IDEAS home Printed from https://ideas.repec.org/a/nat/natcom/v11y2020i1d10.1038_s41467-019-13914-8.html
   My bibliography  Save this article

O-GlcNAc transferase inhibits visceral fat lipolysis and promotes diet-induced obesity

Author

Listed:
  • Yunfan Yang

    (Yale University School of Medicine)

  • Minnie Fu

    (Yale University School of Medicine)

  • Min-Dian Li

    (Yale University School of Medicine
    Yale University School of Medicine)

  • Kaisi Zhang

    (Yale University School of Medicine
    Yale University School of Medicine)

  • Bichen Zhang

    (Yale University School of Medicine
    Yale University School of Medicine)

  • Simeng Wang

    (Yale University School of Medicine)

  • Yuyang Liu

    (Yale University School of Medicine)

  • Weiming Ni

    (Yale University School of Medicine)

  • Qunxiang Ong

    (Yale University School of Medicine)

  • Jia Mi

    (Yale University School of Medicine)

  • Xiaoyong Yang

    (Yale University School of Medicine
    Yale University School of Medicine)

Abstract

Excessive visceral fat accumulation is a primary risk factor for metabolically unhealthy obesity and related diseases. The visceral fat is highly susceptible to the availability of external nutrients. Nutrient flux into the hexosamine biosynthetic pathway leads to protein posttranslational modification by O-linked β-N-acetylglucosamine (O-GlcNAc) moieties. O-GlcNAc transferase (OGT) is responsible for the addition of GlcNAc moieties to target proteins. Here, we report that inducible deletion of adipose OGT causes a rapid visceral fat loss by specifically promoting lipolysis in visceral fat. Mechanistically, visceral fat maintains a high level of O-GlcNAcylation during fasting. Loss of OGT decreases O-GlcNAcylation of lipid droplet-associated perilipin 1 (PLIN1), which leads to elevated PLIN1 phosphorylation and enhanced lipolysis. Moreover, adipose OGT overexpression inhibits lipolysis and promotes diet-induced obesity. These findings establish an essential role for OGT in adipose tissue homeostasis and indicate a unique potential for targeting O-GlcNAc signaling in the treatment of obesity.

Suggested Citation

  • Yunfan Yang & Minnie Fu & Min-Dian Li & Kaisi Zhang & Bichen Zhang & Simeng Wang & Yuyang Liu & Weiming Ni & Qunxiang Ong & Jia Mi & Xiaoyong Yang, 2020. "O-GlcNAc transferase inhibits visceral fat lipolysis and promotes diet-induced obesity," Nature Communications, Nature, vol. 11(1), pages 1-15, December.
  • Handle: RePEc:nat:natcom:v:11:y:2020:i:1:d:10.1038_s41467-019-13914-8
    DOI: 10.1038/s41467-019-13914-8
    as

    Download full text from publisher

    File URL: https://www.nature.com/articles/s41467-019-13914-8
    File Function: Abstract
    Download Restriction: no

    File URL: https://libkey.io/10.1038/s41467-019-13914-8?utm_source=ideas
    LibKey link: if access is restricted and if your library uses this service, LibKey will redirect you to where you can use your library subscription to access this item
    ---><---

    Citations

    Citations are extracted by the CitEc Project, subscribe to its RSS feed for this item.
    as


    Cited by:

    1. Yi Lei & Qiangyun Liu & Binggui Chen & Fangfang Wu & Yiming Li & Xue Dong & Nina Ma & Ziru Wu & Yanfang Zhu & Lu Wang & Yuxin Fu & Yuming Liu & Yinting Song & Mei Du & Heng Zhang & Jidong Zhu & Timoth, 2024. "Protein O-GlcNAcylation coupled to Hippo signaling drives vascular dysfunction in diabetic retinopathy," Nature Communications, Nature, vol. 15(1), pages 1-23, December.

    More about this item

    Statistics

    Access and download statistics

    Corrections

    All material on this site has been provided by the respective publishers and authors. You can help correct errors and omissions. When requesting a correction, please mention this item's handle: RePEc:nat:natcom:v:11:y:2020:i:1:d:10.1038_s41467-019-13914-8. See general information about how to correct material in RePEc.

    If you have authored this item and are not yet registered with RePEc, we encourage you to do it here. This allows to link your profile to this item. It also allows you to accept potential citations to this item that we are uncertain about.

    We have no bibliographic references for this item. You can help adding them by using this form .

    If you know of missing items citing this one, you can help us creating those links by adding the relevant references in the same way as above, for each refering item. If you are a registered author of this item, you may also want to check the "citations" tab in your RePEc Author Service profile, as there may be some citations waiting for confirmation.

    For technical questions regarding this item, or to correct its authors, title, abstract, bibliographic or download information, contact: Sonal Shukla or Springer Nature Abstracting and Indexing (email available below). General contact details of provider: http://www.nature.com .

    Please note that corrections may take a couple of weeks to filter through the various RePEc services.

    IDEAS is a RePEc service. RePEc uses bibliographic data supplied by the respective publishers.