| Literature DB >> 33608456 |
Bin Xie1, Tariq E Khoyratty1, Enas Abu-Shah1, Pablo F Cespedes1, Andrew J MacLean1, Gabriela Pirgova1, Zhiyuan Hu2, Ahmed A Ahmed2, Michael L Dustin1, Irina A Udalova1, Tal I Arnon3.
Abstract
The PI3K pathway plays a key role in B cell activation and is important for the differentiation of Ab producing plasma cells (PCs). Although much is known about the molecular mechanisms that modulate PI3K signaling in B cells, the transcriptional regulation of PI3K expression is poorly understood. In this study, we identify the zinc finger protein Zbtb18 as a transcriptional repressor that directly binds enhancer/promoter regions of genes encoding class I PI3K regulatory subunits, subsequently limiting their expression, dampening PI3K signaling and suppressing PC responses. Following activation, dividing B cells progressively downregulated Zbtb18, allowing gradual amplification of PI3K signals and enhanced development of PCs. Human Zbtb18 displayed similar expression patterns and function in human B cells, acting to inhibit development of PCs. Furthermore, a number of Zbtb18 mutants identified in cancer patients showed loss of suppressor activity, which was also accompanied by impaired regulation of PI3K genes. Taken together, our study identifies Zbtb18 as a repressor of PC differentiation and reveals its previously unappreciated function as a transcription modulator of the PI3K signaling pathway.Entities:
Year: 2021 PMID: 33608456 PMCID: PMC7980533 DOI: 10.4049/jimmunol.2000367
Source DB: PubMed Journal: J Immunol ISSN: 0022-1767 Impact factor: 5.422