5U6H

Solution structure of the zinc fingers 1 and 2 of MBNL1

5U6H の概要

• エントリーDOI: 10.2210/pdb5u6h/pdb
• 関連するPDBエントリー: 5U6L 5U9B
• NMR情報: BMRB: 30207
• 分子名称: Muscleblind-like protein 1, ZINC ION (2 entities in total)
• 機能のキーワード: zinc fingers rna-binding, structure from molmol, rna binding protein
• 由来する生物種: Homo sapiens (Human)
• 細胞内の位置: Nucleus : Q9NR56
• タンパク質・核酸の鎖数: 1
• 化学式量合計: 10708.00

構造登録者

Phukan, P.D.,Park, S.,Martinez-Yamout, M.M.,Zeeb, M.,Dyson, H.J.,Wright, P.E. (登録日: 2016-12-08, 公開日: 2017-08-02, 最終更新日: 2024-05-15)

主引用文献

Park, S.,Phukan, P.D.,Zeeb, M.,Martinez-Yamout, M.A.,Dyson, H.J.,Wright, P.E.
Structural Basis for Interaction of the Tandem Zinc Finger Domains of Human Muscleblind with Cognate RNA from Human Cardiac Troponin T.
Biochemistry, 56:4154-4168, 2017

PubMed Abstract: The human muscleblind-like proteins (MBNL) regulate tissue-specific splicing by targeting cardiac troponin T and other pre-mRNAs; aberrant targeting of CUG and CCUG repeat expansions frequently accompanies the neuromuscular disease myotonic dystrophy. We show, using biolayer interferometry (Octet) and NMR spectroscopy, that the zinc finger domains of MBNL isoform 1 (MBNL1) are necessary and sufficient for binding CGCU sequences within the pre-mRNA of human cardiac troponin T. Protein constructs containing zinc fingers 1 and 2 (zf12) and zinc fingers 3 and 4 (zf34) of MBNL1 each fold into a compact globular tandem zinc finger structure that participates in RNA binding. NMR spectra show that the stoichiometry of the interaction between zf12 or zf34 and the CGCU sequence is 1:1, and that the RNA is single-stranded in the complex. The individual zinc fingers within zf12 or zf34 are nonequivalent: the primary RNA binding surface is formed in each pair by the second zinc finger (zf2 or zf4), which interacts with the CGCU RNA sequence. The NMR structure of the complex between zf12 and a 15-base RNA of sequence GUCUCGCUUUUCCCC, containing a single CGCU element, shows the single-stranded RNA wrapped around zf2 and extending to bind to the C-terminal helix. Bases C101, U102, and U103 make well-defined and highly ordered contacts with the protein, whereas neighboring bases are less well-ordered in the complex. Binding of the MBNL zinc fingers to cardiac troponin T pre-mRNA is specific and relatively simple, unlike the complex multiple dimer-trimer stoichiometries postulated in some previous studies.

PubMed: 28718627
DOI: 10.1021/acs.biochem.7b00484

実験手法

SOLUTION NMR