The structure of helix III in Xenopus oocyte 5 S rRNA:: An RNA stem containing a two-nucleotide bulge

被引:14
作者
Huber, PW [1 ]
Rife, JP
Moore, PB
机构
[1] Univ Notre Dame, Dept Chem & Biochem, Notre Dame, IN 46556 USA
[2] Virginia Commonwealth Univ, Dept Med Chem, Richmond, VA 23298 USA
[3] Virginia Commonwealth Univ, Inst Struct Biol & Drug Discovery, Richmond, VA 23298 USA
[4] Yale Univ, Dept Chem, New Haven, CT 06520 USA
[5] Yale Univ, Dept Mol Biophys & Biochem, New Haven, CT 06520 USA
关键词
5 S rRNA; ribosomal protein L5; bulged nucleotides; NMR spectroscopy;
D O I
10.1006/jmbi.2001.4966
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The solution structure of an oligonucleotide containing the helix Ill sequence from Xenopus oocyte 5 S rRNA has been determined by NMR spectroscopy. Helix III includes two unpaired adenosine residues, flanked on either side by G:C base-pairs, that are required for binding of ribosomal protein L5. The consensus conformation of helix Ill in the context provided by this oligonucleotide has the two adenosine residues located in the miner groove and stacked upon the 3' flanking guanosine residue, consistent with biochemical studies of free 5 S rRNA in solution. A distinct break in stacking that occurs between the first adenosine residue of the bulge and the flanking 5' guanosine residue exposes the base of the adenosine residue in the minor groove and the base of the guanosine residue in the major groove. The major groove of the helix is widened at the site of the unpaired nucleotides and the helix is substantially bent; nonetheless, the G:C base-pairs flanking the bulge are intact. The data indicate that there may be conformational heterogeneity centered in the bulge region. The corresponding adenosine residues in the Haloarcula marismortui 50 S ribosomal subunit form a dinucleotide platform, which is quite different from the motif seen in solution. Thus, the conformation of helix Ill probably changes when 5 S rRNA is incorporated into the ribosome. (C) 2001 Academic Press.
引用
收藏
页码:823 / 832
页数:10
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