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Abstract
<p class="first" id="d1160428e142">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.
</p>