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Volumn 57, Issue 3, 2011, Pages 327-334

Epigenetically immature oocytes lead to loss of imprinting during embryogenesis

Author keywords

DNA methylation; Gene expression; Genomic imprinting; Growing oocyte; Loss of imprinting (LOI)

Indexed keywords

IGF2 PROTEIN, MOUSE; KCNQ1 PROTEIN, MOUSE; MESODERM SPECIFIC TRANSCRIPT PROTEIN; POTASSIUM CHANNEL KCNQ1; PROTEIN; SMALL NUCLEAR RIBONUCLEOPROTEIN; SOMATOMEDIN B;

EID: 79960146308     PISSN: 09168818     EISSN: 13484400     Source Type: Journal    
DOI: 10.1262/jrd.10-145A     Document Type: Article
Times cited : (19)

References (31)
  • 1
    • 0027378582 scopus 로고
    • Role for DNA methylation in genomic imprinting
    • Li E, Beard C, Jaenisch R. Role for DNA methylation in genomic imprinting. Nature 1993; 366: 362-365.
    • (1993) Nature , vol.366 , pp. 362-365
    • Li, E.1    Beard, C.2    Jaenisch, R.3
  • 2
    • 0033615717 scopus 로고    scopus 로고
    • DNA methyltransferases Dnmt3a and Dnmt3b are essential for de novo methylation and mammalian development
    • Okano M, Bell DW, Haber DA, Li E. DNA methyltransferases Dnmt3a and Dnmt3b are essential for de novo methylation and mammalian development. Cell 1999; 99: 247-257.
    • (1999) Cell , vol.99 , pp. 247-257
    • Okano, M.1    Bell, D.W.2    Haber, D.A.3    Li, E.4
  • 3
    • 3042584653 scopus 로고    scopus 로고
    • Essential role for de novo DNA methyltransferase Dnmt3a in paternal and maternal imprinting
    • Kaneda M, Okano M, Hata K, Sado T, Tsujimoto N, Li E, Sasaki H. Essential role for de novo DNA methyltransferase Dnmt3a in paternal and maternal imprinting. Nature 2004; 429: 900-903.
    • (2004) Nature , vol.429 , pp. 900-903
    • Kaneda, M.1    Okano, M.2    Hata, K.3    Sado, T.4    Tsujimoto, N.5    Li, E.6    Sasaki, H.7
  • 4
    • 0035930660 scopus 로고    scopus 로고
    • Dnmt3L and the establishment of maternal genomic imprints
    • Bourc'his D, Xu GL, Lin CS, Bollman B, Bestor TH. Dnmt3L and the establishment of maternal genomic imprints. Science 2001; 294: 2536-2539.
    • (2001) Science , vol.294 , pp. 2536-2539
    • Bourc'his, D.1    Xu, G.L.2    Lin, C.S.3    Bollman, B.4    Bestor, T.H.5
  • 7
    • 33645148785 scopus 로고    scopus 로고
    • Oocyte growth-dependent progression of maternal imprinting in mice
    • Hiura H, Obata Y, Komiyama J, Shirai M, Kono T. Oocyte growth-dependent progression of maternal imprinting in mice. Genes Cells 2006; 11: 353-361.
    • (2006) Genes Cells , vol.11 , pp. 353-361
    • Hiura, H.1    Obata, Y.2    Komiyama, J.3    Shirai, M.4    Kono, T.5
  • 8
    • 0033994867 scopus 로고    scopus 로고
    • Epigenetic modifications necessary for normal development are established during oocyte growth in mice
    • Bao S, Obata Y, Carroll J, Domeki I, Kono T. Epigenetic modifications necessary for normal development are established during oocyte growth in mice. Biol Reprod 2000; 62: 616-621.
    • (2000) Biol Reprod , vol.62 , pp. 616-621
    • Bao, S.1    Obata, Y.2    Carroll, J.3    Domeki, I.4    Kono, T.5
  • 9
    • 49449111926 scopus 로고    scopus 로고
    • Mechanisms of imprinting of the Prader-Willi/Angelman region
    • Horsthemke B, Wagstaff J. Mechanisms of imprinting of the Prader-Willi/Angelman region. Am J Med Genet A 2008; 146A: 2041-2052.
    • (2008) Am J Med Genet A , vol.146 , pp. 2041-2052
    • Horsthemke, B.1    Wagstaff, J.2
  • 10
    • 0037222510 scopus 로고    scopus 로고
    • Association of in vitro fertilization with Beckwith- Wiedemann syndrome and epigenetic alterations of LIT1 and H19
    • DeBaun MR, Niemitz EL, Feinberg AP. Association of in vitro fertilization with Beckwith- Wiedemann syndrome and epigenetic alterations of LIT1 and H19. Am J Hum Genet 2003; 72:156-160.
    • (2003) Am J Hum Genet , vol.72 , pp. 156-160
    • Debaun, M.R.1    Niemitz, E.L.2    Feinberg, A.P.3
  • 12
    • 0038644577 scopus 로고    scopus 로고
    • In vitro fertilization may increase the risk of Beckwith-Wiedemann syndrome related to the abnormal imprinting of the KCN1OT gene
    • Gicquel C, Gaston V, Mandelbaum J, Siffroi JP, Flahault A, Le Bouc Y. In vitro fertilization may increase the risk of Beckwith-Wiedemann syndrome related to the abnormal imprinting of the KCN1OT gene. Am J Hum Genet 2003; 72: 1338-1341.
    • (2003) Am J Hum Genet , vol.72 , pp. 1338-1341
    • Gicquel, C.1    Gaston, V.2    Mandelbaum, J.3    Siffroi, J.P.4    Flahault, A.5    le Bouc, Y.6
  • 14
    • 38849158557 scopus 로고    scopus 로고
    • Long-term effects of in vitro growth of mouse oocytes on their maturation and development
    • Obata Y, Maeda Y, Hatada I, Kono T. Long-term effects of in vitro growth of mouse oocytes on their maturation and development. J Reprod Dev 2007; 53: 1183-1190.
    • (2007) J Reprod Dev , vol.53 , pp. 1183-1190
    • Obata, Y.1    Maeda, Y.2    Hatada, I.3    Kono, T.4
  • 16
    • 33748803926 scopus 로고    scopus 로고
    • Disruption of parental-specific expression of imprinted genes in uniparental fetuses
    • Ogawa H, Wu Q, Komiyama J, Obata Y, Kono T. Disruption of parental-specific expression of imprinted genes in uniparental fetuses. FEBS Lett 2006; 580: 5377-5384.
    • (2006) FEBS Lett , vol.580 , pp. 5377-5384
    • Ogawa, H.1    Wu, Q.2    Komiyama, J.3    Obata, Y.4    Kono, T.5
  • 17
    • 70450162112 scopus 로고    scopus 로고
    • Multilocus methylation analysis in a large cohort of 11p15-related foetal growth disorders (Russell Silver and Beckwith Wiedemann syndromes) reveals simultaneous loss of methylation at paternal and maternal imprinted loci
    • Azzi S, Rossignol S, Steunou V, Sas T, Thibaud N, Danton F, Le Jule M, Heinrichs C, Cabrol S, Gicquel C, Le Bouc Y, Netchine I. Multilocus methylation analysis in a large cohort of 11p15-related foetal growth disorders (Russell Silver and Beckwith Wiedemann syndromes) reveals simultaneous loss of methylation at paternal and maternal imprinted loci. Hum Mol Genet 2009; 18: 4724-4733.
    • (2009) Hum Mol Genet , vol.18 , pp. 4724-4733
    • Azzi, S.1    Rossignol, S.2    Steunou, V.3    Sas, T.4    Thibaud, N.5    Danton, F.6    le Jule, M.7    Heinrichs, C.8    Cabrol, S.9    Gicquel, C.10    le Bouc, Y.11    Netchine, I.12
  • 19
    • 33846157180 scopus 로고    scopus 로고
    • The epigenetic imprinting defect of patients with Beckwith-Wiedemann syndrome born after assisted reproductive technology is not restricted to the 11p15 region
    • Rossignol S, Steunou V, Chalas C, Kerjean A, Rigolet M, Viegas-Pequignot E, Jouannet P, Le Bouc Y, Gicquel C. The epigenetic imprinting defect of patients with Beckwith-Wiedemann syndrome born after assisted reproductive technology is not restricted to the 11p15 region. J Med Genet 2006; 43: 902-907.
    • (2006) J Med Genet , vol.43 , pp. 902-907
    • Rossignol, S.1    Steunou, V.2    Chalas, C.3    Kerjean, A.4    Rigolet, M.5    Viegas-Pequignot, E.6    Jouannet, P.7    le Bouc, Y.8    Gicquel, C.9
  • 20
    • 0023119242 scopus 로고
    • Temporal and regional changes in DNA methylation in the embryonic, extraembryonic and germ cell lineages during mouse embryo development
    • Monk M, Boubelik M, Lehnert S. Temporal and regional changes in DNA methylation in the embryonic, extraembryonic and germ cell lineages during mouse embryo development. Development 1987; 99: 371-382.
    • (1987) Development , vol.99 , pp. 371-382
    • Monk, M.1    Boubelik, M.2    Lehnert, S.3
  • 22
    • 45349108598 scopus 로고    scopus 로고
    • Maternal and zygotic Dnmt1 are necessary and sufficient for the maintenance of DNA methylation imprints during preimplantation development
    • Hirasawa R, Chiba H, Kaneda M, Tajima S, Li E, Jaenisch R, Sasaki H. Maternal and zygotic Dnmt1 are necessary and sufficient for the maintenance of DNA methylation imprints during preimplantation development. Genes Dev 2008; 22: 1607-1616.
    • (2008) Genes Dev , vol.22 , pp. 1607-1616
    • Hirasawa, R.1    Chiba, H.2    Kaneda, M.3    Tajima, S.4    Li, E.5    Jaenisch, R.6    Sasaki, H.7
  • 23
    • 56049114840 scopus 로고    scopus 로고
    • DNA methyltransferase 1o functions during preimplantation development to preclude a profound level of epigenetic variation
    • Cirio MC, Martel J, Mann M, Toppings M, Bartolomei M, Trasler J, Chaillet JR. DNA methyltransferase 1o functions during preimplantation development to preclude a profound level of epigenetic variation. Dev Biol 2008; 324: 139-150.
    • (2008) Dev Biol , vol.324 , pp. 139-150
    • Cirio, M.C.1    Martel, J.2    Mann, M.3    Toppings, M.4    Bartolomei, M.5    Trasler, J.6    Chaillet, J.R.7
  • 25
    • 0028575985 scopus 로고
    • Loss of the imprinted IGF2/cation-independent mannose 6-phosphate receptor results in fetal overgrowth and perinatal lethality
    • Lau MM, Stewart CE, Liu Z, Bhatt H, Rotwein P, Stewart CL. Loss of the imprinted IGF2/cation-independent mannose 6-phosphate receptor results in fetal overgrowth and perinatal lethality. Genes Dev 1994; 8: 2953-2963.
    • (1994) Genes Dev , vol.8 , pp. 2953-2963
    • Lau, M.M.1    Stewart, C.E.2    Liu, Z.3    Bhatt, H.4    Rotwein, P.5    Stewart, C.L.6
  • 27
    • 2942514353 scopus 로고    scopus 로고
    • Loss-of-imprinting of Peg1 in mouse interspecies hybrids is correlated with altered growth
    • Shi W, Lefebvre L, Yu Y, Otto S, Krella A, Orth A, Fundele R. Loss-of-imprinting of Peg1 in mouse interspecies hybrids is correlated with altered growth. Genesis 2004; 39: 65-72.
    • (2004) Genesis , vol.39 , pp. 65-72
    • Shi, W.1    Lefebvre, L.2    Yu, Y.3    Otto, S.4    Krella, A.5    Orth, A.6    Fundele, R.7
  • 28
    • 33847382821 scopus 로고    scopus 로고
    • Alterations in epigenetic modifications during oocyte growth in mice
    • Kageyama S, Liu H, Kaneko N, Ooga M, Nagata M, Aoki F. Alterations in epigenetic modifications during oocyte growth in mice. Reproduction 2007; 133: 85-94.
    • (2007) Reproduction , vol.133 , pp. 85-94
    • Kageyama, S.1    Liu, H.2    Kaneko, N.3    Ooga, M.4    Nagata, M.5    Aoki, F.6
  • 30
    • 0031687985 scopus 로고    scopus 로고
    • Abnormal maternal behaviour and growth retardation associated with loss of the imprinted gene Mest
    • Lefebvre L, Viville S, Barton SC, Ishino F, Keverne EB, Surani MA. Abnormal maternal behaviour and growth retardation associated with loss of the imprinted gene Mest. Nat Genet 1998; 20: 163-169.
    • (1998) Nat Genet , vol.20 , pp. 163-169
    • Lefebvre, L.1    Viville, S.2    Barton, S.C.3    Ishino, F.4    Keverne, E.B.5    Surani, M.A.6
  • 31
    • 0033868543 scopus 로고    scopus 로고
    • Imprint switching for non-random X-chromosome inactivation during mouse oocyte growth
    • Tada T, Obata Y, Tada M, Goto Y, Nakatsuji N, Tan S, Kono T, Takagi N. Imprint switching for non-random X-chromosome inactivation during mouse oocyte growth. Development 2000; 127: 3101-3105.
    • (2000) Development , vol.127 , pp. 3101-3105
    • Tada, T.1    Obata, Y.2    Tada, M.3    Goto, Y.4    Nakatsuji, N.5    Tan, S.6    Kono, T.7    Takagi, N.8


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.