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Phosphoproteomic insights into processes influenced by the kinase-like protein DIA1/C3orf58

Hareza, Agnieszka (author)
International Institute of Molecular and Cell Biology, Warsaw,Warsaw University of Life Sciences
Bakun, Magda (author)
Institute of Biochemistry and Biophysics of the Polish Academy of Sciences
Świderska, Bianka (author)
Institute of Biochemistry and Biophysics of the Polish Academy of Sciences
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Dudkiewicz, Małgorzata (author)
Warsaw University of Life Sciences
Koscielny, Alicja (author)
International Institute of Molecular and Cell Biology, Warsaw
Bajur, Anna (author)
Warsaw University of Life Sciences,International Institute of Molecular and Cell Biology, Warsaw,Max Planck Institute of Molecular Cell Biology and Genetics
Jaworski, Jacek (author)
International Institute of Molecular and Cell Biology, Warsaw
Dadlez, Michał (author)
Institute of Biochemistry and Biophysics of the Polish Academy of Sciences
Pawłowski, Krzysztof (author)
Lund University,Lunds universitet,Institutionen för translationell medicin,Medicinska fakulteten,Department of Translational Medicine,Faculty of Medicine,Warsaw University of Life Sciences
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 (creator_code:org_t)
2018-04-09
2018
English.
In: PeerJ. - : PeerJ. - 2167-8359. ; 2018:4
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Many kinases are still 'orphans,' which means knowledge about their substrates, and often also about the processes they regulate, is lacking. Here, DIA1/C3orf58, a member of a novel predicted kinase-like family, is shown to be present in the endoplasmic reticulum and to influence trafficking via the secretory pathway. Subsequently, DIA1 is subjected to phosphoproteomics analysis to cast light on its signalling pathways. A liquid chromatography-tandem mass spectrometry proteomic approach with phosphopeptide enrichment is applied to membrane fractions of DIA1-overexpressing and control HEK293T cells, and phosphosites dependent on the presence of DIA1 are elucidated. Most of these phosphosites belonged to CK2- and proline-directed kinase types. In parallel, the proteomics of proteins immunoprecipitated with DIA1 reported its probable interactors. This pilot study provides the basis for deeper studies of DIA1 signalling.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Cell- och molekylärbiologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Cell and Molecular Biology (hsv//eng)

Keyword

Mass spectrometry
Novel kinases
Phosphoproteomics
Secretory pathway
Signalling

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