|
|
||||||||
The FASEB Journal, Vol 6, 3186-3192, Copyright © 1992 by The Federation of American Societies for Experimental Biology
REVIEWS |
CP Ehretsmann, AJ Carpousis and HM Krisch
Department of Molecular Biology, University of Geneva, Switzerland.
The fast turnover of mRNA permits rapid changes in the pattern of gene expression. In procaryotes, many enzymes involved in mRNA degradation have been identified and some of these endo- and exo-ribonucleases are now being intensively studied. Some of the structural features of mRNA that influence decay rates have also recently been defined. Although important components of the decay pathway are still elusive, a coherent and simple model for mRNA decay has emerged in the last few years.
This article has been cited by other articles:
![]() |
S. Ghorbel, J. Kormanec, A. Artus, and M.-J. Virolle Transcriptional Studies and Regulatory Interactions between the phoR-phoP Operon and the phoU, mtpA, and ppk Genes of Streptomyces lividans TK24 J. Bacteriol., January 15, 2006; 188(2): 677 - 686. [Abstract] [Full Text] [PDF] |
||||
![]() |
L. Zekri, K. Chebli, H. Tourriere, F. C. Nielsen, T. V. O. Hansen, A. Rami, and J. Tazi Control of Fetal Growth and Neonatal Survival by the RasGAP-Associated Endoribonuclease G3BP Mol. Cell. Biol., October 1, 2005; 25(19): 8703 - 8716. [Abstract] [Full Text] [PDF] |
||||
![]() |
Y. Redko, M. R. Tock, C. J. Adams, V. R. Kaberdin, J. A. Grasby, and K. J. McDowall Determination of the Catalytic Parameters of the N-terminal Half of Escherichia coli Ribonuclease E and the Identification of Critical Functional Groups in RNA Substrates J. Biol. Chem., November 7, 2003; 278(45): 44001 - 44008. [Abstract] [Full Text] [PDF] |
||||
![]() |
V. R. Kaberdin Probing the substrate specificity of Escherichia coli RNase E using a novel oligonucleotide-based assay Nucleic Acids Res., August 15, 2003; 31(16): 4710 - 4716. [Abstract] [Full Text] [PDF] |
||||
![]() |
C. D. Smolke, T. A. Carrier, and J. D. Keasling Coordinated, Differential Expression of Two Genes through Directed mRNA Cleavage and Stabilization by Secondary Structures Appl. Envir. Microbiol., December 1, 2000; 66(12): 5399 - 5405. [Abstract] [Full Text] |
||||
![]() |
K. T. Militello and L. K. Read UTP-Dependent and -Independent Pathways of mRNA Turnover in Trypanosoma brucei Mitochondria Mol. Cell. Biol., April 1, 2000; 20(7): 2308 - 2316. [Abstract] [Full Text] |
||||
![]() |
C. Heck, E. Evguenieva-Hackenberg, A. Balzer, and G. Klug RNase E Enzymes from Rhodobacter capsulatus and Escherichia coli Differ in Context- and Sequence-Dependent In Vivo Cleavage within the Polycistronic puf mRNA J. Bacteriol., December 15, 1999; 181(24): 7621 - 7625. [Abstract] [Full Text] |
||||
![]() |
S. Ghosh and M. P. Deutscher Oligoribonuclease is an essential component of the mRNA decay pathway PNAS, April 13, 1999; 96(8): 4372 - 4377. [Abstract] [Full Text] [PDF] |
||||
![]() |
V. R. Kaberdin, A. Miczak, J. S. Jakobsen, S. Lin-Chao, K. J. McDowall, and A. von Gabain The endoribonucleolytic N-terminal half of Escherichia coli RNase E is evolutionarily conserved in Synechocystis sp. and other bacteria but not the C-terminal half, which is sufficient for degradosome assembly PNAS, September 29, 1998; 95(20): 11637 - 11642. [Abstract] [Full Text] [PDF] |
||||
![]() |
N. F. Vanzo, Y. S. Li, B. Py, E. Blum, C. F. Higgins, L. C. Raynal, H. M. Krisch, and A. J. Carpousis Ribonuclease E organizes the protein interactions in the Escherichia coli RNA degradosome Genes & Dev., September 1, 1998; 12(17): 2770 - 2781. [Abstract] [Full Text] |
||||
![]() |
R. Raya, J. Bardowski, P. S. Andersen, S. D. Ehrlich, and A. Chopin J. Bacteriol., June 15, 1998; 180(12): 3174 - 3180. [Abstract] |
||||
![]() |
F. Claverie-Martin, M. Wang, and S. N. Cohen ARD-1 cDNA from Human Cells Encodes a Site-specific Single-strand Endoribonuclease That Functionally Resembles Escherichia coli RNase E J. Biol. Chem., May 23, 1997; 272(21): 13823 - 13828. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. Yang and D. B. Stern The Spinach Chloroplast Endoribonuclease CSP41 Cleaves the 3'-Untranslated Region of petD mRNA Primarily within Its Terminal Stem-Loop Structure J. Biol. Chem., May 9, 1997; 272(19): 12874 - 12880. [Abstract] [Full Text] [PDF] |
||||
![]() |
G. A. Coburn and G. A. Mackie Overexpression, Purification, and Properties of Escherichia coli Ribonuclease II J. Biol. Chem., January 12, 1996; 271(2): 1048 - 1053. [Abstract] [Full Text] [PDF] |
||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |