Methylation of bacterial release factors RF1 and RF2 is required for normal translation termination in vivo

作者：Mora Liliana; Heurgue Hamard Valerie; de Zamaroczy Miklos; Kervestin Stephanie; Buckingham Richard H^*

来源：JOURNAL OF BIOLOGICAL CHEMISTRY, 2007, 282(49): 35638-35645.

DOI：10.1074/jbc.M706076200

Bacterial release factors RF1 and RF2 are methylated on the Gln residue of a universally conserved tripeptide motif GGQ, which interacts with the peptidyl transferase center of the large ribosomal subunit, triggering hydrolysis of the ester bond in peptidyl-tRNA and releasing the newly synthesized polypeptide from the ribosome. In vitro experiments have shown that the activity of RF2 is stimulated by Gln methylation. The viability of Escherichia coli K12 strains depends on the integrity of the release factor methyltransferase PrmC, because K12 strains are partially deficient in RF2 activity due to the presence of a Thr residue at position 246 instead of Ala. Here, we study in vivo RF1 and RF2 activity at termination codons in competition with programmed frameshifting and the effect of the Ala-246 -> Thr mutation. PrmC inactivation reduces the specific termination activity of RF1 and RF2(Ala-246) by similar to 3- to 4-fold. The mutation Ala-246 -> Thr in RF2 reduces the termination activity in cells similar to 5-fold. After correction for the decrease in level of RF2 due to the autocontrol of RF2 synthesis, the mutation Ala-246 -> Thr reduced RF2 termination activity by similar to 10-fold at UGA codons and UAA codons. PrmC inactivation had no effect on cell growth in rich media but reduced growth considerably on poor carbon sources. This suggests that the expression of some genes needed for optimal growth under such conditions can become growth limiting as a result of inefficient translation termination.

• 出版日期2007-12-7