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Transcriptome-wide analysis reveals GYG2 as a mitochondria-related aging biomarker in human subcutaneous adipose tissue.
Ham, Mira; Cho, Yeonju; Kang, Tae-Wook; Oh, Taeyun; Kim, Hyoung-June; Kim, Kyu-Han.
Afiliação
  • Ham M; R&I Unit, Amorepacific Corporation, Gyeonggi-do, Korea.
  • Cho Y; R&I Unit, Amorepacific Corporation, Gyeonggi-do, Korea.
  • Kang TW; Department of Bioinformatics, The Moagen Inc., Daejeon, Korea.
  • Oh T; Department of Internal Medicine, Institute of Gastroenterology, Yonsei University College of Medicine, Seoul, Korea.
  • Kim HJ; R&I Unit, Amorepacific Corporation, Gyeonggi-do, Korea.
  • Kim KH; R&I Unit, Amorepacific Corporation, Gyeonggi-do, Korea.
Aging Cell ; 23(2): e14049, 2024 Feb.
Article em En | MEDLINE | ID: mdl-38062989
ABSTRACT
Subcutaneous adipose tissue (SAT), a vital energy reservoir and endocrine organ for maintaining systemic glucose, lipid, and energy homeostasis, undergoes significant changes with age. However, among the existing aging-related markers, only few genes are associated with SAT aging. In this study, weighted gene co-expression network analysis was used on a transcriptome of SAT obtained from the Genotype-Tissue Expression portal to identify biologically relevant, SAT-specific, and age-related marker genes. We found modules that exhibited significant changes with age and identified GYG2 as a novel key aging associated gene. The link between GYG2 and mitochondrial function as well as brown/beige adipocytes was supported using additional bioinformatics and experimental analyses. Additionally, we identified PPARG as the transcription factor of GYG2 expression. The newly discovered GYG2 marker can be used to not only determine the age of SAT but also uncover new mechanisms underlying SAT aging.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Gordura Subcutânea / Transcriptoma Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Gordura Subcutânea / Transcriptoma Idioma: En Ano de publicação: 2024 Tipo de documento: Article