+データを開く
-基本情報
登録情報 | データベース: SASBDB / ID: SASDDK5 |
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試料 | Mammalian prion protein mRNA (PrP mRNA wild type) with KCl and pyridostatin (PDS)
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生物種 | human PrP ORF |
引用 | ジャーナル: Sci Rep / 年: 2019 タイトル: Octa-repeat domain of the mammalian prion protein mRNA forms stable A-helical hairpin structure rather than G-quadruplexes. 著者: Andreas Czech / Petr V Konarev / Ingrid Goebel / Dmitri I Svergun / Peter R Wills / Zoya Ignatova / 要旨: Misfolding and aggregation of prion protein (PrP) causes neurodegenerative diseases like Creutzfeldt-Jakob disease (CJD) and scrapie. Besides the consensus that spontaneous conversion of normal ...Misfolding and aggregation of prion protein (PrP) causes neurodegenerative diseases like Creutzfeldt-Jakob disease (CJD) and scrapie. Besides the consensus that spontaneous conversion of normal cellular PrP into misfolded and aggregating PrP is the central event in prion disease, an alternative hypothesis suggests the generation of pathological PrP by rare translational frameshifting events in the octa-repeat domain of the PrP mRNA. Ribosomal frameshifting most commonly relies on a slippery site and an adjacent stable RNA structure to stall translating ribosome. Hence, it is crucial to unravel the secondary structure of the octa-repeat domain of PrP mRNA. Each of the five octa-repeats contains a motif (GGCGGUGGUGGCUGGG) which alone in vitro forms a G-quadruplex. Since the propensity of mRNA to form secondary structure depends on the sequence context, we set to determine the structure of the complete octa-repeat region. We assessed the structure of full-length octa-repeat domain of PrP mRNA using dynamic light scattering (DLS), small angle X-ray scattering (SAXS), circular dichroism (CD) spectroscopy and selective 2'-hydroxyl acylation analysis by primer extension (SHAPE). Our data show that the PrP octa-repeat mRNA forms stable A-helical hairpins with no evidence of G-quadruplex structure even in the presence of G-quadruplex stabilizing agents. |
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-構造の表示
構造ビューア | 分子: MolmilJmol/JSmol |
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-ダウンロードとリンク
-モデル
モデル #1894 | タイプ: dummy / ソフトウェア: (5.0) / ダミー原子の半径: 7.50 A / カイ2乗値: 1.098 / P-value: 0.091063 Omokage検索でこの集合体の類似形状データを探す (詳細) |
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-試料
試料 | 名称: Mammalian prion protein mRNA (PrP mRNA wild type) with KCl and pyridostatin (PDS) 試料濃度: 0.50-4.00 |
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バッファ | 名称: 10 mM Tris buffer with 100 mM KCl and 1 mM PDS / pH: 7.5 |
要素 #1021 | 名称: PrPmRNA / タイプ: RNA / 記述: octo-repeat PrP mRNA / 分子量: 71.89 / 分子数: 2 / 由来: human PrP ORF 配列: AACACUGGGG GCAGCCGAUA CCCGGGGCAG GGCAGCCCUG GAGGCAACCG CUACCCACCU CAGGGCGGUG GUGGCUGGGG GCAGCCUCAU GGUGGUGGCU GGGGGCAGCC UCAUGGUGGU GGCUGGGGGC AGCCCCAUGG UGGUGGCUGG GGACAGCCUC AUGGUGGUGG ...配列: AACACUGGGG GCAGCCGAUA CCCGGGGCAG GGCAGCCCUG GAGGCAACCG CUACCCACCU CAGGGCGGUG GUGGCUGGGG GCAGCCUCAU GGUGGUGGCU GGGGGCAGCC UCAUGGUGGU GGCUGGGGGC AGCCCCAUGG UGGUGGCUGG GGACAGCCUC AUGGUGGUGG CUGGGGUCAA GGAGGUGGCA CCCACCUCAG GGCGGUGGUG GCUGGGGGCC |
-実験情報
ビーム | 設備名称: PETRA III EMBL P12 / 地域: Hamburg / 国: Germany / 線源: X-ray synchrotron / 波長: 0.124 Å / スペクトロメータ・検出器間距離: 3.1 mm | ||||||||||||||||||||||||||||||||||||||||||
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検出器 | 名称: Pilatus 2M | ||||||||||||||||||||||||||||||||||||||||||
スキャン | タイトル: Mammalian prion protein mRNA (PrP mRNA wild type) with KCl and pyridostatin (PDS) 測定日: 2017年6月6日 / 保管温度: 20 °C / セル温度: 20 °C / 照射時間: 0.05 sec. / フレーム数: 20 / 単位: 1/nm /
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距離分布関数 P(R) | ソフトウェア P(R): GNOM 4.6 / ポイント数: 400 /
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結果 | カーブのタイプ: merged
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