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  • Stasyk, TarasUppsala universitet,Ludwiginstitutet för cancerforskning (author)

Phosphoproteome profiling of transforming growth factor (TGF)-beta signaling : abrogation of TGFbeta1-dependent phosphorylation of transcription factor-II-I (TFII-I) enhances cooperation of TFII-I and Smad3 in transcription

  • Article/chapterEnglish2005

Publisher, publication year, extent ...

  • 2005
  • printrdacarrier

Numbers

  • LIBRIS-ID:oai:DiVA.org:uu-74760
  • https://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-74760URI
  • https://doi.org/10.1091/mbc.E05-03-0257DOI

Supplementary language notes

  • Language:English
  • Summary in:English &language:-1_t

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  • Subject category:ref swepub-contenttype
  • Subject category:art swepub-publicationtype

Notes

  • Transforming growth factor-beta (TGFbeta) signaling involves activation of a number of signaling pathways, several of which are controlled by phosphorylation events. Here, we describe a phosphoproteome profiling of MCF-7 human breast epithelial cells treated with TGFbeta1. We identified 32 proteins that change their phosphorylation upon treatment with TGFbeta1; 26 of these proteins are novel targets of TGFbeta1. We show that Smad2 and Smad3 have different effects on the dynamics of TGFbeta1-induced protein phosphorylation. The identified proteins belong to nine functional groups, e.g., proteins regulating RNA processing, cytoskeletal rearrangements, and proteasomal degradation. To evaluate the proteomics findings, we explored the functional importance of TGFbeta1-dependent phosphorylation of one of the targets, i.e., transcription factor-II-I (TFII-I). We confirmed that TGFbeta1 stimulated TFII-I phosphorylation at serine residues 371 and 743. Abrogation of the phosphorylation by replacement of Ser371 and Ser743 with alanine residues resulted in enhanced complex formation between TFII-I and Smad3, and enhanced cooperation between TFII-I and Smad3 in transcriptional regulation, as evaluated by a microarray-based measurement of expression of endogenous cyclin D2, cyclin D3, and E2F2 genes, and by a luciferase reporter assay. Thus, TGFbeta1-dependent phosphorylation of TFII-I may modulate TGFbeta signaling at the transcriptional level.

Subject headings and genre

  • MEDICINE
  • MEDICIN

Added entries (persons, corporate bodies, meetings, titles ...)

  • Dubrovska, AnnaUppsala universitet,Ludwiginstitutet för cancerforskning(Swepub:uu)andub498 (author)
  • Lomnytska, MartaUppsala universitet,Ludwiginstitutet för cancerforskning(Swepub:uu)marlo829 (author)
  • Yakymovych, IhorUppsala universitet,Ludwiginstitutet för cancerforskning(Swepub:uu)ihoryaky (author)
  • Wernstedt, ChristerUppsala universitet,Ludwiginstitutet för cancerforskning(Swepub:uu)chrisws (author)
  • Heldin, Carl-HenrikUppsala universitet,Ludwiginstitutet för cancerforskning(Swepub:uu)carlheld (author)
  • Hellman, UlfUppsala universitet,Ludwiginstitutet för cancerforskning(Swepub:uu)ulfhm (author)
  • Souchelnytskyi, SerhiyUppsala universitet,Ludwiginstitutet för cancerforskning(Swepub:uu)sergsouc (author)
  • Uppsala universitetLudwiginstitutet för cancerforskning (creator_code:org_t)

Related titles

  • In:Molecular Biology of the Cell16:10, s. 4765-47801059-15241939-4586

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