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Shared PPARα/γ Target Genes Regulate Brown Adipocyte Thermogenic Function
Author(s) -
Yachen Shen,
Yvonne Su,
Francisco J. Silva,
Angela H. Weller,
Jaimarie SostreColón,
Paul M. Titchenell,
David J. Steger,
Patrick Seale,
Raymond E. Soccio
Publication year - 2020
Publication title -
cell reports
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 6.264
H-Index - 154
eISSN - 2639-1856
pISSN - 2211-1247
DOI - 10.1016/j.celrep.2020.02.032
Subject(s) - brown adipose tissue , biology , adipocyte , peroxisome proliferator activated receptor , function (biology) , thermogenesis , regulator , gene , microbiology and biotechnology , receptor , transcriptome , nuclear receptor , adipose tissue , gene expression , genetics , endocrinology , transcription factor
Brown adipose tissue (BAT) generates heat to maintain body temperature and suppress obesity. Agonists for nuclear receptors PPARα and PPARγ both affect brown adipocyte function, yet the interplay between these factors in BAT is uncertain. Here, we report that PPARα shares most genomic binding sites with PPARγ, and these common binding sites are more related to BAT function than PPARγ-selective sites without PPARα. Integrating PPARα and PPARγ genomic occupancy with cold-responsive BAT transcriptomes identifies a subset of 16 genes with potential relevance to BAT function. Among these, we focused on the lysosomal protease cathepsin Z (CTSZ) and showed it is necessary for mitochondrial respiration in both mouse and human brown adipocytes. Thus, CTSZ is a shared PPARα/γ target gene in BAT and a regulator of brown adipocyte thermogenic function.

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