FTO mediates LINE1 m 6 A demethylation and chromatin regulation in mESCs and mouse development DOI
Jiangbo Wei, Xianbin Yu, Lei Yang

и другие.

Science, Год журнала: 2022, Номер 376(6596), С. 968 - 973

Опубликована: Май 5, 2022

-methyladenosine (m

Язык: Английский

Where, When, and How: Context-Dependent Functions of RNA Methylation Writers, Readers, and Erasers DOI Creative Commons
Hailing Shi, Jiangbo Wei, Chuan He

и другие.

Molecular Cell, Год журнала: 2019, Номер 74(4), С. 640 - 650

Опубликована: Май 1, 2019

Язык: Английский

Процитировано

1478

The role of m6A RNA methylation in cancer DOI Creative Commons
Ting Sun, Ruiyan Wu, Liang Ming

и другие.

Biomedicine & 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

745

Small-Molecule Targeting of Oncogenic FTO Demethylase in Acute Myeloid Leukemia DOI Creative Commons
Yue Huang, Rui Su, Yue Sheng

и другие.

Cancer Cell, Год журнала: 2019, Номер 35(4), С. 677 - 691.e10

Опубликована: Апрель 1, 2019

Язык: Английский

Процитировано

689

m6A mRNA demethylase FTO regulates melanoma tumorigenicity and response to anti-PD-1 blockade DOI Creative Commons
Seungwon Yang, Jiangbo Wei, Yan‐Hong Cui

и другие.

Nature 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

582

m 6 A RNA methylation: from mechanisms to therapeutic potential DOI Open Access
P. Cody He, Chuan He

The EMBO Journal, Год журнала: 2021, Номер 40(3)

Опубликована: Янв. 20, 2021

Язык: Английский

Процитировано

505

The emerging role of RNA modifications in the regulation of mRNA stability DOI Creative Commons

Sung Ho Boo,

Yoon Ki Kim

Experimental & 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

422

The human 18S rRNA m6A methyltransferase METTL5 is stabilized by TRMT112 DOI Creative Commons

Nhan van Tran,

Felix G.M. Ernst, Ben R Hawley

и другие.

Nucleic 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

403

A comprehensive review of m6A/m6Am RNA methyltransferase structures DOI Creative Commons
Stephanie Oerum, Vincent Meynier, Marjorie Catala

и другие.

Nucleic 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

359

The RNA modification N6-methyladenosine as a novel regulator of the immune system DOI
Ziv Shulman,

Noam Stern‐Ginossar

Nature Immunology, Год журнала: 2020, Номер 21(5), С. 501 - 512

Опубликована: Апрель 13, 2020

Язык: Английский

Процитировано

330

RNA modifications regulating cell fate in cancer DOI
Sylvain Delaunay, Michaela Frye

Nature Cell Biology, Год журнала: 2019, Номер 21(5), С. 552 - 559

Опубликована: Май 1, 2019

Язык: Английский

Процитировано

311