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转录组学和蛋白质组学中的剪接变体和同工型鉴定。

Identification of Splice Variants and Isoforms in Transcriptomics and Proteomics.

机构信息

Department of Molecular Biosciences, Northwestern University, Evanston, Illinois, USA; email:

Proteomics Center of Excellence, Northwestern University, Evanston, Illinois, USA.

出版信息

Annu Rev Biomed Data Sci. 2023 Aug 10;6:357-376. doi: 10.1146/annurev-biodatasci-020722-044021.

Abstract

Alternative splicing is pivotal to the regulation of gene expression and protein diversity in eukaryotic cells. The detection of alternative splicing events requires specific omics technologies. Although short-read RNA sequencing has successfully supported a plethora of investigations on alternative splicing, the emerging technologies of long-read RNA sequencing and top-down mass spectrometry open new opportunities to identify alternative splicing and protein isoforms with less ambiguity. Here, we summarize improvements in short-read RNA sequencing for alternative splicing analysis, including percent splicing index estimation and differential analysis. We also review the computational methods used in top-down proteomics analysis regarding proteoform identification, including the construction of databases of protein isoforms and statistical analyses of search results. While many improvements in sequencing and computational methods will result from emerging technologies, there should be future endeavors to increase the effectiveness, integration, and proteome coverage of alternative splicing events.

摘要

可变剪接对于真核细胞中基因表达和蛋白质多样性的调控至关重要。可变剪接事件的检测需要特定的组学技术。尽管短读长 RNA 测序已成功支持了大量关于可变剪接的研究,但新兴的长读长 RNA 测序和自上而下的质谱技术为识别可变剪接和具有较少歧义的蛋白质异构体提供了新的机会。在这里,我们总结了短读长 RNA 测序在可变剪接分析方面的改进,包括外显子百分比估计和差异分析。我们还回顾了自上而下的蛋白质组学分析中用于蛋白质异构体鉴定的计算方法,包括蛋白质异构体数据库的构建和搜索结果的统计分析。虽然新兴技术将带来测序和计算方法的许多改进,但未来仍应努力提高可变剪接事件的有效性、整合性和蛋白质组覆盖范围。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4498/10840079/b47e5c0b121b/nihms-1962383-f0001.jpg

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