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Crosstalk between histone/DNA modifications and RNA N6-methyladenosine modification.
Wang, Yushuai; Huang, Huilin; Chen, Jianjun; Weng, Hengyou.
Affiliation
  • Wang Y; Guangzhou National Laboratory, Guangzhou 510005, China.
  • Huang H; Sun Yat-sen University Cancer Center, State Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer Medicine, Guangzhou 510060, China.
  • Chen J; Department of Systems Biology, Beckman Research Institute of City of Hope, Monrovia, CA 91016, USA; Gehr Family Center for Leukemia Research & City of Hope Comprehensive Cancer Center, City of Hope, Duarte, CA 91010, USA. Electronic address: jianchen@coh.org.
  • Weng H; Guangzhou National Laboratory, Guangzhou 510005, China; Bioland Laboratory (Guangzhou Regenerative Medicine and Health Guangdong Laboratory), Guangzhou 510005, China; The First Affiliated Hospital, State Key Laboratory of Respiratory Diseases, Guangzhou Medical University, Guangzhou 510005, China. E
Curr Opin Genet Dev ; 86: 102205, 2024 Jun.
Article in En | MEDLINE | ID: mdl-38776766
ABSTRACT
N6-methyladenosine (m6A) is the most prevalent internal RNA modification in eukaryotic messenger RNAs (mRNAs), regulating gene expression at the transcription and post-transcription levels. Complex interplay between m6A and other well-studied epigenetic modifications, including histone modifications and DNA modification, has been extensively reported in recent years. The crosstalk between RNA m6A modification and histone/DNA modifications plays a critical role in establishing the chromatin state for the precise and specific fine-tuning of gene expression and undoubtedly has profound impacts on both physiological and pathological processes. In this review, we discuss the crosstalk between RNA m6A modification and histone/DNA modifications, emphasizing their sophisticated communications and the mechanisms underlying to gain a comprehensive view of the biological relevance of m6A-based epigenetic network.
Subject(s)

Full text: 1 Database: MEDLINE Main subject: Histones / Adenosine / Epigenesis, Genetic Language: En Journal: Curr Opin Genet Dev Journal subject: GENETICA Year: 2024 Type: Article Affiliation country: China

Full text: 1 Database: MEDLINE Main subject: Histones / Adenosine / Epigenesis, Genetic Language: En Journal: Curr Opin Genet Dev Journal subject: GENETICA Year: 2024 Type: Article Affiliation country: China