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本文引用的文献

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Methionine secreted by tumor-associated pericytes supports cancer stem cells in clear cell renal carcinoma.肿瘤相关周细胞分泌的蛋氨酸支持透明细胞肾细胞癌中的癌症干细胞。
Cell Metab. 2024 Apr 2;36(4):778-792.e10. doi: 10.1016/j.cmet.2024.01.018. Epub 2024 Feb 19.
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Rewiring of RNA methylation by the oncometabolite fumarate in renal cell carcinoma.肾细胞癌中癌代谢物富马酸酯对RNA甲基化的重编程
NAR Cancer. 2024 Feb 7;6(1):zcae004. doi: 10.1093/narcan/zcae004. eCollection 2024 Mar.
3
Ascorbic Acid Reprograms Epigenome and Epitranscriptome by Reducing Fe(III) in the Catalytic Cycle of Dioxygenases.抗坏血酸通过在双加氧酶催化循环中还原Fe(III)来重编程表观基因组和表位转录组。
ACS Chem Biol. 2024 Jan 19;19(1):129-140. doi: 10.1021/acschembio.3c00567. Epub 2023 Dec 15.
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Zika virus remodelled ER membranes contain proviral factors involved in redox and methylation pathways.寨卡病毒重塑的内质网膜包含参与氧化还原和甲基化途径的前病毒因子。
Nat Commun. 2023 Dec 5;14(1):8045. doi: 10.1038/s41467-023-43665-6.
5
Beyond energy and growth: the role of metabolism in developmental signaling, cell behavior and diapause.超越能量和生长:代谢在发育信号转导、细胞行为和休眠中的作用。
Development. 2023 Oct 15;150(20). doi: 10.1242/dev.201610. Epub 2023 Oct 26.
6
Nitric oxide inhibits FTO demethylase activity to regulate N-methyladenosine mRNA methylation.一氧化氮抑制 FTO 去甲基酶活性以调节 N-甲基腺苷 mRNA 甲基化。
Redox Biol. 2023 Nov;67:102928. doi: 10.1016/j.redox.2023.102928. Epub 2023 Oct 14.
7
Xanthine derivatives inhibit FTO in an L-ascorbic acid-dependent manner.黄嘌呤衍生物以 L-抗坏血酸依赖的方式抑制 FTO。
Chem Commun (Camb). 2023 Sep 7;59(72):10809-10812. doi: 10.1039/d3cc02484a.
8
The Proteins of mRNA Modification: Writers, Readers, and Erasers.mRNA 修饰蛋白:书写者、阅读者和擦除者。
Annu Rev Biochem. 2023 Jun 20;92:145-173. doi: 10.1146/annurev-biochem-052521-035330. Epub 2023 Apr 17.
9
scmA-seq reveals single-cell landscapes of the dynamic mA during oocyte maturation and early embryonic development.scmA-seq 揭示了卵母细胞成熟和早期胚胎发育过程中动态 mA 的单细胞图谱。
Nat Commun. 2023 Jan 19;14(1):315. doi: 10.1038/s41467-023-35958-7.
10
Transcriptome-wide profiling and quantification of N-methyladenosine by enzyme-assisted adenosine deamination.通过酶辅助腺苷脱氨酶对 N6-甲基腺苷进行转录组范围的谱分析和定量。
Nat Biotechnol. 2023 Jul;41(7):993-1003. doi: 10.1038/s41587-022-01587-6. Epub 2023 Jan 2.

代谢指挥棒:指挥 N6-甲基腺苷书写和擦除的舞蹈。

The metabolic baton: conducting the dance of N6-methyladenosine writing and erasing.

机构信息

Laboratory of Cell Biology, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, MD, USA.

Laboratory of Cell Biology, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, MD, USA.

出版信息

Curr Opin Genet Dev. 2024 Jun;86:102206. doi: 10.1016/j.gde.2024.102206. Epub 2024 May 23.

DOI:10.1016/j.gde.2024.102206
PMID:38788488
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11212039/
Abstract

The modification N6-methyladenosine (mA) plays an important role in determining the functional output of gene expression programs. Throughout the transcriptome, the levels of mA are tightly regulated by the opposing activities of methyltransferases and demethylases, as well as the interaction of modified transcripts with mA-dependent RNA-binding proteins that modulate transcript stability, often referred to as writers, erasers, and readers. The enzymatic activities of both writers and erasers are tightly linked to the cellular metabolic environment, as these enzymatic reactions rely on metabolism intermediaries as cofactors. In this review, we highlight the examples of intersection between metabolism and mA-dependent gene regulation and discuss the different contexts where this interaction plays important roles.

摘要

N6-甲基腺苷(m6A)的修饰在决定基因表达程序的功能输出方面起着重要作用。在整个转录组中,m6A 的水平受到甲基转移酶和去甲基酶的拮抗活性以及修饰转录本与依赖 m6A 的 RNA 结合蛋白相互作用的严格调节,这些蛋白通常被称为写作酶、擦除酶和阅读酶,它们可以调节转录本的稳定性。写作酶和擦除酶的酶促活性都与细胞代谢环境紧密相关,因为这些酶促反应依赖代谢中间产物作为辅助因子。在这篇综述中,我们强调了代谢和 m6A 依赖性基因调控之间的交叉实例,并讨论了这种相互作用在不同背景下发挥重要作用的情况。