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

AUTOR(ES)

Jenkins, Bethany D.

FONTE

Oxford University Press

RESUMO

Group II introns are catalytic RNAs that have been proposed to be the evolutionary precursors to the spliceosome. Most group II 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 pthts 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.

Documentos Relacionados

• Peptidyl-tRNA hydrolase from Sulfolobus solfataricus
• Group II intron splicing factors derived by diversification of an ancient RNA-binding domain
• Peptidyl-tRNA hydrolase is involved in lambda inhibition of host protein synthesis.
• A physiological connection between tmRNA and peptidyl-tRNA hydrolase functions in Escherichia coli
• Visualizing the solvent-inaccessible core of a group II intron ribozyme