Translational repression mechanisms in prokaryotes.

Mol Microbiol

Department of Chemistry, Program in Biological Chemistry, Bates College, 5 Andrews Road, Lewiston, Maine 04240, USA.

Published: June 2003

Translational repression results from a complex choreography of macromolecular interactions interfering with the formation of translational initiation complexes. The relationship between the rate and extent of formation of these interactions to form repressed mRNA complexes determines the extent of repression. A novel analysis of repression mechanisms is presented here and it indicates that the reversibility of repressed complex formation influences the steady state balance of the distribution of translationally active and inactive complexes and therefore has an impact on the efficiency of repression. Reviewed here is evidence for three distinct translational repression mechanisms, regulating expression of the transcription factor sigma32, threonine tRNA synthetase and ribosomal proteins on the alpha operon in Escherichia coli. Efficient regulation of expression in these systems makes use of specific mRNA structures in quite different ways.

Download full-text PDF

Source
http://dx.doi.org/10.1046/j.1365-2958.2003.03517.xDOI Listing

Publication Analysis

Top Keywords

translational repression
12
repression mechanisms
12
repression
5
translational
4
mechanisms prokaryotes
4
prokaryotes translational
4
repression complex
4
complex choreography
4
choreography macromolecular
4
macromolecular interactions
4

Similar Publications

Subcellular spatial regulation of immunity-induced phosphorylation of RIN4 links PAMP-triggered immunity to Exo70B1.

Front Plant Sci

December 2024

Department of Plant, Soil and Microbial Sciences, Michigan State University, East Lansing, MI, United States.

RIN4 is a crucial regulator of plant immunity, playing a role in both PAMP-triggered immunity (PTI) and effector-triggered immunity (ETI). While the impact of post-translational modifications (PTMs) on RIN4 has been extensively studied, their specific effects on plant immune response regulation and the underlying mechanisms have remained unclear. In this study, we investigated the phosphorylation of RIN4 at threonine-166 (RIN4) in transgenic lines expressing various RIN4 variants.

View Article and Find Full Text PDF

Receptor kinase LecRK-I.9 regulates cell wall remodelling during lateral root formation in Arabidopsis.

J Exp Bot

December 2024

Laboratoire de Recherche en Sciences Végétales, Université de Toulouse, CNRS, UPS, Toulouse INP, F-31320, Auzeville-Tolosane, France.

Assembling and remodelling the cell wall is essential for plant development. Cell wall dynamics is controlled by cell wall proteins, polysaccharide biosynthesis, and a variety of sensor and receptor systems. LecRK-I.

View Article and Find Full Text PDF

Natural variation in an HD-ZIP factor identifies its role in controlling apple leaf cuticular wax deposition.

Dev Cell

December 2024

State Key Laboratory for Crop Stress Resistance and High-Efficiency Production, College of Horticulture, Northwest A&F University, Yangling, China. Electronic address:

Natural variation is an invaluable genetic resource for plant trait improvement. Here, we performed a genome-wide association study (GWAS) analysis and identified MdHDG5, which controls apple leaf cuticular wax. An A-to-G single-nucleotide polymorphism (SNP) on the HDG5 promoter is associated with HDG5 expression and hexacosanol content (a component of leaf cuticular wax).

View Article and Find Full Text PDF

The effective and translational strategy to regenerate knee meniscal fibrocartilage remained challenging. Herein, we first identified vascular smooth muscle cells (VSMCs) transdifferentiated into fibrochondrocytes and participated in spontaneous meniscal regeneration using smooth muscle cell lineage tracing transgenic mice meniscal defect model. Then, we identified low-intensity pulsed ultrasound (LIPUS) acoustic stimulus enhanced fibrochondrogenic transdifferentiation of VSMCs in vitro and in vivo.

View Article and Find Full Text PDF

Bromodomain and extra-terminal domain (BET) proteins, including BRD4, bind acetylated chromatin and co-activate gene transcription. A BET inhibitor, JQ1, prevents and reverses pathological cardiac remodeling in preclinical models of heart failure. However, the underlying cellular mechanisms by which JQ1 improves cardiac structure and function remain poorly defined.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!