Systematically Learning of Internal Ribosome Entry Site and Prediction by Machine Learning

Junhui Wang, Purdue University

Abstract

Internal ribosome entry sites (IRES) are segments of the mRNA found in untranslated regions, which can recruit the ribosome and initiate translation independently of the more widely used 5’ cap dependent translation initiation mechanism. IRES play an important role in conditions where has been 5’ cap dependent translation initiation blocked or repressed. They have been found to play important roles in viral infection, cellular apoptosis, and response to other external stimuli. It has been suggested that about 10% of mRNAs, both viral and cellular, can utilize IRES. But due to the limitations of IRES bicistronic assay, which is a gold standard for identifying IRES, relatively few IRES have been definitively described and functionally validated compared to the potential overall population. Viral and cellular IRES may be mechanistically different, but this is difficult to analyze because the mechanistic differences are still not very clearly defined. Identifying additional IRES is an important step towards better understanding IRES mechanisms. Development of a new bioinformatics tool that can accurately predict IRES from sequence would be a significant step forward in identifying IRES-based regulation, and in elucidating IRES mechanism. This dissertation systematically studies the features which can distinguish IRES from nonIRES sequences. Sequence features such as kmer words, and structural features such as predicted MFE of folding, QMFE, and sequence/structure triplets are evaluated as possible discriminative features. Those potential features incorporated into an IRES classifier based on XGBboost, a machine learning model, to classify novel sequences as belong to IRES or nonIRES groups. The XGBoost model performs better than previous predictors, with higher accuracy and lower computational time. The number of features in the model has been greatly reduced, compared to previous predictors, by adding global kmer and structural features. The trained XGBoost model has been implemented as the first high-throughput bioinformatics tool for IRES prediction, IRESpy. This website provides a public tool for all IRES researchers and can be used in other genomics applications such as gene annotation and analysis of differential gene expression.

Degree

Ph.D.

Advisors

Gribskov, Purdue University.

Subject Area

Genetics|Virology

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