Abstract

Doc number: 29

Abstract

Background: Hox proteins are transcription factors involved in crucial processes during animal development. Their mode of action remains scantily documented. While other families of transcription factors, like Smad or Stat, are known cell signaling transducers, such a function has never been squarely addressed for Hox proteins.

Results: To investigate the mode of action of mammalian Hoxa1, we characterized its interactome by a systematic yeast two-hybrid screening against ~12,200 ORF-derived polypeptides. Fifty nine interactors were identified of which 45 could be confirmed by affinity co-purification in animal cell lines. Many Hoxa1 interactors are proteins involved in cell-signaling transduction, cell adhesion and vesicular trafficking. Forty-one interactions were detectable in live cells by Bimolecular Fluorescence Complementation which revealed distinctive intracellular patterns for these interactions consistent with the selective recruitment of Hoxa1 by subgroups of partner proteins at vesicular, cytoplasmic or nuclear compartments.

Conclusions: The characterization of the Hoxa1 interactome presented here suggests unexplored roles for Hox proteins in cell-to-cell communication and cell physiology.

Details

Title
Protein interactions of the transcription factor Hoxa1
Author
Lambert, Barbara; Vandeputte, Julie; Remacle, Sophie; Bergiers, Isabelle; Simonis, Nicolas; Twizere, Jean-Claude; Vidal, Marc; Rezsohazy, René
Pages
29
Publication year
2012
Publication date
2012
Publisher
BioMed Central
e-ISSN
1471213X
Source type
Scholarly Journal
Language of publication
English
ProQuest document ID
1221240900
Copyright
© 2012 Lambert et al.; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.