Literature DB >> 19360674

Feasibility and relevance of examining lymphoblastoid cell lines to study role of microRNAs in autism.

Zohreh Talebizadeh1, Merlin G Butler, Mariana F Theodoro.   

Abstract

To assess the feasibility and relevance of using lymphoblastoid cell lines to study the role of noncoding RNAs in the etiology of autism, we evaluated global expression profiling of 470 mature human microRNAs from six subjects with autism compared with six matched controls. Differential expression (either higher or lower) for 9 of the 470 microRNAs was observed in our autism samples compared with controls. Potential target genes for these microRNAs were identified using computer tools, which included several autism susceptibility genes. Our preliminary results indicate microRNAs should be considered and evaluated in the etiology of autism. In addition, analysis of this class of noncoding RNAs in lymphoblastoid cells has the potential to reveal at least a subset of brain-related microRNAs implicated in autism. Subsequently, this model system should allow for detection of complex subtle changes in susceptibility genes/pathways contributing to autism.

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Year:  2008        PMID: 19360674      PMCID: PMC2768334          DOI: 10.1002/aur.33

Source DB:  PubMed          Journal:  Autism Res        ISSN: 1939-3806            Impact factor:   5.216


  59 in total

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6.  Numerous microRNPs in neuronal cells containing novel microRNAs.

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7.  A genomewide screen of 345 families for autism-susceptibility loci.

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9.  Gene expression profiling of lymphoblastoid cell lines from monozygotic twins discordant in severity of autism reveals differential regulation of neurologically relevant genes.

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10.  Microarray analysis of microRNA expression in the developing mammalian brain.

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  59 in total

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Review 7.  MicroRNA-132, -134, and -138: a microRNA troika rules in neuronal dendrites.

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Review 8.  MicroRNAs in psychiatric and neurodevelopmental disorders.

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9.  Investigation of post-transcriptional gene regulatory networks associated with autism spectrum disorders by microRNA expression profiling of lymphoblastoid cell lines.

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