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-Structure paper
| タイトル | Bacterial reverse transcriptase synthesizes long poly(A)-rich cDNA for antiphage defense. |
|---|---|
| ジャーナル・号・ページ | Science, Vol. 388, Issue 6753, Page eads4639, Year 2025 |
| 掲載日 | 2025年6月19日 |
 著者 | Xin-Yi Song / Yushan Xia / Jun-Tao Zhang / Yu-Jun Liu / Hua Qi / Xin-Yang Wei / Hailiang Hu / Yu Xia / Xue Liu / Ying-Fei Ma / Ning Jia /  |
| PubMed 要旨 | Prokaryotic defense-associated reverse transcriptases (DRTs) were recently identified with antiviral functions; however, their functional mechanisms remain largely unexplored. Here we show that DRT9 ...Prokaryotic defense-associated reverse transcriptases (DRTs) were recently identified with antiviral functions; however, their functional mechanisms remain largely unexplored. Here we show that DRT9 forms a hexameric complex with its upstream noncoding RNA (ncRNA) to mediate antiphage defense by inducing cell growth arrest through abortive infection. Upon phage infection, the phage-encoded ribonucleotide reductase NrdAB complex increases intracellular deoxyadenosine triphosphate levels, activating DRT9 to synthesize long, polyadenylate [poly(A)]-rich single-stranded complementary DNA (cDNA), which likely sequesters the essential phage single-stranded DNA binding (SSB) protein and disrupts phage propagation. We further determined the cryo-electron microscopy structure of the DRT9-ncRNA hexamer complex, providing mechanistic insights into its cDNA synthesis. These findings highlight the diversity of RT-based antiviral defense mechanisms, expand our understanding of RT biological functions, and provide a structural basis for developing DRT9-based biotechnological tools. |
 リンク | Science / PubMed:40310939 |
| 手法 | EM (単粒子) |
| 解像度 | 2.59 - 2.62 Å |
| 構造データ | EMDB-60724, PDB-9ioa: EMDB-60725, PDB-9iob: |
| 由来 |
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 キーワード | ANTIVIRAL PROTEIN/RNA / RNA BINDING / PROTEIN-RNA COMPLEX / ANTIVIRAL PROTEIN-RNA complex |
escherichia coli (大腸菌)
