Science, Год журнала: 2022, Номер 376(6596), С. 968 - 973
Опубликована: Май 5, 2022
-methyladenosine (m
Язык: Английский
Science, Год журнала: 2022, Номер 376(6596), С. 968 - 973
Опубликована: Май 5, 2022
-methyladenosine (m
Язык: Английский
Molecular Cell, Год журнала: 2019, Номер 74(4), С. 640 - 650
Опубликована: Май 1, 2019
Язык: Английский
Процитировано
1478Biomedicine & Pharmacotherapy, Год журнала: 2019, Номер 112, С. 108613 - 108613
Опубликована: Фев. 19, 2019
N6-methyladenosine (m6A), the most abundant internal modification of RNA in eukaryotic cells, has gained increasing attention recent years. The m6A affects multiple aspects metabolism, ranging from processing, nuclear export, translation to decay. Emerging evidence suggests that methylation plays a critical role cancer through various mechanisms. Moreover, provided more possibilities for early diagnosis and treatment cancers. In this review, we focus on m6A-associated mechanisms functions several major malignancies summarize dual as well its prospects cancer.
Язык: Английский
Процитировано
745Cancer Cell, Год журнала: 2019, Номер 35(4), С. 677 - 691.e10
Опубликована: Апрель 1, 2019
Язык: Английский
Процитировано
689Nature Communications, Год журнала: 2019, Номер 10(1)
Опубликована: Июнь 25, 2019
Melanoma is one of the most deadly and therapy-resistant cancers. Here we show that N
Язык: Английский
Процитировано
582The EMBO Journal, Год журнала: 2021, Номер 40(3)
Опубликована: Янв. 20, 2021
Язык: Английский
Процитировано
505Experimental & Molecular Medicine, Год журнала: 2020, Номер 52(3), С. 400 - 408
Опубликована: Март 1, 2020
Many studies have highlighted the importance of tight regulation mRNA stability in control gene expression. largely depends on nucleotide sequence, which affects secondary and tertiary structures mRNAs, accessibility various RNA-binding proteins to mRNAs. Recent advances high-throughput RNA-sequencing techniques resulted elucidation important roles played by modifications sequences regulating stability. To date, hundreds different RNA been characterized. Among them, several modifications, including N
Язык: Английский
Процитировано
422Nucleic Acids Research, Год журнала: 2019, Номер 47(15), С. 7719 - 7733
Опубликована: Июль 12, 2019
Abstract N6-methyladenosine (m6A) has recently been found abundantly on messenger RNA and shown to regulate most steps of mRNA metabolism. Several important m6A methyltransferases have described functionally structurally, but the enzymes responsible for installing one residue each subunit human ribosomes at sites eluded identification over 30 years. Here, we identify METTL5 as enzyme 18S rRNA modification confirm ZCCHC4 28S enzyme. We show that must form a heterodimeric complex with TRMT112, known methyltransferase activator, gain metabolic stability in cells. provide first atomic resolution structure METTL5–TRMT112, supporting its RNA-binding mode differs distinctly from other methyltransferases. On basis similarities DNA methyltransferase, propose METTL5–TRMT112 acts by extruding adenosine be modified double-stranded nucleic acid.
Язык: Английский
Процитировано
403Nucleic Acids Research, Год журнала: 2021, Номер 49(13), С. 7239 - 7255
Опубликована: Апрель 26, 2021
Abstract Gene expression is regulated at many levels including co- or post-transcriptionally, where chemical modifications are added to RNA on riboses and bases. Expression control via has been termed ‘epitranscriptomics’ keep with the related ‘epigenomics’ for DNA modification. One such modification N6-methylation found adenosine (m6A) 2′-O-methyladenosine (m6Am) in most types of RNA. The can affect fold, stability, degradation cellular interaction(s) modified RNA, implicating it processes as splicing, translation, export decay. multiple roles played by this explains why m6A misregulation connected human cancers. m6A/m6Am writer enzymes methyltransferases (MTases). Structures available functionally characterized MTases from (m6A mRNA, snRNA, rRNA m6Am mRNA MTases), zebrafish (m6Am MTase) bacteria MTase). For each these MTases, we describe their overall domain organization, active site architecture substrate binding. We identify areas that remain be investigated, propose yet unexplored routes structural characterization MTase:substrate complexes, highlight common elements should described future MTase structures.
Язык: Английский
Процитировано
359Nature Immunology, Год журнала: 2020, Номер 21(5), С. 501 - 512
Опубликована: Апрель 13, 2020
Язык: Английский
Процитировано
330Nature Cell Biology, Год журнала: 2019, Номер 21(5), С. 552 - 559
Опубликована: Май 1, 2019
Язык: Английский
Процитировано
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