Inferring the gene network underlying the branching of tomato inflorescence.

The architecture of tomato inflorescence strongly affects flower production and subsequent crop yield. To understand the genetic activities involved, insight into the underlying network of genes that initiate and control the sympodial growth in the tomato is essential. In this paper, we show how the...

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Main Authors: Laura Astola, Hans Stigter, Aalt D J van Dijk, Raymond van Daelen, Jaap Molenaar
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2014-01-01
Series:PLoS ONE
Online Access:https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/24699171/?tool=EBI
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spelling doaj-6a697374ad30486289d78a638b18e9cf2021-03-03T20:14:55ZengPublic Library of Science (PLoS)PLoS ONE1932-62032014-01-0194e8968910.1371/journal.pone.0089689Inferring the gene network underlying the branching of tomato inflorescence.Laura AstolaHans StigterAalt D J van DijkRaymond van DaelenJaap MolenaarThe architecture of tomato inflorescence strongly affects flower production and subsequent crop yield. To understand the genetic activities involved, insight into the underlying network of genes that initiate and control the sympodial growth in the tomato is essential. In this paper, we show how the structure of this network can be derived from available data of the expressions of the involved genes. Our approach starts from employing biological expert knowledge to select the most probable gene candidates behind branching behavior. To find how these genes interact, we develop a stepwise procedure for computational inference of the network structure. Our data consists of expression levels from primary shoot meristems, measured at different developmental stages on three different genotypes of tomato. With the network inferred by our algorithm, we can explain the dynamics corresponding to all three genotypes simultaneously, despite their apparent dissimilarities. We also correctly predict the chronological order of expression peaks for the main hubs in the network. Based on the inferred network, using optimal experimental design criteria, we are able to suggest an informative set of experiments for further investigation of the mechanisms underlying branching behavior.https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/24699171/?tool=EBI
collection DOAJ
language English
format Article
sources DOAJ
author Laura Astola
Hans Stigter
Aalt D J van Dijk
Raymond van Daelen
Jaap Molenaar
spellingShingle Laura Astola
Hans Stigter
Aalt D J van Dijk
Raymond van Daelen
Jaap Molenaar
Inferring the gene network underlying the branching of tomato inflorescence.
PLoS ONE
author_facet Laura Astola
Hans Stigter
Aalt D J van Dijk
Raymond van Daelen
Jaap Molenaar
author_sort Laura Astola
title Inferring the gene network underlying the branching of tomato inflorescence.
title_short Inferring the gene network underlying the branching of tomato inflorescence.
title_full Inferring the gene network underlying the branching of tomato inflorescence.
title_fullStr Inferring the gene network underlying the branching of tomato inflorescence.
title_full_unstemmed Inferring the gene network underlying the branching of tomato inflorescence.
title_sort inferring the gene network underlying the branching of tomato inflorescence.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2014-01-01
description The architecture of tomato inflorescence strongly affects flower production and subsequent crop yield. To understand the genetic activities involved, insight into the underlying network of genes that initiate and control the sympodial growth in the tomato is essential. In this paper, we show how the structure of this network can be derived from available data of the expressions of the involved genes. Our approach starts from employing biological expert knowledge to select the most probable gene candidates behind branching behavior. To find how these genes interact, we develop a stepwise procedure for computational inference of the network structure. Our data consists of expression levels from primary shoot meristems, measured at different developmental stages on three different genotypes of tomato. With the network inferred by our algorithm, we can explain the dynamics corresponding to all three genotypes simultaneously, despite their apparent dissimilarities. We also correctly predict the chronological order of expression peaks for the main hubs in the network. Based on the inferred network, using optimal experimental design criteria, we are able to suggest an informative set of experiments for further investigation of the mechanisms underlying branching behavior.
url https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/24699171/?tool=EBI
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AT hansstigter inferringthegenenetworkunderlyingthebranchingoftomatoinflorescence
AT aaltdjvandijk inferringthegenenetworkunderlyingthebranchingoftomatoinflorescence
AT raymondvandaelen inferringthegenenetworkunderlyingthebranchingoftomatoinflorescence
AT jaapmolenaar inferringthegenenetworkunderlyingthebranchingoftomatoinflorescence
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