晨间信号Morning Signal
《科学》 第393卷 第6817期 · 2026年9月17日 · 中文解读

VIPR系统通过非连续几何三链体实现RNA引导的DNA识别

MicROBiOlOGY VIPR RNA- guided DNA recognition by noncontiguous geometric triplex formation · Peter H. Yoon, Trevor A. Docter, Zeyuan Terry Zhang, Kenneth Loi, Santiago C. Lopez, Luis E. Valentin-Alvarado, Owen T. Tuck, Stephen G. Brohawn, Jennifer A. Doudna
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本文通过21个冷冻电镜结构揭示了VIPR系统如何利用非连续配对规则和几何三链体实现RNA引导的DNA识别与转录沉默。
原文开头
VIPR RNA- guided DNA recognition by noncontiguous geometric triplex formation Peter H. Yoon1,2†, Trevor A. Docter1†, Zeyuan Terry Zhang2,3†, Kenneth Loi1,2, Santiago C. Lopez1,2, Luis E. Valentin- Alvarado1,2, Owen T. Tuck1,2, Stephen G. Brohawn1,3,4,5, Jennifer A. Doudna1,2,3,5,6,7,8,9* Viral interference programmable repeat (VIpr) systems use a noncontiguous code for rNA- guided transcriptional silencing. How the Vipr protein and a VIpr rNA (vrrNA) comprising alternating GGY and NN segments achieve precise DNA targeting is unknown. Here, we present 21 cryo–electron microscopy structures that help explain the mechanism of target engagement. Vipr protomers oligomerize along the vrrNA to form a right- handed helical filament, sequestering each GGY motif and positioning the adjacent NN bases for target base pairing. …
摘自《科学》(Science)第393卷 第6817期 · 2026年9月17日,Peter H. Yoon, Trevor A. Docter, Zeyuan Terry Zhang, Kenneth Loi, Santiago C. Lopez, Luis E. Valentin-Alvarado, Owen T. Tuck, Stephen G. Brohawn, Jennifer A. Doudna。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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