Muscleblind protein, MBNL1/EXP, binds specifically to CHHG repeats

被引:134
作者
Kino, Y [1 ]
Mori, D [1 ]
Oma, Y [1 ]
Takeshita, Y [1 ]
Sasagawa, N [1 ]
Ishiura, S [1 ]
机构
[1] Univ Tokyo, Dept Life Sci, Grad Sch Arts & Sci, Meguro Ku, Tokyo 1538902, Japan
基金
日本学术振兴会;
关键词
D O I
10.1093/hmg/ddh056
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Myotonic dystrophy (DM) type 1 is caused by an expansion of a CTG repeat in the DMPK gene and type 2 by a CCTG repeat in the ZNF9 gene. Previous reports have suggested that transcripts containing expanded CUG/CCUG repeats might have toxic gain-of-function effects, probably affecting the function of RNA-binding proteins in the pathogenesis of DM. Here, it was attempted to compare the RNA-binding properties of three proteins, CUG-BP, MBNL1/EXP and PKR, which have previously been suggested to interact with CUG repeats. MBNL1, but not CUG-BP or PKR, interacted with both CUG and CCUG repeats in a yeast three-hybrid system. By using various synthetic RNAs, it was found that MBNL1 specifically interacts with repetitive sequences summarized as CHHG and CHG repeats, where H is A, U or C. Interestingly, MBNL1 did not interact with a genuine double-stranded RNA comprising CAG/CUG repeats, suggesting that MBNL1 prefers bulge-containing double-stranded RNAs. Deletion analysis indicates a difference in RNA-binding abilities among splice variants of MBNL1. It was also found that MBNL1 can bind to repetitive motifs in ZNF9, which contain a minimal length of CCUG repeats with non-CCUG insertions.
引用
收藏
页码:495 / 507
页数:13
相关论文
共 53 条
[1]   Cis and trans effects of the myotonic dystrophy (DM) mutation in a cell culture model [J].
Amack, JD ;
Paguio, AP ;
Mahadevan, MS .
HUMAN MOLECULAR GENETICS, 1999, 8 (11) :1975-1984
[2]   Mutant DMPK 3′-UTR transcripts disrupt C2C12 myogenic differentiation by compromising MyoD [J].
Amack, JD ;
Reagan, SR ;
Mahadevan, MS .
JOURNAL OF CELL BIOLOGY, 2002, 159 (03) :419-429
[3]   The myotonic dystrophy expanded CUG repeat tract is necessary but not sufficient to disrupt C2C12 myoblast differentiation [J].
Amack, JD ;
Mahadevan, MS .
HUMAN MOLECULAR GENETICS, 2001, 10 (18) :1879-1887
[4]   The muscleblind gene participates in the organization of Z-bands and epidermal attachments of Drosophila muscles and is regulated by Dmef2 [J].
Artero, R ;
Prokop, A ;
Paricio, N ;
Begemann, G ;
Pueyo, I ;
Mlodzik, M ;
Perez-Alonso, M ;
Baylies, MK .
DEVELOPMENTAL BIOLOGY, 1998, 195 (02) :131-143
[5]  
Begemann G, 1997, DEVELOPMENT, V124, P4321
[6]   Analyzing mRNA-protein complexes using a yeast three-hybrid system [J].
Bernstein, DS ;
Buter, N ;
Stumpf, C ;
Wickens, M .
METHODS, 2002, 26 (02) :123-141
[7]   DMPK dosage alterations result in atrioventricular conduction abnormalities in a mouse myotonic dystrophy model [J].
Berul, CI ;
Maguire, CT ;
Aronovitz, MJ ;
Greenwood, J ;
Miller, C ;
Gehrmann, J ;
Housman, D ;
Mendelsohn, ME ;
Reddy, S .
JOURNAL OF CLINICAL INVESTIGATION, 1999, 103 (04) :R1-R7
[8]   Minor-groove recognition of double-stranded RNA by the double-stranded RNA-binding domain from the RNA-activated protein kinase PKR [J].
Bevilacqua, PC ;
Cech, TR .
BIOCHEMISTRY, 1996, 35 (31) :9983-9994
[9]   MOLECULAR-BASIS OF MYOTONIC-DYSTROPHY - EXPANSION OF A TRINUCLEOTIDE (CTG) REPEAT AT THE 3' END OF A TRANSCRIPT ENCODING A PROTEIN-KINASE FAMILY MEMBER [J].
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 .
CELL, 1992, 68 (04) :799-808
[10]   Muscle-specific alternative splicing of myotubularin-related 1 gene is impaired in DM1 muscle cells [J].
Buj-Bello, A ;
Furling, D ;
Tronchère, H ;
Laporte, J ;
Lerouge, T ;
Butler-Browne, GS ;
Mandel, JL .
HUMAN MOLECULAR GENETICS, 2002, 11 (19) :2297-2307