011) Dynamic maintenance of asymmetric meiotic spindle position through Arp2/3-complex-driven cytoplasmic streaming in mouse oocytes. Nat Cell Biol 13:1252–1258
Yu LZ, Xiong B, Gao WX, Wang CM, Zhong ZS, Huo LJ, Wang Q, Hou Y, Liu K, Liu XJ, Schatten H, Chen DY, Sun QY (2007) MEK1/2 regulates microtubule organization, spindle pole tethering and asymmetric division during mouse oocyte meiotic maturation. Cell Cycle 6:330–338
Zernicka-Goetz M, Huang S (2010) Stochasticity versus determinism in development: a false dichotomy? Nat Rev Genet 11:743–744
Zernicka-Goetz M, Verlhac M-H, Géraud G, Kubiak JZ (1997) Protein phosphatases control MAP kinase activation and microtubule organization during rat oocyte maturation. Eur J Cell Biol 72:30–38
Zhang YZ, Ouyang YC, Hou Y, Schatten H, Chen DY, Sun QY (2008) Mitochondrial behavior during oogenesis in zebrafish: a confocal microscopy analysis. Dev Growth Differ 50:189–201
Zhang CH, Wang ZB, Quan S, Huang X, Tong JS, Ma JY, Guo L, Wei YC, Ouyang YC, Hou Y, Xing FQ, Sun QY (2011) GM130, a cis-Golgi protein, regulates meiotic spindle assembly and asymmetric division in mouse oocyte. Cell Cycle 10:1861–1870
Zhong ZS, Huo LJ, Liang CC, Chen DY, Sun QY (2005) Small GTPase RhoA is required for ooplasmic segregation and spindle rotation, but not for spindle organization and chromosome separation during mouse oocyte maturation, fertilization, and early cleavage. Mol Reprod Dev 41:256–261
Zhou RR, Wang B, Wang J, Schatten H, Zhang YZ (2010) Is the mitochondrial cloud the selection machinery for preferentially transmitting wild-type mtDNA between generations? Rewinding Müller’s ratchet efficiently. Curr Genet 56:101–107
Zigmond SH (2004) Formin-induced nucleation of actin filaments. Curr Opin Cell Biol 16:99–105
Zuchero JB, Coutts AS, Quinlan ME, Thangue NB, Mullins RD (2009) p53-cofactor JMY is a multifunctional actin nucleation factor. Nat Cell Biol 11:451–459
Acknowledgements
We are grateful to Guillaume Halet for reading the manuscript and valuable discussions. While writing this article, MK was supported by NSF grant 0904186 and JZK by ARC.
Author information
Authors and Affiliations
Corresponding author
Editor information
Editors and Affiliations
Rights and permissions
Copyright information
© 2012 Springer-Verlag Berlin Heidelberg
About this chapter
Cite this chapter
Kloc, M., Ghobrial, R.M., Borsuk, E., Kubiak, J.Z. (2012). Polarity and Asymmetry During Mouse Oogenesis and Oocyte Maturation. In: Kubiak, J. (eds) Mouse Development. Results and Problems in Cell Differentiation, vol 55. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-30406-4_2
Download citation
DOI: https://doi.org/10.1007/978-3-642-30406-4_2
Published:
Publisher Name: Springer, Berlin, Heidelberg
Print ISBN: 978-3-642-30405-7
Online ISBN: 978-3-642-30406-4
eBook Packages: Biomedical and Life SciencesBiomedical and Life Sciences (R0)