한빛사논문
Ki-Jun Yoon1,2,*, Yoon Ki Kim1,3,4,*
1Department of Biological Sciences, Korea Advanced Institute of Science and Technology (KAIST), Daejeon 34141, Republic of Korea
2KAIST Stem Cell Center, KAIST, Daejeon 34141, Republic of Korea
3Creative Research Initiatives Center for Molecular Biology of Translation, Korea University, Seoul, Republic of Korea
4Division of Life Sciences, Korea University, Seoul 02841, Republic of Korea
*Corresponding author.
Abstract
A recent study by Hu et al. describes N6-methyladenosine (m6A)-selective allyl chemical labeling and sequencing (m6A-SAC-seq), which allows for quantitative, stoichiometric, and positional analyses of m6A at single-nucleotide resolution across the whole transcriptome level. Information on the m6A stoichiometry will provide additional layers of gene regulatory pathways mediated by m6A modification during diverse molecular, cellular, and physiological events.
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