Profiling temporal lncRNA dynamics in keratinocyte differentiation
50th FEBS Congress, Maastricht, Hollanda, 4 - 08 Temmuz 2026, ss.85, (Özet Bildiri)
- Yayın Türü: Bildiri / Özet Bildiri
- Basıldığı Şehir: Maastricht
- Basıldığı Ülke: Hollanda
- Sayfa Sayıları: ss.85
- Karadeniz Teknik Üniversitesi Adresli: Evet
Özet
Rationale: The epidermis is the first barrier protecting the body from the external environment, and its development and mainten- ance are tightly regulated by epigenetic mechanisms controlling the temporal dynamics of gene expression. Long non-coding RNAs (lncRNAs) have emerged as key epigenetic modulators of epidermal homeostasis and keratinocyte differentiation. However, a comprehensive temporal characterization of lncRNA expression during keratinocyte differentiation has not yet been conducted. Methods: For this purpose, we utilized an in vitro calcium- induced keratinocyte differentiation model using HaCaT cell line to profile lncRNA expression across stem cell-like, early, and late differentiation stages. Following RNA-sequencing, differentially expressed genes (DEGs) at early and late differentiation stages compared to the stem cell-like stage were identified using DESeq2. Annotation and filtering were performed based on Ensembl (GRCh38.p14), genomic location and structural features of lncRNAs were analyzed using BioMart.
Results: DEG analysis revealed a progressive increase in the number of differentially expressed lncRNAs during early (84 DEGs) and late (321 DEGs) keratinocyte differentiation stages compared to stem cell-like stage. Among them, the most promi- nent lncRNAs at the late differentiation stage were CERNA2, COLCA1, LINC01776, LNCOG, and SLC8A1-AS1 (log2FC ≥ 6; adj p ≤ 1 9 105). Notably, the identified differentially expressed lncRNAs were enriched on chromosome 1, which harbors the Epidermal Differentiation Complex gene cluster at 1q21.3 and were classified as antisense (~44%) or intergenic (~33%). Conclusions: Together, our data reveal characterization of lncRNAs associated with keratinocyte differentiation, highlight the potential role of epigenetic regulation of this process, and nominate novel candidates for future functional studies.
Funding: TUBITAK (grant no. 118Z124).