Recruitment of a peptidyl-tRNA hydrolase as a facilitator of group II intron splicing in chloroplasts

被引:97
作者
Jenkins, BD [1 ]
Barkan, A [1 ]
机构
[1] Univ Oregon, Inst Mol Biol, Eugene, OR 97403 USA
关键词
catalytic RNA; group II intron; plastid; RNA chaperone; splicing;
D O I
10.1093/emboj/20.4.872
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
Group II introns are catalytic RNAs that have been proposed to be the evolutionary precursors to the spliceosome, Most group LI introns require accessory factors to splice efficiently in vivo, but few such factors have been identified, We have cloned the maize nuclear gene crs2, which is required for the splicing of nine group II introns in chloroplasts, CRS2 is related to peptidyl-tRNA hydrolase enzymes. However, CRS2 expression failed to rescue an Escherichia coli pth(ts) mutant and CRS2 lacks several conserved amino acids that are important for the activity of the E.coli enzyme, indicating that it may lack peptidyl-tRNA hydrolase activity, CRS2 is localized to the chloroplast stroma, where it is found in a large salt-stable complex that contains RNA. CRS2 co-sediments with group II intron RNA during centrifugation of stroma through sucrose gradients, suggesting that CRS2 facilitates splicing via direct interaction with intron RNA. Sequence comparisons indicate how evolutionary tinkering may have allowed an enzyme that interacts with peptidyl-tRNAs to acquire a function in group II intron splicing.
引用
收藏
页码:872 / 879
页数:8
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