| Literature DB >> 27117867 |
Zhigang Miao1, Ning Xin2, Bin Wei3, Xiaodong Hua4, Gaocai Zhang1, Cuihua Leng1, Chenyu Zhao1, Di Wu1, Jizhen Li5, Wei Ge6, Miao Sun7, Xingshun Xu8.
Abstract
5-hydroxymethylcytosine (5hmC) is considered as a novel DNA modification and plays an important role in cancer, stem cells, and developmental diseases. In this study, we demonstrated the existence of RNA 5hmC modification in mouse brain RNA by using a dot blot analysis method. Our data indicated that 5hmC modification in RNA samples was less than that in DNA samples. Further, we optimized the conditions for 5hmC detection in RNA samples such as DNase treatment, denature reagents, denature time, sample air-dry time, and the cross-linking time between RNA and membrane. Our results demonstrated that DNase treatment and denature reagents were two important factors that affected the 5hmC detection in RNA samples. By using the optimal conditions for RNA 5hmC detection, we found that the brainstem, the hippocampus, and the cerebellum had high levels of 5hmC modification and 5mC modification in RNA. Finally, we found that RNA 5hmC modification decreased in MPTP-induced Parkinson's disease model in mice. These suggest that 5hmC modification in RNA might play an important regulative role on protein or microRNA expression in these brain tissues. Because DNA 5hmC modification plays an important role in neural differentiation and development as well as neurological diseases, the significance of 5hmC modification in RNA in different neurological diseases needs further investigation. In summary, our study demonstrated for the first time the abundance of 5hmC modification in brain RNA by using a dot blot analysis method and proved that dot blot analysis is a useful method for 5hmC detection in RNA samples.Entities:
Keywords: 5-Hydroxymethylcytosine; 5-Methylcytosine; Dot blot; Method; RNA
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Year: 2016 PMID: 27117867 DOI: 10.1016/j.brainres.2016.04.055
Source DB: PubMed Journal: Brain Res ISSN: 0006-8993 Impact factor: 3.252