Please use this identifier to cite or link to this item: https://doi.org/10.1186/1471-2148-10-157
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dc.titleFunctional conservation of a forebrain enhancer from the elephant shark (Callorhinchus milii ) in zebrafish and mice
dc.contributor.authorMacDonald, R.B
dc.contributor.authorDebiais-Thibaud, M
dc.contributor.authorMartin, K
dc.contributor.authorPoitras, L
dc.contributor.authorTay, B.-H
dc.contributor.authorVenkatesh, B
dc.contributor.authorEkker, M
dc.date.accessioned2020-10-27T11:38:47Z
dc.date.available2020-10-27T11:38:47Z
dc.date.issued2010
dc.identifier.citationMacDonald, R.B, Debiais-Thibaud, M, Martin, K, Poitras, L, Tay, B.-H, Venkatesh, B, Ekker, M (2010). Functional conservation of a forebrain enhancer from the elephant shark (Callorhinchus milii ) in zebrafish and mice. BMC Evolutionary Biology 10 (1) : 157. ScholarBank@NUS Repository. https://doi.org/10.1186/1471-2148-10-157
dc.identifier.issn14712148
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/181667
dc.description.abstractAbstract. Background. The phylogenetic position of the elephant shark (Callorhinchus milii ) is particularly relevant to study the evolution of genes and gene regulation in vertebrates. Here we examine the evolution of Dlx homeobox gene regulation during vertebrate embryonic development with a particular focus on the forebrain. We first identified the elephant shark sequence orthologous to the URE2 cis -regulatory element of the mouse Dlx1/Dlx2 locus (herein named CmURE2). We then conducted a comparative study of the sequence and enhancer activity of CmURE2 with that of orthologous regulatory sequences from zebrafish and mouse. Results. The CmURE2 sequence shows a high percentage of identity with its mouse and zebrafish counterparts but is overall more similar to mouse URE2 (MmURE2) than to zebrafish URE2 (DrURE2). In transgenic zebrafish and mouse embryos, CmURE2 displayed enhancer activity in the forebrain that overlapped with that of DrURE2 and MmURE2. However, we detected notable differences in the activity of the three sequences in the diencephalon. Outside of the forebrain, CmURE2 shows enhancer activity in areas such as the pharyngeal arches and dorsal root ganglia where its' counterparts are also active. Conclusions. Our transgenic assays show that part of the URE2 enhancer activity is conserved throughout jawed vertebrates but also that new characteristics have evolved in the different groups. Our study demonstrates that the elephant shark is a useful outgroup to study the evolution of regulatory mechanisms in vertebrates and to address how changes in the sequence of cis -regulatory elements translate into changes in their regulatory activity. © 2010 MacDonald et al; licensee BioMed Central Ltd.
dc.rightsAttribution 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.sourceUnpaywall 20201031
dc.subjectbioassay
dc.subjectcyprinid
dc.subjectevolutionary biology
dc.subjectgenetic analysis
dc.subjectphylogenetics
dc.subjectrodent
dc.subjectshark
dc.subjectCallorhinchus milii
dc.subjectChondrichthyes
dc.subjectDanio rerio
dc.subjectGnathostomata (vertebrate)
dc.subjectMus
dc.subjectVertebrata
dc.subjectanimal
dc.subjectarticle
dc.subjectDNA sequence
dc.subjectenhancer region
dc.subjectforebrain
dc.subjectgene expression regulation
dc.subjectgenetics
dc.subjecthomeobox
dc.subjectmolecular evolution
dc.subjectmolecular genetics
dc.subjectmouse
dc.subjectnucleotide sequence
dc.subjectprenatal development
dc.subjectsequence alignment
dc.subjectshark
dc.subjecttransgenic animal
dc.subjectzebra fish
dc.subjectAnimals
dc.subjectAnimals, Genetically Modified
dc.subjectBase Sequence
dc.subjectConserved Sequence
dc.subjectEnhancer Elements, Genetic
dc.subjectEvolution, Molecular
dc.subjectGene Expression Regulation, Developmental
dc.subjectGenes, Homeobox
dc.subjectMice
dc.subjectMolecular Sequence Data
dc.subjectProsencephalon
dc.subjectSequence Alignment
dc.subjectSequence Analysis, DNA
dc.subjectSharks
dc.subjectZebrafish
dc.typeArticle
dc.contributor.departmentPAEDIATRICS
dc.description.doi10.1186/1471-2148-10-157
dc.description.sourcetitleBMC Evolutionary Biology
dc.description.volume10
dc.description.issue1
dc.description.page157
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