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Cooperative Tertiary Interaction Network Guides RNA Folding
被引:79
作者:
Behrouzi, Reza
[1
]
Roh, Joon Ho
[2
,3
]
Kilburn, Duncan
[1
]
Briber, R. M.
[2
]
Woodson, Sarah A.
[1
]
机构:
[1] Johns Hopkins Univ, TC Jenkins Dept Biophys, Baltimore, MD 21218 USA
[2] Univ Maryland, Dept Mat Sci & Engn, College Pk, MD 20742 USA
[3] Natl Inst Stand & Technol, Ctr Neutron Res, Gaithersburg, MD 20899 USA
来源:
基金:
美国国家卫生研究院;
关键词:
GROUP-I RIBOZYME;
TETRAHYMENA-THERMOPHILA RIBOZYME;
COMPARATIVE SEQUENCE;
CRYSTAL-STRUCTURE;
STRUCTURAL BASIS;
CORE HELICES;
ACTIVE-SITE;
INTRON;
STABILITY;
COLLAPSE;
D O I:
10.1016/j.cell.2012.01.057
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:
Noncoding RNAs form unique 3D structures, which perform many regulatory functions. To understand how RNAs fold uniquely despite a small number of tertiary interaction motifs, we mutated the major tertiary interactions in a group I ribozyme by single-base substitutions. The resulting perturbations to the folding energy landscape were measured using SAXS, ribozyme activity, hydroxyl radical footprinting, and native PAGE. Double-and triple-mutant cycles show that most tertiary interactions have a small effect on the stability of the native state. Instead, the formation of core and peripheral structural motifs is cooperatively linked in near-native folding intermediates, and this cooperativity depends on the native helix orientation. The emergence of a cooperative interaction network at an early stage of folding suppresses nonnative structures and guides the search for the native state. We suggest that cooperativity in noncoding RNAs arose from natural selection of architectures conducive to forming a unique, stable fold.
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页码:348 / 357
页数:10
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