KIAA1429-mediated M(6)A methylation inhibits osteoclast differentiation via stabilizing Lrp4 mRNA and protects against osteoporosis.

N(6)-methyladenosine (m(6)A) is a novel epigenetic modification that has been reported to be involved in the progression of osteoporosis (OP), providing new insights into the pathogenesis of OP. The methyltransferases KIAA1429 [also known as virus-like m(6)A methyltransferase-associated protein (VIRMA)] participates in various essential biological processes by regulating target gene expression levels. However, the function of KIAA1429-mediated m(6)A modification in OP progression remains unclear. This study aimed to investigate the biological roles and potential underlying mechanisms of KIAA1429 in OP and osteoclast differentiation. scRNA-seq combined with bulk RNA-seq screening for the differential gene KIAA1429. Analysis of clinical data confirmed KIAA1429 expression and its clinical significance in OP. KIAA1429 inhibited osteoclast differentiation in vitro and reduced bone resorption in ovariectomized (OVX) mice. Mechanistically, LRP4 was identified as a downstream target of KIAA1429. KIAA1429 mediated the m(6)A modification of Lrp4 mRNA, and then YT521-B homology-domain-containing protein 1 (YTHDC1) increased Lrp4 stability and expression. In addition, LRP4 enhancement recruited TNFAIP3, which inactivated NF-κB signaling. This novel mechanism of NF-κB signaling pathway inhibition by enhanced KIAA1429/YTHDC1-coupled Lrp4 transcription during osteoclast differentiation highlights the potential of KIAA1429 as a novel predictive biomarker and therapeutic target for OP progression.