Mutation screening of brain-expressed X-chromosomal miRNA genes in 464 patients with nonsyndromic X-linked mental retardation

被引:21
作者
Chen, Wei
Jensen, Lars R.
Gecz, Jozef
Fryns, Jean-Pierre
Moraine, Claude
de Brouwer, Arjan
Chelly, Jamel
Moser, Bettina
Ropers, H. Hilger
Kuss, Andreas W.
机构
[1] Max Planck Inst Mol Genet, D-14195 Berlin, Germany
[2] Womens & Childrens Hosp, Dept Med Genet, Adelaide, SA, Australia
[3] Univ Louvain, Ctr Human Genet, Louvain, Belgium
[4] Hop Bretonneau, Serv Genet, Tours, France
[5] Hop Bretonneau, INSERM, U316, Tours, France
[6] Radboud Univ Nijmegen, Med Ctr, Dept Human Genet, Nijmegen, Netherlands
[7] Fac Med Cochin, INSERM, Paris, France
关键词
miRNA; X-linked mental retardation; genetic modifier; mutation; brain;
D O I
10.1038/sj.ejhg.5201758
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
MiRNAs are small noncoding RNAs that control the expression of target genes at the post-transcriptional level and have been reported to modulate various biological processes. Their function as regulatory factors in gene expression renders them attractive candidates for harbouring genetic variants with subtle effects on IQ. In an attempt to investigate the potential role of miRNAs in the aetiology of X-linked mental retardation, we have examined all 13 known, brain-expressed X-chromosomal miRNAs in a cohort of 464 patients with non-syndromic X-linked MR and found four nucleotide changes in three different pre-miRNA hairpins. All the observed changes appear to be functionally neutral which, taken together with the rarity of detected nucleotide changes in miRNA genes, may reflect strong selection and thus underline the functional importance of miRNAs.
引用
收藏
页码:375 / 378
页数:4
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