Abstract:
BACKGROUND:MECP2, the gene mutated in the majority of Rett syndrome cases, is a transcriptional regulator that can activate or repress transcription. Although the transcription regulatory function of MECP2 has been known for over a decade, it remains unclear how transcriptional dysregulation leads to the neurodevelopmental disorder. Notably, little convergence was previously observed between the genes abnormally expressed in the brain of Rett syndrome mouse models and those identified in human studies. METHODS:Here we carried out a comprehensive transcriptome analysis of human brain tissue from Rett syndrome brain using both RNA-seq and microarrays. RESULTS:We identified over two hundred differentially expressed genes, and identified the complement C1Q complex genes (C1QA, C1QB and C1QC) as a point of convergence between gene expression changes in human and mouse Rett syndrome brain. CONCLUSIONS:The results of our study support a role for alterations in the expression level of C1Q complex genes in RTT pathogenesis.
journal_name
BMC Genomicsjournal_title
BMC genomicsauthors
Lin P,Nicholls L,Assareh H,Fang Z,Amos TG,Edwards RJ,Assareh AA,Voineagu Idoi
10.1186/s12864-016-2746-7subject
Has Abstractpub_date
2016-06-06 00:00:00pages
427issn
1471-2164pii
10.1186/s12864-016-2746-7journal_volume
17pub_type
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