A probabilistic model for the evolution of RNA structure

<p>Abstract</p> <p>Background</p> <p>For the purposes of finding and aligning noncoding RNA gene- and <it>cis</it>-regulatory elements in multiple-genome datasets, it is useful to be able to derive multi-sequence stochastic grammars (and hence multiple align...

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Main Author: Holmes Ian
Format: Article
Language:English
Published: BMC 2004-10-01
Series:BMC Bioinformatics
Online Access:http://www.biomedcentral.com/1471-2105/5/166
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spelling doaj-286cc0ac0df846bfb6ab554566e0f8cb2020-11-25T01:05:49ZengBMCBMC Bioinformatics1471-21052004-10-015116610.1186/1471-2105-5-166A probabilistic model for the evolution of RNA structureHolmes Ian<p>Abstract</p> <p>Background</p> <p>For the purposes of finding and aligning noncoding RNA gene- and <it>cis</it>-regulatory elements in multiple-genome datasets, it is useful to be able to derive multi-sequence stochastic grammars (and hence multiple alignment algorithms) systematically, starting from hypotheses about the various kinds of random mutation event and their rates.</p> <p>Results</p> <p>Here, we consider a highly simplified evolutionary model for RNA, called "The TKF91 Structure Tree" (following Thorne, Kishino and Felsenstein's 1991 model of sequence evolution with indels), which we have implemented for pairwise alignment as proof of principle for such an approach. The model, its strengths and its weaknesses are discussed with reference to four examples of functional ncRNA sequences: a riboswitch (guanine), a zipcode (nanos), a splicing factor (U4) and a ribozyme (RNase P). As shown by our visualisations of posterior probability matrices, the selected examples illustrate three different signatures of natural selection that are highly characteristic of ncRNA: (i) co-ordinated basepair substitutions, (ii) co-ordinated basepair indels and (iii) whole-stem indels.</p> <p>Conclusions</p> <p>Although all three types of mutation "event" are built into our model, events of type (i) and (ii) are found to be better modeled than events of type (iii). Nevertheless, we hypothesise from the model's performance on pairwise alignments that it would form an adequate basis for a prototype multiple alignment and genefinding tool.</p> http://www.biomedcentral.com/1471-2105/5/166
collection DOAJ
language English
format Article
sources DOAJ
author Holmes Ian
spellingShingle Holmes Ian
A probabilistic model for the evolution of RNA structure
BMC Bioinformatics
author_facet Holmes Ian
author_sort Holmes Ian
title A probabilistic model for the evolution of RNA structure
title_short A probabilistic model for the evolution of RNA structure
title_full A probabilistic model for the evolution of RNA structure
title_fullStr A probabilistic model for the evolution of RNA structure
title_full_unstemmed A probabilistic model for the evolution of RNA structure
title_sort probabilistic model for the evolution of rna structure
publisher BMC
series BMC Bioinformatics
issn 1471-2105
publishDate 2004-10-01
description <p>Abstract</p> <p>Background</p> <p>For the purposes of finding and aligning noncoding RNA gene- and <it>cis</it>-regulatory elements in multiple-genome datasets, it is useful to be able to derive multi-sequence stochastic grammars (and hence multiple alignment algorithms) systematically, starting from hypotheses about the various kinds of random mutation event and their rates.</p> <p>Results</p> <p>Here, we consider a highly simplified evolutionary model for RNA, called "The TKF91 Structure Tree" (following Thorne, Kishino and Felsenstein's 1991 model of sequence evolution with indels), which we have implemented for pairwise alignment as proof of principle for such an approach. The model, its strengths and its weaknesses are discussed with reference to four examples of functional ncRNA sequences: a riboswitch (guanine), a zipcode (nanos), a splicing factor (U4) and a ribozyme (RNase P). As shown by our visualisations of posterior probability matrices, the selected examples illustrate three different signatures of natural selection that are highly characteristic of ncRNA: (i) co-ordinated basepair substitutions, (ii) co-ordinated basepair indels and (iii) whole-stem indels.</p> <p>Conclusions</p> <p>Although all three types of mutation "event" are built into our model, events of type (i) and (ii) are found to be better modeled than events of type (iii). Nevertheless, we hypothesise from the model's performance on pairwise alignments that it would form an adequate basis for a prototype multiple alignment and genefinding tool.</p>
url http://www.biomedcentral.com/1471-2105/5/166
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