Suppr超能文献

用于解决癌症中异常mRNA翻译的下一代测序技术。

Next generation sequencing technologies to address aberrant mRNA translation in cancer.

作者信息

Román Ángel-Carlos, Benítez Dixan A, Díaz-Pizarro Alba, Del Valle-Del Pino Nuria, Olivera-Gómez Marcos, Cumplido-Laso Guadalupe, Carvajal-González Jose M, Mulero-Navarro Sonia

机构信息

Departamento de Bioquímica y Biología Molecular y Genética, Universidad de Extremadura. Avda. de Elvas s/n, 06071 Badajoz, Spain.

出版信息

NAR Cancer. 2024 May 15;6(2):zcae024. doi: 10.1093/narcan/zcae024. eCollection 2024 Jun.

Abstract

In this review, we explore the transformative impact of next generation sequencing technologies in the realm of translatomics (the study of how translational machinery acts on a genome-wide scale). Despite the expectation of a direct correlation between mRNA and protein content, the complex regulatory mechanisms that affect this relationship remark the limitations of standard RNA-seq approaches. Then, the review characterizes crucial techniques such as polysome profiling, ribo-seq, trap-seq, proximity-specific ribosome profiling, rnc-seq, tcp-seq, qti-seq and scRibo-seq. All these methods are summarized within the context of cancer research, shedding light on their applications in deciphering aberrant translation in cancer cells. In addition, we encompass databases and bioinformatic tools essential for researchers that want to address translatome analysis in the context of cancer biology.

摘要

在本综述中,我们探讨了新一代测序技术在翻译组学领域(即研究翻译机制如何在全基因组范围内发挥作用)所带来的变革性影响。尽管人们期望mRNA与蛋白质含量之间存在直接关联,但影响这种关系的复杂调控机制凸显了标准RNA测序方法的局限性。随后,该综述对多核糖体谱分析、核糖体测序、trap-seq、邻近特异性核糖体谱分析、rnc-seq、tcp-seq、qti-seq和单细胞核糖体测序等关键技术进行了描述。所有这些方法都在癌症研究的背景下进行了总结,阐明了它们在解读癌细胞异常翻译方面的应用。此外,我们还涵盖了对于想要在癌症生物学背景下进行翻译组分析的研究人员至关重要的数据库和生物信息学工具。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f4b/11094761/7a8f55d0b611/zcae024figgra1.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验