Unraveling the Hierarchy of cis and trans Factors That Determine the DNA Binding by Peroxisome Proliferator-Activated Receptor γ

Author:

Nagy Gergely1,Daniel Bence23,Cuaranta-Monroy Ixchelt1,Nagy Laszlo123

Affiliation:

1. Department of Biochemistry and Molecular Biology, Faculty of Medicine, University of Debrecen, Debrecen, Hungary

2. Johns Hopkins University School of Medicine, Department of Medicine, Institute for Fundamental Biomedical Research, Johns Hopkins All Children’s Hospital, Saint Petersburg, Florida, USA

3. Johns Hopkins University School of Medicine, Department of Biological Chemistry, Institute for Fundamental Biomedical Research, Johns Hopkins All Children’s Hospital, Saint Petersburg, Florida, USA

Abstract

Peroxisome proliferator-activated receptor γ (PPARγ) is a nuclear receptor essential for adipocyte development and the maintenance of the alternatively polarized macrophage phenotype. Biochemical studies have established that as an obligate heterodimer with retinoid X receptor (RXR), PPARγ binds directly repeated nuclear receptor half sites spaced by one nucleotide (direct repeat 1 [DR1]). However, it has not been analyzed systematically and genome-wide how cis factors such as the sequences of DR1s and adjacent sequences and trans factors such as cobinding lineage-determining transcription factors (LDTFs) contribute to the direct binding of PPARγ in different cellular contexts.

Funder

HHS | National Institutes of Health

European Commission

American Heart Association

Emberi Eroforrások Minisztériuma

NKFI | Hungarian Scientific Research Fund

Publisher

American Society for Microbiology

Subject

Cell Biology,Molecular Biology

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