Variants in PRKCE and KLC1, Potential Negative Regulators of Type I Psoriasis

Abstract Background: Psoriasis is a multifactorial disease with a complex genetic predisposition. The pathophysiology of psoriasis is associated with genetic variants, especially in negative regulatory genes. To better characterize gene variants in psoriasis and identify the relationship between clinical characteristics and variant genes in its pathogenesis. DNA was extracted from 282 type Ⅰ psoriasis patients and purified, and 13 variable genes were amplified and sequenced using the Sanger method. Results: Among the 13 investigated genes, the variants frequencies of protein kinase C epsilon (PRKCE) (c.240T>C, 35.9% vs 47.7%, P< .05) and kinesin light chain 1 (KLC1) (c.216A>G, 2.9% vs 98.1%, P< .01) were significantly lower in patients than in normal Asian individuals. Additionally, we found considerable differences in the relationship between variants in genes CADM2, JPH2, SPTLC3 and clinical characteristics stratified by medical history and family history. Moreover, MEGF6 gene variants (39.52% vs. 22.50%, χ2=3.83, p < .05) showed a stronger association with the group as mild (PASI≤10) than with the group as heavy. Conclusions: Our results provide a comprehensive correlation analysis of negative regulatory genes that are regulated in psoriasis. This integrated analysis offers novel insight into the pathogenic mechanisms involved in psoriasis.