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Next-generation Drosophila protein interactome map and its functional implications.
Bhat, Guruharsha; Li, Kejie; Locke, George; Theodorou, Marina; Kilambi, Krishna; Hori, Kazuya; Ho, Diana; Obar, Robert; Williams, Leah; Parzen, Hannah; Dephoure, Noah; Braun, Craig; Muskavitch, Marc; Celniker, Susan E; Gygi, Steven; Artavanis-Tsakonas, Spyros.
Afiliação
  • Bhat G; Department of Cell Biology, Harvard Medical School, Boston, MA, USA; Biogen, 225 Binney St, Cambridge, MA 02142, USA.
  • Li K; Biogen, 225 Binney St, Cambridge, MA 02142, USA; Triveni Bio, Watertown, MA, USA.
  • Locke G; Biogen, 225 Binney St, Cambridge, MA 02142, USA; Senda Biosciences, Cambridge, MA, USA.
  • Theodorou M; Department of Cell Biology, Harvard Medical School, Boston, MA, USA; Biogen, 225 Binney St, Cambridge, MA 02142, USA; Nereid Therpaeutics, Boston, MA 02210, USA.
  • Kilambi K; Biogen, 225 Binney St, Cambridge, MA 02142, USA; Pfizer, Cambridge, MA, USA.
  • Hori K; Department of Cell Biology, Harvard Medical School, Boston, MA, USA; University of Fukui, Fukui, Japan.
  • Ho D; Department of Cell Biology, Harvard Medical School, Boston, MA, USA.
  • Obar R; Department of Cell Biology, Harvard Medical School, Boston, MA, USA.
  • Williams L; Department of Cell Biology, Harvard Medical School, Boston, MA, USA.
  • Parzen H; Department of Cell Biology, Harvard Medical School, Boston, MA, USA.
  • Dephoure N; Department of Cell Biology, Harvard Medical School, Boston, MA, USA.
  • Braun C; Department of Cell Biology, Harvard Medical School, Boston, MA, USA.
  • Muskavitch M; Department of Cell Biology, Harvard Medical School, Boston, MA, USA.
  • Celniker SE; Biological Systems and Engineering Division, Lawrence Berkeley National Laboratory, Berkeley, CA, USA.
  • Gygi S; Department of Cell Biology, Harvard Medical School, Boston, MA, USA.
  • Artavanis-Tsakonas S; Department of Cell Biology, Harvard Medical School, Boston, MA, USA. Electronic address: artavanis@hms.harvard.edu.
Dev Cell ; 2024 Jun 27.
Article em En | MEDLINE | ID: mdl-38944040
ABSTRACT
We describe a next-generation Drosophila protein interaction map-"DPIM2"-established from affinity purification-mass spectrometry of 5,805 baits, covering the largest fraction of the Drosophila proteome. The network contains 32,668 interactions among 3,644 proteins, organized into 632 clusters representing putative functional modules. Our analysis expands the pool of known protein interactions in Drosophila, provides annotation for poorly studied genes, and postulates previously undescribed protein interaction relationships. The predictive power and functional relevance of this network are probed through the lens of the Notch signaling pathway, and we find that newly identified members of complexes that include known Notch modifiers can also modulate Notch signaling. DPIM2 allows direct comparisons with a recently published human protein interaction network, defining the existence of functional interactions conserved across species. Thus, DPIM2 defines a valuable resource for predicting protein co-complex memberships and functional associations as well as generates functional hypotheses regarding specific protein interactions.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Dev Cell Assunto da revista: EMBRIOLOGIA Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Dev Cell Assunto da revista: EMBRIOLOGIA Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Estados Unidos
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