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Volumn 6, Issue 1, 2011, Pages 95-102

Epigenetic investigation of variably X chromosome inactivated genes in monozygotic female twins discordant for primary biliary cirrhosis

Author keywords

Autoimmune cholangitis; DNA methylation; Gene promoter; Gene regulation; X chromosome inactivation

Indexed keywords

DNA; MESSENGER RNA;

EID: 78651238248     PISSN: 15592294     EISSN: 15592308     Source Type: Journal    
DOI: 10.4161/epi.6.1.13405     Document Type: Article
Times cited : (77)

References (39)
  • 1
    • 56749133320 scopus 로고    scopus 로고
    • The autoimmunologist: Geoepidemiology, a new center of gravity and prime time for autoimmunity
    • Shoenfeld Y, Selmi C, Zimlichman E, Gershwin ME. The autoimmunologist: geoepidemiology, a new center of gravity and prime time for autoimmunity. J Autoimmun 2008; 31:15-18.
    • (2008) J Autoimmun , vol.31 , pp. 15-18
    • Shoenfeld, Y.1    Selmi, C.2    Zimlichman, E.3    Gershwin, M.E.4
  • 2
    • 48449102199 scopus 로고    scopus 로고
    • The unfinished business of primary biliary cirrhosis
    • Selmi C, Zuin M, Gershwin ME. The unfinished business of primary biliary cirrhosis. J Hepatol 2008; 49:451-460.
    • (2008) J Hepatol , vol.49 , pp. 451-460
    • Selmi, C.1    Zuin, M.2    Gershwin, M.E.3
  • 6
    • 34548303660 scopus 로고    scopus 로고
    • Preferential X chromosome loss but random inactivation characterize primary biliary cirrhosis
    • Miozzo M, Selmi C, Gentilin B, Grati FR, Sirchia S, Oertelt S, et al. Preferential X chromosome loss but random inactivation characterize primary biliary cirrhosis. Hepatology 2007; 46:456-462.
    • (2007) Hepatology , vol.46 , pp. 456-462
    • Miozzo, M.1    Selmi, C.2    Gentilin, B.3    Grati, F.R.4    Sirchia, S.5    Oertelt, S.6
  • 7
    • 4143103585 scopus 로고    scopus 로고
    • Primary biliary cirrhosis in monozygotic and dizygotic twins: Genetics, epigenetics and environment
    • Selmi C, Mayo MJ, Bach N, Ishibashi H, Invernizzi P, Gish RG, et al. Primary biliary cirrhosis in monozygotic and dizygotic twins: genetics, epigenetics and environment. Gastroenterology 2004; 127:485-492.
    • (2004) Gastroenterology , vol.127 , pp. 485-492
    • Selmi, C.1    Mayo, M.J.2    Bach, N.3    Ishibashi, H.4    Invernizzi, P.5    Gish, R.G.6
  • 9
    • 15244353967 scopus 로고    scopus 로고
    • Willard HF X-inactivation profile reveals extensive variability in X-linked gene expression in females
    • Carrel L, Willard HF X-inactivation profile reveals extensive variability in X-linked gene expression in females. Nature 2005; 434:400-404.
    • (2005) Nature , vol.434 , pp. 400-404
    • Carrel, L.1
  • 11
    • 0036856355 scopus 로고    scopus 로고
    • MethPrimer: Designing primers for methylation PCRs
    • Li LC, Dahiya R. MethPrimer: designing primers for methylation PCRs. Bioinformatics 2002; 18:1427-1431.
    • (2002) Bioinformatics , vol.18 , pp. 1427-1431
    • Li, L.C.1    Dahiya, R.2
  • 13
    • 0026678490 scopus 로고
    • Methylation of HpaII and HhaI sites near the polymorphic CAG repeat in the human androgen-receptor gene correlates with X chromosome inactivation
    • Allen RC, Zoghbi HY, Moseley AB, Rosenblatt HM, Belmont J W Methylation of HpaII and HhaI sites near the polymorphic CAG repeat in the human androgen-receptor gene correlates with X chromosome inactivation. Am J Hum Genet 1992; 51:1229-1239.
    • (1992) Am J Hum Genet , vol.51 , pp. 1229-1239
    • Allen, R.C.1    Zoghbi, H.Y.2    Moseley, A.B.3    Rosenblatt, H.M.4    Belmont, J.W.5
  • 14
    • 67149095289 scopus 로고    scopus 로고
    • Primary biliary cirrhosis associated with HLA, IL12A and IL12RB2 variants
    • Hirschfield GM, Liu X, Xu C, Lu Y, Xie G, Lu Y, et al. Primary biliary cirrhosis associated with HLA, IL12A and IL12RB2 variants. N Engl J Med 2009; 360:2544-2555.
    • (2009) N Engl J Med , vol.360 , pp. 2544-2555
    • Hirschfield, G.M.1    Liu, X.2    Xu, C.3    Lu, Y.4    Xie, G.5    Lu, Y.6
  • 15
    • 70450169678 scopus 로고    scopus 로고
    • Epigenetic profiling of somatic tissues from human autopsy specimens identifies tissue- and individual-specific DNA methylation patterns
    • Byun HM, Siegmund KD, Pan F, Weisenberger DJ, Kanel G, Laird PW, et al. Epigenetic profiling of somatic tissues from human autopsy specimens identifies tissue- and individual-specific DNA methylation patterns. Hum Mol Genet 2009; 18:4808-4817.
    • (2009) Hum Mol Genet , vol.18 , pp. 4808-4817
    • Byun, H.M.1    Siegmund, K.D.2    Pan, F.3    Weisenberger, D.J.4    Kanel, G.5    Laird, P.W.6
  • 16
    • 0034326284 scopus 로고    scopus 로고
    • Large-scale methylation analysis of human genomic DNA reveals tissue-specific differences between the methylation profiles of genes and pseudogenes
    • Grunau C, Hindermann W, Rosenthal A. Large-scale methylation analysis of human genomic DNA reveals tissue-specific differences between the methylation profiles of genes and pseudogenes. Hum Mol Genet 2000; 9:2651-2663.
    • (2000) Hum Mol Genet , vol.9 , pp. 2651-2663
    • Grunau, C.1    Hindermann, W.2    Rosenthal, A.3
  • 17
    • 33847304609 scopus 로고    scopus 로고
    • Gene body-specific methylation on the active X chromosome
    • Hellman A, Chess A. Gene body-specific methylation on the active X chromosome. Science 2007; 315:1141-1143.
    • (2007) Science , vol.315 , pp. 1141-1143
    • Hellman, A.1    Chess, A.2
  • 21
    • 59149084538 scopus 로고    scopus 로고
    • The human colon cancer methy-lome shows similar hypo- and hypermethylation at conserved tissue-specific CpG island shores
    • Irizarry RA, Ladd-Acosta C, Wen B, Wu Z, Montano C, Onyango P, et al. The human colon cancer methy-lome shows similar hypo- and hypermethylation at conserved tissue-specific CpG island shores. Nat Genet 2009; 41:178-186.
    • (2009) Nat Genet , vol.41 , pp. 178-186
    • Irizarry, R.A.1    Ladd-Acosta, C.2    Wen, B.3    Wu, Z.4    Montano, C.5    Onyango, P.6
  • 22
  • 25
    • 0026345201 scopus 로고
    • Difference in early development of presumed monozygotic twins with Rett syndrome
    • Bruck I, Philippart M, Giraldi D, Antoniuk S. Difference in early development of presumed monozygotic twins with Rett syndrome. Am J Med Genet 1991; 39:415-417.
    • (1991) Am J Med Genet , vol.39 , pp. 415-417
    • Bruck, I.1    Philippart, M.2    Giraldi, D.3    Antoniuk, S.4
  • 26
    • 0028902950 scopus 로고
    • Studies of X inactivation and isodisomy in twins provide further evidence that the X chromosome is not involved in Rett syndrome
    • Migeon BR, Dunn MA, Thomas G, Schmeckpeper BJ, Naidu S. Studies of X inactivation and isodisomy in twins provide further evidence that the X chromosome is not involved in Rett syndrome. Am J Hum Genet 1995; 56:647-653.
    • (1995) Am J Hum Genet , vol.56 , pp. 647-653
    • Migeon, B.R.1    Dunn, M.A.2    Thomas, G.3    Schmeckpeper, B.J.4    Naidu, S.5
  • 27
    • 34247095504 scopus 로고    scopus 로고
    • Reduced MeCP2 expression is frequent in autism frontal cortex and correlates with aberrant MECP2 promoter methylation
    • Nagarajan RP, Hogart AR, Gwye Y, Martin MR, LaSalle JM. Reduced MeCP2 expression is frequent in autism frontal cortex and correlates with aberrant MECP2 promoter methylation. Epigenetics 2006; 1: 1-11.
    • (2006) Epigenetics , vol.1 , pp. 1-11
    • Nagarajan, R.P.1    Hogart, A.R.2    Gwye, Y.3    Martin, M.R.4    Lasalle, J.M.5
  • 29
    • 18444407168 scopus 로고    scopus 로고
    • Discordant KCNQ1OT1 imprinting in sets of monozygotic twins discordant for Beckwith-Wiedemann syndrome
    • Weksberg R, Shuman C, Caluseriu O, Smith AC, Fei YL, Nishikawa J, et al. Discordant KCNQ1OT1 imprinting in sets of monozygotic twins discordant for Beckwith-Wiedemann syndrome. Hum Mol Genet 2002; 11:1317-1325.
    • (2002) Hum Mol Genet , vol.11 , pp. 1317-1325
    • Weksberg, R.1    Shuman, C.2    Caluseriu, O.3    Smith, A.C.4    Fei, Y.L.5    Nishikawa, J.6
  • 30
    • 52649109709 scopus 로고    scopus 로고
    • Monozygotic female twins discordant for Silver-Russell syndrome and hypomethylation of the H19-DMR
    • Yamazawa K, Kagami M, Fukami M, Matsubara K, Ogata T Monozygotic female twins discordant for Silver-Russell syndrome and hypomethylation of the H19-DMR. J Hum Genet 2008; 53:950-955.
    • (2008) J Hum Genet , vol.53 , pp. 950-955
    • Yamazawa, K.1    Kagami, M.2    Fukami, M.3    Matsubara, K.4    Ogata, T.5
  • 31
    • 34548398164 scopus 로고    scopus 로고
    • Primer: Epigenetics of autoimmunity
    • Richardson B. Primer: epigenetics of autoimmunity. Nat Clin Pract Rheumatol 2007; 3:521-527.
    • (2007) Nat Clin Pract Rheumatol , vol.3 , pp. 521-527
    • Richardson, B.1
  • 33
    • 23044514626 scopus 로고    scopus 로고
    • Chromosome-wide and promoter-specific analyses identify sites of differential DNA methylation in normal and transformed human cells
    • Weber M, Davies JJ, Wittig D, Oakeley EJ, Haase M, Lam WL, et al. Chromosome-wide and promoter-specific analyses identify sites of differential DNA methylation in normal and transformed human cells. Nat Genet 2005; 37:853-862.
    • (2005) Nat Genet , vol.37 , pp. 853-862
    • Weber, M.1    Davies, J.J.2    Wittig, D.3    Oakeley, E.J.4    Haase, M.5    Lam, W.L.6
  • 34
    • 33747871713 scopus 로고    scopus 로고
    • Sadee W Allelic mRNA expression of X-linked monoamine oxidase a (MAOA) in human brain: Dissection of epigenetic and genetic factors
    • Pinsonneault JK, Papp AC, Sadee W Allelic mRNA expression of X-linked monoamine oxidase a (MAOA) in human brain: dissection of epigenetic and genetic factors. Hum Mol Genet 2006; 15:2636-2649.
    • (2006) Hum Mol Genet , vol.15 , pp. 2636-2649
    • Pinsonneault, J.K.1    Papp, A.C.2
  • 35
    • 0031259748 scopus 로고    scopus 로고
    • Genomic structure of a novel chloride channel gene, CLIC2, in Xq28
    • Heiss NS, Poustka A. Genomic structure of a novel chloride channel gene, CLIC2, in Xq28. Genomics, 1997; 45:224-228.
    • (1997) Genomics , vol.45 , pp. 224-228
    • Heiss, N.S.1    Poustka, A.2
  • 37
    • 0029916122 scopus 로고    scopus 로고
    • Human peptidyl-prolyl isomerase essential for regulation of mitosis
    • Lu KP, Hanes SD, Hunter T A human peptidyl-prolyl isomerase essential for regulation of mitosis. Nature 1996; 380:544-547.
    • (1996) Nature , vol.380 , pp. 544-547
    • Lu, K.P.1    Hanes, S.D.2    Hunter, T.A.3
  • 39
    • 0036382919 scopus 로고    scopus 로고
    • The N-terminal basic domain of human parvulin hPar14 is responsible for the entry to the nucleus and high-affinity DNA-binding
    • Surmacz TA, Bayer E, Rahfeld JU, Fischer G, Bayer P. The N-terminal basic domain of human parvulin hPar14 is responsible for the entry to the nucleus and high-affinity DNA-binding. J Mol Biol 2002; 321:235-247.
    • (2002) J Mol Biol , vol.321 , pp. 235-247
    • Surmacz, T.A.1    Bayer, E.2    Rahfeld, J.U.3    Fischer, G.4    Bayer, P.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.