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Omics · study · 2026

Effect of PPARγ2 acetylation in at lysine 382 in mouse beige adipocyte differentiation

Listed in NCBI GEO

PPARr is a master regulator of adipogenesis which undergo different post translational modification during adipogenesis.

Description

This post translational modification of PPARγ control unique subset of genes rather full PPARr target genes. Recently we reported that SIRT7 deacetylate PPARr2 at lysine 382 residue and regulate lipogenesis in C3H10T1/2 cells.

Here, we investigate this SIRT7-mediated PPARγ2 lysine deacetylation in mouse beige adipocyte differentiation of subcutaneous white AT (scWAT) stromal vascular fraction (SVF) cell line. At first we prepared PPARr2 K382 acetylation (KQ) and deacetylation (KR) mimicking mutant expressing mouse scWAT SVF cell line. After beige adipocyte differentiation, we isolated total RNA at day 2 and performed RNA-seq analysis.

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From keywords
Life Sciences
Inferred from text
RNA sequencing 65%
Provenance · 1 source records, 8 field assertions
SourceKeyLast seenRaw
NCBI GEOGSE31785913 d agoJSON v1
FieldAssertionExtractorEvidence
access_levelsource · NCBI GEOconnector:ncbi_geo@1.0.0
concepts[field].local:field:life-sciencesmapping · NCBI GEOconnector:ncbi_geo@1.0.0
concepts[method].geo_series_type:expression-profiling-by-high-throughput-sequencingsource · NCBI GEOconnector:ncbi_geo@1.0.0/gdstype
concepts[modality].local:modality:rna-seqenrichment · NCBI GEOkeyword-concept-rules@1.0.0title+description (65%)
concepts[organism].NCBITaxon:10090source · NCBI GEOconnector:ncbi_geo@1.0.0/taxon
descriptionsource · NCBI GEOconnector:ncbi_geo@1.0.0/summary
publication_datesource · NCBI GEOconnector:ncbi_geo@1.0.0
titlesource · NCBI GEOconnector:ncbi_geo@1.0.0/title