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LIBRIS Formathandbok  (Information om MARC21)
FältnamnIndikatorerMetadata
00005798naa a2200457 4500
001oai:DiVA.org:uu-435716
003SwePub
008210301s2021 | |||||||||||000 ||eng|
024a https://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-4357162 URI
024a https://doi.org/10.1186/s12864-020-07329-92 DOI
040 a (SwePub)uu
041 a engb eng
042 9 SwePub
072 7a ref2 swepub-contenttype
072 7a art2 swepub-publicationtype
100a Lindner, Melanieu Netherlands Inst Ecol NIOO KNAW, Dept Anim Ecol, POB 50, NL-6700 AB Wageningen, Netherlands.;Univ Groningen, Groningen Inst Evolutionary Life Sci GELI FES, Chronobiol Unit, Groningen, Netherlands.4 aut
2451 0a Temporal changes in DNA methylation and RNA expression in a small song bird :b within- and between-tissue comparisons
264 c 2021-01-07
264 1b BioMed Central (BMC),c 2021
338 a electronic2 rdacarrier
520 a Background: DNA methylation is likely a key mechanism regulating changes in gene transcription in traits that show temporal fluctuations in response to environmental conditions. To understand the transcriptional role of DNA methylation we need simultaneous within-individual assessment of methylation changes and gene expression changes over time. Within-individual repeated sampling of tissues, which are essential for trait expression is, however, unfeasible (e.g. specific brain regions, liver and ovary for reproductive timing). Here, we explore to what extend between-individual changes in DNA methylation in a tissue accessible for repeated sampling (red blood cells (RBCs)) reflect such patterns in a tissue unavailable for repeated sampling (liver) and how these DNA methylation patterns are associated with gene expression in such inaccessible tissues (hypothalamus, ovary and liver). For this, 18 great tit (Parus major) females were sacrificed at three time points (n=6 per time point) throughout the pre-laying and egg-laying period and their blood, hypothalamus, ovary and liver were sampled.Results: We simultaneously assessed DNA methylation changes (via reduced representation bisulfite sequencing) and changes in gene expression (via RNA-seq and qPCR) over time. In general, we found a positive correlation between changes in CpG site methylation in RBCs and liver across timepoints. For CpG sites in close proximity to the transcription start site, an increase in RBC methylation over time was associated with a decrease in the expression of the associated gene in the ovary. In contrast, no such association with gene expression was found for CpG site methylation within the gene body or the 10kb up- and downstream regions adjacent to the gene body.Conclusion: Temporal changes in DNA methylation are largely tissue-general, indicating that changes in RBC methylation can reflect changes in DNA methylation in other, often less accessible, tissues such as the liver in our case. However, associations between temporal changes in DNA methylation with changes in gene expression are mostly tissue- and genomic location-dependent. The observation that temporal changes in DNA methylation within RBCs can relate to changes in gene expression in less accessible tissues is important for a better understanding of how environmental conditions shape traits that temporally change in expression in wild populations.
650 7a NATURVETENSKAPx Biologix Genetik0 (SwePub)106092 hsv//swe
650 7a NATURAL SCIENCESx Biological Sciencesx Genetics0 (SwePub)106092 hsv//eng
653 a DNA methylation
653 a RNA expression
653 a Tissue-specific and tissue-general temporal changes
653 a Accessible and inaccessible tissues
653 a Great tit
700a Verhagen, Ireneu Netherlands Inst Ecol NIOO KNAW, Dept Anim Ecol, POB 50, NL-6700 AB Wageningen, Netherlands.;Wageningen Univ & Res, Wageningen, Netherlands.4 aut
700a Viitaniemi, Heidi M.u Univ Helsinki, Organismal & Evolutionary Biol Res Programme, Helsinki, Finland.;Czech Acad Sci, Inst Vertebrate Biol, Prague, Czech Republic.;Univ Turku, Dept Biol, Turku, Finland.4 aut
700a Laine, Veronika N.u Netherlands Inst Ecol NIOO KNAW, Dept Anim Ecol, POB 50, NL-6700 AB Wageningen, Netherlands.;Univ Helsinki, Finnish Museum Nat Hist, Helsinki, Finland.4 aut
700a Visser, Marcel E.u Netherlands Inst Ecol NIOO KNAW, Dept Anim Ecol, POB 50, NL-6700 AB Wageningen, Netherlands.;Univ Groningen, Groningen Inst Evolutionary Life Sci GELI FES, Chronobiol Unit, Groningen, Netherlands.4 aut
700a Husby, Arild,c Associate Senior Lectureru Uppsala universitet,Evolutionsbiologi,Univ Helsinki, Organismal & Evolutionary Biol Res Programme, Helsinki, Finland.;NTNU, Ctr Biodivers Dynam, Dept Biol, Trondheim, Norway.4 aut0 (Swepub:uu)arihu528
700a van Oers, Keesu Netherlands Inst Ecol NIOO KNAW, Dept Anim Ecol, POB 50, NL-6700 AB Wageningen, Netherlands.4 aut
710a Netherlands Inst Ecol NIOO KNAW, Dept Anim Ecol, POB 50, NL-6700 AB Wageningen, Netherlands.;Univ Groningen, Groningen Inst Evolutionary Life Sci GELI FES, Chronobiol Unit, Groningen, Netherlands.b Netherlands Inst Ecol NIOO KNAW, Dept Anim Ecol, POB 50, NL-6700 AB Wageningen, Netherlands.;Wageningen Univ & Res, Wageningen, Netherlands.4 org
773t BMC Genomicsd : BioMed Central (BMC)g 22:1q 22:1x 1471-2164
856u https://doi.org/10.1186/s12864-020-07329-9y Fulltext
856u https://uu.diva-portal.org/smash/get/diva2:1532281/FULLTEXT01.pdfx primaryx Raw objecty fulltext:print
856u https://bmcgenomics.biomedcentral.com/track/pdf/10.1186/s12864-020-07329-9
8564 8u https://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-435716
8564 8u https://doi.org/10.1186/s12864-020-07329-9

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