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Volumn 135, Issue 2, 2016, Pages 185-192

Incorporation of 5-ethynyl-2′-deoxyuridine (EdU) as a novel strategy for identification of the skewed X inactivation pattern in balanced and unbalanced X-rearrangements

Author keywords

[No Author keywords available]

Indexed keywords

EDOXUDINE; 5-ETHYNYL-2'-DEOXYURIDINE; DEOXYURIDINE;

EID: 84954404502     PISSN: 03406717     EISSN: 14321203     Source Type: Journal    
DOI: 10.1007/s00439-015-1622-x     Document Type: Article
Times cited : (18)

References (34)
  • 1
    • 0026678490 scopus 로고
    • Methylation of Hpall and Hhal Sites Near the Polymorphic CAG Repeat in the Human Androgen-Receptor Gene Correlates with X Chromosome Inactivation
    • PID: 1281384, COI: 1:CAS:528:DyaK3sXhvV2htL4%3D
    • Allen RC, Zoghbi HY, Moseley AB, Rosenblatt HM, Belmont JW (1992) Methylation of Hpall and Hhal Sites Near the Polymorphic CAG Repeat in the Human Androgen-Receptor Gene Correlates with X Chromosome Inactivation. Am J Hum Genet 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
  • 2
    • 48249090474 scopus 로고    scopus 로고
    • Cryptic mosaicism involving a second chromosome X in patients with Turner syndrome
    • PID: 18545811
    • Araújo A, Ramos ES (2008) Cryptic mosaicism involving a second chromosome X in patients with Turner syndrome. Braz J Med Biol Res 41:368–372
    • (2008) Braz J Med Biol Res , vol.41 , pp. 368-372
    • Araújo, A.1    Ramos, E.S.2
  • 3
    • 85045484695 scopus 로고
    • A morphological distinction between neurones of the male and female, and the behaviour of the nucleolar satellite during accelerated nucleoprotein synthesis
    • PID: 18120749, COI: 1:STN:280:DyaH1M%2Fit1entw%3D%3D
    • Barr ML, Bertram EG (1949) A morphological distinction between neurones of the male and female, and the behaviour of the nucleolar satellite during accelerated nucleoprotein synthesis. Nature 163:676–677. doi:10.1038/163676a0
    • (1949) Nature , vol.163 , pp. 676-677
    • Barr, M.L.1    Bertram, E.G.2
  • 4
    • 0029881774 scopus 로고    scopus 로고
    • Differential underacetylation of histones H2A, H3 and H4 on the inactive X chromosome in human female cells
    • PID: 8655133, COI: 1:CAS:528:DyaK28XivFait7k%3D
    • Belyaev ND, Keohane AM, Turner BM (1996) Differential underacetylation of histones H2A, H3 and H4 on the inactive X chromosome in human female cells. Hum Genet 97:573–578
    • (1996) Hum Genet , vol.97 , pp. 573-578
    • Belyaev, N.D.1    Keohane, A.M.2    Turner, B.M.3
  • 5
    • 84897476274 scopus 로고    scopus 로고
    • Reactivation of capital HA, Cyrillic chromosome upon reprogramming leads to changes in the replication pattern and 5hmC accumulation
    • PID: 23982752, COI: 1:CAS:528:DC%2BC2cXltl2jsLw%3D
    • Bogomazova AN, Lagarkova MA, Panova AV, Nekrasov ED, Kiselev SL (2014) Reactivation of capital HA, Cyrillic chromosome upon reprogramming leads to changes in the replication pattern and 5hmC accumulation. Chromosoma 123:117–128. doi:10.1007/s00412-013-0433-x
    • (2014) Chromosoma , vol.123 , pp. 117-128
    • Bogomazova, A.N.1    Lagarkova, M.A.2    Panova, A.V.3    Nekrasov, E.D.4    Kiselev, S.L.5
  • 6
    • 38149097805 scopus 로고    scopus 로고
    • No evidence that skewing of X chromosome inactivation patterns is transmitted to offspring in humans
    • PID: 18097474, COI: 1:CAS:528:DC%2BD1cXksFOkuw%3D%3D
    • Bolduc V, Chagnon P, Provost S, Dubé MP, Belisle C, Gingras M, Mollica L, Busque L (2008) No evidence that skewing of X chromosome inactivation patterns is transmitted to offspring in humans. J Clin Invest 118:333–341. doi:10.1172/JCI33166
    • (2008) J Clin Invest , vol.118 , pp. 333-341
    • Bolduc, V.1    Chagnon, P.2    Provost, S.3    Dubé, M.P.4    Belisle, C.5    Gingras, M.6    Mollica, L.7    Busque, L.8
  • 8
    • 0026456701 scopus 로고
    • The human XIST gene: analysis of a 17 kb inactive X-specific RNA that contains conserved repeats and is highly localized within the nucleus
    • PID: 1423611, COI: 1:CAS:528:DyaK3sXisVyrs7Y%3D
    • Brown CJ, Hendrich BD, Rupert JL, Lafrenière RG, Xing Y, Lawrence J, Willard HF (1992) The human XIST gene: analysis of a 17 kb inactive X-specific RNA that contains conserved repeats and is highly localized within the nucleus. Cell 71:527–542
    • (1992) Cell , vol.71 , pp. 527-542
    • Brown, C.J.1    Hendrich, B.D.2    Rupert, J.L.3    Lafrenière, R.G.4    Xing, Y.5    Lawrence, J.6    Willard, H.F.7
  • 9
    • 47549090286 scopus 로고    scopus 로고
    • Detection of S-phase cell cycle progression using 5-ethynyl-2′-deoxyuridine incorporation with click chemistry, an alternative to using 5-bromo-2′-deoxyuridine antibodies
    • PID: 18533904, COI: 1:CAS:528:DC%2BD1cXnsl2gsr0%3D
    • Buck SB, Bradford J, Gee KR, Agnew BJ, Clark ST, Salic A (2008) Detection of S-phase cell cycle progression using 5-ethynyl-2′-deoxyuridine incorporation with click chemistry, an alternative to using 5-bromo-2′-deoxyuridine antibodies. Biotechniques 44:927–929. doi:10.2144/000112812
    • (2008) Biotechniques , vol.44 , pp. 927-929
    • Buck, S.B.1    Bradford, J.2    Gee, K.R.3    Agnew, B.J.4    Clark, S.T.5    Salic, A.6
  • 11
    • 0001109234 scopus 로고
    • The Lyon–Beutler hypothesis and isochromosome X patients with Turner Syndrome
    • Gartler SM, Sparkes RS (1963) The Lyon–Beutler hypothesis and isochromosome X patients with Turner Syndrome. Lancet 282:411. doi:10.1016/S0140-6736(63)93096-4
    • (1963) Lancet , vol.282 , pp. 411
    • Gartler, S.M.1    Sparkes, R.S.2
  • 12
    • 1842615143 scopus 로고    scopus 로고
    • Molecular cytogenetic analysis of a de novo balanced X;autosome translocation: evidence for predominant inactivation of the derivative X chromosome in a girl with multiple malformations
    • PID: 15054834
    • Gläser B, Shirneshan K, Bink K, Wirth J, Kehrer-Sawatzki H, Bartz U, Zoll B, Bohlander SK (2004) Molecular cytogenetic analysis of a de novo balanced X;autosome translocation: evidence for predominant inactivation of the derivative X chromosome in a girl with multiple malformations. Am J Med Genet A 126A:229–236. doi:10.1002/ajmg.a.20584
    • (2004) Am J Med Genet A , vol.126A , pp. 229-236
    • Gläser, B.1    Shirneshan, K.2    Bink, K.3    Wirth, J.4    Kehrer-Sawatzki, H.5    Bartz, U.6    Zoll, B.7    Bohlander, S.K.8
  • 13
    • 80055027547 scopus 로고    scopus 로고
    • Replication banding patterns in human chromosomes detected using 5-ethynyl-2′-deoxyuridine Incorporation
    • PID: 22096263, COI: 1:CAS:528:DC%2BC3MXhsFChtrfF
    • Hoshi O, Ushiki T (2011) Replication banding patterns in human chromosomes detected using 5-ethynyl-2′-deoxyuridine Incorporation. Acta Histochem Cytochem 44:233–237. doi:10.1267/ahc.11029
    • (2011) Acta Histochem Cytochem , vol.44 , pp. 233-237
    • Hoshi, O.1    Ushiki, T.2
  • 14
    • 0022586282 scopus 로고
    • Analysis of spreading of inactivation in eight X autosome translocations utilizing the high resolution RBG technique
    • PID: 3957346, COI: 1:STN:280:DyaL287ms1Cqtw%3D%3D
    • Keitges EA, Palmer CG (1986) Analysis of spreading of inactivation in eight X autosome translocations utilizing the high resolution RBG technique. Hum Genet 72:231–236
    • (1986) Hum Genet , vol.72 , pp. 231-236
    • Keitges, E.A.1    Palmer, C.G.2
  • 15
    • 0015824058 scopus 로고
    • Microfluorometric detection of deoxyribonucleic acid replication in human metaphase chromosomes
    • PID: 4128545, COI: 1:CAS:528:DyaE2cXmvVSjsA%3D%3D
    • Latt SA (1973) Microfluorometric detection of deoxyribonucleic acid replication in human metaphase chromosomes. Proc Natl Acad Sci USA 70:3395–3399
    • (1973) Proc Natl Acad Sci USA , vol.70 , pp. 3395-3399
    • Latt, S.A.1
  • 16
    • 69249235745 scopus 로고    scopus 로고
    • Lessons from X-chromosome inactivation: long ncRNA as guides and tethers to the epigenome
    • PID: 19684108, COI: 1:CAS:528:DC%2BD1MXhtVegurnK
    • Lee JT (2009) Lessons from X-chromosome inactivation: long ncRNA as guides and tethers to the epigenome. Genes Dev 23:1831–1842. doi:10.1101/gad.1811209
    • (2009) Genes Dev , vol.23 , pp. 1831-1842
    • Lee, J.T.1
  • 17
    • 7144223296 scopus 로고
    • Gene action in the X-chromosome of the mouse (Mus musculus L.)
    • PID: 13764598, COI: 1:STN:280:DyaF3c%2FosVGksw%3D%3D
    • Lyon MF (1961) Gene action in the X-chromosome of the mouse (Mus musculus L.). Nature 190:372–373. doi:10.1038/190372a0
    • (1961) Nature , vol.190 , pp. 372-373
    • Lyon, M.F.1
  • 18
    • 0020367269 scopus 로고
    • X-autosome translocations: cytogenetic characteristics and their consequences
    • PID: 7152515, COI: 1:STN:280:DyaL3s7gslWmtw%3D%3D
    • Mattei MG, Mattei JF, Ayme S, Giraud F (1982) X-autosome translocations: cytogenetic characteristics and their consequences. Hum Genet 61:295–309
    • (1982) Hum Genet , vol.61 , pp. 295-309
    • Mattei, M.G.1    Mattei, J.F.2    Ayme, S.3    Giraud, F.4
  • 19
    • 84943353489 scopus 로고    scopus 로고
    • Chromosome domain architecture and dynamic organization of the fission yeast genome
    • PID: 26096785
    • Mizuguchi T, Barrowman J, Grewal SS (2015) Chromosome domain architecture and dynamic organization of the fission yeast genome. FEBS Lett. doi:10.1016/j.febslet.2015.06.008
    • (2015) FEBS Lett
    • Mizuguchi, T.1    Barrowman, J.2    Grewal, S.S.3
  • 23
    • 84856676842 scopus 로고    scopus 로고
    • Spread of X-chromosome inactivation into chromosome 15 is associated with Prader–Willi syndrome phenotype in a boy with a t(X;15)(p21.1;q11.2) translocation
    • PID: 21735174
    • Sakazume S, Ohashi H, Sasaki Y, Harada N, Nakanishi K, Sato H, Emi M, Endoh K, Sohma R, Kido Y, Toshiro N, Kubota T (2012) Spread of X-chromosome inactivation into chromosome 15 is associated with Prader–Willi syndrome phenotype in a boy with a t(X;15)(p21.1;q11.2) translocation. Hum Genet 131:121–130
    • (2012) Hum Genet , vol.131 , pp. 121-130
    • Sakazume, S.1    Ohashi, H.2    Sasaki, Y.3    Harada, N.4    Nakanishi, K.5    Sato, H.6    Emi, M.7    Endoh, K.8    Sohma, R.9    Kido, Y.10    Toshiro, N.11    Kubota, T.12
  • 24
    • 0042471801 scopus 로고    scopus 로고
    • CpG dinucleotide methylation patterns in the human androgen receptor gene and X-chromosome inactivation in peripheral blood leukocytes of phenotypically normal women
    • Sato K, Uehara S, Hashiyada M, Nabeshima H, Sugawara J, Terada Y, Yaegashi N, Okamura K (2004) CpG dinucleotide methylation patterns in the human androgen receptor gene and X-chromosome inactivation in peripheral blood leukocytes of phenotypically normal women. J Hum Genet 48:374–379. doi:10.1002/ajmg.a.30256
    • (2004) J Hum Genet , vol.48 , pp. 374-379
    • Sato, K.1    Uehara, S.2    Hashiyada, M.3    Nabeshima, H.4    Sugawara, J.5    Terada, Y.6    Yaegashi, N.7    Okamura, K.8
  • 25
    • 0024353550 scopus 로고
    • Investigation of the “variable spreading” of X inactivation into a translocated autosome
    • PID: 2731936, COI: 1:STN:280:DyaL1M3nslegtw%3D%3D
    • Schanz S, Steinbach P (1989) Investigation of the “variable spreading” of X inactivation into a translocated autosome. Hum Genet 82:244–248
    • (1989) Hum Genet , vol.82 , pp. 244-248
    • Schanz, S.1    Steinbach, P.2
  • 26
    • 0028912530 scopus 로고
    • Replication banding and molecular studies of a mosaic, unbalanced dic(X;15)(Xpter+Xq26.1::15pll+15qter)
    • PID: 7604850, COI: 1:STN:280:DyaK2MzivVGrsQ%3D%3D
    • Scheuerle A, Zenger-Hain JL, Dyke DLV, Ledbetter DH, Greenberg F, Shaffer LG (1995) Replication banding and molecular studies of a mosaic, unbalanced dic(X;15)(Xpter+Xq26.1:15pll+15qter). Am J Med Genet 56:403–408
    • (1995) Am J Med Genet , vol.56 , pp. 403-408
    • Scheuerle, A.1    Zenger-Hain, J.L.2    Dyke, D.L.V.3    Ledbetter, D.H.4    Greenberg, F.5    Shaffer, L.G.6
  • 27
    • 33846783183 scopus 로고    scopus 로고
    • Phenotype in X chromosome rearrangements: pitfalls of X inactivation study
    • PID: 16690229, COI: 1:CAS:528:DC%2BD2sXhs1Sntbo%3D
    • Schluth C, Cossée M, Girard-Lemaire F, Carelle N, Dollfus H, Jeandidier E, Flori E (2007) Phenotype in X chromosome rearrangements: pitfalls of X inactivation study. Pathol Biol 55:29–36. doi:10.1016/j.patbio.2006.04.003
    • (2007) Pathol Biol , vol.55 , pp. 29-36
    • Schluth, C.1    Cossée, M.2    Girard-Lemaire, F.3    Carelle, N.4    Dollfus, H.5    Jeandidier, E.6    Flori, E.7
  • 29
    • 84908519191 scopus 로고    scopus 로고
    • The sister chromatid exchange (SCE) assay
    • PID: 24623246, COI: 1:CAS:528:DC%2BC2MXnt1Cktbo%3D
    • Stults DM, Killen MW, Pierce AJ (2014) The sister chromatid exchange (SCE) assay. Methods Mol Biol 1105:439–455. doi:10.1007/978-1-62703-739-6_32
    • (2014) Methods Mol Biol , vol.1105 , pp. 439-455
    • Stults, D.M.1    Killen, M.W.2    Pierce, A.J.3
  • 32
    • 0017126281 scopus 로고
    • Analysis of deoxyribonucleic acid replication in human X chromosomes by fluorescence microscopy
    • PID: 1266850, COI: 1:CAS:528:DyaE28Xkt12lt78%3D
    • Willard HF, Latt SA (1976) Analysis of deoxyribonucleic acid replication in human X chromosomes by fluorescence microscopy. Am J Hum Genet 28:213–227
    • (1976) Am J Hum Genet , vol.28 , pp. 213-227
    • Willard, H.F.1    Latt, S.A.2
  • 33
    • 3042724653 scopus 로고    scopus 로고
    • Attenuated phenotype in a child with trisomy for 1q due to unbalanced X;1 translocation [46, X, der(X), t(X;1)(q28;q32.1)]
    • Yatsenko SA, Sahoo T, Rosenkranz M, Mendonza-Londono R, Naeem R, Scaglia F (2004) Attenuated phenotype in a child with trisomy for 1q due to unbalanced X;1 translocation [46, X, der(X), t(X;1)(q28;q32.1)]. Am J Med Genet A 128:72–77. doi:10.1002/ajmg.a.30094
    • (2004) Am J Med Genet A , vol.128 , pp. 72-77
    • Yatsenko, S.A.1    Sahoo, T.2    Rosenkranz, M.3    Mendonza-Londono, R.4    Naeem, R.5    Scaglia, F.6
  • 34
    • 84908193685 scopus 로고    scopus 로고
    • Spread of X inactivation on chromosome 15 is associated with a more severe phenotype in a girl with an unbalanced t(X; 15) translocation
    • COI: 1:CAS:528:DC%2BC2cXhsFyjtLfP
    • Yeung KS, Chee YY, Luk HM, Kan ASY, Tnag MHY, Lau ET, Shuen AY, Lo IFM, Chan KYK, Chung BHY (2014) Spread of X inactivation on chromosome 15 is associated with a more severe phenotype in a girl with an unbalanced t(X; 15) translocation. Am J Med Genet A 164:2521–2528. doi:10.1002/ajmg.a.36670
    • (2014) Am J Med Genet A , vol.164 , pp. 2521-2528
    • Yeung, K.S.1    Chee, Y.Y.2    Luk, H.M.3    Kan, A.S.Y.4    Tnag, M.H.Y.5    Lau, E.T.6    Shuen, A.Y.7    Lo, I.F.M.8    Chan, K.Y.K.9    Chung, B.H.Y.10


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.