Crystal structure of a luteoviral RNA pseudoknot and model for a minimal ribosomal frameshifting motif

被引:48
作者
Pallan, PS
Marshall, WS
Harp, J
Jewett, FC
Wawrzak, Z
Brown, BA
Rich, A
Egli, M
机构
[1] Vanderbilt Univ, Sch Med, Dept Biochem, Nashville, TN 37232 USA
[2] Dharmacon Inc, Lafayette, CO 80026 USA
[3] Wake Forest Univ, Dept Chem, DND CAT, Winston Salem, NC 27109 USA
[4] Argonne Natl Lab, Synchrotron Res Ctr, Adv Photon Source, Argonne, IL 60439 USA
[5] MIT, Dept Biol, Cambridge, MA 02139 USA
关键词
D O I
10.1021/bi051061i
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
To understand the role of structural elements of RNA pseudoknots in controlling the extent of -1-type ribosomal frameshifting, we determined the crystal structure of a high-efficiency frameshifting mutant of the pseudoknot from potato leaf roll virus (PLRV). Correlations of the structure with available in vitro frameshifting data for PLRV pseudoknot mutants implicate sequence and length of a stem-loop linker as modulators of frameshifting efficiency. Although the sequences and overall structures of the RNA pseudoknots from PLRV and beet western yellow virus (BWYV) are similar, nucleotide deletions in the linker and adjacent minor groove loop abolish frameshifting only with the latter. Conversely, mutant PLRV pseudoknots with up to four nucleotides deleted in this region exhibit nearly wild-type frameshifting efficiencies. The crystal structure helps rationalize the different tolerances for deletions in the PLRV and BWYV RNAs, and we have used it to build a three-dimensional model of the PRLV pseudoknot with a four-nucleotide deletion. The resulting structure defines a minimal RNA pseudoknot motif composed of 22 nucleotides capable of stimulating -1-type ribosomal frameshifts.
引用
收藏
页码:11315 / 11322
页数:8
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