| Literature DB >> 15713678 |
Olga V Shpanchenko1, Maria I Zvereva, Pavel V Ivanov, Elizaveta Y Bugaeva, Alexey S Rozov, Alexey A Bogdanov, Markus Kalkum, Leif A Isaksson, Knud H Nierhaus, Olga A Dontsova.
Abstract
tmRNA (transfer messenger RNA) is a unique molecule used by all bacteria to rescue stalled ribosomes and to mark unfinished peptides with a specific degradation signal. tmRNA is recruited by arrested ribosomes in which it facilitates the translational switch from cellular mRNA to the mRNA part of tmRNA. Small protein B (SmpB) is a key partner for the trans-translation activity of tmRNA both in vivo and in vitro. It was shown that SmpB acts at the initiation step of the trans-translation process by facilitating tmRNA aminoacylation and binding to the ribosome. Little is known about the subsequent steps of trans-translation. Here we demonstrated the first example of an investigation of tmRNA.ribosome complexes at different stages of trans-translation. Our results show that the structural element at the position of tmRNA pseudoknot 3 remains intact during the translation of the mRNA module of tmRNA and that it is localized on the surface of the ribosome. At least one SmpB molecule remains bound to a ribosome.tmRNA complex isolated from the cell when translation is blocked at different positions within the mRNA part of tmRNA.Mesh:
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Year: 2005 PMID: 15713678 DOI: 10.1074/jbc.M409094200
Source DB: PubMed Journal: J Biol Chem ISSN: 0021-9258 Impact factor: 5.157