| Literature DB >> 26711009 |
Yaxue Zeng1, Bing Yao2, Jaehoon Shin3, Li Lin2, Namshik Kim1, Qifeng Song4, Shuang Liu4, Yijing Su1, Junjie U Guo5, Luoxiu Huang2, Jun Wan6, Hao Wu7, Jiang Qian6, Xiaodong Cheng8, Heng Zhu4, Guo-li Ming9, Peng Jin10, Hongjun Song11.
Abstract
Lin28, a well-known RNA-binding protein, regulates diverse cellular properties. All physiological functions of Lin28A characterized so far have been attributed to its repression of let-7 miRNA biogenesis or modulation of mRNA translational efficiency. Here we show that Lin28A directly binds to a consensus DNA sequence in vitro and in mouse embryonic stem cells in vivo. ChIP-seq and RNA-seq reveal enrichment of Lin28A binding around transcription start sites and a positive correlation between its genomic occupancy and expression of many associated genes. Mechanistically, Lin28A recruits 5-methylcytosine-dioxygenase Tet1 to genomic binding sites to orchestrate 5-methylcytosine and 5-hydroxymethylcytosine dynamics. Either Lin28A or Tet1 knockdown leads to dysregulated DNA methylation and expression of common target genes. These results reveal a surprising role for Lin28A in transcriptional regulation via epigenetic DNA modifications and have implications for understanding mechanisms underlying versatile functions of Lin28A in mammalian systems.Entities:
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Year: 2015 PMID: 26711009 PMCID: PMC4779955 DOI: 10.1016/j.molcel.2015.11.020
Source DB: PubMed Journal: Mol Cell ISSN: 1097-2765 Impact factor: 17.970