Evidence map›Paper›PMID 21059250›Full record

ArticleAlgorithms for molecular biology : AMB2010

Estimating the evidence of selection and the reliability of inference in unigenic evolution.

Andrew D Fernandes, Benjamin P Kleinstiver, David R Edgell, Lindi M Wahl, Gregory B Gloor

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Article in Algorithms for molecular biology : AMB, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 authors.

Andrew D FernandesDepartment of Biochemistry, The University of Western Ontario, N6A 5C1 Canada. andrew@fernandes.org.
Benjamin P Kleinstiver
David R Edgell
Lindi M Wahl
Gregory B Gloor

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundUnigenic evolution is a large-scale mutagenesis experiment used to identify residues that are potentially important for protein function. Both currently-used methods for the analysis of unigenic evolution data analyze 'windows' of contiguous sites, a strategy that increases statistical power but incorrectly assumes that functionally-critical sites are contiguous. In addition, both methods require the questionable assumption of asymptotically-large sample size due to the presumption of approximate normality.

resultsWe develop a novel approach, termed the Evidence of Selection (EoS), removing the assumption that functionally important sites are adjacent in sequence and and explicitly modelling the effects of limited sample-size. Precise statistical derivations show that the EoS score can be easily interpreted as an expected log-odds-ratio between two competing hypotheses, namely, the hypothetical presence or absence of functional selection for a given site. Using the EoS score, we then develop selection criteria by which functionally-important yet non-adjacent sites can be identified. An approximate power analysis is also developed to estimate the reliability of inference given the data. We validate and demonstrate the the practical utility of our method by analysis of the homing endonuclease I-Bmol, comparing our predictions with the results of existing methods.

conclusionsOur method is able to assess both the evidence of selection at individual amino acid sites and estimate the reliability of those inferences. Experimental validation with I-Bmol proves its utility to identify functionally-important residues of poorly characterized proteins, demonstrating increased sensitivity over previous methods without loss of specificity. With the ability to guide the selection of precise experimental mutagenesis conditions, our method helps make unigenic analysis a more broadly applicable technique with which to probe protein function. AVAILABILITY: Software to compute, plot, and summarize EoS data is available as an open-source package called 'unigenic' for the 'R' programming language at http://www.fernandes.org/txp/article/13/an-analytical-framework-for-unigenic-evolution.

Identifiers

PMID21059250
PMCPMC2994857

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