4.6 Article

Dynamics of the Ternary Complex Formed by c-Myc Interactor JPO2, Transcriptional Co- activator LEDGF/p75, and Chromatin

Journal

JOURNAL OF BIOLOGICAL CHEMISTRY
Volume 289, Issue 18, Pages 12494-12506

Publisher

AMER SOC BIOCHEMISTRY MOLECULAR BIOLOGY INC
DOI: 10.1074/jbc.M113.525964

Keywords

Chromatin; Coactivator Transcription; Fluorescence Correlation Spectroscopy; Integrase; Protein Dynamics; Protein-Protein Interactions; Transcription Factors; JPO2; LEDGF; p75; PogZ

Funding

  1. Bijzonder Onderzoeksfonds (BOF) KU Leuven
  2. Fonds voor Wetenschappelijk Onderzoek in Vlaanderen (FWO)
  3. European Union (EU) (Framework Programme 7 (FP7) Combined Highly Active Anti-Retroviral Microbicides (CHAARM))
  4. Research Foundation Flanders (FWO Vlaanderen)
  5. agency for Innovation by Science and Technology (IWT Flanders)

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Background: The function of transcription factors can be investigated by monitoring their movement inside the nucleus of cells with biophysical techniques. Results: A model for interaction of JPO2 with chromatin in the absence and presence of its interaction partner LEDGF/p75 is proposed. Conclusion: JPO2 adopts the dynamics of LEDGF/p75. Significance: Our approach is generic for the study of transcription factor dynamics. Lens epithelium-derived growth factor (LEDGF/p75) is a transcriptional co-activator involved in targeting human immunodeficiency virus (HIV) integration and the development of MLL fusion-mediated acute leukemia. A previous study revealed that LEDGF/p75 dynamically scans the chromatin, and upon interaction with HIV-1 integrase, their complex is locked on chromatin. At present, it is not known whether LEDGF/p75-mediated chromatin locking is typical for interacting proteins. Here, we employed continuous photobleaching and fluorescence correlation and cross-correlation spectroscopy to investigate in vivo chromatin binding of JPO2, a LEDGF/p75- and c-Myc-interacting protein involved in transcriptional regulation. In the absence of LEDGF/p75, JPO2 performs chromatin scanning inherent to transcription factors. However, whereas the dynamics of JPO2 chromatin binding are decelerated upon interaction with LEDGF/p75, very strong locking of their complex onto chromatin is absent. Similar results were obtained with the domesticated transposase PogZ, another cellular interaction partner of LEDGF/p75. We furthermore show that diffusive JPO2 can oligomerize; that JPO2 and LEDGF/p75 interact directly and specifically in vivo through the specific interaction domain of JPO2 and the C-terminal domain of LEDGF/p75, comprising the integrase-binding domain; and that modulation of JPO2 dynamics requires a functional PWWP domain in LEDGF/p75. Our results suggest that the dynamics of the LEDGF/p75-chromatin interaction depend on the specific partner and that strong chromatin locking is not a property of all LEDGF/p75-binding proteins.

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