001     136030
005     20240423115935.0
024 7 _ |a 10.1371/journal.pcbi.1000569
|2 doi
024 7 _ |a pmid:19936059
|2 pmid
024 7 _ |a pmc:PMC2774268
|2 pmc
024 7 _ |a 1553-734X
|2 ISSN
024 7 _ |a 1553-7358
|2 ISSN
024 7 _ |a altmetric:4707274
|2 altmetric
037 _ _ |a DZNE-2020-02352
041 _ _ |a English
082 _ _ |a 610
100 1 _ |a Wittmann, Dominik M
|0 P:(DE-HGF)0
|b 0
245 _ _ |a Spatial analysis of expression patterns predicts genetic interactions at the mid-hindbrain boundary.
260 _ _ |a San Francisco, Calif.
|c 2009
|b Public Library of Science
264 _ 1 |3 online
|2 Crossref
|b Public Library of Science (PLoS)
|c 2009-11-20
336 7 _ |a article
|2 DRIVER
336 7 _ |a Output Types/Journal article
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336 7 _ |a Journal Article
|b journal
|m journal
|0 PUB:(DE-HGF)16
|s 1713863109_10934
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336 7 _ |a ARTICLE
|2 BibTeX
336 7 _ |a JOURNAL_ARTICLE
|2 ORCID
336 7 _ |a Journal Article
|0 0
|2 EndNote
520 _ _ |a The isthmic organizer mediating differentiation of mid- and hindbrain during vertebrate development is characterized by a well-defined pattern of locally restricted gene expression domains around the mid-hindbrain boundary (MHB). This pattern is established and maintained by a regulatory network between several transcription and secreted factors that is not yet understood in full detail. In this contribution we show that a Boolean analysis of the characteristic spatial gene expression patterns at the murine MHB reveals key regulatory interactions in this network. Our analysis employs techniques from computational logic for the minimization of Boolean functions. This approach allows us to predict also the interplay of the various regulatory interactions. In particular, we predict a maintaining, rather than inducing, effect of Fgf8 on Wnt1 expression, an issue that remained unclear from published data. Using mouse anterior neural plate/tube explant cultures, we provide experimental evidence that Fgf8 in fact only maintains but does not induce ectopic Wnt1 expression in these explants. In combination with previously validated interactions, this finding allows for the construction of a regulatory network between key transcription and secreted factors at the MHB. Analyses of Boolean, differential equation and reaction-diffusion models of this network confirm that it is indeed able to explain the stable maintenance of the MHB as well as time-courses of expression patterns both under wild-type and various knock-out conditions. In conclusion, we demonstrate that similar to temporal also spatial expression patterns can be used to gain information about the structure of regulatory networks. We show, in particular, that the spatial gene expression patterns around the MHB help us to understand the maintenance of this boundary on a systems level.
536 _ _ |a 342 - Disease Mechanisms and Model Systems (POF3-342)
|0 G:(DE-HGF)POF3-342
|c POF3-342
|f POF III
|x 0
542 _ _ |i 2009-11-20
|2 Crossref
|u http://creativecommons.org/licenses/by/4.0/
588 _ _ |a Dataset connected to CrossRef, PubMed,
650 _ 7 |a Fgf8 protein, mouse
|2 NLM Chemicals
650 _ 7 |a Wnt1 Protein
|2 NLM Chemicals
650 _ 7 |a Wnt1 protein, mouse
|2 NLM Chemicals
650 _ 7 |a Fibroblast Growth Factor 8
|0 148997-75-5
|2 NLM Chemicals
650 _ 2 |a Algorithms
|2 MeSH
650 _ 2 |a Animals
|2 MeSH
650 _ 2 |a Brain: embryology
|2 MeSH
650 _ 2 |a Brain: metabolism
|2 MeSH
650 _ 2 |a Brain Mapping: methods
|2 MeSH
650 _ 2 |a Computational Biology: methods
|2 MeSH
650 _ 2 |a Diffusion
|2 MeSH
650 _ 2 |a Fibroblast Growth Factor 8: genetics
|2 MeSH
650 _ 2 |a Gene Expression Profiling: methods
|2 MeSH
650 _ 2 |a Gene Expression Regulation, Developmental
|2 MeSH
650 _ 2 |a Mice
|2 MeSH
650 _ 2 |a Mice, Inbred C57BL
|2 MeSH
650 _ 2 |a Models, Biological
|2 MeSH
650 _ 2 |a Models, Statistical
|2 MeSH
650 _ 2 |a Transcription, Genetic
|2 MeSH
650 _ 2 |a Wnt1 Protein: genetics
|2 MeSH
700 1 _ |a Blöchl, Florian
|0 P:(DE-HGF)0
|b 1
700 1 _ |a Trümbach, Dietrich
|0 P:(DE-2719)9000367
|b 2
|u dzne
700 1 _ |a Wurst, Wolfgang
|0 P:(DE-2719)2000028
|b 3
|u dzne
700 1 _ |a Prakash, Nilima
|0 P:(DE-2719)9000256
|b 4
|u dzne
700 1 _ |a Theis, Fabian J
|0 P:(DE-HGF)0
|b 5
|e Corresponding author
773 1 8 |a 10.1371/journal.pcbi.1000569
|b : Public Library of Science (PLoS), 2009-11-20
|n 11
|p e1000569
|3 journal-article
|2 Crossref
|t PLoS Computational Biology
|v 5
|y 2009
|x 1553-7358
773 _ _ |a 10.1371/journal.pcbi.1000569
|g Vol. 5, no. 11, p. e1000569 -
|0 PERI:(DE-600)2193340-6
|n 11
|q 5:11|p e1000569
|t PLoS Computational Biology
|v 5
|y 2009
|x 1553-7358
856 4 _ |u https://journals.plos.org/ploscompbiol/article?id=10.1371/journal.pcbi.1000569
856 7 _ |2 Pubmed Central
|u http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2774268
856 4 _ |u https://pub.dzne.de/record/136030/files/DZNE-2020-02352.pdf
|y OpenAccess
856 4 _ |u https://pub.dzne.de/record/136030/files/DZNE-2020-02352.pdf?subformat=pdfa
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910 1 _ |a Deutsches Zentrum für Neurodegenerative Erkrankungen
|0 I:(DE-588)1065079516
|k DZNE
|b 2
|6 P:(DE-2719)9000367
910 1 _ |a Deutsches Zentrum für Neurodegenerative Erkrankungen
|0 I:(DE-588)1065079516
|k DZNE
|b 3
|6 P:(DE-2719)2000028
910 1 _ |a Deutsches Zentrum für Neurodegenerative Erkrankungen
|0 I:(DE-588)1065079516
|k DZNE
|b 4
|6 P:(DE-2719)9000256
913 1 _ |a DE-HGF
|b Gesundheit
|l Erkrankungen des Nervensystems
|1 G:(DE-HGF)POF3-340
|0 G:(DE-HGF)POF3-342
|3 G:(DE-HGF)POF3
|2 G:(DE-HGF)POF3-300
|4 G:(DE-HGF)POF
|v Disease Mechanisms and Model Systems
|x 0
914 1 _ |y 2009
915 _ _ |a DBCoverage
|0 StatID:(DE-HGF)0200
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915 _ _ |a Creative Commons Attribution CC BY (No Version)
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LibraryCollectionCLSMajorCLSMinorLanguageAuthor
Marc 21