Abstract

BackgroundMost organisms cannot be cultivated, as they live in unique ecological conditions that cannot be mimicked in the lab. Understanding the functionality of those organisms’ genes and their interactions by performing large-scale measurements of transcription levels, protein-protein interactions or metabolism, is extremely difficult and, in some cases, impossible. Thus, efficient algorithms for deciphering genome functionality based only on the genomic sequences with no other experimental measurements are needed.ResultsIn this study, we describe a novel algorithm that infers gene networks that we name Common Substring Network (CSN). The algorithm enables inferring novel regulatory relations among genes based only on the genomic sequence of a given organism and partial homolog/ortholog-based functional annotation. It can specifically infer the functional annotation of genes with unknown homology.This approach is based on the assumption that related genes, not necessarily homologs, tend to share sub-sequences, which may be related to common regulatory mechanisms, similar functionality of encoded proteins, common evolutionary history, and more.We demonstrate that CSNs, which are based on S. cerevisiae and E. coli genomes, have properties similar to ‘traditional’ biological networks inferred from experiments. Highly expressed genes tend to have higher degree nodes in the CSN, genes with similar protein functionality tend to be closer, and the CSN graph exhibits a power-law degree distribution. Also, we show how the CSN can be used for predicting gene interactions and functions.ConclusionsThe reported results suggest that ‘silent’ code inside the transcript can help to predict central features of biological networks and gene function. This approach can help researchers to understand the genome of novel microorganisms, analyze metagenomic data, and can help to decipher new gene functions.AvailabilityOur MATLAB implementation of CSN is available at https://www.cs.tau.ac.il/~tamirtul/CSN-Autogen

Highlights

  • Most organisms cannot be cultivated, as they live in unique ecological conditions that cannot be mimicked in the lab

  • By implementing our algorithm on all S. cerevisiae and E. coli genes, and generating the complete genomic map, which is based solely on its Deoxyribonucleic Acid [DNA] sequence, we demonstrate that our approach gives meaningful predictions

  • Developing a comprehensive sequence-based network - the Common Substring Network (CSN) The CSN network is constructed by calculating the resemblance scores between all pairs of genes based on their nucleotide sequences (Fig. 1a, box (i)

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Summary

Introduction

Most organisms cannot be cultivated, as they live in unique ecological conditions that cannot be mimicked in the lab. In a small number of well-studied model organisms, various experimental tools such as gene expression measurements [18, 19], protein-protein interactions [PPI] measurements [20,21,22], genetic interaction measurements [23,24,25], and others, have been combined to decipher the functionality of genes and the way they work together. Even for those model organisms there are still many open questions regarding the exact functionality of genes [16, 26,27,28], and for most organisms, these data is still limited The conventional approach is based on the homology of proteins, but it cannot be implemented for deciphering the functionality of novel genes with no well-studied homologs

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