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-Structure paper
タイトル | Cryo-EM structures of Escherichia coli Ec86 retron complexes reveal architecture and defence mechanism. |
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ジャーナル・号・ページ | Nat Microbiol, Vol. 7, Issue 9, Page 1480-1489, Year 2022 |
掲載日 | 2022年8月18日 |
著者 | Yanjing Wang / Zeyuan Guan / Chen Wang / Yangfan Nie / Yibei Chen / Zhaoyang Qian / Yongqing Cui / Han Xu / Qiang Wang / Fen Zhao / Delin Zhang / Pan Tao / Ming Sun / Ping Yin / Shuangxia Jin / Shan Wu / Tingting Zou / |
PubMed 要旨 | First discovered in the 1980s, retrons are bacterial genetic elements consisting of a reverse transcriptase and a non-coding RNA (ncRNA). Retrons mediate antiphage defence in bacteria but their ...First discovered in the 1980s, retrons are bacterial genetic elements consisting of a reverse transcriptase and a non-coding RNA (ncRNA). Retrons mediate antiphage defence in bacteria but their structure and defence mechanisms are unknown. Here, we investigate the Escherichia coli Ec86 retron and use cryo-electron microscopy to determine the structures of the Ec86 (3.1 Å) and cognate effector-bound Ec86 (2.5 Å) complexes. The Ec86 reverse transcriptase exhibits a characteristic right-hand-like fold consisting of finger, palm and thumb subdomains. Ec86 reverse transcriptase reverse-transcribes part of the ncRNA into satellite, multicopy single-stranded DNA (msDNA, a DNA-RNA hybrid) that we show wraps around the reverse transcriptase electropositive surface. In msDNA, both inverted repeats are present and the 3' sides of the DNA/RNA chains are close to the reverse transcriptase active site. The Ec86 effector adopts a two-lobe fold and directly binds reverse transcriptase and msDNA. These findings offer insights into the structure-function relationship of the retron-effector unit and provide a structural basis for the optimization of retron-based genome editing systems. |
リンク | Nat Microbiol / PubMed:35982312 |
手法 | EM (単粒子) |
解像度 | 2.51 - 3.12 Å |
構造データ | EMDB-31827, PDB-7v9u: EMDB-33226, PDB-7xjg: |
化合物 | ChemComp-MG: |
由来 |
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キーワード | TRANSFERASE/DNA/RNA / Reverse transcriptase / RNA BINDING PROTEIN / TRANSFERASE-DNA-RNA complex / RNA BINDING PROTEIN/DNA/RNA / RNA BINDING PROTEIN-DNA-RNA complex |