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dc.contributor.authorGjuvsland, Arne Bjørke
dc.contributor.authorWang, Yunpeng
dc.contributor.authorPlahte, Erik
dc.contributor.authorOmholt, Stig W
dc.date.accessioned2017-12-08T13:18:41Z
dc.date.available2017-12-08T13:18:41Z
dc.date.created2014-01-06T09:50:35Z
dc.date.issued2013
dc.identifier.citationFrontiers in Genetics. 2013, 4 .nb_NO
dc.identifier.issn1664-8021
dc.identifier.urihttp://hdl.handle.net/11250/2469811
dc.description.abstractIt was recently shown that monotone gene action, i.e., order-preservation between allele content and corresponding genotypic values in the mapping from genotypes to phenotypes, is a prerequisite for achieving a predictable parent-offspring relationship across the whole allele frequency spectrum. Here we test the consequential prediction that the design principles underlying gene regulatory networks are likely to generate highly monotone genotype-phenotype maps. To this end we present two measures of the monotonicity of a genotype-phenotype map, one based on allele substitution effects, and the other based on isotonic regression. We apply these measures to genotype-phenotype maps emerging from simulations of 1881 different 3-gene regulatory networks. We confirm that in general, genotype-phenotype maps are indeed highly monotonic across network types. However, regulatory motifs involving incoherent feedforward or positive feedback, as well as pleiotropy in the mapping between genotypes and gene regulatory parameters, are clearly predisposed for generating non-monotonicity. We present analytical results confirming these deep connections between molecular regulatory architecture and monotonicity properties of the genotype-phenotype map. These connections seem to be beyond reach by the classical distinction between additive and non-additive gene action.nb_NO
dc.language.isoengnb_NO
dc.publisherFrontiers Medianb_NO
dc.rightsNavngivelse 4.0 Internasjonal*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/deed.no*
dc.titleMonotonicity is a key feature of genotype-phenotype mapsnb_NO
dc.typeJournal articlenb_NO
dc.typePeer reviewednb_NO
dc.description.versionpublishedVersionnb_NO
dc.source.pagenumber15nb_NO
dc.source.volume4nb_NO
dc.source.journalFrontiers in Geneticsnb_NO
dc.identifier.doi10.3389/fgene.2013.00216
dc.identifier.cristin1083963
dc.relation.projectNorges forskningsråd: 178901nb_NO
dc.relation.projectNotur/NorStore: NN4653Knb_NO
dc.description.localcode© 2013 Gjuvsland, Wang, Plahte and Omholt. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). This Document is Protected by copyright and was first published by Frontiers. All rights reserved. it is reproduced with permission.nb_NO
cristin.unitcode194,66,10,0
cristin.unitnameInstitutt for biologi
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode1


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