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151.
152.
In the early stages of infection, gaining control of the cellular protein synthesis machinery including its ribosomes is the ultimate combat objective for a virus. To successfully replicate, viruses unequivocally need to usurp and redeploy this machinery for translation of their own mRNA. In response, the host triggers global shutdown of translation while paradoxically allowing swift synthesis of antiviral proteins as a strategy to limit collateral damage. This fundamental conflict at the level of translational control defines the outcome of infection. As part of this special issue on molecular mechanisms of early virus–host cell interactions, we review the current state of knowledge regarding translational control during viral infection with specific emphasis on protein kinase RNA-activated and mammalian target of rapamycin-mediated mechanisms. We also describe recent technological advances that will allow unprecedented insight into how viruses and host cells battle for ribosomes. 相似文献
153.
Fabien Sénéchal Mélanie L'Enfant Jean-Marc Domon Emeline Rosiau Marie-Jeanne Crépeau Ogier Surcouf Juan Esquivel-Rodriguez Paulo Marcelo Alain Mareck Fran?ois Guérineau Hyung-Rae Kim Jozef Mravec Estelle Bonnin Elisabeth Jamet Daisuke Kihara Patrice Lerouge Marie-Christine Ralet Jér?me Pelloux Catherine Rayon 《The Journal of biological chemistry》2015,290(38):23320-23335
Pectin methylesterases (PMEs) catalyze the demethylesterification of homogalacturonan domains of pectin in plant cell walls and are regulated by endogenous pectin methylesterase inhibitors (PMEIs). In Arabidopsis dark-grown hypocotyls, one PME (AtPME3) and one PMEI (AtPMEI7) were identified as potential interacting proteins. Using RT-quantitative PCR analysis and gene promoter::GUS fusions, we first showed that AtPME3 and AtPMEI7 genes had overlapping patterns of expression in etiolated hypocotyls. The two proteins were identified in hypocotyl cell wall extracts by proteomics. To investigate the potential interaction between AtPME3 and AtPMEI7, both proteins were expressed in a heterologous system and purified by affinity chromatography. The activity of recombinant AtPME3 was characterized on homogalacturonans (HGs) with distinct degrees/patterns of methylesterification. AtPME3 showed the highest activity at pH 7.5 on HG substrates with a degree of methylesterification between 60 and 80% and a random distribution of methyl esters. On the best HG substrate, AtPME3 generates long non-methylesterified stretches and leaves short highly methylesterified zones, indicating that it acts as a processive enzyme. The recombinant AtPMEI7 and AtPME3 interaction reduces the level of demethylesterification of the HG substrate but does not inhibit the processivity of the enzyme. These data suggest that the AtPME3·AtPMEI7 complex is not covalently linked and could, depending on the pH, be alternately formed and dissociated. Docking analysis indicated that the inhibition of AtPME3 could occur via the interaction of AtPMEI7 with a PME ligand-binding cleft structure. All of these data indicate that AtPME3 and AtPMEI7 could be partners involved in the fine tuning of HG methylesterification during plant development. 相似文献
154.
Astrid-Kim Raimbault Yasmine Zuily-Fodil Alain Soler Maria H. Cruz de Carvalho 《Journal of plant physiology》2013
A full-length cDNA encoding a putative aspartic acid protease (AcAP1) was isolated for the first time from the flesh of pineapple (Ananas comosus) fruit. The deduced sequence of AcAP1 showed all the common features of a typical plant aspartic protease phytepsin precursor. Analysis of AcAP1 gene expression under postharvest chilling treatment in two pineapple varieties differing in their resistance to blackheart development revealed opposite trends. The resistant variety showed an up-regulation of AcAP1 precursor gene expression whereas the susceptible showed a down-regulation in response to postharvest chilling treatment. The same trend was observed regarding specific AP enzyme activity in both varieties. Taken together our results support the involvement of AcAP1 in postharvest chilling stress resistance in pineapple fruits. 相似文献
155.
156.
Alain E. Reinberg 《Chronobiology international》1993,10(4):235-237
157.
Target-dependent on/off switch increases ribozyme fidelity 总被引:2,自引:0,他引:2
158.
159.
Since the invention of the Petri dish, there have been continuous efforts to improve efficiency in microbial cultivation.
These efforts were devoted to the attainment for diverse growth conditions, simulation of in situ conditions and achievement
of high-throughput rates. As a result, prokaryotes catalysing novel redox reactions as well as representatives of abundant,
but not-yet cultured taxa, were isolated. Significant insights into microbial physiology have been made by studying the small
number of prokaryotes already cultured. However, despite these numerous breakthroughs, microbial cultivation is still a low-throughput
process. The main hindrance to cultivation is likely due to the prevailing lack of knowledge on targeted species. In this
review, we focus on the limiting factors surrounding cultivation. We discuss several cultivation obstacles, including the
loss of microbial cell–cell communication following species isolation. Future research directions, including the refinement
of culture media, strategies based on cell–cell communication and high-throughput innovations, are reviewed. We further propose
that a combination of these approaches is urgently required to promote cultivation of uncultured species, thereby dawning
a new era in the field. 相似文献
160.