Literature DB >> 12535525

The critical role of the universally conserved A2602 of 23S ribosomal RNA in the release of the nascent peptide during translation termination.

Norbert Polacek1, Maria J Gomez, Koichi Ito, Liqun Xiong, Yoshikazu Nakamura, Alexander Mankin.   

Abstract

The ribosomal peptidyl transferase center is responsible for two fundamental reactions, peptide bond formation and nascent peptide release, during the elongation and termination phases of protein synthesis, respectively. We used in vitro genetics to investigate the functional importance of conserved 23S rRNA nucleotides located in the peptidyl transferase active site for transpeptidation and peptidyl-tRNA hydrolysis. While mutations at A2451, U2585, and C2063 (E. coli numbering) did not significantly affect either of the reactions, substitution of A2602 with C or its deletion abolished the ribosome ability to promote peptide release but had little effect on transpeptidation. This indicates that the mechanism of peptide release is distinct from that of peptide bond formation, with A2602 playing a critical role in peptide release during translation termination.

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Year:  2003        PMID: 12535525     DOI: 10.1016/s1097-2765(02)00825-0

Source DB:  PubMed          Journal:  Mol Cell        ISSN: 1097-2765            Impact factor:   17.970


  37 in total

1.  Interference probing of rRNA with snoRNPs: a novel approach for functional mapping of RNA in vivo.

Authors:  Ben Liu; Maurille J Fournier
Journal:  RNA       Date:  2004-07       Impact factor: 4.942

2.  Structure of the 70S ribosome bound to release factor 2 and a substrate analog provides insights into catalysis of peptide release.

Authors:  Hong Jin; Ann C Kelley; David Loakes; V Ramakrishnan
Journal:  Proc Natl Acad Sci U S A       Date:  2010-04-26       Impact factor: 11.205

3.  Comprehensive genetic selection revealed essential bases in the peptidyl-transferase center.

Authors:  Neuza Satomi Sato; Naomi Hirabayashi; Ilana Agmon; Ada Yonath; Tsutomu Suzuki
Journal:  Proc Natl Acad Sci U S A       Date:  2006-10-10       Impact factor: 11.205

4.  Two distinct components of release factor function uncovered by nucleophile partitioning analysis.

Authors:  Jeffrey J Shaw; Rachel Green
Journal:  Mol Cell       Date:  2007-11-09       Impact factor: 17.970

5.  Peptidyl-CCA deacylation on the ribosome promoted by induced fit and the O3'-hydroxyl group of A76 of the unacylated A-site tRNA.

Authors:  Miljan Simonović; Thomas A Steitz
Journal:  RNA       Date:  2008-09-25       Impact factor: 4.942

6.  Peptide release on the ribosome depends critically on the 2' OH of the peptidyl-tRNA substrate.

Authors:  Julie L Brunelle; Jeffrey J Shaw; Elaine M Youngman; Rachel Green
Journal:  RNA       Date:  2008-06-20       Impact factor: 4.942

Review 7.  Modulating the activity of the peptidyl transferase center of the ribosome.

Authors:  Malte Beringer
Journal:  RNA       Date:  2008-03-27       Impact factor: 4.942

8.  The 2'-OH group of the peptidyl-tRNA stabilizes an active conformation of the ribosomal PTC.

Authors:  Hani S Zaher; Jeffrey J Shaw; Scott A Strobel; Rachel Green
Journal:  EMBO J       Date:  2011-05-06       Impact factor: 11.598

9.  Different substrate-dependent transition states in the active site of the ribosome.

Authors:  Stephan Kuhlenkoetter; Wolfgang Wintermeyer; Marina V Rodnina
Journal:  Nature       Date:  2011-07-31       Impact factor: 49.962

10.  Conjugation with polyamines enhances the antibacterial and anticancer activity of chloramphenicol.

Authors:  Ourania N Kostopoulou; Ekaterini C Kouvela; George E Magoulas; Thomas Garnelis; Ioannis Panagoulias; Maria Rodi; Georgios Papadopoulos; Athanasia Mouzaki; George P Dinos; Dionissios Papaioannou; Dimitrios L Kalpaxis
Journal:  Nucleic Acids Res       Date:  2014-06-17       Impact factor: 16.971

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