RNA leaching of transcription factors disrupts transcription in myotonic dystrophy

被引:121
作者
Ebralidze, A
Wang, Y
Petkova, V
Ebralidse, K
Junghans, RP
机构
[1] Harvard Univ, Sch Med, Harvard Inst Human Genet, Biotherapeut Dev Lab, Boston, MA 02215 USA
[2] Beth Israel Deaconess Med Ctr, Div Hematol Oncol, Boston, MA 02215 USA
关键词
D O I
10.1126/science.1088679
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Myotonic dystrophy type 1 (DM1) is caused by a CUG(n) expansion (n approximate to 50 to 5000) in the 3' untranslated region of the mRNA of the DM protein kinase gene. We show that mutant RNA binds and sequesters transcription factors (TFs), with up to 90% depletion of selected TFs from active chromatin. Diverse genes are consequently reduced in expression, including the ion transporter CIC-1, which has been implicated in myotonia. When TF specificity protein 1 (Sp1) was overexpressed in DM1-affected cells, low levels of messenger RNA for CIC-1 were restored to normal. Transcription factor leaching from chromatin by mutant RNA provides a potentially unifying pathomechanistic explanation for this disease.
引用
收藏
页码:383 / 387
页数:5
相关论文
共 27 条
  • [1] Trichothiodystrophy, a transcription syndrome
    Bergmann, E
    Egly, JM
    [J]. TRENDS IN GENETICS, 2001, 17 (05) : 279 - 286
  • [2] MOLECULAR-BASIS OF MYOTONIC-DYSTROPHY - EXPANSION OF A TRINUCLEOTIDE (CTG) REPEAT AT THE 3' END OF A TRANSCRIPT ENCODING A PROTEIN-KINASE FAMILY MEMBER
    BROOK, JD
    MCCURRACH, ME
    HARLEY, HG
    BUCKLER, AJ
    CHURCH, D
    ABURATANI, H
    HUNTER, K
    STANTON, VP
    THIRION, JP
    HUDSON, T
    SOHN, R
    ZEMELMAN, B
    SNELL, RG
    RUNDLE, SA
    CROW, S
    DAVIES, J
    SHELBOURNE, P
    BUXTON, J
    JONES, C
    JUVONEN, V
    JOHNSON, K
    HARPER, PS
    SHAW, DJ
    HOUSMAN, DE
    [J]. CELL, 1992, 68 (04) : 799 - 808
  • [3] Loss of the muscle-specific chloride channel in type 1 myotonic dystrophy due to misregulated alternative splicing
    Charlet-B, N
    Savkur, RS
    Singh, G
    Philips, AV
    Grice, EA
    Cooper, TA
    [J]. MOLECULAR CELL, 2002, 10 (01) : 45 - 53
  • [4] Expansion of a CUG trinucleotide repeat in the 3' untranslated region of myotonic dystrophy protein kinase transcripts results in nuclear retention of transcripts
    Davis, BM
    McCurrach, ME
    Taneja, KL
    Singer, RH
    Housman, DE
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (14) : 7388 - 7393
  • [5] Sp1 and TAFII130 transcriptional activity disrupted in early Huntington's disease
    Dunah, AW
    Jeong, H
    Griffin, A
    Kim, YM
    Standaert, DG
    Hersch, SM
    Mouradian, MM
    Young, AB
    Tanese, N
    Krainc, D
    [J]. SCIENCE, 2002, 296 (5576) : 2238 - 2243
  • [6] EBRALIDZE A, UNPUB
  • [7] Myotonic dystrophy type 2
    Finsterer, J
    [J]. EUROPEAN JOURNAL OF NEUROLOGY, 2002, 9 (05) : 441 - 447
  • [8] Perspectives: Neurodegeneration - A glutamine-rich trail leads to transcription factors
    Freiman, RN
    Tjian, R
    [J]. SCIENCE, 2002, 296 (5576) : 2149 - 2150
  • [9] Inappropriate gene activation in FSHD: A repressor complex binds a chromosomal repeat deleted in dystrophic muscle
    Gabellini, D
    Green, MR
    Tupler, R
    [J]. CELL, 2002, 110 (03) : 339 - 348
  • [10] Abnormal myotonic dystrophy protein kinase levels produce only mild myopathy in mice
    Jansen, G
    Groenen, PJTA
    Bachner, D
    Jap, PHK
    Coerwinkel, M
    Oerlemans, F
    vandenBroek, W
    Gohlsch, B
    Pette, D
    Plomp, JJ
    Molenaar, PC
    Nederhoff, MGJ
    vanEchteld, CJA
    Dekker, M
    Berns, A
    Hameister, H
    Wieringa, B
    [J]. NATURE GENETICS, 1996, 13 (03) : 316 - 324