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.
ReferencesLawsonKA, MenesesJJ, PedersenRA. Clonal analysis of epiblast fate during germ layer formation in the mouse embryo. Development, 1991, 113, 891–911LawsonKA, HageWJ. Clonal analysis of the origin of primordial germ cells in the mouse. Ciba Found Symp, 1994, 182, 68–84GinsburgM, SnowMH, McLarenA. Primordial germ cells in the mouse embryo during gastrulation. Development, 1990, 110, 521–528BuehrM. The primordial germ cells of mammals: some current perspectives. Exp Cell Res, 1997, 232, 194–207ChiquoineAD. The identification, origin, and migration of the primordial germ cells in the mouse embryo. Anat Rec, 1954, 118, 135–146HahnelAC, RappoleeDA, MillanJL, ManesT, ZiomekCA, TheodosiouNG et al. Two alkaline phosphatase genes are expressed during early development in the mouse embryo. Development, 1990, 110, 555–564MacGregorGR, ZambrowiczBP, SorianoP. Tissue non-specific alkaline phosphatase is expressed in both embryonic and extraembryonic lineages during mouse embryogenesis but is not required for migration of primordial germ cells. Development, 1995, 121, 1487–1496MatsuiY, ZseboK, HoganBL. Derivation of pluripotential embryonic stem cells from murine primordial germ cells in culture. Cell, 1992, 70, 841–847ResnickJL, BixlerLS, ChengL, DonovanPJ. Long-term proliferation of mouse primordial germ cells in culture. Nature, 1992, 359, 550–551SchattenH, SunQ-Y. The functional significance of centrosomes in mammalian meiosis, fertilization, development, nuclear transfer, and stem cell differentiation. Environ Mol Mutagen, 2009, 50, 620–636DeanW, Ferguson-SmithA. Genomic imprinting: mother maintains methylation marks. Curr Biol, 2001, 11, R527–R530FulkaH, MrazekM, TeplaO, FulkaJ. DNA methylation pattern in human zygotes and developing embryos. Reproduction, 2004, 128, 703–708Reis SilvaAR, AdenotP, DanielN, ArchillaC, PeynotN, LucciCM et al. Dynamics of DNA methylation levels in maternal and paternal rabbit genomes after fertilization. Epigenetics, 2011, 6, 987–993OkamotoI, OtteAP, AllisCD, ReinbergD, HeardE. Epigenetic dynamics of imprinted X inactivation during early mouse development. Science, 2004, 303, 644–649OkamotoI, PatratC, ThépotD, PeynotN, FauqueP, DanielN et al. Eutherian mammals use diverse strategies to initiate X-chromosome inactivation during development. Nature, 2011, 472, 370–374BrownCJ, WillardHF. The human X-inactivation centre is not required for maintenance of X-chromosome inactivation. Nature, 1994, 368, 154–156RackKA, ChellyJ, GibbonsRJ, RiderS, BenjaminD, LafreniéreRG et al. Absence of the XIST gene from late-replicating isodicentric X chromosomes in leukaemia. Hum Mol Genet, 1994, 3, 1053–1059RayPF, WinstonRM, HandysideAH. XIST expression from the maternal X chromosome in human male preimplantation embryos at the blastocyst stage. Hum Mol Genet, 1997, 6, 1323–1327RossantJ. Developmental biology: a mouse is not a cow. Nature, 2011, 471, 457–458ChawengsaksophakK, JamesR, HammondVE, KöntgenF, BeckF. Homeosis and intestinal tumours in Cdx2 mutant mice. Nature, 1997, 386, 84–87NicholsJ, ZevnikB, AnastassiadisK, NiwaH, Klewe-NebeniusD, ChambersI et al. Formation of pluripotent stem cells in the mammalian embryo depends on the POU transcription factor Oct4. Cell, 1998, 95, 379–391StrumpfD, MaoC-A, YamanakaY, RalstonA, ChawengsaksophakK, BeckF et al. Cdx2 is required for correct cell fate specification and differentiation of trophectoderm in the mouse blastocyst. Development, 2005, 132, 2093–2102GrabarekJB, ZyzyńskaK, SaizN, PiliszekA, FrankenbergS, NicholsJ et al. Differential plasticity of epiblast and primitive endoderm precursors within the ICM of the early mouse embryo. Development, 2012, 139, 129–1393231774BergDK, SmithCS, PeartonDJ, WellsDN, BroadhurstR, DonnisonM et al. Trophectoderm lineage determination in cattle. Dev Cell, 2011, 20, 244–255DietrichJ-E, HiiragiT. Stochastic patterning in the mouse pre-implantation embryo. Development, 2007, 134, 4219–4231PalmieriSL, PeterW, HessH, ScholerHR. Oct-4 transcription factor is differentially expressed in the mouse embryo during establishment of the first two extraembryonic cell lineages involved in implantation. Dev Biol, 1994, 166, 259–267CauffmanG, LiebaersI, SteirteghemA, VeldeH. POU5F1 isoforms show different expression patterns in human embryonic stem cells and preimplantation embryos. Stem Cells, 2006, 24, 2685–2691ChenL, YabuuchiA, EminliS, TakeuchiA, LuC-W, HochedlingerK et al. Cross-regulation of the Nanog and Cdx2 promoters. Cell Res, 2009, 19, 1052–1061HarveyAJ, ArmantDR, BavisterBD, NicholsSM, BrennerCA. Inner cell mass localization of NANOG precedes OCT3/4 in rhesus monkey blastocysts. Stem Cells Dev, 2009, 18, 1451–14583016202KirchhofN, CarnwathJW, LemmeE, AnastassiadisK, SchölerH, NiemannH. Expression pattern of Oct-4 in preimplantation embryos of different species. Biol Reprod, 2000, 63, 1698–1705KuijkEW, PuyL, TolHTA, OeiCHY, HaagsmanHP, ColenbranderB et al. Differences in early lineage segregation between mammals. Dev Dyn, 2008, 237, 918–927MitalipovSM, KuoH-C, HenneboldJD, WolfDP. Oct-4 expression in pluripotent cells of the rhesus monkey. Biol Reprod, 2003, 69, 1785–1792PantD, KeeferCL. Expression of pluripotency-related genes during bovine inner cell mass explant culture. Cloning Stem Cells, 2009, 11, 355–365EijkMJ, RooijenMA, ModinaS, ScesiL, FolkersG, TolHT et al. Molecular cloning, genetic mapping, and developmental expression of bovine POU5F1. Biol Reprod, 1999, 60, 1093–1103NiakanKK, EgganK. Analysis of human embryos from zygote to blastocyst reveals distinct gene expression patterns relative to the mouse. Dev Biol, 2013, 375, 54–64SelwoodL, JohnsonMH. Trophoblast and hypoblast in the monotreme, marsupial and eutherian mammal: evolution and origins. BioEssays, 2006, 28, 128–145ViebahnCThe anterior margin of the mammalian gastrula: comparative and phylogenetic aspects of its role in axis formation and head induction. Curr Top Dev Biol, 1999AmsterdamElsevier63–103GuillomotM. Cellular interactions during implantation in domestic ruminants. J Reprod Fertil Suppl, 1995, 49, 39–51HerrmannBG. Expression pattern of the Brachyury gene in whole-mount TWis/TWis mutant embryos. Development, 1991, 113(3)913–917HueI, RenardJP, ViebahnC. Brachyury is expressed in gastrulating bovine embryos well ahead of implantation. Dev Genes Evol, 2001, 211, 157–159Flechon JE. Morphological aspects of embryonic disc at the time of its appearance in the blastocyst of farm mammals [Sow, ewe and rabbit, scanning electron microscopy]. Scanning Electron Microscope (USA). 1978;2:541–6.BarendsPM, StrobandHW, TaverneN, te KronnieG, LeënMP, BlommersPC. Integrity of the preimplantation pig blastocyst during expansion and loss of polar trophectoderm (Rauber cells) and the morphology of the embryoblast as an indicator for developmental stage. J Reprod Fertil, 1989, 87, 715–726VejlstedM, DuY, VajtaG, Maddox-HyttelP. Post-hatching development of the porcine and bovine embryo—defining criteria for expected development in vivo and in vitro. Theriogenology, 2006, 65, 153–165BeddingtonRS, RobertsonEJ. Axis development and early asymmetry in mammals. Cell, 1999, 96, 195–209NicholsJ, SmithA. Pluripotency in the embryo and in culture. Cold Spring Harb Perspect Biol, 2012, 4(8)a0081283405859De Felici M. Origin, migration and proliferation of human primordial germ cells. In: Oogenesis. Berlin: Springer; 2013. p. 19–37.Viebahn C. Epithelio-mesenchymal transformation during formation of the mesoderm in the mammalian embryo. Acta Anat. 1995;154(1):79–97.ViebahnC, StortzC, MitchellSA, BlumM. Low proliferative and high migratory activity in the area of Brachyury expressing mesoderm progenitor cells in the gastrulating rabbit embryo. Development, 2002, 129, 2355–2365IdkowiakJ, WeisheitG, PlitznerJ, ViebahnC. Hypoblast controls mesoderm generation and axial patterning in the gastrulating rabbit embryo. Dev Genes Evol, 2004, 214, 591–605OhinataY, PayerB, O'CarrollD, AncelinK, OnoY, SanoM et al. Blimp1 is a critical determinant of the germ cell lineage in mice. Nature, 2005, 436(7048)207–213OhinataY, OhtaH, ShigetaM, YamanakaK, WakayamaT, SaitouM. A signaling principle for the specification of the germ cell lineage in mice. Cell, 2009, 137, 571–584LiuP, WakamiyaM, SheaMJ, AlbrechtU, BehringerRR, BradleyA. Requirement for Wnt3 in vertebrate axis formation. Nat Genet, 1999, 22, 361–365AramakiS, HayashiK, KurimotoK, OhtaH, YabutaY, IwanariH et al. A mesodermal factor, T, specifies mouse germ cell fate by directly activating germline determinants. Dev Cell, 2013, 27, 516–529HopfC, ViebahnC, PüschelB. BMP signals and the transcriptional repressor BLIMP1 during germline segregation in the mammalian embryo. Dev Genes Evol, 2011, 221, 209–2233192270BehringerRR, WakamiyaM, TsangTE, TamPP. A flattened mouse embryo: leveling the playing field. Genesis, 2000, 28, 23–30MagnúsdóttirE, DietmannS, MurakamiK, GünesdoganU, TangF, BaoS et al. A tripartite transcription factor network regulates primordial germ cell specification in mice. Nat Cell Biol, 2013, 15, 905–9153796875BortvinA, GoodheartM, LiaoM, PageDC. Dppa3/Pgc7/stella is a maternal factor and is not required for germ cell specification in mice. BMC Dev Biol, 2004, 4, 2362866YeomYI, FuhrmannG, OvittCE, BrehmA, OhboK, GrossM et al. Germline regulatory element of Oct-4 specific for the totipotent cycle of embryonal cells. Development, 1996, 122, 881–894YoshimizuT, SugiyamaN, FeliceM, YeomYI, OhboK, MasukoK et al. Germline-specific expression of the Oct-4/green fluorescent protein (GFP) transgene in mice. Dev Growth Differ, 1999, 41, 675–684OkamuraD, TokitakeY, NiwaH, MatsuiY. Requirement of Oct3/4 function for germ cell specification. Dev Biol, 2008, 317, 576–584KehlerJ, TolkunovaE, KoschorzB, PesceM, GentileL, BoianiM et al. Oct4 is required for primordial germ cell survival. EMBO Rep, 2004, 5, 1078–10831299174HartAH, HartleyL, IbrahimM, RobbL. Identification, cloning and expression analysis of the pluripotency promoting Nanog genes in mouse and human. Dev Dyn, 2004, 230, 187–198HatanoS-Y, TadaM, KimuraH, YamaguchiS, KonoT, NakanoT et al. Pluripotential competence of cells associated with Nanog activity. Mech Dev, 2005, 122, 67–79AcamporaD, GiovannantonioLG, SimeoneA. Otx2 is an intrinsic determinant of the embryonic stem cell state and is required for transition to a stable epiblast stem cell condition. Development, 2012, 140, 43–55YamaguchiS, KimuraH, TadaM, NakatsujiN, TadaT. Nanog expression in mouse germ cell development. Gene Expr Patterns, 2005, 5, 639–646ChambersI, SilvaJ, ColbyD, NicholsJ, NijmeijerB, RobertsonM et al. Nanog safeguards pluripotency and mediates germline development. Nature, 2007, 450, 1230–1234YamaguchiS, KurimotoK, YabutaY, SasakiH, NakatsujiN, SaitouM et al. Conditional knockdown of Nanog induces apoptotic cell death in mouse migrating primordial germ cells. Development, 2009, 136, 4011–4020CampoloF, GoriM, FavaroR, NicolisS, PellegriniM, BottiF et al. Essential role of Sox2 for the establishment and maintenance of the germ cell line. Stem Cells, 2013, 31, 1408–1421Schäfer-HaasA, ViebahnC. The term cell epitope PG-2 is expressed in primordial germ cells and in hypoblast cells of the gastrulating rabbit embryo. Anat Embryol, 2000, 202, 13–23HyttelP, KamstrupKM, HyldigS. From hatching into fetal life in the pig. Acta Scientiae Veterinariae, 2011, 39(Suppl 1)s203–s221TakagiY, TalbotNC, RexroadCE, PurselVG. Identification of pig primordial germ cells by immunocytochemistry and lectin binding. Mol Reprod Dev, 1997, 46, 567–580MartinsDS, AmbrósioCE, SaraivaNZ, WenceslauCV, MoriniAC, KerkisI et al. Early development and putative primordial germ cells characterization in dogs. Reprod Domest Anim, 2011, 46, e62–e66LeddaS, BoglioloL, BebbereD, AriuF, PirinoS. Characterization, isolation and culture of primordial germ cells in domestic animals: recent progress and insights from the ovine species. Theriogenology, 2010, 74, 534–543WitschiE. Migration of germ cells of human embryos from the yolk sac to the primitive gonadal folds. Contr Embryol Carnegie Inst, 1948, 209, 67–80JongJ, StoopH, GillisA, GurpR, GeijnG-J, BoerM et al. Differential expression of SOX17 and SOX2 in germ cells and stem cells has biological and clinical implications. J Pathol, 2008, 215, 21–30EvansMJ, KaufmanMH. Establishment in culture of pluripotential cells from mouse embryos. Nature, 1981, 292, 154–156MartinGR. Isolation of a pluripotent cell line from early mouse embryos cultured in medium conditioned by teratocarcinoma stem cells. Proc Natl Acad Sci USA, 1981, 78, 7634–7638349323ThomsonJA, KalishmanJ, GolosTG, DurningM, HarrisCP, BeckerRA et al. Isolation of a primate embryonic stem cell line. Proc Natl Acad Sci USA, 1995, 92, 7844–784841242ThomsonJA, KalishmanJ, GolosTG, DurningM, HarrisCP, HearnJP. Pluripotent cell lines derived from common marmoset (Callithrix jacchus) blastocysts. Biol Reprod, 1996, 55, 254–259ThomsonJA, Itskovitz-EldorJ, ShapiroSS, WaknitzMA, SwiergielJJ, MarshallVS et al. Embryonic stem cell lines derived from human blastocysts. Science, 1998, 282, 1145–1147FangZF, GaiH, HuangYZ, LiSG, ChenXJ, ShiJJ et al. Rabbit embryonic stem cell lines derived from fertilized, parthenogenetic or somatic cell nuclear transfer embryos. Exp Cell Res, 2006, 312, 3669–3682WangS, TangX, NiuY, ChenH, LiB, LiT et al. Generation and characterization of rabbit embryonic stem cells. Stem Cells, 2007, 25, 481–489HondaA, HiroseM, InoueK, OgonukiN, MikiH, ShimozawaN et al. Stable embryonic stem cell lines in rabbits: potential small animal models for human research. Reprod Biomed Online, 2008, 17, 706–715Nowak-ImialekM, KuesW, CarnwathJW, NiemannH. Pluripotent stem cells and reprogrammed cells in farm animals. Microsc Microanal, 2011, 17, 474–497BronsIGM, Smithers, TrotterMWB, Rugg-GunnP, SunB, Chuva de Sousa LopesSM et al. Derivation of pluripotent epiblast stem cells from mammalian embryos. Nature, 2007, 448, 191–195TesarPJ, ChenowethJG, BrookFA, DaviesTJ, EvansEP, MackDL et al. New cell lines from mouse epiblast share defining features with human embryonic stem cells. Nature, 2007, 448, 196–199KakegawaR, TeramuraT, TakeharaT, AnzaiM, MitaniT, MatsumotoK et al. Isolation and culture of rabbit primordial germ cells. J Reprod Dev, 2008, 54, 352–357TakahashiK, YamanakaS. Induction of pluripotent stem cells from mouse embryonic and adult fibroblast cultures by defined factors. Cell, 2006, 126, 663–676TakahashiK, TanabeK, OhnukiM, NaritaM, IchisakaT, TomodaK et al. Induction of pluripotent stem cells from adult human fibroblasts by defined factors. Cell, 2007, 131, 861–872LiuH, ZhuF, YongJ, ZhangP, HouP, LiH et al. Generation of induced pluripotent stem cells from adult rhesus monkey fibroblasts. Cell Stem Cell, 2008, 3, 587–590HondaA, HiroseM, HatoriM, MatobaS, MiyoshiH, InoueK et al. Generation of induced pluripotent stem cells in rabbits: potential experimental models for human regenerative medicine. J Biol Chem, 2010, 285, 31362–313692951210GillichA, HayashiK. Switching stem cell state through programmed germ cell reprogramming. Differentiation, 2011, 81, 281–291ChiaN-Y, ChanY-S, FengB, LuX, OrlovYL, MoreauD et al. A genome-wide RNAi screen reveals determinants of human embryonic stem cell identity. Nature, 2010, 468, 316–320BergeD, KurekD, BlauwkampT, KooleW, MaasA, ErogluE et al. Embryonic stem cells require Wnt proteins to prevent differentiation to epiblast stem cells. Nat Cell Biol, 2011, 13(9)1070–10754157727DaheronL, OpitzSL, ZaehresH, LenschMW, LenschWM, AndrewsPW et al. LIF/STAT3 signaling fails to maintain self-renewal of human embryonic stem cells. Stem Cells, 2004, 22, 770–778HumphreyRK, BeattieGM, LopezAD, BucayN, KingCC, FirpoMT, Rose-JohnS, HayekA. Maintenance of pluripotency in human embryonic stem cells is STAT3 independent. Stem Cells, 2004, 22(4)522–530BrandenbergerR, KhrebtukovaI, ThiesRS, MiuraT, JingliC, PuriR et al. MPSS profiling of human embryonic stem cells. BMC Dev Biol, 2004, 4, 10514702RhoJ-Y, YuK, HanJ-S, ChaeJ-I, KooD-B, YoonH-S et al. Transcriptional profiling of the developmentally important signalling pathways in human embryonic stem cells. Hum Reprod, 2006, 21, 405–412XuR-H, ChenX, LiDS, LiR, AddicksGC, GlennonC et al. BMP4 initiates human embryonic stem cell differentiation to trophoblast. Nat Biotechnol, 2002, 20, 1261–1264SumiT, TsuneyoshiN, NakatsujiN, SuemoriH. Defining early lineage specification of human embryonic stem cells by the orchestrated balance of canonical Wnt/beta-catenin, Activin/Nodal and BMP signaling. Development, 2008, 135, 2969–2979GreberB, WuG, BernemannC, JooJY, HanDW, KoK et al. Conserved and divergent roles of FGF signaling in mouse epiblast stem cells and human embryonic stem cells. Cell Stem Cell, 2010, 6, 215–226YingQ-L, WrayJ, NicholsJ, Batlle-MoreraL, DobleB, WoodgettJ et al. The ground state of embryonic stem cell self-renewal. Nature, 2008, 453, 519–523ParkJ-K, KimH-S, UhK-J, ChoiK-H, KimH-M, LeeT et al. Primed pluripotent cell lines derived from various embryonic origins and somatic cells in pig. PLoS ONE, 2013, 8, e524813543426AlberioR, CroxallN, AllegrucciC. Pig epiblast stem cells depend on activin/nodal signaling for pluripotency and self-renewal. Stem Cells Dev, 2010, 19, 1627–16363129689HondaA, HiroseM, OguraA. Basic FGF and Activin/Nodal but not LIF signaling sustain undifferentiated status of rabbit embryonic stem cells. Exp Cell Res, 2009, 315, 2033–2042WatanabeK, UenoM, KamiyaD, NishiyamaA, MatsumuraM, WatayaT et al. A ROCK inhibitor permits survival of dissociated human embryonic stem cells. Nat Biotechnol., 2007, 25, 681–686NakatsujiN, SuemoriH. Embryonic stem cell lines of nonhuman primates. ScientificWorldJournal, 2002, 2, 1762–1773WhitworthDJ, OvchinnikovDA, WolvetangEJ. Generation and characterization of LIF-dependent canine induced pluripotent stem cells from adult dermal fibroblasts. Stem Cells Dev, 2012, 21, 2288–2297TurnpennyL, BrickwoodS, SpallutoCM, PiperK, CameronIT, WilsonDI et al. Derivation of human embryonic germ cells: an alternative source of pluripotent stem cells. Stem Cells, 2003, 21, 598–609ShamblottMJ, AxelmanJ, WangS, BuggEM, LittlefieldJW, DonovanPJ et al. Derivation of pluripotent stem cells from cultured human primordial germ cells. Proc Natl Acad Sci USA, 1998, 95, 13726–1373124887MitalipovS, KuoH-C, ByrneJ, ClepperL, MeisnerL, JohnsonJ et al. Isolation and characterization of novel rhesus monkey embryonic stem cell lines. Stem Cells, 2006, 24, 2177–2186MüllerT, FleischmannG, EildermannK, Mätz-RensingK, HornPA, SasakiE et al. A novel embryonic stem cell line derived from the common marmoset monkey (Callithrix jacchus) exhibiting germ cell-like characteristics. Hum Reprod, 2009, 24, 1359–1372HatoyaS, ToriiR, KondoY, OkunoT, KobayashiK, WijewardanaV et al. Isolation and characterization of embryonic stem-like cells from canine blastocysts. Mol Reprod Dev, 2006, 73, 298–305WestFD, TerlouwSL, KwonDJ, MumawJL, DharaSK, HasneenK et al. Porcine induced pluripotent stem cells produce chimeric offspring. Stem Cells Dev, 2010, 19, 1211–1220De Los AngelesA, LohY-H, TesarPJ, DaleyGQ. Accessing naïve human pluripotency. Curr Opin Genet Dev, 2012, 22, 272–2824171054GillichA, BaoS, GraboleN, HayashiK, TrotterMWB, PasqueV et al. Epiblast stem cell-based system reveals reprogramming synergy of germline factors. Cell Stem Cell, 2012, 10, 425–4393343665HannaJ, ChengAW, SahaK, KimJ, LengnerCJ, SoldnerF et al. Human embryonic stem cells with biological and epigenetic characteristics similar to those of mouse ESCs. Proc Natl Acad Sci USA, 2010, 107, 9222–92272889088WangW, YangJ, LiuH, LuD, ChenX, ZenonosZ et al. Rapid and efficient reprogramming of somatic cells to induced pluripotent stem cells by retinoic acid receptor gamma and liver receptor homolog 1. Proc Natl Acad Sci USA, 2011, 108, 18283–182883215025WareCB, WangL, MechamBH, ShenL, NelsonAM, BarM et al. Histone deacetylase inhibition elicits an evolutionarily conserved self-renewal program in embryonic stem cells. Cell Stem Cell, 2009, 4, 359–3692719860GafniO, WeinbergerL, MansourAA, ManorYS, ChomskyE, Ben-YosefD et al. Derivation of novel human ground state naive pluripotent stem cells. Nature, 2013, 504, 282–286ChanY-S, GökeJ, NgJ-H, LuX, GonzalesKAU, TanC-P et al. Induction of a human pluripotent state with distinct regulatory circuitry that resembles preimplantation epiblast. Cell Stem Cell, 2013, 13, 663–675HondaA, HatoriM, HiroseM, HondaC, IzuH, InoueK et al. Naive-like conversion overcomes the limited differentiation capacity of induced pluripotent stem cells. J Biol Chem, 2013, 288, 26157–261663764818FujishiroS-H, NakanoK, MizukamiY, AzamiT, AraiY, MatsunariH et al. Generation of naive-like porcine-induced pluripotent stem cells capable of contributing to embryonic and fetal development. Stem Cells Dev, 2013, 22, 473–4823549629TangF, BarbacioruC, NordmanE, BaoS, LeeC, WangX et al. Deterministic and stochastic allele specific gene expression in single mouse blastomeres. PLoS ONE, 2011, 6(6)e212083121735YanL, YangM, GuoH, YangL, WuJ, LiR et al. Single-cell RNA-Seq profiling of human preimplantation embryos and embryonic stem cells. Nat Struct Mol Biol, 2013, 20, 1131–1139ImamuraM, HikabeO, LinZY-C, OkanoH. Generation of germ cells in vitro in the era of induced pluripotent stem cells. Mol Reprod Dev, 2014, 81, 2–19HayashiK, OhtaH, KurimotoK, AramakiS, SaitouM. Reconstitution of the mouse germ cell specification pathway in culture by pluripotent stem cells. Cell, 2011, 146, 519–532HayashiK, OgushiS, KurimotoK, ShimamotoS, OhtaH, SaitouM. Offspring from oocytes derived from in vitro primordial germ cell-like cells in mice. Science, 2012, 338, 971–975NakakiF, HayashiK, OhtaH, KurimotoK, YabutaY, SaitouM. Induction of mouse germ-cell fate by transcription factors in vitro. Nature, 2013, 501, 222–226JulatonVTA, Reijo PeraRA. NANOS3 function in human germ cell development. Hum Mol Genet, 2011, 20, 2238–22503090199KeeK, AngelesVT, FloresM, NguyenHN, Reijo PeraRA. Human DAZL, DAZ and BOULE genes modulate primordial germ-cell and haploid gamete formation. Nature, 2009, 462, 222–2253133736TeramuraT, TakeharaT, KawataN, FujinamiN, MitaniT, TakenoshitaM et al. Primate embryonic stem cells proceed to early gametogenesis in vitro. Cloning Stem Cells, 2007, 9, 144–156YamauchiK, HasegawaK, ChumaS, NakatsujiN, SuemoriH. In vitro germ cell differentiation from cynomolgus monkey embryonic stem cells. PLoS ONE, 2009, 4, e53382671468FukunagaN, TeramuraT, OnoderaY, TakeharaT, FukudaK, HosoiY. Leukemia inhibitory factor (LIF) enhances germ cell differentiation from primate embryonic stem cells. Cell Reprogram, 2010, 12(4)369–376GilbertSFDevelopmental biology, 2010MassachusettsSinauer Associates
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.
Germ cells are unique cell types that generate a totipotent zygote upon fertilization, giving rise to the next generation in mammals and many other multicellular organisms. How germ cells acquire this ability has been of considerable interest. In mammals, primordial germ cells (PGCs), the precursors of sperm and oocytes, are specified around the time of gastrulation. PGCs are induced by signals from the surrounding extra-embryonic tissues to the equipotent epiblast cells that give rise to all cell types. Currently, the mechanism of PGC specification in mammals is best understood from studies in mice. Following implantation, the epiblast cells develop as an egg cylinder while the extra-embryonic ectoderm cells which are the source of important signals for PGC specification are located over the egg cylinder. However, in most cases, including humans, the epiblast cells develop as a planar disc, which alters the organization and the source of the signaling for cell fates. This, in turn, might have an effect on the precise mechanism of PGC specification in vivo as well as in vitro using pluripotent embryonic stem cells. Here, we discuss how the key early embryonic differences between rodents and other mammals may affect the establishment of the pluripotency network in vivo and in vitro, and consequently the basis for PGC specification, particularly from pluripotent embryonic stem cells in vitro.
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
Germ cell specification and pluripotency in mammals: a perspective from early embryogenesis
Author
Irie, Naoko 1 ; Tang, Walfred W C 1 ; M. Azim Surani 1
1 Wellcome Trust/Cancer Research UK, Gurdon Institute, University of Cambridge, Cambridge, UK