FIH‐1 engages novel binding partners to positively influence epithelial proliferation via p63. Issue 1 (25th November 2019)

• Record Type: Journal Article
• Authors: Kaplan, Nihal; Dong, Ying; Wang, Sijia; Yang, Wending; Park, Jong Kook; Wang, Junyi; Fiolek, Elaina; Perez White, Bethany; Chandel, Navdeep S.; Peng, Han; Lavker, Robert M.
• Is Part Of: FASEB journal. Volume 34:Issue 1(2020)
• Page Start: 525
• Page End: 539
• Publication Date: 2019-11-25
• Subjects: ASPP2 -- epidermis -- GADD45α -- limbal and corneal epithelia; Biology -- Periodicals; Biology, Experimental -- Periodicals; 570
• DOI: 10.1096/fj.201901512R
• Languages: English
• ISSNs: 0892-6638

Abstract

Abstract: Whereas much is known about the genes regulated by ΔNp63α in keratinocytes, how ΔNp63α is regulated is less clear. During studies with the hydroxylase, factor inhibiting hypoxia‐inducible factor 1 (FIH‐1), we observed increases in epidermal ΔNp63α expression along with proliferative capacity in a conditional FIH‐1 transgenic mouse. Conversely, loss of FIH‐1 in vivo and in vitro attenuated ΔNp63α expression. To elucidate the FIH‐1/p63 relationship, BioID proteomics assays identified FIH‐1 binding partners that had the potential to regulate p63 expression. FIH‐1 interacts with two previously unknown partners, Plectin1 and signal transducer and activator of transcription 1 (STAT1) leading to the regulation of ΔNp63α expression. Two known interactors of FIH‐1, apoptosis‐stimulating of P53 protein 2 (ASPP2) and histone deacetylase 1 (HDAC1), were also identified. Knockdown of ASPP2 upregulated ΔNp63α and reversed the decrease in ΔNp63α by FIH‐1 depletion. Additionally, FIH‐1 regulates growth arrest and DNA damage‐45 alpha (GADD45α), a negative regulator of ΔNp63α by interacting with HDAC1. GADD45α knockdown rescued reduction in ΔNp63α by FIH‐1 depletion. Collectively, our data reveal that FIH‐1 positively regulates ΔNp63α in keratinocytes via variety of signaling partners: (a) Plectin1/STAT1, (b) ASPP2, and (c) HDAC1/GADD45α signaling pathways.