A ubiquitin-like protein encoded by the "noncoding" RNA TINCR promotes keratinocyte proliferation and wound healing.
Akihiro NitaAkinobu MatsumotoRonghao TangChisa ShiraishiKazuya IchiharaDaisuke SaitoMikita SuyamaTomoharu YasudaGaku TsujiMasutaka FurueBumpei KatayamaToshiyuki OzawaTeruasa MurataTeruki DainichiKenji KabashimaAtsushi HatanoMasaki MatsumotoKeiichi I NakayamaPublished in: PLoS genetics (2021)
Although long noncoding RNAs (lncRNAs) are transcripts that do not encode proteins by definition, some lncRNAs actually contain small open reading frames that are translated. TINCR (terminal differentiation-induced ncRNA) has been recognized as a lncRNA that contributes to keratinocyte differentiation. However, we here show that TINCR encodes a ubiquitin-like protein that is well conserved among species and whose expression was confirmed by the generation of mice harboring a FLAG epitope tag sequence in the endogenous open reading frame as well as by targeted proteomics. Forced expression of this protein promoted cell cycle progression in normal human epidermal keratinocytes, and mice lacking this protein manifested a delay in skin wound healing associated with attenuated cell cycle progression in keratinocytes. We termed this protein TINCR-encoded ubiquitin-like protein (TUBL), and our results reveal a role for TINCR in the regulation of keratinocyte proliferation and skin regeneration that is dependent on TUBL.
Keyphrases
- wound healing
- cell cycle
- cell proliferation
- binding protein
- small molecule
- poor prognosis
- protein protein
- amino acid
- endothelial cells
- minimally invasive
- signaling pathway
- working memory
- high glucose
- high fat diet induced
- stem cells
- transcription factor
- gene expression
- cancer therapy
- insulin resistance
- drug delivery
- single cell
- long noncoding rna
- monoclonal antibody
- induced pluripotent stem cells
- label free