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

被引:0
|
作者
Wei Chen
Lars R Jensen
Jozef Gecz
Jean-Pierre Fryns
Claude Moraine
Arjan de Brouwer
Jamel Chelly
Bettina Moser
H Hilger Ropers
Andreas W Kuss
机构
[1] Max Planck Institute for Molecular Genetics,Department of Genetic Medicine
[2] Women's and Children's Hospital,Department of Human Genetics
[3] Centre for Human Genetics,undefined
[4] University of Leuven,undefined
[5] Service de Génétique et INSERM U316,undefined
[6] Hôpital Bretonneau,undefined
[7] Radboud University Medical Centre,undefined
[8] INSERM 129-ICGM,undefined
[9] Faculté de Médecine Cochin,undefined
来源
European Journal of Human Genetics | 2007年 / 15卷
关键词
MiRNA; X-linked mental retardation; genetic modifier; mutation; brain;
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学科分类号
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.
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页码:375 / 378
页数:3
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