Advertisement
JBC

HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Submit a Letter to Editor
Right arrow Alert me when this article is cited
Right arrow Alert me when eLetters are posted
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrowRequest Permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Meinnel, T.
Right arrow Articles by Blanquet, S.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Meinnel, T.
Right arrow Articles by Blanquet, S.
Social Bookmarking
 Add to CiteULike   Add to Complore   Add to Connotea   Add to Del.icio.us   Add to Digg   Add to Reddit   Add to Technorati  
What's this?

Volume 270, Number 26, Issue of June 30, pp. 15908-15914, 1995
©1995 by The American Society for Biochemistry and Molecular Biology, Inc.
Maturation of Pre-tRNA by Escherichia coli RNase P Is Specified by a Guanosine of the 5`-Flanking Sequence

Thierry Meinnel , Sylvain Blanquet

The C/A base pair at the top of the acceptor stem of Escherichia coli tRNA accounts for several of the specialized roles of this tRNA in translation initiation. According to the rules of RNA substrate recognition by RNase P, the C/A pair is likely to disfavor the 5`-maturation of pre-tRNA. Indeed, in contrast to other E. coli tRNA species, tRNA was not properly matured when overproduced from a multicopy expression vector. Half of the recovered tRNA retained an extension at the 5` side. Such a defect of tRNA processing could be cured by changing bases C and A by a Watson-Crick base pair or by non-paired bases, provided one of them was a G. It could also be compensated by either (i) overexpression of RNase P or (ii) introduction within the plasmid of one out of the three 5`-flanking sequences naturally occurring in the four E. coli tRNA genes. The effect of these flanking sequences on the maturation of tRNA could be accounted for by the presence of a G located 2 bases upstream from C. Notably, this G is the only residue that is conserved in the 5`-flanking sequences of all four E. coli tRNA genes.




Add to CiteULike CiteULike   Add to Complore Complore   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us   Add to Digg Digg   Add to Reddit Reddit   Add to Technorati Technorati    What's this?


This article has been cited by other articles:


Home page
Nucleic Acids ResHome page
R. Villet, M. Fonvielle, P. Busca, M. Chemama, A. P. Maillard, J.-E. Hugonnet, L. Dubost, A. Marie, N. Josseaume, S. Mesnage, et al.
Idiosyncratic features in tRNAs participating in bacterial cell wall synthesis
Nucleic Acids Res., November 29, 2007; 35(20): 6870 - 6883.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
J.-M. Guillon, S. Heiss, J. Soutourina, Y. Mechulam, S. Laalami, M. Grunberg-Manago, and S. Blanquet
Interplay of Methionine tRNAs with Translation Elongation Factor Tu and Translation Initiation Factor 2in Escherichia coli
J. Biol. Chem., September 13, 1996; 271(37): 22321 - 22325.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 All ASBMB Journals   Molecular and Cellular Proteomics 
 Journal of Lipid Research   ASBMB Today 
Copyright © 1995 by the American Society for Biochemistry and Molecular Biology.
Advertisement
spacer
Advertisement
Advertisement