Genome ResearchGenomicsPeer-reviewed journal article
Improved Prokaryotic Gene Prediction Yields Insights into Transcription and Translation Mechanisms on Whole Genome Scale
Alexandre LomsadzeiD, Karl Gemayel, Shiyuyun Tang, Mark Yu. BorodovskyiD
Abstract
In a conventional view of the prokaryotic genome organization promoters precede operons and RBS sites with Shine-Dalgarno consensus precede genes. However, recent experimental research suggesting a more diverse view motivated us to develop an algorithm with improved gene-finding accuracy. We describe GeneMarkS-2, an ab initio algorithm that uses a model derived by self-training for finding species-specific (native) genes, along with an array of pre-computed heuristic models designed to identify harder-to-detect genes (likely horizontally transferred). Importantly, we designed GeneMarkS-2 to identify several types of distinct sequence patterns (signals) involved in gene expression control, among them the patterns characteristic for leaderless transcription as well as non-canonical RBS patterns. To assess the accuracy of GeneMarkS-2 we used genes validated by COG annotation, proteomics experiments, and N-terminal protein sequencing. We observed that GeneMarkS-2 performed better on average in all accuracy measures when compared with the current state-of-the-art gene prediction tools. Furthermore, the screening of [~]5,000 representative prokaryotic genomes made by GeneMarkS-2 predicted frequent leaderless transcription in both archaea and bacteria. We also observed that the RBS sites in some species with leadered transcription did not necessarily exhibit the Shine-Dalgarno consensus. The modeling of different types of sequence motifs regulating gene expression prompted a division of prokaryotic genomes into five categories with distinct sequence patterns around the gene starts.\n\n[Supplemental material is available for this article].
- organism: bacteria (other)
- assay: whole-genome sequencing
- research focus: gene regulatory network inference
- research focus: variant calling
- research focus: benchmarking
- research focus: database / resource
- approach: statistical model
- Citations
- 235
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