Predicting lncRNA-Protein Interaction With Weighted Graph-Regularized Matrix Factorization

被引:2
|
作者
Sun, Xibo [1 ]
Cheng, Leiming [2 ]
Liu, Jinyang [3 ,4 ]
Xie, Cuinan [3 ,4 ]
Yang, Jiasheng [5 ]
Li, Fu [6 ]
机构
[1] Yidu Cent Hosp Weifang, Weifang, Peoples R China
[2] Huaibei Kuanggong Zong Yiyuan, Huaibei, Peoples R China
[3] Geneis Beijing Co Ltd, Beijing, Peoples R China
[4] Qingdao Geneis Inst Big Data Min & Precis Med, Qingdao, Peoples R China
[5] Changsha Med Univ, Academician Workstn, Changsha, Peoples R China
[6] Hainan Med Univ, Dept Thorac Surg, Affiliated Hosp 2, Haikou, Hainan, Peoples R China
关键词
lncRNA-protein interaction; weighted graph-regularized matrix factorization; lncRNA similarity; protein similarity; SFPQ; SNHG3; PRPF31; POOR-PROGNOSIS;
D O I
10.3389/fgene.2021.690096
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Long non-coding RNAs (lncRNAs) are widely concerned because of their close associations with many key biological activities. Though precise functions of most lncRNAs are unknown, research works show that lncRNAs usually exert biological function by interacting with the corresponding proteins. The experimental validation of interactions between lncRNAs and proteins is costly and time-consuming. In this study, we developed a weighted graph-regularized matrix factorization (LPI-WGRMF) method to find unobserved lncRNA-protein interactions (LPIs) based on lncRNA similarity matrix, protein similarity matrix, and known LPIs. We compared our proposed LPI-WGRMF method with five classical LPI prediction methods, that is, LPBNI, LPI-IBNRA, LPIHN, RWR, and collaborative filtering (CF). The results demonstrate that the LPI-WGRMF method can produce high-accuracy performance, obtaining an AUC score of 0.9012 and AUPR of 0.7324. The case study showed that SFPQ, SNHG3, and PRPF31 may associate with Q9NUL5, Q9NUL5, and Q9UKV8 with the highest linking probabilities and need to further experimental validation.
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页数:8
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