晨间信号Morning Signal
《科学》 第391卷 第6784期 · 2026年1月29日 · 中文解读

DNA-蛋白质交联通过cGAS-STING通路驱动早衰和胚胎致死

DNA-protein cross-links promote cGAS-STING–driven premature aging and embryonic lethality
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该研究揭示了SPRTN蛋白酶在修复DNA-蛋白质交联(DPC)中的关键作用,并证明未修复的DPC会激活cGAS-STING先天免疫通路,导致早衰和胚胎致死。
原文开头
Full article and list of author affiliations: https://doi.org/10.1126/ science.adx9445 Ines Tomaskovic†, Cristian Prieto-Garcia†, et al. INTRODUCTION: DNA-protein cross-links (DPCs) are highly toxic lesions in which proteins become covalently attached to DNA, blocking essential processes such as replication and transcription. To maintain genome stability, cells rely on specialized repair mechanisms that remove DPCs. The protease SPRTN was the first enzyme identified to resolve these lesions by cleaving the protein component from DNA. Although SPRTN’s function has been well-documented during DNA replication, its role in other phases of the cell cycle remains less understood. Importantly, inherited inactivating mutations in SPRTN cause Ruijs-Aalfs progeria syndrome (RJALS), a rare disorder marked by premature aging and early-onset liver cancer. …
摘自《科学》(Science)第391卷 第6784期 · 2026年1月29日。仅引用开头一小段供了解文章,版权归原刊所有,全文请阅读原刊。
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