Subcellular Spatial Transcriptomes: Emerging Frontier for Understanding Gene Regulation.

Furqan M Fazal, Howard Y Chang
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Abstract

RNAs are trafficked and localized with exquisite precision inside the cell. Studies of candidate messenger RNAs have shown the vital importance of RNA subcellular location in development and cellular function. New sequencing- and imaging-based methods are providing complementary insights into subcellular localization of RNAs transcriptome-wide. APEX-seq and ribosome profiling as well as proximity-labeling approaches have revealed thousands of transcript isoforms are localized to distinct cytotopic locations, including locations that defy biochemical fractionation and hence were missed by prior studies. Sequences in the 3' and 5' untranslated regions (UTRs) serve as "zip codes" to direct transcripts to particular locales, and it is clear that intronic and retrotransposable sequences within transcripts have been co-opted by cells to control localization. Molecular motors, nuclear-to-cytosol RNA export, liquid-liquid phase separation, RNA modifications, and RNA structure dynamically shape the subcellular transcriptome. Location-based RNA regulation continues to pose new mysteries for the field, yet promises to reveal insights into fundamental cell biology and disease mechanisms.

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亚细胞空间转录组:理解基因调控的新兴前沿。
rna在细胞内被精确地运输和定位。对候选信使RNA的研究表明,RNA亚细胞定位在发育和细胞功能中至关重要。新的基于测序和成像的方法为rna转录组的亚细胞定位提供了补充的见解。APEX-seq和核糖体分析以及接近性标记方法已经揭示了数千种转录异构体定位于不同的细胞位位置,包括不符合生化分离的位置,因此被先前的研究遗漏。3'和5'非翻译区(utr)中的序列就像“邮政编码”一样,将转录本引导到特定的区域,很明显,转录本中的内含子序列和反转录转座序列已经被细胞选择来控制定位。分子马达,核-胞质RNA输出,液-液相分离,RNA修饰和RNA结构动态塑造亚细胞转录组。基于位置的RNA调控继续为该领域带来新的谜团,但有望揭示基本细胞生物学和疾病机制的见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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