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Volumn 46, Issue 6, 2014, Pages 551-557

The noncoding RNA IPW regulates the imprinted DLK1-DIO3 locus in an induced pluripotent stem cell model of Prader-Willi syndrome

Author keywords

[No Author keywords available]

Indexed keywords

UNTRANSLATED RNA;

EID: 84901638082     PISSN: 10614036     EISSN: 15461718     Source Type: Journal    
DOI: 10.1038/ng.2968     Document Type: Article
Times cited : (117)

References (32)
  • 1
    • 79960530899 scopus 로고    scopus 로고
    • Genomic imprinting: The emergence of an epigenetic paradigm
    • Ferguson-Smith, A.C. Genomic imprinting: the emergence of an epigenetic paradigm. Nat. Rev. Genet. 12, 565-575 (2011).
    • (2011) Nat. Rev. Genet. , vol.12 , pp. 565-575
    • Ferguson-Smith, A.C.1
  • 3
    • 30844442607 scopus 로고    scopus 로고
    • The snoRNA HBII-52 regulates alternative splicing of the serotonin receptor 2C
    • Kishore, S. & Stamm, S. The snoRNA HBII-52 regulates alternative splicing of the serotonin receptor 2C. Science 311, 230-232 (2006).
    • (2006) Science , vol.311 , pp. 230-232
    • Kishore, S.1    Stamm, S.2
  • 4
    • 84868152631 scopus 로고    scopus 로고
    • Long noncoding RNAs with snoRNA ends
    • Yin, Q.F. et al. Long noncoding RNAs with snoRNA ends. Mol. Cell 48, 219-230 (2012).
    • (2012) Mol. Cell , vol.48 , pp. 219-230
    • Yin, Q.F.1
  • 5
    • 72849144528 scopus 로고    scopus 로고
    • Clone-and gene-specific aberrations of parental imprinting in human induced pluripotent stem cells
    • Pick, M. et al. Clone-and gene-specific aberrations of parental imprinting in human induced pluripotent stem cells. Stem Cells 27, 2686-2690 (2009).
    • (2009) Stem Cells , vol.27 , pp. 2686-2690
    • Pick, M.1
  • 6
    • 36248966518 scopus 로고    scopus 로고
    • Induction of pluripotent stem cells from adult human fibroblasts by defined factors
    • Takahashi, K. et al. Induction of pluripotent stem cells from adult human fibroblasts by defined factors. Cell 131, 861-872 (2007).
    • (2007) Cell , vol.131 , pp. 861-872
    • Takahashi, K.1
  • 7
    • 79958791356 scopus 로고    scopus 로고
    • Global analysis of parental imprinting in human parthenogenetic induced pluripotent stem cells
    • Stelzer, Y., Yanuka, O. & Benvenisty, N. Global analysis of parental imprinting in human parthenogenetic induced pluripotent stem cells. Nat. Struct. Mol. Biol. 18, 735-741 (2011).
    • (2011) Nat. Struct. Mol. Biol. , vol.18 , pp. 735-741
    • Stelzer, Y.1    Yanuka, O.2    Benvenisty, N.3
  • 8
    • 84881452590 scopus 로고    scopus 로고
    • Identification of novel imprinted differentially methylated regions by global analysis of human-parthenogenetic-induced pluripotent stem cells
    • Stelzer, Y. et al. Identification of novel imprinted differentially methylated regions by global analysis of human-parthenogenetic-induced pluripotent stem cells. Stem Cell Reports 1, 79-89 (2013).
    • (2013) Stem Cell Reports , vol.1 , pp. 79-89
    • Stelzer, Y.1
  • 9
    • 77956214743 scopus 로고    scopus 로고
    • Differential modeling of fragile X syndrome by human embryonic stem cells and induced pluripotent stem cells
    • Urbach, A., Bar-Nur, O., Daley, G.Q. & Benvenisty, N. Differential modeling of fragile X syndrome by human embryonic stem cells and induced pluripotent stem cells. Cell Stem Cell 6, 407-411 (2010).
    • (2010) Cell Stem Cell , vol.6 , pp. 407-411
    • Urbach, A.1    Bar-Nur, O.2    Daley, G.Q.3    Benvenisty, N.4
  • 10
    • 84889257291 scopus 로고    scopus 로고
    • Involvement of parental imprinting in the antisense regulation of onco-miR-372-373
    • Stelzer, Y., Sagi, I. & Benvenisty, N. Involvement of parental imprinting in the antisense regulation of onco-miR-372-373. Nat. Commun. 4, 2724 (2013).
    • (2013) Nat. Commun. , vol.4 , pp. 2724
    • Stelzer, Y.1    Sagi, I.2    Benvenisty, N.3
  • 11
    • 0038419811 scopus 로고    scopus 로고
    • Imprinted microRNA genes transcribed antisense to a reciprocally imprinted retrotransposon-like gene
    • Seitz, H. et al. Imprinted microRNA genes transcribed antisense to a reciprocally imprinted retrotransposon-like gene. Nat. Genet. 34, 261-262 (2003).
    • (2003) Nat. Genet. , vol.34 , pp. 261-262
    • Seitz, H.1
  • 12
    • 84864506177 scopus 로고    scopus 로고
    • Accumulation of instability in serial differentiation and reprogramming of parthenogenetic human cells
    • Vassena, R. et al. Accumulation of instability in serial differentiation and reprogramming of parthenogenetic human cells. Hum. Mol. Genet. 21, 3366-3373 (2012).
    • (2012) Hum. Mol. Genet. , vol.21 , pp. 3366-3373
    • Vassena, R.1
  • 13
    • 68749097161 scopus 로고    scopus 로고
    • A deletion of the HBII-85 class of small nucleolar RNAs (snoRNAs) is associated with hyperphagia, obesity and hypogonadism
    • de Smith, A.J. et al. A deletion of the HBII-85 class of small nucleolar RNAs (snoRNAs) is associated with hyperphagia, obesity and hypogonadism. Hum. Mol. Genet. 18, 3257-3265 (2009).
    • (2009) Hum. Mol. Genet. , vol.18 , pp. 3257-3265
    • De Smith, A.J.1
  • 14
    • 77958486211 scopus 로고    scopus 로고
    • Paternally inherited microdeletion at 15q11.2 confirms a significant role for the SNORD116 C/D box snoRNA cluster in Prader-Willi syndrome
    • Duker, A.L. et al. Paternally inherited microdeletion at 15q11.2 confirms a significant role for the SNORD116 C/D box snoRNA cluster in Prader-Willi syndrome. Eur. J. Hum. Genet. 18, 1196-1201 (2010).
    • (2010) Eur. J. Hum. Genet. , vol.18 , pp. 1196-1201
    • Duker, A.L.1
  • 15
    • 44349191455 scopus 로고    scopus 로고
    • Prader-Willi phenotype caused by paternal deficiency for the HBII-85 C/D box small nucleolar RNA cluster
    • Sahoo, T. et al. Prader-Willi phenotype caused by paternal deficiency for the HBII-85 C/D box small nucleolar RNA cluster. Nat. Genet. 40, 719-721 (2008).
    • (2008) Nat. Genet. , vol.40 , pp. 719-721
    • Sahoo, T.1
  • 16
    • 0028124726 scopus 로고
    • Identification of a novel paternally expressed gene in the Prader-Willi syndrome region
    • Wevrick, R., Kerns, J.A. & Francke, U. Identification of a novel paternally expressed gene in the Prader-Willi syndrome region. Hum. Mol. Genet. 3, 1877-1882 (1994).
    • (1994) Hum. Mol. Genet. , vol.3 , pp. 1877-1882
    • Wevrick, R.1    Kerns, J.A.2    Francke, U.3
  • 17
    • 62249133709 scopus 로고    scopus 로고
    • Chromatin signature reveals over a thousand highly conserved large non-coding RNAs in mammals
    • Guttman, M. et al. Chromatin signature reveals over a thousand highly conserved large non-coding RNAs in mammals. Nature 458, 223-227 (2009).
    • (2009) Nature , vol.458 , pp. 223-227
    • Guttman, M.1
  • 18
    • 80052869283 scopus 로고    scopus 로고
    • LincRNAs act in the circuitry controlling pluripotency and differentiation
    • Guttman, M. et al. lincRNAs act in the circuitry controlling pluripotency and differentiation. Nature 477, 295-300 (2011).
    • (2011) Nature , vol.477 , pp. 295-300
    • Guttman, M.1
  • 19
    • 34250729138 scopus 로고    scopus 로고
    • Functional demarcation of active and silent chromatin domains in human HOX loci by noncoding RNAs
    • Rinn, J.L. et al. Functional demarcation of active and silent chromatin domains in human HOX loci by noncoding RNAs. Cell 129, 1311-1323 (2007).
    • (2007) Cell , vol.129 , pp. 1311-1323
    • Rinn, J.L.1
  • 20
    • 67650921949 scopus 로고    scopus 로고
    • Many human large intergenic noncoding RNAs associate with chromatin-modifying complexes and affect gene expression
    • Khalil, A.M. et al. Many human large intergenic noncoding RNAs associate with chromatin-modifying complexes and affect gene expression. Proc. Natl. Acad. Sci. USA 106, 11667-11672 (2009).
    • (2009) Proc. Natl. Acad. Sci. USA , vol.106 , pp. 11667-11672
    • Khalil, A.M.1
  • 21
    • 53249098795 scopus 로고    scopus 로고
    • A maternal-zygotic effect gene, Zfp57, maintains both maternal and paternal imprints
    • Li, X. et al. A maternal-zygotic effect gene, Zfp57, maintains both maternal and paternal imprints. Dev. Cell 15, 547-557 (2008).
    • (2008) Dev. Cell , vol.15 , pp. 547-557
    • Li, X.1
  • 22
    • 14044256546 scopus 로고    scopus 로고
    • In vitro and in vivo analyses of a Phe/Tyr switch controlling product specificity of histone lysine methyltransferases
    • Collins, R.E. et al. In vitro and in vivo analyses of a Phe/Tyr switch controlling product specificity of histone lysine methyltransferases. J. Biol. Chem. 280, 5563-5570 (2005).
    • (2005) J. Biol. Chem. , vol.280 , pp. 5563-5570
    • Collins, R.E.1
  • 23
    • 50149108172 scopus 로고    scopus 로고
    • The promise of human induced pluripotent stem cells for research and therapy
    • Nishikawa, S., Goldstein, R.A. & Nierras, C.R. The promise of human induced pluripotent stem cells for research and therapy. Nat. Rev. Mol. Cell Biol. 9, 725-729 (2008).
    • (2008) Nat. Rev. Mol. Cell Biol. , vol.9 , pp. 725-729
    • Nishikawa, S.1    Goldstein, R.A.2    Nierras, C.R.3
  • 24
    • 84870156157 scopus 로고    scopus 로고
    • IPSC disease modeling
    • Soldner, F. & Jaenisch, R. Medicine. iPSC disease modeling. Science 338, 1155-1156 (2012).
    • (2012) Science , vol.338 , pp. 1155-1156
    • Soldner, F.1    Jaenisch, R.M.2
  • 25
    • 78049303170 scopus 로고    scopus 로고
    • Induced pluripotent stem cell models of the genomic imprinting disorders Angelman and Prader-Willi syndromes
    • Chamberlain, S.J. et al. Induced pluripotent stem cell models of the genomic imprinting disorders Angelman and Prader-Willi syndromes. Proc. Natl. Acad. Sci. USA 107, 17668-17673 (2010).
    • (2010) Proc. Natl. Acad. Sci. USA , vol.107 , pp. 17668-17673
    • Chamberlain, S.J.1
  • 26
    • 78650051022 scopus 로고    scopus 로고
    • Induced pluripotent stem cells can be used to model the genomic imprinting disorder Prader-Willi syndrome
    • Yang, J. et al. Induced pluripotent stem cells can be used to model the genomic imprinting disorder Prader-Willi syndrome. J. Biol. Chem. 285, 40303-40311 (2010).
    • (2010) J. Biol. Chem. , vol.285 , pp. 40303-40311
    • Yang, J.1
  • 27
    • 80052978224 scopus 로고    scopus 로고
    • Integrative annotation of human large intergenic noncoding RNAs reveals global properties and specific subclasses
    • Cabili, M.N. et al. Integrative annotation of human large intergenic noncoding RNAs reveals global properties and specific subclasses. Genes Dev. 25, 1915-1927 (2011).
    • (2011) Genes Dev. , vol.25 , pp. 1915-1927
    • Cabili, M.N.1
  • 28
    • 0032837374 scopus 로고    scopus 로고
    • Towards a molecular understanding of Prader-Willi and Angelman syndromes
    • Mann, M.R. & Bartolomei, M.S. Towards a molecular understanding of Prader-Willi and Angelman syndromes. Hum. Mol. Genet. 8, 1867-1873 (1999).
    • (1999) Hum. Mol. Genet. , vol.8 , pp. 1867-1873
    • Mann, M.R.1    Bartolomei, M.S.2
  • 29
    • 12344264924 scopus 로고    scopus 로고
    • Maternal uniparental disomy chromosome 14: Case report and literature review
    • Falk, M.J., Curtis, C.A., Bass, N.E., Zinn, A.B. & Schwartz, S. Maternal uniparental disomy chromosome 14: case report and literature review. Pediatr. Neurol. 32, 116-120 (2005).
    • (2005) Pediatr. Neurol. , vol.32 , pp. 116-120
    • Falk, M.J.1    Curtis, C.A.2    Bass, N.E.3    Zinn, A.B.4    Schwartz, S.5
  • 30
    • 0032850551 scopus 로고    scopus 로고
    • Maternal uniparental disomy for chromosome 14 in a boy with a normal karyotype
    • Hordijk, R. et al. Maternal uniparental disomy for chromosome 14 in a boy with a normal karyotype. J. Med. Genet. 36, 782-785 (1999).
    • (1999) J. Med. Genet. , vol.36 , pp. 782-785
    • Hordijk, R.1
  • 31
    • 73949156905 scopus 로고    scopus 로고
    • Maternal uniparental disomy 14 syndrome demonstrates Prader-Willi syndrome-like phenotype
    • Hosoki, K. et al. Maternal uniparental disomy 14 syndrome demonstrates Prader-Willi syndrome-like phenotype. J. Pediatr. 155, 900-903 (2009).
    • (2009) J. Pediatr , vol.155 , pp. 900-903
    • Hosoki, K.1
  • 32
    • 0035093826 scopus 로고    scopus 로고
    • Evolution of imprinting mechanisms: The battle of the sexes begins in the zygote
    • Reik, W. & Walter, J. Evolution of imprinting mechanisms: the battle of the sexes begins in the zygote. Nat. Genet. 27, 255-256 (2001).
    • (2001) Nat. Genet. , vol.27 , pp. 255-256
    • Reik, W.1    Walter, J.2


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