Science (New York, N.Y.) · 2026
A noncontiguous code for RNA-guided DNA recognition at the origin of CRISPR-Cas.
СтатьяНазвание и аннотация: Перевод в очереди
Обработка статьи · этапы, ошибки и управление
Загрузка состояния…
Ошибки и ограничения
История · было → стало
Состояние обновляется каждые 5 секунд, пока блок открыт. Процент показывается только там, где известен объём работы. Пауза останавливает продолжение этапа; текущий запрос к источнику может завершиться.
Yoon Peter H, Loi Kenneth J, Zhang Zeyuan Terry, Docter Trevor A, Lopez Santiago C, Langeberg Conner J, Ur-Rehman Muhammad Moez, Vohra Kamakshi, Zhou Zehan, Esain-Garcia Isabel, Trinidad Marena I, Shi Honglue, Boger Ron, Wang Peter Y, Adler Benjamin A, Brohawn Stephen G, Doudna Jennifer A
Аннотация
CRISPR-Cas provides RNA-mediated adaptive immunity, but how its first RNA-guided effector arose is unclear. In this study, we report the discovery of Viral Interference Programmable Repeat (VIPR) systems consisting of a Vipr protein ancestral to the earliest CRISPR-Cas effectors and VIPR RNAs (vrRNAs) comprising alternating GGY/NN motifs. Unlike canonical guide RNAs that pair with target nucleic acids through contiguous complementarity, vrRNAs recognize double-stranded DNA through a noncontiguous code in which the variable NN dinucleotides collectively specify a gapped target sequence. Natural vrRNA targets suggest that VIPR systems act against competing phages, and we demonstrate programmable phage defense by redirecting the complex for transcriptional repression. These results suggest that adaptive immunity originated from ancient warfare between viruses, revealing a previously unidentified logic for encoding information in sequence.