Global quantitative proteomics reveals novel factors in the ecdysone signaling pathway in Drosophila melanogaster. Issue 4 (14th January 2015)
- Record Type:
- Journal Article
- Title:
- Global quantitative proteomics reveals novel factors in the ecdysone signaling pathway in Drosophila melanogaster. Issue 4 (14th January 2015)
- Main Title:
- Global quantitative proteomics reveals novel factors in the ecdysone signaling pathway in Drosophila melanogaster
- Authors:
- Sap, Karen A.
Bezstarosti, Karel
Dekkers, Dick H. W.
van den Hout, Mirjam
van Ijcken, Wilfred
Rijkers, Erikjan
Demmers, Jeroen A. A.
Krijgsveld, Jeroen - Abstract:
- <abstract abstract-type="main"> <title> <x xml:space="preserve">Abstract</x> </title> <p>The ecdysone signaling pathway plays a major role in various developmental transitions in insects. Recent advances in the understanding of ecdysone action have relied to a large extent on the application of molecular genetic tools in <italic>Drosophila</italic>. Here, we used a comprehensive quantitative SILAC MS‐based approach to study the global, dynamic proteome of a <italic>Drosophila</italic> cell line to investigate how hormonal signals are transduced into specific cellular responses. Global proteome data after ecdysone treatment after various time points were then integrated with transcriptome data. We observed a substantial overlap in terms of affected targets between the dynamic proteome and transcriptome, although there were some clear differences in timing effects. Also, downregulation of several specific mRNAs did not always correlate with downregulation of their corresponding protein counterparts, and in some cases there was no correlation between transcriptome and proteome dynamics whatsoever. In addition, we performed a comprehensive interactome analysis of EcR, the major target of ecdysone. Proteins copurified with EcR include factors involved in transcription, chromatin remodeling, ecdysone signaling, ecdysone biosynthesis, and other signaling pathways. Novel ecdysone‐responsive proteins identified in this study might link previously unknown proteins to the ecdysone<abstract abstract-type="main"> <title> <x xml:space="preserve">Abstract</x> </title> <p>The ecdysone signaling pathway plays a major role in various developmental transitions in insects. Recent advances in the understanding of ecdysone action have relied to a large extent on the application of molecular genetic tools in <italic>Drosophila</italic>. Here, we used a comprehensive quantitative SILAC MS‐based approach to study the global, dynamic proteome of a <italic>Drosophila</italic> cell line to investigate how hormonal signals are transduced into specific cellular responses. Global proteome data after ecdysone treatment after various time points were then integrated with transcriptome data. We observed a substantial overlap in terms of affected targets between the dynamic proteome and transcriptome, although there were some clear differences in timing effects. Also, downregulation of several specific mRNAs did not always correlate with downregulation of their corresponding protein counterparts, and in some cases there was no correlation between transcriptome and proteome dynamics whatsoever. In addition, we performed a comprehensive interactome analysis of EcR, the major target of ecdysone. Proteins copurified with EcR include factors involved in transcription, chromatin remodeling, ecdysone signaling, ecdysone biosynthesis, and other signaling pathways. Novel ecdysone‐responsive proteins identified in this study might link previously unknown proteins to the ecdysone signaling pathway and might be novel targets for developmental studies. To our knowledge, this is the first time that ecdysone signaling is studied by global quantitative proteomics. All MS data have been deposited in the ProteomeXchange with identifier PXD001455 (<ext-link ext-link-type="uri" xlink:href="http://proteomecentral.proteomexchange.org/dataset/PXD001455" xlink:type="simple" xmlns:xlink="http://www.w3.org/1999/xlink">http://proteomecentral.proteomexchange.org/dataset/PXD001455</ext-link>).</p> </abstract> … (more)
- Is Part Of:
- Proteomics. Volume 15:Issue 4(2015:Feb.)
- Journal:
- Proteomics
- Issue:
- Volume 15:Issue 4(2015:Feb.)
- Issue Display:
- Volume 15, Issue 4 (2015)
- Year:
- 2015
- Volume:
- 15
- Issue:
- 4
- Issue Sort Value:
- 2015-0015-0004-0000
- Page Start:
- 725
- Page End:
- 738
- Publication Date:
- 2015-01-14
- Subjects:
- Proteins -- Separation -- Periodicals
Bioinformatics -- Periodicals
Proteomics -- Periodicals
Genomes -- Periodicals
Molecular genetics -- Periodicals
572.605 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1615-9861 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/pmic.201400308 ↗
- Languages:
- English
- ISSNs:
- 1615-9853
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 6936.178000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 3860.xml