| First Author | Li Y | Year | 2020 |
| Journal | EMBO Rep | Volume | 21 |
| Issue | 5 | Pages | e48566 |
| PubMed ID | 32239614 | Mgi Jnum | J:292743 |
| Mgi Id | MGI:6448862 | Doi | 10.15252/embr.201948566 |
| Citation | Li Y, et al. (2020) Regulation of epidermal differentiation through KDF1-mediated deubiquitination of IKKalpha. EMBO Rep 21(5):e48566 |
| abstractText | Progenitor cells at the basal layer of skin epidermis play an essential role in maintaining tissue homeostasis and enhancing wound repair in skin. The proliferation, differentiation, and cell death of epidermal progenitor cells have to be delicately regulated, as deregulation of this process can lead to many skin diseases, including skin cancers. However, the underlying molecular mechanisms involved in skin homeostasis remain poorly defined. In this study, with quantitative proteomics approach, we identified an important interaction between KDF1 (keratinocyte differentiation factor 1) and IKKalpha (IkappaB kinase alpha) in differentiating skin keratinocytes. Ablation of either KDF1 or IKKalpha in mice leads to similar but striking abnormalities in skin development, particularly in skin epidermal differentiation. With biochemical and mouse genetics approach, we further demonstrate that the interaction of IKKalpha and KDF1 is essential for epidermal differentiation. To probe deeper into the mechanisms, we find that KDF1 associates with a deubiquitinating protease USP7 (ubiquitin-specific peptidase 7), and KDF1 can regulate skin differentiation through deubiquitination and stabilization of IKKalpha. Taken together, our study unravels an important molecular mechanism underlying epidermal differentiation and skin tissue homeostasis. |
