Structural analysis of genomic and proteomic signatures reveal dynamic expression of intrinsically disordered regions in breast cancer

被引:0
|
作者
Zatorski, Nicole [1 ]
Sun, Yifei [1 ]
Elmas, Abdulkadir [2 ]
Dallago, Christian [3 ,4 ]
Karl, Timothy [4 ]
Stein, David [1 ]
Rost, Burkhard [4 ]
Huang, Kuan-Lin [2 ]
Walsh, Martin [1 ]
Schlessinger, Avner [1 ]
机构
[1] Icahn Sch Med Mt Sinai, Dept Pharmacol Sci, One Gustave Levey Pl, New York, NY 10029 USA
[2] Icahn Sch Med Mt Sinai, Dept Genet & Genom Sci, One Gustave Levey Pl, New York, NY 10029 USA
[3] NVIDIA GmbH, Einsteinstr 172, D-81677 Munich, Germany
[4] Tech Univ Munich TUM, Fac Informat Bioinformat & Computat Biol, D-85748 Garching, Germany
基金
美国国家卫生研究院;
关键词
features; Feature selection trained; tissue; regions; repurposing; PROTEIN FUNCTION; CONNECTIVITY MAP; LOCALIZATION; PREDICTION; DOMAINS;
D O I
10.1016/j.isci.2024.110640
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Structural features of proteins capture underlying information about protein evolution and function, which enhances the analysis of proteomic and transcriptomic data. Here, we develop Structural Analysis of Gene and protein Expression Signatures (SAGES), a method that describes expression data using features calculated from sequence-based prediction methods and 3D structural models. We used SAGES, along with machine learning, to characterize tissues from healthy individuals and those with breast cancer. We analyzed gene expression data from 23 breast cancer patients and genetic mutation data from the Catalog of Somatic Mutations In Cancer database as well as 17 breast tumor protein expression profiles. We identified prominent expression of intrinsically disordered regions in breast cancer proteins as well as relationships between drug perturbation signatures and breast cancer disease signatures. Our results suggest that SAGES is generally applicable to describe diverse biological phenomena including disease states and drug effects.
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页数:17
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