Academic Journal

Topological Characterization of Human and Mouse m5C Epitranscriptome Revealed by Bisulfite Sequencing

التفاصيل البيبلوغرافية
العنوان: Topological Characterization of Human and Mouse m5C Epitranscriptome Revealed by Bisulfite Sequencing
المؤلفون: Zhen Wei, Subbarayalu Panneerdoss, Santosh Timilsina, Jingting Zhu, Tabrez A. Mohammad, Zhi-Liang Lu, João Pedro de Magalhães, Yidong Chen, Rong Rong, Yufei Huang, Manjeet K. Rao, Jia Meng
المصدر: International Journal of Genomics, Vol 2018 (2018)
بيانات النشر: Wiley, 2018.
سنة النشر: 2018
المجموعة: LCC:Genetics
مصطلحات موضوعية: Genetics, QH426-470
الوصف: Background. Compared with the well-studied 5-methylcytosine (m5C) in DNA, the role and topology of epitranscriptome m5C remain insufficiently characterized. Results. Through analyzing transcriptome-wide m5C distribution in human and mouse, we show that the m5C modification is significantly enriched at 5′ untranslated regions (5′UTRs) of mRNA in human and mouse. With a comparative analysis of the mRNA and DNA methylome, we demonstrate that, like DNA methylation, transcriptome m5C methylation exhibits a strong clustering effect. Surprisingly, an inverse correlation between mRNA and DNA m5C methylation is observed at CpG sites. Further analysis reveals that RNA m5C methylation level is positively correlated with both RNA expression and RNA half-life. We also observed that the methylation level of mitochondrial RNAs is significantly higher than RNAs transcribed from the nuclear genome. Conclusions. This study provides an in-depth topological characterization of transcriptome-wide m5C modification by associating RNA m5C methylation patterns with transcriptional expression, DNA methylations, RNA stabilities, and mitochondrial genome.
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 2314-436X
2314-4378
Relation: https://doaj.org/toc/2314-436X; https://doaj.org/toc/2314-4378
DOI: 10.1155/2018/1351964
URL الوصول: https://doaj.org/article/271b300dce334098acc2ce7c40c02218
رقم الانضمام: edsdoj.271b300dce334098acc2ce7c40c02218
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:2314436X
23144378
DOI:10.1155/2018/1351964