An analysis of single amino acid repeats as use case for application specific background models

Abstract

BackgroundSequence analysis aims to identify biologically relevant signals against a backdrop of functionally meaningless variation. Increasingly, it is recognized that the quality of the background model directly affects the performance of analyses. State-of-the-art approaches rely on classical sequence models that are adapted to the studied dataset. Although performing well in the analysis of globular protein domains, these models break down in regions of stronger compositional bias or low complexity. While these regions are typically filtered, there is increasing anecdotal evidence of functional roles. This motivates an exploration of more complex sequence models and application-specific approaches for the investigation of biased regions.ResultsTraditional Markov-chains and application-specific regression models are compared using the example of predicting runs of single amino acids, a particularly simple class of biased regions. Cross-fold validation experiments reveal that the alternative regression models capture the multi-variate trends well, despite their low dimensionality and in contrast even to higher-order Markov-predictors. We show how the significance of unusual observations can be computed for such empirical models. The power of a dedicated model in the detection of biologically interesting signals is then demonstrated in an analysis identifying the unexpected enrichment of contiguous leucine-repeats in signal-peptides. Considering different reference sets, we show how the question examined actually defines what constitutes the 'background'. Results can thus be highly sensitive to the choice of appropriate model training sets. Conversely, the choice of reference data determines the questions that can be investigated in an analysis.ConclusionsUsing a specific case of studying biased regions as an example, we have demonstrated that the construction of application-specific background models is both necessary and feasible in a challenging sequence analysis situation.

Deciphering Peptide-Protein Interactions via Composition-Based Prediction: A Case Study with Survivin/BIRC5

“…Over billions of years, organisms have leveraged fundamental physical principles, exemplified by signal peptides like nuclear localization signals with significant compositional biases 89 . Such peptides, despite low information content, hold substantial abstract signal value due to their unique enrichment in specific functional groups, as seen in the PKKKRKV segment found in the SV40 Large T-antigen.…”

Deciphering peptide-protein interactions via composition-based prediction: a case study with survivin/BIRC5

“…Over billions of years, organisms have leveraged fundamental physical principles, exemplified by signal peptides like nuclear localization signals with significant compositional biases [99]. Despite low information content, such peptides hold substantial abstract signal value due to their unique enrichment in specific functional groups, as seen in the PKKKRKV segment found in the SV40 Large T-antigen.…”