<scp>METTL14</scp> affects <scp>UVB</scp>‐induced human dermal fibroblasts photoaging via <scp>miR</scp>‐100‐3p biogenesis in an <scp>m⁶A</scp>‐dependent manner

Abstract

Abstract Exposure to ultraviolet radiation can lead to skin photoaging, which increases the risk of skin tumors. This study aims to investigate how microRNA m 6 A modification contributes to skin photoaging. This study found that skin fibroblasts exposed to a single UVB dose of 30 mJ/cm 2 exhibited characteristics of photoaging. The m 6 A level of total RNA decreased in photoaged cells with a down‐regulated level of METTL14, and overexpression of METTL14 displayed a photoprotective function. Moreover, miR‐100‐3p was a downstream target of METTL14. And METTL14 could affect pri‐miR‐100 processing to mature miR‐100‐3p in an m 6 A‐dependent manner via DGCR8. Furthermore, miR‐100‐3p targeted at 3′ end untranslated region of ERRFI1 mRNA with an inhibitory effect on translation. Additionally, photoprotective effects of overexpression of METTL14 were reversed by miR‐100‐3p inhibitor or overexpression of ERRFI1. In UVB‐induced photoaging of human skin fibroblasts, METTL14‐dependent m 6 A can regulate miR‐100‐3p maturation via DGCR8 and affect skin fibroblasts photoaging through miR‐100‐3p/ERRFI1 axis.