You may have access to the free features available through My Research. You can save searches, save documents, create alerts and more. Please log in through your library or institution to check if you have access.
You may have access to different export options including Google Drive and Microsoft OneDrive and citation management tools like RefWorks and EasyBib. Try logging in through your library or institution to get access to these tools.
REFERENCESHammondJ.
Recovery and culture of tubal mouse ova.
Nature1949; 163: 28–29.
KaufmanMH,
SachsL.
Complete preimplantation development in culture of parthenogenetic mouse embryos.
J Embryol Exp Morph1976; 35: 179–190.
GoddardMJ,
PrattHP.
Control of events during early cleavage of the mouse embryo: an analysis of the ‘two-cell block’.
J Embryol Exp Morph1983; 73: 111–133.
WhittenWK,
BiggersJD.
Complete development in vitro of the pre-implantation stages of the mouse in a simple chemically defined medium.
J Reprod Fertil1968; 17: 399–401.
Muggleton-HarrisA,
WhittinghamDG,
WilsonL.
Cytoplasmic control of preimplantation development in vitro in the mouse.
Nature1982; 299: 460–462.
AbramczukJ,
SolterD,
KoprowskiH.
The beneficial effect EDTA on development of mouse one-cell embryos in chemically defined medium.
Dev Biol1977; 61: 378–383.
ChatotCL,
ZiomekCA,
BavisterBD,
LewisJL,
TorresI.
An improved culture medium supports development of random-bred one-cell mouse embryos in vitro.
J Reprod Fertil1989; 86: 679–688.
HaraguchiS,
NaitoK,
SatoE.
Phosphate exposure during the late one-cell and early two-cell stages induces a time-specific decrease in cyclin B and cdc25B mRNAs in AKR/N mouse embryos in vitro.
Zygote1999; 7: 87–93.
BiggersJD,
GwatkinRLB,
BrinsterRL.
Development of mouse embryos in organ culture of fallopian tubes on a chemically defined medium.
Nature1962; 194: 747–749.
MinamiN,
BavisterBD,
IritaniA.
Development of hamster two-cell embryos in the isolated mouse oviduct in organ culture system.
Gamete Res1988; 19: 235–240.
BellierS,
ChastantS,
AdenotP,
VincentM,
RenardJP,
BensaudeO.
Nuclear translocation and carboxyl-terminal domain phosphorylation of RNA polymerase II delineate the two phases of zygotic gene activation in mammalian embryos.
EMBO J1997; 16: 6250–6262.
LathamKE,
SolterD,
SchultzRM.
Acquisition of a transcriptionally permissive state during the one-cell stage of mouse embryogenesis.
Dev Biol1992; 149: 457–462.
MatsumotoK,
AnzaiM,
NakagataN,
TakahashiA,
TakahashiY,
MiyataK.
Onset of paternal gene activation in early mouse embryos fertilized with transgenic mouse sperm.
Mol Reprod Dev1994; 39: 136–140.
RamPT,
SchultzRM.
Reporter gene expression in G2 of the one-cell mouse embryo.
Dev Biol1993; 156: 552–556.
TemelesGL,
RamPT,
RothsteinJL,
SchultzRM.
Expression patterns of novel genes during mouse preimplantation embryogenesis.
Mol Reprod Dev1994; 37: 121–129.
BouniolC,
NguyenE,
DebeyP.
Endogenous transcription occurs at the one-cell stage in the mouse embryo.
Exp Cell Res1995; 218: 57–62.
ChristiansE,
CampionE,
ThompsonEM,
RenardJP.
Expression of the HSP 70.1 gene, a landmark of early zygotic activity in the mouse embryo, is restricted to the first burst of transcription.
Development1995; 121: 113–122.
AokiF,
WorradDM,
SchultzRM.
Regulation of transcriptional activity during the first and second cell cycles in the preimplantation mouse embryo.
Dev Biol1997; 181: 296–307.
FlachG,
JohnsonMH,
BraudePR,
TaylorRA,
BoltonVN.
The transition from maternal to embryonic control in the two-cell mouse embryo.
EMBO J1982; 1: 681–686.
LathamKE,
SolterD,
SchultzRM.
Activation of a two-cell stage-specific gene following transfer of heterologous nuclei into enucleated mouse embryos.
Mol Reprod Dev1991; 30: 182–186.
BensaudeO,
BabinetC,
MorangeM,
JacobF.
Heat shock proteins, first major products of zygotic gene activity in mouse embryo.
Nature1983; 305: 331–333.
ConoverJC,
TemelesGL,
ZimmermannJW,
BurkeB,
SchultzRM.
Stage-specific expression of a family of proteins that are major products of zygotic gene activation in the mouse embryo.
Dev Biol1991; 144: 392–404.
DavisWJ,
De SousaPA,
SchultzRM.
Transient expression of translation initiation factor eIF-4C during the two-cell stage of the preimplantation mouse embryo: identification by mRNA differential display and the role of DNA replication in zygotic gene activation.
Dev Biol1996; 174: 190–201.
LathamKE,
RambhatlaL,
HayashizakiY,
ChapmanVM.
Stage-specific induction and regulation by genomic imprinting of the mouse U2afbp-rs gene during preimplantation development.
Dev Biol1995; 168: 670–676.
SchultzRM.
Regulation of zygotic gene activation in the mouse.
Bioessays1993; 15: 531–538.
MajumderS,
DePamphilisML.
A unique role for enhancers is revealed during early mouse development.
Bioessays1995; 17: 879–889.
NothiasJY,
MajumderS,
KanekoKJ,
DePamphilisML.
Regulation of gene expression at the beginning of mammalian development.
J Biol Chem1995; 270: 22077–22080.
HeneryCC,
MirandaM,
WiekowskiM,
WilmutI,
DePamphilisML.
Repression of gene expression at the beginning of mouse development.
Dev Biol1995; 169: 448–460.
HamataniT,
CarterMG,
SharovAA,
KoMS.
Dynamics of global gene expression changes during mouse preimplantation development.
Dev Cell2004; 6: 117–131.
HowlettSK,
WebbM,
MaroB,
JohnsonMH.
Meiosis II, mitosis I and the linking interphase: a study of the cytoskeleton in the fertilised mouse egg.
Cytobios1985; 43: 295–305.
TaylorKD,
PikoL.
Patterns of mRNA prevalence and expression of B1 and B2 transcripts in early mouse embryos.
Development1987; 101: 877–892.
LathamKE,
GarrelsJI,
ChangC,
SolterD.
Quantitative analysis of protein synthesis in mouse embryos. I. Extensive reprogramming at the one- and two-cell stages.
Development1991; 112: 921–932.
TelfordNA,
WatsonAJ,
SchultzGA.
Transition from maternal to embryonic control in early mammalian development: a comparison of several species.
Mol Reprod Dev1990; 26: 90–100.
MatzukMM,
BurnsKH,
ViveirosMM,
EppigJJ.
Intercellular communication in the mammalian ovary: oocytes carry the conversation.
Science2002; 296: 2178–2180.
DongJ,
AlbertiniDF,
NishimoriK,
KumarTR,
LuN,
MatzukMM.
Growth differentiation factor-9 is required during early ovarian folliculogenesis.
Nature1996; 383: 531–535.
MatzukMM.
Revelations of ovarian follicle biology from gene knockout mice.
Mol Cell Endocrinol2000; 163: 61–66.
CarabatsosMJ,
ElvinJ,
MatzukMM,
AlbertiniDF.
Characterization of oocyte and follicle development in growth differentiation factor-9-deficient mice.
Dev Biol1998; 204: 373–384.
McGrathSA,
EsquelaAF,
LeeSJ.
Oocyte-specific expression of growth/differentiation factor-9.
Mol Endocrinol1995; 9: 131–136.
DubeJL,
WangP,
ElvinJ,
LyonsKM,
CelesteAJ,
MatzukMM.
The bone morphogenetic protein 15 gene is X-linked and expressed in oocytes.
Mol Endocrinol1998; 12: 1809–1817.
SmithP,
OWS,
CorriganKAet al.Ovarian morphology and endocrine characteristics of female sheep fetuses that are heterozygous or homozygous for the inverdale prolificacy gene (fecX1).
Biol Reprod1997; 57: 1183–1192.
Braw-TalR,
McNattyKP,
SmithPet al.Ovaries of ewes homozygous for the X-linked Inverdale gene (FecXI) are devoid of secondary and tertiary follicles but contain many abnormal structures.
Biol Reprod1993; 49: 895–907.
YanC,
WangP,
DeMayoJet al.Synergistic roles of bone morphogenetic protein 15 and growth differentiation factor 9 in ovarian function.
Mol Endocrinol2001; 15: 854–866.
LyonsKM,
PeltonRW,
HoganBL.
Patterns of expression of murine Vgr-1 and BMP-2a RNA suggest that transforming growth factor-beta-like genes coordinately regulate aspects of embryonic development.
Genes Dev1989; 3: 1657–1668.
SchmidP,
CoxD,
Van_der_PuttenH,
McMasterGK,
BilbeG.
Expression of TGF-beta s and TGF-beta type II receptor mRNAs in mouse folliculogenesis: stored maternal TGF-beta 2 message in oocytes.
Biochem Biophys Res Commun1994; 201: 649–656.
ValveE,
PenttilaTL,
ParankoJ,
HarkonenP.
FGF-8 is expressed during specific phases of rodent oocyte and spermatogonium development.
Biochem Biophys Res Commun1997; 232: 173–177.
CarabatsosMJ,
SellittoC,
GoodenoughDA,
AlbertiniDF.
Oocyte-granulosa cell heterologous gap junctions are required for the coordination of nuclear and cytoplasmic meiotic competence.
Dev Biol2000; 226: 167–179.
EppigJJ,
WigglesworthK,
PendolaFL.
The mammalian oocyte orchestrates the rate of ovarian follicular development.
Proc Natl Acad Sci USA2002; 99: 2890–2894.
SoyalSM,
AmlehA,
DeanJ.
FIGalpha, a germ cell-specific transcription factor required for ovarian follicle formation.
Development2000; 127: 4645–4654.
EpifanoO,
LiangLF,
FamilariM,
MoosMC,
DeanJ.
Coordinate expression of the three zona pellucida genes during mouse oogenesis.
Development1995; 121: 1947–1956.
LiangL,
SoyalSM,
DeanJ.
FIGalpha, a germ cell specific transcription factor involved in the coordinate expression of the zona pellucida genes.
Development1997; 124: 4939–4947.
NewportJ,
KirschnerM.
A major developmental transition in early Xenopus embryos: I. characterization and timing of cellular changes at the midblastula stage.
Cell1982; 30: 675–686.
MorisatoD,
AndersonKV.
Signaling pathways that establish the dorsal-ventral pattern of the Drosophila embryo.
Annu Rev Genet1995; 29: 371–399.
DeanJ.
Oocyte-specific genes regulate follicle formation, fertility and early mouse development.
J Reprod Immunol2002; 53: 171–180.
BurnsKH,
ViveirosMM,
RenYet al.Roles of NPM2 in chromatin and nucleolar organization in oocytes and embryos.
Science2003; 300: 633–636.
ChristiansE,
DavisAA,
ThomasSD,
BenjaminIJ.
Maternal-effect of Hsf1 on reproductive success.
Nature2000; 407: 693–694.
GurtuVE,
VermaS,
GrossmannAH,
LiskayRM,
SkarnesWC,
BakerSM.
Maternal-effect for DNA mismatch repair in the mouse.
Genetics2002; 160: 271–277.
HowellCY,
BestorTH,
DingFet al.Genomic imprinting disrupted by a maternal-effect mutation in the Dnmt1 gene.
Cell2001; 104: 829–838.
PayerB,
SaitouM,
BartonSCet al.Stella is a maternal-effect gene required for normal early development in mice.
Curr Biol2003; 13: 2110–2117.
RamosSB,
StumpoDJ,
KenningtonEAet al.The CCCH tandem zinc-finger protein Zfp36l2 is crucial for female fertility and early embryonic development.
Development2004; 131: 4883–4893.
TongZB,
GoldL,
PfeiferKEet al.Mater, a maternal-effect gene required for early embryonic development in mice.
Nat Genet2000; 26: 267–268.
WuX,
ViveirosMM,
EppigJJ,
BaiY,
FitzpatrickSL,
MatzukMM.
Zygote arrest 1 (Zar1) is a novel maternal-effect gene critical for the oocyte-to-embryo transition.
Nat Genet2003; 33: 187–191.
TongZB,
NelsonLM.
A mouse gene encoding an oocyte antigen associated with autoimmune premature ovarian failure.
Endocrinology1999; 140: 3720–3726.
MertineitC,
YoderJA,
TaketoT,
LairdDW,
TraslerJM,
BestorTH.
Sex-specific exons control DNA methyltransferase in mammalian germ cells.
Development1998; 125: 889–897.
XuZ,
KopfGS,
SchultzRM.
Involvement of inositol 1,4,5-trisphosphate-mediated Ca2+ release in early and late events of mouse egg activation.
Development1994; 120: 1851–1859.
LaiWS,
CarballoE,
ThornJM,
KenningtonEA,
BlackshearPJ.
Interactions of CCCH zinc finger proteins with mRNA. Binding of tristetraprolin-related zinc finger proteins to Au-rich elements and destabilization of mRNA.
J Biol Chem2000; 275: 17827–17837.
YanW,
RajkovicA,
ViveirosMM,
BurnsKH,
EppigJJ,
MatzukMM.
Identification of Gasz, an Evolutionarily Conserved Gene Expressed Exclusively in Germ Cells and Encoding a Protein with Four Ankyrin Repeats, a Sterile-alpha Motif, and a Basic Leucine Zipper.
Mol Endocrinol2002; 16: 1168–1184.
YanW,
MaL,
ZilinskiCA,
MatzukMM.
Identification and characterization of evolutionarily conserved pufferfish, zebrafish, and frog orthologs of GASZ.
Biol Reprod2004; 70: 1619–1625.
SuzumoriN,
YanC,
MatzukMM,
RajkovicA.
Nobox is a homeobox-encoding gene preferentially expressed in primordial and growing oocytes.
Mech Dev2002; 111: 137–141.
RajkovicA,
PangasSA,
BallowD,
SuzumoriN,
MatzukMM.
NOBOX deficiency disrupts early folliculogenesis and oocyte-specific gene expression.
Science2004; 305: 1157–1159.
MinamiN,
SasakiK,
AizawaA,
MiyamotoM,
ImaiH.
Analysis of gene expression in mouse two-cell embryos using fluorescein differential display: comparison of culture environments.
Biol Reprod2001; 64: 30–35.
MinamiN,
AizawaA,
IharaR,
MiyamotoM,
OhashiA,
ImaiH.
Oogenesin is a novel mouse protein expressed in oocytes and early cleavage-stage embryos.
Biol Reprod2003; 69: 1736–1742.
DadeS,
CallebautI,
MermillodP,
MongetP.
Identification of a new expanding family of genes characterized by atypical LRR domains. Localization of a cluster preferentially expressed in oocyte.
FEBS Lett2003; 555: 533–538.
TsukamotoS,
IharaR,
AizawaAet al.Oog1, an oocyte-specific protein, interacts with Ras and Ras-signaling proteins during early embryogenesis.
Biochem Biophys Res Commun2006; 343: 1105–1112.
AlbrightCF,
GiddingsBW,
LiuJ,
VitoM,
WeinbergRA.
Characterization of a guanine nucleotide dissociation stimulator for a ras-related GTPase.
EMBO J1993; 12: 339–347.
KikuchiA,
DemoSD,
YeZH,
ChenYW,
WilliamsLT.
RalGDS family members interact with the effector loop of ras p21.
Mol Cell Biol1994; 14: 7483–7491.
HaberlandJ,
GerkeV.
Conserved charged residues in the leucine-rich repeat domain of the Ran GTPase activating protein are required for Ran binding and GTPase activation.
Biochem J1999; 343 Part 3: 653–662.
DadeS,
CallebautI,
PaillissonA,
BontouxM,
Dalbies-TranR,
MongetP.
In silico identification and structural features of six new genes similar to MATER specifically expressed in the oocyte.
Biochem Biophys Res Commun2004; 324: 547–553.
PaillissonA,
DadeS,
CallebautIet al.Identification, characterization and metagenome analysis of oocyte-specific genes organized in clusters in the mouse genome.
BMC Genomics2005; 6: 76.
You have requested "on-the-fly" machine translation of selected content from our databases. This functionality is provided solely for your convenience and is in no way intended to replace human translation. Show full disclaimer
Neither ProQuest nor its licensors make any representations or warranties with respect to the translations. The translations are automatically generated "AS IS" and "AS AVAILABLE" and are not retained in our systems. PROQUEST AND ITS LICENSORS SPECIFICALLY DISCLAIM ANY AND ALL EXPRESS OR IMPLIED WARRANTIES, INCLUDING WITHOUT LIMITATION, ANY WARRANTIES FOR AVAILABILITY, ACCURACY, TIMELINESS, COMPLETENESS, NON-INFRINGMENT, MERCHANTABILITY OR FITNESS FOR A PARTICULAR PURPOSE. Your use of the translations is subject to all use restrictions contained in your Electronic Products License Agreement and by using the translation functionality you agree to forgo any and all claims against ProQuest or its licensors for your use of the translation functionality and any output derived there from. Hide full disclaimer
Longer documents can take a while to translate. Rather than keep you waiting, we have only translated the first few paragraphs. Click the button below if you want to translate the rest of the document.
Studies on oocyte-specific genes are important in understanding the genetic pathways essential for folliculogenesis, oogenesis and early embryogenesis. Although the molecular mechanisms regulating oocyte growth and embryo development in mammals have partially been unraveled by gene knockout studies, many aspects concerning reproduction remain to be determined. Development of mammalian embryos starts with the fusion of sperm and egg. After fertilization, the first major developmental transition, maternal to zygotic transition, occurs at the specific stages of preimplantation development in each mammal. The transition is called zygotic gene activation (ZGA) or embryonic genome activation. The ZGA is one of the most important events that occur during preimplantation development; however, the mechanism of the event remains unknown. Because the development until the transition is maintained by maternally inherited proteins and transcripts stored in the oocytes, it is highly likely that these products play an important role in the initiation of ZGA. Several maternal-effects genes that are specifically expressed in oocytes have been identified and their involvement in preimplantation development has been revealed. Therefore, to study oocyte-specific gene regulation would help not only to understand the precise mechanisms of mammalian development, but also to show the mechanisms of reproductive disorders, such as premature ovarian failure and infertility. (Reprod Med Biol 2006; 5: 175–182)
You have requested "on-the-fly" machine translation of selected content from our databases. This functionality is provided solely for your convenience and is in no way intended to replace human translation. Show full disclaimer
Neither ProQuest nor its licensors make any representations or warranties with respect to the translations. The translations are automatically generated "AS IS" and "AS AVAILABLE" and are not retained in our systems. PROQUEST AND ITS LICENSORS SPECIFICALLY DISCLAIM ANY AND ALL EXPRESS OR IMPLIED WARRANTIES, INCLUDING WITHOUT LIMITATION, ANY WARRANTIES FOR AVAILABILITY, ACCURACY, TIMELINESS, COMPLETENESS, NON-INFRINGMENT, MERCHANTABILITY OR FITNESS FOR A PARTICULAR PURPOSE. Your use of the translations is subject to all use restrictions contained in your Electronic Products License Agreement and by using the translation functionality you agree to forgo any and all claims against ProQuest or its licensors for your use of the translation functionality and any output derived there from. Hide full disclaimer
Longer documents can take a while to translate. Rather than keep you waiting, we have only translated the first few paragraphs. Click the button below if you want to translate the rest of the document.
Details
Title
Role of oocyte-specific genes in the development of mammalian embryos
Author
Tsukamoto, Satoshi 1
1 Laboratory of Reproductive Biology, Graduate School of Agriculture, Kyoto University, Kyoto, Japan