NAD+激酶
染色质
RNA聚合酶Ⅱ
生物
转录调控
发起人
增强子
PARP1
抄写(语言学)
基因表达调控
染色质免疫沉淀
基因表达
细胞生物学
基因
聚ADP核糖聚合酶
遗传学
聚合酶
酶
生物化学
语言学
哲学
作者
Yessenia Cedeño-Cedeño,Samuel J. Taylor,Matthew J. Gamble,Ulrich Steidl,Robert A. Coleman
出处
期刊:
[Cold Spring Harbor Laboratory]
日期:2025-05-06
标识
DOI:10.1101/2025.04.30.651499
摘要
SUMMARY Gene expression relies on transcriptional bursts driven by dynamic chromatin-modifying enzymes that depend on metabolites like NAD⁺. Depletion of NAD + contributes to cancer, metabolic disorders, and aging, emphasizing the significance of tight regulation of NAD + production in the cell. NMNAT1, a nuclear NAD⁺-synthetase enzyme, supports chromatin-modifying enzymes such as PARP1 and SIRT1; however, its direct role in transcriptional regulation remains unclear. Using integrated multi-omics, we present the first high-resolution, genome-wide study of NMNAT1’s regulatory functions. We demonstrate that NMNAT1 binds to the promoters and enhancers of actively transcribed genes involved in DNA replication, cell cycle progression, and chromatin regulation. RNA-seq and CUT&Tag analyses indicate reduced RNA Polymerase II occupancy at downregulated genes in NMNAT1 knockout cells, implicating NMNAT1 in transcriptional activation through Pol II engagement. These findings position NMNAT1 as a key node linking localized NAD⁺ production to gene-specific transcription, offering new insights into metabolic regulation of gene expression.
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