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-Structure paper
タイトル | Structural basis of RNA-induced autoregulation of the DExH-type RNA helicase maleless. |
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ジャーナル・号・ページ | Mol Cell, Vol. 83, Issue 23, Page 4318-4333.e10, Year 2023 |
掲載日 | 2023年12月7日 |
著者 | Pravin Kumar Ankush Jagtap / Marisa Müller / Anna E Kiss / Andreas W Thomae / Karine Lapouge / Martin Beck / Peter B Becker / Janosch Hennig / |
PubMed 要旨 | RNA unwinding by DExH-type helicases underlies most RNA metabolism and function. It remains unresolved if and how the basic unwinding reaction of helicases is regulated by auxiliary domains. We ...RNA unwinding by DExH-type helicases underlies most RNA metabolism and function. It remains unresolved if and how the basic unwinding reaction of helicases is regulated by auxiliary domains. We explored the interplay between the RecA and auxiliary domains of the RNA helicase maleless (MLE) from Drosophila using structural and functional studies. We discovered that MLE exists in a dsRNA-bound open conformation and that the auxiliary dsRBD2 domain aligns the substrate RNA with the accessible helicase tunnel. In an ATP-dependent manner, dsRBD2 associates with the helicase module, leading to tunnel closure around ssRNA. Furthermore, our structures provide a rationale for blunt-ended dsRNA unwinding and 3'-5' translocation by MLE. Structure-based MLE mutations confirm the functional relevance of our model for RNA unwinding. Our findings contribute to our understanding of the fundamental mechanics of auxiliary domains in DExH helicase MLE, which serves as a model for its human ortholog and potential therapeutic target, DHX9/RHA. |
リンク | Mol Cell / PubMed:37989319 |
手法 | EM (単粒子) |
解像度 | 2.86 - 4.24 Å |
構造データ | EMDB-15931, PDB-8b9g: EMDB-15932, PDB-8b9i: EMDB-15933, PDB-8b9j: EMDB-15934, PDB-8b9k: EMDB-15935, PDB-8b9l: EMDB-17703, PDB-8pjb: EMDB-17711, PDB-8pjj: |
化合物 | ChemComp-ADP: ChemComp-ALF: ChemComp-HOH: ChemComp-MG: |
由来 |
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キーワード | RNA BINDING PROTEIN / RNA Helicase / Drosophila dosage compensation |