このアイテムのアクセス数: 116
このアイテムのファイル:
ファイル | 記述 | サイズ | フォーマット | |
---|---|---|---|---|
s41467-023-44217-8.pdf | 2.84 MB | Adobe PDF | 見る/開く |
完全メタデータレコード
DCフィールド | 値 | 言語 |
---|---|---|
dc.contributor.author | Fujita, Ken-ichi | en |
dc.contributor.author | Ito, Misa | en |
dc.contributor.author | Irie, Midori | en |
dc.contributor.author | Harada, Kotaro | en |
dc.contributor.author | Fujiwara, Naoko | en |
dc.contributor.author | Ikeda, Yuya | en |
dc.contributor.author | Yoshioka, Hanae | en |
dc.contributor.author | Yamazaki, Tomohiro | en |
dc.contributor.author | Kojima, Masaki | en |
dc.contributor.author | Mikami, Bunzo | en |
dc.contributor.author | Mayeda, Akila | en |
dc.contributor.author | Masuda, Seiji | en |
dc.contributor.alternative | 藤田, 賢一 | ja |
dc.contributor.alternative | 伊藤, 慶紗 | ja |
dc.contributor.alternative | 入江, みどり | ja |
dc.contributor.alternative | 原田, 光太郎 | ja |
dc.contributor.alternative | 藤原, 奈央子 | ja |
dc.contributor.alternative | 池田, 宥哉 | ja |
dc.contributor.alternative | 吉岡, 英恵 | ja |
dc.contributor.alternative | 山崎, 智弘 | ja |
dc.contributor.alternative | 小島, 正樹 | ja |
dc.contributor.alternative | 三上, 文三 | ja |
dc.contributor.alternative | 前田, 明 | ja |
dc.contributor.alternative | 増田, 誠司 | ja |
dc.date.accessioned | 2024-01-18T04:09:18Z | - |
dc.date.available | 2024-01-18T04:09:18Z | - |
dc.date.issued | 2024-01-15 | - |
dc.identifier.uri | http://hdl.handle.net/2433/286644 | - |
dc.description | mRNAを核から細胞質へ輸送するバルクmRNA輸送体の構成因子を解明 がんの早期発見や予後の予測に役立つ可能性のある研究成果. 京都大学プレスリリース. 2024-01-16. | ja |
dc.description.abstract | mRNA export is an essential pathway for the regulation of gene expression. In humans, closely related RNA helicases, UAP56 and URH49, shape selective mRNA export pathways through the formation of distinct complexes, known as apo-TREX and apo-AREX complexes, and their subsequent remodeling into similar ATP-bound complexes. Therefore, defining the unidentified components of the apo-AREX complex and elucidating the molecular mechanisms underlying the formation of distinct apo-complexes is key to understanding their functional divergence. In this study, we identify additional apo-AREX components physically and functionally associated with URH49. Furthermore, by comparing the structures of UAP56 and URH49 and performing an integrated analysis of their chimeric mutants, we exhibit unique structural features that would contribute to the formation of their respective complexes. This study provides insights into the specific structural and functional diversification of these two helicases that diverged from the common ancestral gene Sub2. | en |
dc.language.iso | eng | - |
dc.publisher | Springer Nature | en |
dc.rights | © The Author(s) 2024 | en |
dc.rights | This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. | en |
dc.rights.uri | http://creativecommons.org/licenses/by/4.0/ | - |
dc.subject | RNA transport | en |
dc.subject | X-ray crystallography | en |
dc.title | Structural differences between the closely related RNA helicases, UAP56 and URH49, fashion distinct functional apo-complexes | en |
dc.type | journal article | - |
dc.type.niitype | Journal Article | - |
dc.identifier.jtitle | Nature Communications | en |
dc.identifier.volume | 15 | - |
dc.relation.doi | 10.1038/s41467-023-44217-8 | - |
dc.textversion | publisher | - |
dc.identifier.artnum | 455 | - |
dc.address | Division of Integrated Life Sciences, Graduate School of Biostudies, Kyoto University; Division of Gene Expression Mechanism, Center for Medical Science, Fujita Health University; Division of Cancer Stem Cell, National Cancer Center Research Institute | en |
dc.address | Division of Integrated Life Sciences, Graduate School of Biostudies, Kyoto University | en |
dc.address | Division of Integrated Life Sciences, Graduate School of Biostudies, Kyoto University | en |
dc.address | Division of Integrated Life Sciences, Graduate School of Biostudies, Kyoto University | en |
dc.address | Division of Integrated Life Sciences, Graduate School of Biostudies, Kyoto University | en |
dc.address | Division of Integrated Life Sciences, Graduate School of Biostudies, Kyoto University | en |
dc.address | Division of Integrated Life Sciences, Graduate School of Biostudies, Kyoto University | en |
dc.address | Division of Integrated Life Sciences, Graduate School of Biostudies, Kyoto University | en |
dc.address | School of Life Sciences, Tokyo University of Pharmacy and Life Sciences | en |
dc.address | Research Institute for Sustainable Humanosphere, Kyoto University; Institute of Advanced Energy, Kyoto University | en |
dc.address | Division of Gene Expression Mechanism, Center for Medical Science, Fujita Health University | en |
dc.address | Division of Integrated Life Sciences, Graduate School of Biostudies, Kyoto University; Department of Food Science and Nutrition, Faculty of Agriculture Kindai University; Agricultural Technology and Innovation Research Institute, Kindai University; Antiaging Center, Kindai University | en |
dc.identifier.pmid | 38225262 | - |
dc.relation.url | https://www.kyoto-u.ac.jp/ja/research-news/2024-01-16-1 | - |
dcterms.accessRights | open access | - |
datacite.awardNumber | 26292053 | - |
datacite.awardNumber | 17K19232 | - |
datacite.awardNumber | 19K22280 | - |
datacite.awardNumber | 19H02884 | - |
datacite.awardNumber | 21K19078 | - |
datacite.awardNumber | 22H02264 | - |
datacite.awardNumber | 19K15807 | - |
datacite.awardNumber.uri | https://kaken.nii.ac.jp/grant/KAKENHI-PROJECT-26292053/ | - |
datacite.awardNumber.uri | https://kaken.nii.ac.jp/grant/KAKENHI-PROJECT-17K19232/ | - |
datacite.awardNumber.uri | https://kaken.nii.ac.jp/grant/KAKENHI-PROJECT-19K22280/ | - |
datacite.awardNumber.uri | https://kaken.nii.ac.jp/grant/KAKENHI-PROJECT-19H02884/ | - |
datacite.awardNumber.uri | https://kaken.nii.ac.jp/grant/KAKENHI-PROJECT-21K19078/ | - |
datacite.awardNumber.uri | https://kaken.nii.ac.jp/grant/KAKENHI-PROJECT-22H02264/ | - |
datacite.awardNumber.uri | https://kaken.nii.ac.jp/grant/KAKENHI-PROJECT-19K15807/ | - |
dc.identifier.eissn | 2041-1723 | - |
jpcoar.funderName | 日本学術振興会 | ja |
jpcoar.funderName | 日本学術振興会 | ja |
jpcoar.funderName | 日本学術振興会 | ja |
jpcoar.funderName | 日本学術振興会 | ja |
jpcoar.funderName | 日本学術振興会 | ja |
jpcoar.funderName | 日本学術振興会 | ja |
jpcoar.funderName | 日本学術振興会 | ja |
jpcoar.awardTitle | 真核細胞におけるmRNA輸送基盤の解明とアプライドmRNAバイオテクロジー | ja |
jpcoar.awardTitle | カルシウムシグナリングによる選択的mRNAスプライシング制御原理の新規解明 | ja |
jpcoar.awardTitle | 活性フラボノイドによる選択的mRNAスプライシング制御の分子機構解明と応用展開 | ja |
jpcoar.awardTitle | 真核細胞におけるmRNA核外輸送体の分子進化による輸送体多様化の分子基盤の解明 | ja |
jpcoar.awardTitle | スプライシング阻害活性をモデルとした食品化合物の迅速探索・評価法の開発と応用展開 | ja |
jpcoar.awardTitle | ヒトにおける核内mRNA輸送経路の多様化とその生理的意義の解明 | ja |
jpcoar.awardTitle | mRNA輸送因子UAP56とURH49による選択的mRNA輸送基盤の統合的解析 | ja |
出現コレクション: | 学術雑誌掲載論文等 |

このアイテムは次のライセンスが設定されています: クリエイティブ・コモンズ・ライセンス