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Biomedicines. 2024 May 16;12(5):1110. doi: 10.3390/biomedicines12051110.
2
Accurate structure prediction of biomolecular interactions with AlphaFold 3.利用 AlphaFold 3 进行生物分子相互作用的精确结构预测。
Nature. 2024 Jun;630(8016):493-500. doi: 10.1038/s41586-024-07487-w. Epub 2024 May 8.
3
Metabolic regulation of mRNA splicing.mRNA 剪接的代谢调控。
Trends Cell Biol. 2024 Sep;34(9):756-770. doi: 10.1016/j.tcb.2024.02.002. Epub 2024 Mar 1.
4
mA mRNA Modifications in Glioblastoma: Emerging Prognostic Biomarkers and Therapeutic Targets.胶质母细胞瘤中的mRNA修饰:新兴的预后生物标志物和治疗靶点
Cancers (Basel). 2024 Feb 9;16(4):727. doi: 10.3390/cancers16040727.
5
Methyltransferase-like 3 mediated RNA m A modifications in the reproductive system: Potentials for diagnosis and therapy.甲基转移酶样蛋白 3 介导的生殖系统中 RNA mA 修饰:用于诊断和治疗的潜力。
J Cell Mol Med. 2024 Feb;28(4):e18128. doi: 10.1111/jcmm.18128.
6
The RNA mA writer METTL3 in tumor microenvironment: emerging roles and therapeutic implications.肿瘤微环境中的 RNA mA 书写酶 METTL3:新兴作用和治疗意义。
Front Immunol. 2024 Jan 22;15:1335774. doi: 10.3389/fimmu.2024.1335774. eCollection 2024.
7
The role of m6A epigenetic modifications in tumor coding and non-coding RNA processing.m6A 表观遗传修饰在肿瘤编码和非编码 RNA 加工中的作用。
Cell Commun Signal. 2023 Dec 15;21(1):355. doi: 10.1186/s12964-023-01385-w.
8
METTL16-mediated N6-methyladenosine modification of Soga1 enables proper chromosome segregation and chromosomal stability in colorectal cancer.METTL16 介导的 Soga1 的 N6-甲基腺苷修饰可使结直肠癌中染色体正确分离和染色体稳定。
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9
Comparative RNA-Seq Analysis Revealed Tissue-Specific Splicing Variations during the Generation of the PDX Model.比较 RNA-Seq 分析揭示了 PDX 模型生成过程中组织特异性剪接变化。
Int J Mol Sci. 2023 Nov 30;24(23):17001. doi: 10.3390/ijms242317001.
10
N6-Methyladenosine Methylation of mRNA in Cell Apoptosis.mRNA 在细胞凋亡中的 N6-甲基腺苷甲基化。
Mol Neurobiol. 2024 Jul;61(7):3934-3948. doi: 10.1007/s12035-023-03813-x. Epub 2023 Dec 2.

对 m6A 转录组动态的新认识:杂交测序鉴定出 m6A 写入器 METTL3/14 的新型 mRNAs。

New insights into the dynamics of m6A epitranscriptome: hybrid-seq identifies novel mRNAs of the m6A writers METTL3/14.

机构信息

Department of Biochemistry & Molecular Biology, National & Kapodistrian University of Athens, Athens, 15701, Greece.

出版信息

Epigenomics. 2024;16(17):1159-1174. doi: 10.1080/17501911.2024.2390818. Epub 2024 Sep 3.

DOI:10.1080/17501911.2024.2390818
PMID:39225157
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11457658/
Abstract

N6-methyladenosine (m6A), a prevalent mRNA modification, is dynamically regulated by methyltransferases, including METTL3 and METTL14. In the current study, we employed a custom hybrid-seq method to identify novel / transcripts, explore their protein-coding capacities and predict the putative role of the METTL isoforms. Demultiplexing of the hybrid-seq barcoded datasets unraveled the expression patterns of the newly identified mRNAs in major malignancies as well as in non-malignant cells, providing a deeper understanding of the methylation pathways. Open reading frame query revealed novel METTL3/14 isoforms, broadening our perspective for the structural diversity within METTL family. Our findings offer significant insights into the intricate transcriptional landscape of /, shedding light on the regulatory mechanisms underlying methylation in mRNAs.

摘要

N6-甲基腺苷(m6A)是一种普遍存在的 mRNA 修饰物,其动态调控由甲基转移酶完成,包括 METTL3 和 METTL14。在本研究中,我们采用定制的混合测序方法鉴定新的 / 转录本,探索其编码蛋白的能力,并预测 METTL 同工型的潜在作用。混合测序条形码数据集的解复用揭示了新鉴定的 mRNA 在主要恶性肿瘤以及非恶性细胞中的表达模式,深入了解了甲基化途径。开放阅读框查询揭示了新的 METTL3/14 同工型,拓宽了我们对 METTL 家族结构多样性的认识。我们的研究结果为 / 的复杂转录图谱提供了重要的见解,揭示了 mRNA 中甲基化的调控机制。