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利用当前组学技术揭示可变剪接对蛋白质组的影响。

Uncovering the impacts of alternative splicing on the proteome with current omics techniques.

机构信息

The John Curtin School of Medical Research, Australian National University, Canberra, Australian Capital Territory, Australia.

EMBL Australia Partner Laboratory Network and the Australian National University, Canberra, Australian Capital Territory, Australia.

出版信息

Wiley Interdiscip Rev RNA. 2022 Jul;13(4):e1707. doi: 10.1002/wrna.1707. Epub 2022 Jan 3.

Abstract

The high-throughput sequencing of cellular RNAs has underscored a broad effect of isoform diversification through alternative splicing on the transcriptome. Moreover, the differential production of transcript isoforms from gene loci has been recognized as a critical mechanism in cell differentiation, organismal development, and disease. Yet, the extent of the impact of alternative splicing on protein production and cellular function remains a matter of debate. Multiple experimental and computational approaches have been developed in recent years to address this question. These studies have unveiled how molecular changes at different steps in the RNA processing pathway can lead to differences in protein production and have functional effects. New and emerging experimental technologies open exciting new opportunities to develop new methods to fully establish the connection between messenger RNA expression and protein production and to further investigate how RNA variation impacts the proteome and cell function. This article is categorized under: RNA Processing > Splicing Regulation/Alternative Splicing Translation > Regulation RNA Evolution and Genomics > Computational Analyses of RNA.

摘要

细胞 RNA 的高通量测序强调了通过选择性剪接对转录组产生广泛的异构体多样化效应。此外,从基因座产生转录体异构体已被认为是细胞分化、生物发育和疾病的关键机制。然而,选择性剪接对蛋白质产生和细胞功能的影响程度仍然存在争议。近年来已经开发了多种实验和计算方法来解决这个问题。这些研究揭示了 RNA 处理途径中不同步骤的分子变化如何导致蛋白质产生的差异,并具有功能影响。新出现的实验技术为开发新方法提供了令人兴奋的新机会,这些方法可以充分建立信使 RNA 表达与蛋白质产生之间的联系,并进一步研究 RNA 变异如何影响蛋白质组和细胞功能。本文属于以下类别:RNA 加工 > 剪接调控/选择性剪接 翻译 > 调控 RNA 进化和基因组学 > 对 RNA 的计算分析。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d66/9542554/54c7a971bf5d/WRNA-13-e1707-g004.jpg

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