piRNAs Warrant Investigation in Rett Syndrome: An Omics Perspective

التفاصيل البيبلوغرافية
العنوان: piRNAs Warrant Investigation in Rett Syndrome: An Omics Perspective
المؤلفون: Alka Saxena, Dave Tang, Piero Carninci
المصدر: Disease Markers, Vol 33, Iss 5, Pp 261-275 (2012)
Disease markers
بيانات النشر: Hindawi Limited, 2012.
سنة النشر: 2012
مصطلحات موضوعية: endocrine system, congenital, hereditary, and neonatal diseases and abnormalities, Transcription, Genetic, Methyl-CpG-Binding Protein 2, Clinical Biochemistry, Mice, Cerebellum, mental disorders, Genetics, Rett Syndrome, Animals, Humans, RNA, Small Interfering, Molecular Biology, MeCP2, lcsh:R5-920, urogenital system, Biochemistry (medical), General Medicine, nervous system diseases, short RNAs, Long Interspersed Nucleotide Elements, piRNAs, Mutation, Other, lcsh:Medicine (General), LINE 1
الوصف: Mutations in the MECP2 gene are found in a large proportion of girls with Rett Syndrome. Despite extensive research, the principal role of MeCP2 protein remains elusive. Is MeCP2 a regulator of genes, acting in concert with co-activators and co-repressors, predominantly as an activator of target genes or is it a methyl CpG binding protein acting globally to change the chromatin state and to supress transcription from repeat elements? If MeCP2 has no specific targets in the genome, what causes the differential expression of specific genes in the Mecp2 knockout mouse brain? We discuss the discrepancies in current data and propose a hypothesis to reconcile some differences in the two viewpoints. Since transcripts from repeat elements contribute to piRNA biogenesis, we propose that piRNA levels may be higher in the absence of MeCP2 and that increased piRNA levels may contribute to the mis-regulation of some genes seen in the Mecp2 knockout mouse brain. We provide preliminary data showing an increase in piRNAs in the Mecp2 knockout mouse cerebellum. Our investigation suggests that global piRNA levels may be elevated in the Mecp2 knockout mouse cerebellum and strongly supports further investigation of piRNAs in Rett syndrome.
وصف الملف: text/xhtml
اللغة: English
تدمد: 1875-8630
0278-0240
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::11be6615c0409abe9a4df995b1bb0bdc
https://doaj.org/article/6aebc73c220f4722bbed3d45509eae3d
Rights: OPEN
رقم الانضمام: edsair.doi.dedup.....11be6615c0409abe9a4df995b1bb0bdc
قاعدة البيانات: OpenAIRE