分子生物学
IVD分子诊断
细胞培养与分析
蛋白研究
细胞因子
重组蛋白
抗体
高通量测序建库
病原检测UCF系列
生物医药
工具酶
抑制剂激活剂与常用试剂
仪器
耗材

HSPA1A and DNAJB1 regulate NELF condensate dynamics to safeguard transcriptional recovery under heat stress

Shuyao Jiang, Zixuan Jia, Wenxuan Zhu, Yu Liu, Huanyi Fu, Feifeng Zhu, Zhuo Li, Jiaye Yang, Yiying Zhu, Zhongxing Sun, Tianyi Zhu, Xuebo Quan, Huipeng Jiao, Kai Huang, Zhibing Wu, Wei Zou, Bing Yang, Yi Lu, Long Zhang, Fangfang Zhou, Dong Fang, Huasong Lu

Journal:MOLECULAR CELL

IF:16.6

DOI:10.1016/j.molcel.2026.01.015

PMID:41653920

Published:2026-02-06

research field:分子生物学伴侣蛋白生物学转录调控细胞生物学应激反应

Abstract

Promoter-proximal pausing by negative elongation factor (NELF) establishes a critical checkpoint for RNA polymerase II (RNA Pol II) transcription. Heat shock (HS) induces NELF to form nuclear condensates, yet how their dynamics are regulated and coupled to transcriptional adaptation remains unclear. Using a nanobody-based proximity labeling strategy (NbPro), we identify the molecular chaperones HSPA1A and DNAJB1 as key regulators of NELF condensate dynamics. Although dispensable for initial HS-induced transcriptional repression, chaperone-mediated regulation is required for efficient transcriptional reactivation during recovery. Mechanistically, DNAJB1 recognizes NELFA’s tentacle domain and facilitates HSPA1A recruitment, thereby preventing aberrant aggregation and enabling timely condensate disassembly. Disruption of NELF condensate dynamics leads to persistent NELFA phosphorylation, impaired chromatin association, destabilized RNA Pol II pausing, and premature release of non-productive RNA Pol II complexes. Together, these findings reveal a chaperone-dependent mechanism that governs NELF condensate dynamics and highlight promoter-proximal pausing as a checkpoint to prevent immature RNA Pol II escape, rather than merely a means of transcriptional repression.

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