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Identification of Splice Variants and Isoforms in Transcriptomics and Proteomics
被引:17
|作者:
Su, Taojunfeng
[1
]
Hollas, Michael A. R.
[2
]
Fellers, Ryan T.
[2
]
Kelleher, Neil L.
[1
,2
,3
]
机构:
[1] Northwestern Univ, Dept Mol Biosci, Evanston, IL 60208 USA
[2] Northwestern Univ, Prote Ctr Excellence, Evanston, IL USA
[3] Northwestern Univ, Dept Chem, Evanston, IL USA
来源:
ANNUAL REVIEW OF BIOMEDICAL DATA SCIENCE
|
2023年
/
6卷
基金:
美国国家卫生研究院;
关键词:
alternative splicing;
short-read RNA-seq;
long-read RNA-seq;
top-down mass spectrometry;
protein isoform;
proteoform;
TOP-DOWN PROTEOMICS;
PROTEIN IDENTIFICATION;
MESSENGER-RNA;
INTRON RETENTION;
PROTEOFORM ATLAS;
READ ALIGNMENT;
SOFTWARE TOOL;
BOTTOM-UP;
QUANTIFICATION;
ASSOCIATION;
D O I:
10.1146/annurev-biodatasci-020722-044021
中图分类号:
Q [生物科学];
学科分类号:
07 ;
0710 ;
09 ;
摘要:
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.
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页码:357 / 376
页数:20
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