Predicting Yeast Synthetic Lethal Genetic Interactions using Short Polypeptide Clusters

被引:0
|
作者
Li, Bo [1 ]
Zhang, Yuehua [1 ]
Srimani, Pradip K. [1 ]
Luo, Feng [1 ]
机构
[1] Clemson Univ, Sch Comp, Clemson, SC 29634 USA
关键词
synthetic lethal; polypeptide; genetic interaction; GENOME; PRINCIPLES; NETWORKS; DELETION;
D O I
10.1109/BIBM.2011.21
中图分类号
TP39 [计算机的应用];
学科分类号
081203 ; 0835 ;
摘要
Synthetic lethal genetic interactions (SLGI) among proteins have been widely used to define functional relationships between proteins and pathways. However, the molecular mechanism of synthetic lethal genetic interactions is still unclear. In this study we used the clusters of short polypeptide sequences, which are typically shorter than the classically defined protein domains, to characterize the functionalities of proteins. We developed a framework to identify significant short polypeptide clusters from yeast protein sequences. We then used these short polypeptide clusters as features to predict SLGIs. Both cross-validation and evaluation on experimental data sets showed that the short polypeptide clusters based approach is superior to the previous protein domain based approach. The short polypeptide clusters based approach provides significantly higher coverage for predicting SLGIs. Moreover, the short polypeptide clusters based approach produced less false positive predictions.
引用
收藏
页码:185 / 190
页数:6
相关论文
共 50 条
  • [21] Inferring synthetic lethal interactions from mutual exclusivity of genetic events in cancer
    Sriganesh Srihari
    Jitin Singla
    Limsoon Wong
    Mark A. Ragan
    Biology Direct, 10
  • [22] Chemical-genetic Screens for Synthetic Lethal Interactions in Pancreatic Ductal Adenocarcinomas
    Caffa, I.
    Soncini, D.
    Ansaldi, F.
    Provenzani, A.
    Castiglioni, I.
    Patrone, F.
    Ballestrero, A.
    Nencioni, A.
    EUROPEAN JOURNAL OF CANCER, 2012, 48 : 52 - 52
  • [23] Chemical-genetic Screenings for Synthetic-lethal Interactions in Breast Cancer
    Soncini, D.
    Caffa, I.
    Zoppoli, G.
    Petrone, F.
    Ballestrero, A.
    Nencioni, A.
    EUROPEAN JOURNAL OF CANCER, 2011, 47 : S151 - S151
  • [24] Combining proteomics and genetic screens to identify KRAS synthetic lethal interactions.
    Sheth, S.
    Cook, Danielle R.
    Strasser, Samantha D.
    Martin, Timothy D.
    Menon, Sneha
    Popow, Olesja
    Paulo, Joao A.
    Elledge, Steve J.
    Haigis, Kevin M.
    MOLECULAR CANCER RESEARCH, 2020, 18 (05) : 58 - 58
  • [25] Synthetic lethal interactions in yeast reveal functional roles of J protein co-chaperones
    Gillies, Anne T.
    Taylor, Rebecca
    Gestwicki, Jason E.
    MOLECULAR BIOSYSTEMS, 2012, 8 (11) : 2901 - 2908
  • [26] Revealing hidden relationships among yeast genes involved in chromosome segregation using systematic synthetic lethal and synthetic dosage lethal screens
    Baetz, Kristin
    Measday, Vivien
    Andrews, Brenda
    CELL CYCLE, 2006, 5 (06) : 592 - 595
  • [27] STUDIES OF SYNTHETIC POLYPEPTIDE-WATER INTERACTIONS USING MONOLAYER TECHNIQUES
    MALCOLM, BR
    JOURNAL OF POLYMER SCIENCE PART C-POLYMER SYMPOSIUM, 1971, (34): : 87 - &
  • [28] Genetic and environmental context dependency confounds identification of KRAS synthetic lethal interactions.
    Ku, Angel
    Hu, Hsien-Ming
    Kongara, Sameera
    Zhao, Xin
    Di, Wu
    McCormick, Frank
    Balmain, Allan
    Bandyopadhyay, Sourav
    MOLECULAR CANCER RESEARCH, 2020, 18 (05) : 72 - 72
  • [29] Global investigation of protein-protein interactions in yeast Saccharomyces cerevisiae using re-occurring short polypeptide sequences
    Pitre, S.
    North, C.
    Alamgir, M.
    Jessulat, M.
    Chan, A.
    Luo, X.
    Green, J. R.
    Dumontier, M.
    Dehne, F.
    Golshani, A.
    NUCLEIC ACIDS RESEARCH, 2008, 36 (13) : 4286 - 4294
  • [30] STUDIES OF SYNTHETIC POLYPEPTIDE-WATER INTERACTIONS USING MONOLAYER TECHNIQUES - COLL
    MALCOLM, BR
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 1970, (SEP): : 70 - &