Translational control of photosynthetic gene expression in phototrophic eukaryotes

2008 ◽  
Vol 133 (3) ◽  
pp. 507-515 ◽  
Author(s):  
Lutz Wobbe ◽  
Christian Schwarz ◽  
Jörg Nickelsen ◽  
Olaf Kruse
2012 ◽  
Vol 2012 ◽  
pp. 1-10 ◽  
Author(s):  
Godfrey Grech ◽  
Marieke von Lindern

Organisation of RNAs into functional subgroups that are translated in response to extrinsic and intrinsic factors underlines a relatively unexplored gene expression modulation that drives cell fate in the same manner as regulation of the transcriptome by transcription factors. Recent studies on the molecular mechanisms of inflammatory responses and haematological disorders indicate clearly that the regulation of mRNA translation at the level of translation initiation, mRNA stability, and protein isoform synthesis is implicated in the tight regulation of gene expression. This paper outlines how these posttranscriptional control mechanisms, including control at the level of translation initiation factors and the role of RNA binding proteins, affect hematopoiesis. The clinical relevance of these mechanisms in haematological disorders indicates clearly the potential therapeutic implications and the need of molecular tools that allow measurement at the level of translational control. Although the importance of miRNAs in translation control is well recognised and studied extensively, this paper will exclude detailed account of this level of control.


2005 ◽  
Vol 135 (3) ◽  
pp. 367-375 ◽  
Author(s):  
Ali K. Reiter ◽  
Stephen J. Crozier ◽  
Scot R. Kimball ◽  
Leonard S. Jefferson

1989 ◽  
Vol 13 (3-4) ◽  
pp. 469-479 ◽  
Author(s):  
Niklas Langstrom ◽  
Anders Eriksson ◽  
Bengt Winblad ◽  
William Wallace

Development ◽  
2002 ◽  
Vol 129 (14) ◽  
pp. 3325-3334 ◽  
Author(s):  
Ira E. Clark ◽  
Krista C. Dobi ◽  
Heather K. Duchow ◽  
Anna N. Vlasak ◽  
Elizabeth R. Gavis

Translational repression of maternal nanos (nos) mRNA by a cis-acting Translational Control Element (TCE) in the nos 3′UTR is critical for anterior-posterior patterning of the Drosophila embryo. We show, through ectopic expression experiments, that the nos TCE is capable of repressing gene expression at later stages of development in neuronal cells that regulate the molting cycle. Our results predict additional targets of TCE-mediated repression within the nervous system. They also suggest that mechanisms that regulate maternal mRNAs, like TCE-mediated repression, may function more widely during development to spatially or temporally control gene expression.


1993 ◽  
Vol 102 (4) ◽  
pp. 1085-1093 ◽  
Author(s):  
J. L. Wang ◽  
J. J. Long ◽  
T. Hotchkiss ◽  
J. O. Berry

2013 ◽  
Vol 117 (1-3) ◽  
pp. 91-120 ◽  
Author(s):  
James O. Berry ◽  
Pradeep Yerramsetty ◽  
Amy M. Zielinski ◽  
Christopher M. Mure

2005 ◽  
Vol 33 (3) ◽  
pp. 474-476 ◽  
Author(s):  
B. Suess

We have developed conditional gene expression systems based on engineered small-molecule-binding riboswitches. Tetracycline-dependent regulation can be imposed on an mRNA in yeast by inserting an aptamer in its 5′-untranslated region. Biochemical and genetic analyses determined that binding of the ligand tetracycline leads to a pseudoknot-like linkage within the aptamer structure, thereby inhibiting the initial steps of translation. A second translational control element was designed by combining a theophylline aptamer with a communication module for which a 1 nt slipping mechanism had been proposed. This structural element was inserted close to the bacterial ribosomal binding site at a position just interfering with translation in the non-ligand-bound form. Addition of the ligand then shifts the inhibitory element to a distance that permits efficient translation.


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