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Epitranscriptomic Code and Its Alterations in Human Disease
DOI:10.1016/j.molmed.2018.07.010.png)
摘要
En 中文
Innovations in epitranscriptomics have resulted in the identification of more than 160 RNA modifications to date. These developments, together with the recent discovery of writers, readers, and erasers of modifications occurring across a wide range of RNAs and tissue types, have led to a surge in integrative approaches for transcriptome-wide mapping of modifications and protein-RNA interaction profiles of epitranscriptome players. RNA modification maps and crosstalk between them have begun to elucidate the role of modifications as signaling switches, entertaining the notion of an epitranscriptomic code as a driver of the post-transcriptional fate of RNA. Emerging single-molecule sequencing technologies and development of antibodies specific to various RNA modifications could enable charting of transcript-specific epitranscriptomic marks across cell types and their alterations in disease.
Keyword:
DYNAMIC N-1-METHYLADENOSINE METHYLOME
RECESSIVE INTELLECTUAL DISABILITY
MESSENGER-RNA TRANSLATION
BINDING PROTEIN ABP140
OBESITY-ASSOCIATED FTO
CELL SELF-RENEWAL
NONCODING RNA
BREAST-CANCER
RIBONUCLEIC-ACIDS
NUCLEAR-RNA
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13.8
论文数:
2.6K
被引数:
1.4W
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引用论文
Reprogramming of tRNA modifications controls the oxidative stress response by codon-biased translation of proteins
NATURE COMMUNICATIONS
IF15.7

