메뉴 건너뛰기




Volumn 6, Issue 8, 2011, Pages

Quantification of age-dependent somatic CAG repeat instability in Hdh CAG knock-in mice reveals different expansion dynamics in striatum and liver

Author keywords

[No Author keywords available]

Indexed keywords

GENOMIC DNA; HDH PROTEIN, MOUSE; NERVE PROTEIN; NUCLEAR PROTEIN;

EID: 80052288666     PISSN: None     EISSN: 19326203     Source Type: Journal    
DOI: 10.1371/journal.pone.0023647     Document Type: Article
Times cited : (58)

References (28)
  • 1
  • 3
    • 0027480960 scopus 로고
    • A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes. The Huntington's Disease Collaborative Research Group
    • Huntington's disease collaborative research group
    • Huntington's disease collaborative research group (1993) A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes. The Huntington's Disease Collaborative Research Group. Cell 72: 971-983.
    • (1993) Cell , vol.72 , pp. 971-983
  • 4
    • 0027176364 scopus 로고
    • The relationship between trinucleotide (CAG) repeat length and clinical features of Huntington's disease
    • Andrew SE, Goldberg YP, Kremer B, Telenius H, Theilmann J, et al. (1993) The relationship between trinucleotide (CAG) repeat length and clinical features of Huntington's disease. Nat Genet 4: 398-403.
    • (1993) Nat Genet , vol.4 , pp. 398-403
    • Andrew, S.E.1    Goldberg, Y.P.2    Kremer, B.3    Telenius, H.4    Theilmann, J.5
  • 5
    • 0027240431 scopus 로고
    • Trinucleotide repeat length instability and age of onset in Huntington's disease
    • Duyao M, Ambrose C, Myers R, Novelletto A, Persichetti F, et al. (1993) Trinucleotide repeat length instability and age of onset in Huntington's disease. Nat Genet 4: 387-392.
    • (1993) Nat Genet , vol.4 , pp. 387-392
    • Duyao, M.1    Ambrose, C.2    Myers, R.3    Novelletto, A.4    Persichetti, F.5
  • 6
    • 0027261537 scopus 로고
    • Relationship between trinucleotide repeat expansion and phenotypic variation in Huntington's disease
    • Snell RG, MacMillan JC, Cheadle JP, Fenton I, Lazarou LP, et al. (1993) Relationship between trinucleotide repeat expansion and phenotypic variation in Huntington's disease. Nat Genet 4: 393-397.
    • (1993) Nat Genet , vol.4 , pp. 393-397
    • Snell, R.G.1    MacMillan, J.C.2    Cheadle, J.P.3    Fenton, I.4    Lazarou, L.P.5
  • 7
    • 0346752132 scopus 로고    scopus 로고
    • Dramatic tissue-specific mutation length increases are an early molecular event in Huntington disease pathogenesis
    • Kennedy L, Evans E, Chen CM, Craven L, Detloff PJ, et al. (2003) Dramatic tissue-specific mutation length increases are an early molecular event in Huntington disease pathogenesis. Hum Mol Genet 12: 3359-3367.
    • (2003) Hum Mol Genet , vol.12 , pp. 3359-3367
    • Kennedy, L.1    Evans, E.2    Chen, C.M.3    Craven, L.4    Detloff, P.J.5
  • 8
    • 0032938295 scopus 로고    scopus 로고
    • Length-dependent gametic CAG repeat instability in the Huntington's disease knock-in mouse
    • Wheeler VC, Auerbach W, White JK, Srinidhi J, Auerbach A, et al. (1999) Length-dependent gametic CAG repeat instability in the Huntington's disease knock-in mouse. Hum Mol Genet 8: 115-122.
    • (1999) Hum Mol Genet , vol.8 , pp. 115-122
    • Wheeler, V.C.1    Auerbach, W.2    White, J.K.3    Srinidhi, J.4    Auerbach, A.5
  • 9
    • 0035882460 scopus 로고    scopus 로고
    • Age-dependent and tissue-specific CAG repeat instability occurs in mouse knock-in for a mutant Huntington's disease gene
    • Ishiguro H, Yamada K, Sawada H, Nishii K, Ichino N, et al. (2001) Age-dependent and tissue-specific CAG repeat instability occurs in mouse knock-in for a mutant Huntington's disease gene. J Neurosci Res 65: 289-297.
    • (2001) J Neurosci Res , vol.65 , pp. 289-297
    • Ishiguro, H.1    Yamada, K.2    Sawada, H.3    Nishii, K.4    Ichino, N.5
  • 10
    • 0034641887 scopus 로고    scopus 로고
    • Dramatic mutation instability in HD mouse striatum: does polyglutamine load contribute to cell-specific vulnerability in Huntington's disease?
    • Kennedy L, Shelbourne PF, (2000) Dramatic mutation instability in HD mouse striatum: does polyglutamine load contribute to cell-specific vulnerability in Huntington's disease? Hum Mol Genet 9: 2539-2544.
    • (2000) Hum Mol Genet , vol.9 , pp. 2539-2544
    • Kennedy, L.1    Shelbourne, P.F.2
  • 11
    • 78951494319 scopus 로고    scopus 로고
    • Defining Genetic Factors That Modulate Intergenerational CAG Repeat Instability in Drosophila melanogaster
    • Jung J, van Jaarsveld MT, Shieh SY, Xu K, Bonini NM, (2011) Defining Genetic Factors That Modulate Intergenerational CAG Repeat Instability in Drosophila melanogaster. Genetics 187: 61-71.
    • (2011) Genetics , vol.187 , pp. 61-71
    • Jung, J.1    van Jaarsveld, M.T.2    Shieh, S.Y.3    Xu, K.4    Bonini, N.M.5
  • 12
    • 77952255626 scopus 로고    scopus 로고
    • A novel approach to investigate tissue-specific trinucleotide repeat instability
    • Lee JM, Zhang J, Su AI, Walker JR, Wiltshire T, et al. (2010) A novel approach to investigate tissue-specific trinucleotide repeat instability. BMC Syst Biol 4: 29.
    • (2010) BMC Syst Biol , vol.4 , pp. 29
    • Lee, J.M.1    Zhang, J.2    Su, A.I.3    Walker, J.R.4    Wiltshire, T.5
  • 13
    • 0037321290 scopus 로고    scopus 로고
    • Mismatch repair gene Msh2 modifies the timing of early disease in Hdh(Q111) striatum
    • Wheeler VC, Lebel LA, Vrbanac V, Teed A, te Riele H, et al. (2003) Mismatch repair gene Msh2 modifies the timing of early disease in Hdh(Q111) striatum. Hum Mol Genet 12: 273-281.
    • (2003) Hum Mol Genet , vol.12 , pp. 273-281
    • Wheeler, V.C.1    Lebel, L.A.2    Vrbanac, V.3    Teed, A.4    te Riele, H.5
  • 14
    • 57449091694 scopus 로고    scopus 로고
    • Intergenerational and striatal CAG repeat instability in Huntington's disease knock-in mice involve different DNA repair genes
    • Dragileva E, Hendricks A, Teed A, Gillis T, Lopez ET, et al. (2009) Intergenerational and striatal CAG repeat instability in Huntington's disease knock-in mice involve different DNA repair genes. Neurobiol Dis 33: 37-47.
    • (2009) Neurobiol Dis , vol.33 , pp. 37-47
    • Dragileva, E.1    Hendricks, A.2    Teed, A.3    Gillis, T.4    Lopez, E.T.5
  • 15
    • 68049113685 scopus 로고    scopus 로고
    • Somatic expansion of the Huntington's disease CAG repeat in the brain is associated with an earlier age of disease onset
    • Swami M, Hendricks AE, Gillis T, Massood T, Mysore J, et al. (2009) Somatic expansion of the Huntington's disease CAG repeat in the brain is associated with an earlier age of disease onset. Hum Mol Genet 18: 3039-3047.
    • (2009) Hum Mol Genet , vol.18 , pp. 3039-3047
    • Swami, M.1    Hendricks, A.E.2    Gillis, T.3    Massood, T.4    Mysore, J.5
  • 17
    • 34447324387 scopus 로고    scopus 로고
    • Triplet repeat mutation length gains correlate with cell-type specific vulnerability in Huntington disease brain
    • Shelbourne PF, Keller-McGandy C, Bi WL, Yoon SR, Dubeau L, et al. (2007) Triplet repeat mutation length gains correlate with cell-type specific vulnerability in Huntington disease brain. Hum Mol Genet 16: 1133-1142.
    • (2007) Hum Mol Genet , vol.16 , pp. 1133-1142
    • Shelbourne, P.F.1    Keller-McGandy, C.2    Bi, W.L.3    Yoon, S.R.4    Dubeau, L.5
  • 20
    • 0032708840 scopus 로고    scopus 로고
    • Msh2 deficiency prevents in vivo somatic instability of the CAG repeat in Huntington disease transgenic mice
    • Manley K, Shirley TL, Flaherty L, Messer A, (1999) Msh2 deficiency prevents in vivo somatic instability of the CAG repeat in Huntington disease transgenic mice. Nat Genet 23: 471-473.
    • (1999) Nat Genet , vol.23 , pp. 471-473
    • Manley, K.1    Shirley, T.L.2    Flaherty, L.3    Messer, A.4
  • 21
    • 78650706363 scopus 로고    scopus 로고
    • Continuous and periodic expansion of CAG repeats in Huntington's disease R6/1 mice
    • Mollersen L, Rowe AD, Larsen E, Rognes T, Klungland A, (2010) Continuous and periodic expansion of CAG repeats in Huntington's disease R6/1 mice. PLoS Genet 6: e1001242.
    • (2010) PLoS Genet , vol.6
    • Mollersen, L.1    Rowe, A.D.2    Larsen, E.3    Rognes, T.4    Klungland, A.5
  • 22
    • 33745593763 scopus 로고    scopus 로고
    • Genetic background modifies nuclear mutant huntingtin accumulation and HD CAG repeat instability in Huntington's disease knock-in mice
    • Lloret A, Dragileva E, Teed A, Espinola J, Fossale E, et al. (2006) Genetic background modifies nuclear mutant huntingtin accumulation and HD CAG repeat instability in Huntington's disease knock-in mice. Hum Mol Genet 15: 2015-2024.
    • (2006) Hum Mol Genet , vol.15 , pp. 2015-2024
    • Lloret, A.1    Dragileva, E.2    Teed, A.3    Espinola, J.4    Fossale, E.5
  • 23
    • 34249337762 scopus 로고    scopus 로고
    • OGG1 initiates age-dependent CAG trinucleotide expansion in somatic cells
    • Kovtun IV, Liu Y, Bjoras M, Klungland A, Wilson SH, et al. (2007) OGG1 initiates age-dependent CAG trinucleotide expansion in somatic cells. Nature 447: 447-452.
    • (2007) Nature , vol.447 , pp. 447-452
    • Kovtun, I.V.1    Liu, Y.2    Bjoras, M.3    Klungland, A.4    Wilson, S.H.5
  • 24
    • 34547830208 scopus 로고    scopus 로고
    • Somatic CTG*CAG repeat instability in a mouse model for myotonic dystrophy type 1 is associated with changes in cell nuclearity and DNA ploidy
    • van den Broek WJ, Wansink DG, Wieringa B, (2007) Somatic CTG*CAG repeat instability in a mouse model for myotonic dystrophy type 1 is associated with changes in cell nuclearity and DNA ploidy. BMC Mol Biol 8: 61.
    • (2007) BMC Mol Biol , vol.8 , pp. 61
    • van den Broek, W.J.1    Wansink, D.G.2    Wieringa, B.3
  • 25
    • 0031056685 scopus 로고    scopus 로고
    • Instability of highly expanded CAG repeats in mice transgenic for the Huntington's disease mutation
    • Mangiarini L, Sathasivam K, Mahal A, Mott R, Seller M, et al. (1997) Instability of highly expanded CAG repeats in mice transgenic for the Huntington's disease mutation. Nat Genet 15: 197-200.
    • (1997) Nat Genet , vol.15 , pp. 197-200
    • Mangiarini, L.1    Sathasivam, K.2    Mahal, A.3    Mott, R.4    Seller, M.5
  • 26
    • 68449096617 scopus 로고    scopus 로고
    • The insulin/Akt pathway controls a specific cell division program that leads to generation of binucleated tetraploid liver cells in rodents
    • Celton-Morizur S, Merlen G, Couton D, Margall-Ducos G, Desdouets C, (2009) The insulin/Akt pathway controls a specific cell division program that leads to generation of binucleated tetraploid liver cells in rodents. J Clin Invest 119: 1880-1887.
    • (2009) J Clin Invest , vol.119 , pp. 1880-1887
    • Celton-Morizur, S.1    Merlen, G.2    Couton, D.3    Margall-Ducos, G.4    Desdouets, C.5
  • 27
    • 0034163497 scopus 로고    scopus 로고
    • Long glutamine tracts cause nuclear localization of a novel form of huntingtin in medium spiny striatal neurons in HdhQ92 and HdhQ111 knock-in mice
    • Wheeler VC, White JK, Gutekunst CA, Vrbanac V, Weaver M, et al. (2000) Long glutamine tracts cause nuclear localization of a novel form of huntingtin in medium spiny striatal neurons in HdhQ92 and HdhQ111 knock-in mice. Hum Mol Genet 9: 503-513.
    • (2000) Hum Mol Genet , vol.9 , pp. 503-513
    • Wheeler, V.C.1    White, J.K.2    Gutekunst, C.A.3    Vrbanac, V.4    Weaver, M.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.