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Sökning: WFRF:(Daub M.) > Promoter Usage and ...

LIBRIS Formathandbok  (Information om MARC21)
FältnamnIndikatorerMetadata
00002795naa a2200373 4500
001oai:prod.swepub.kib.ki.se:139087231
003SwePub
008240701s2018 | |||||||||||000 ||eng|
024a http://kipublications.ki.se/Default.aspx?queryparsed=id:1390872312 URI
024a https://doi.org/10.1038/s41598-018-30702-42 DOI
040 a (SwePub)ki
041 a engb eng
042 9 SwePub
072 7a ref2 swepub-contenttype
072 7a art2 swepub-publicationtype
100a Alhendi, AMN4 aut
2451 0a Promoter Usage and Dynamics in Vascular Smooth Muscle Cells Exposed to Fibroblast Growth Factor-2 or Interleukin-1β
264 c 2018-09-03
264 1b Springer Science and Business Media LLC,c 2018
520 a Smooth muscle cells (SMC) in blood vessels are normally growth quiescent and transcriptionally inactive. Our objective was to understand promoter usage and dynamics in SMC acutely exposed to a prototypic growth factor or pro-inflammatory cytokine. Using cap analysis gene expression (FANTOM5 project) we report differences in promoter dynamics for immediate-early genes (IEG) and other genes when SMC are exposed to fibroblast growth factor-2 or interleukin-1β. Of the 1871 promoters responding to FGF2 or IL-1β considerably more responded to FGF2 (68.4%) than IL-1β (18.5%) and 13.2% responded to both. Expression clustering reveals sets of genes induced, repressed or unchanged. Among IEG responding rapidly to FGF2 or IL-1β were FOS, FOSB and EGR-1, which mediates human SMC migration. Motif activity response analysis (MARA) indicates most transcription factor binding motifs in response to FGF2 were associated with a sharp induction at 1 h, whereas in response to IL-1β, most motifs were associated with a biphasic change peaking generally later. MARA revealed motifs for FOS_FOS{B,L1}_JUN{B,D} and EGR-1..3 in the cluster peaking 1 h after FGF2 exposure whereas these motifs were in clusters peaking 1 h or later in response to IL-1β. Our findings interrogating CAGE data demonstrate important differences in promoter usage and dynamics in SMC exposed to FGF2 or IL-1β.
700a Patrikakis, M4 aut
700a Daub, COu Karolinska Institutet4 aut
700a Kawaji, H4 aut
700a Itoh, M4 aut
700a de Hoon, M4 aut
700a Carninci, P4 aut
700a Hayashizaki, Y4 aut
700a Arner, E4 aut
700a Khachigian, LM4 aut
710a Karolinska Institutet4 org
773t Scientific reportsd : Springer Science and Business Media LLCg 8:1, s. 13164-q 8:1<13164-x 2045-2322
856u https://doi.org/10.1038/s41598-018-30702-4
8564 8u http://kipublications.ki.se/Default.aspx?queryparsed=id:139087231
8564 8u https://doi.org/10.1038/s41598-018-30702-4

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