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Wang, Tao

0000-0002-4837-6854

Mayo Clinic

Laboratory of Protein Structure and Function, Institute of Medicine and Pharmacy, Qiqihar Medical University, Qiqihar, Heilongjiang 161006, China.

Citations 1

MCM2-7 proteins promote NF-κB transcriptional activity through cooperative promoter recruitment
Hong, Xian , Sui, Ming , Li, Qiang , Lu, Yan-Ji, Nie, Yong-Hong, Li, Y Z, YUE, Xin-xin, Xu, Jing , Billadeau, Daniel, Wang, Tao, Deng, Zhi-Hui , Wang, Tao , Li, Wenhua

Bioscience Reports | June 11, 2026 | Volume: 46 | Issue: 7 | Pages: No page available

10.1042/bsr20260337 Get It

Abstract The minichromosome maintenance 2-7 (MCM2-7) proteins form a hexameric protein complex that is the structural core of replicative helicase, which is essential for accurate DNA replication. While their role in replication is well-established, the biological functions of excess chromatin-bound MCM2-7 proteins remain unclear. Here, we identify a transcriptional regulatory function of MCM2-7 through its interaction with nuclear factor κB (NF-κB) p65. We demonstrate that MCM2-7 proteins and NF-κB p65 reciprocally recruit each other to target gene promoters. Consequently, MCM2-7 proteins facilitate the localization of RNA Pol II to NF-κB target gene promoters and along the gene body, thereby promoting transcription of NF-κB target genes. These findings reveal MCM2-7 proteins promote NF-κB target gene transcription by facilitating p65 and RNA Pol II recruitment, offering a potential avenue for fine-tuning NF-κB target gene transcription.