The role of DEAD-box RNA helicase p68 (DDX5) in the development and treatment of breast cancer

2018 ◽  
Vol 234 (5) ◽  
pp. 5478-5487 ◽  
Author(s):  
Vida Hashemi ◽  
Ali Masjedi ◽  
Bita Hazhir-karzar ◽  
Asghar Tanomand ◽  
Siamak Sandoghchian Shotorbani ◽  
...  
2020 ◽  
Vol 11 (7) ◽  
pp. 1846-1858 ◽  
Author(s):  
Xiudi Wang ◽  
Peipei Li ◽  
Chenying Wang ◽  
Dagui Zhang ◽  
Linghui Zeng ◽  
...  

2013 ◽  
Vol 4 (4) ◽  
pp. 369-385 ◽  
Author(s):  
Ricardo Soto-Rifo ◽  
Théophile Ohlmann

2011 ◽  
Vol 39 (2) ◽  
pp. 679-683 ◽  
Author(s):  
Martina Schröder

Human DDX3 is a DEAD (Asp-Glu-Ala-Asp)-box RNA helicase that appears to be a prime target for viral manipulation. While two viruses that manifest major global health threats, HIV and HCV (hepatitis C virus), utilize DDX3 for their replication, other viruses inhibit DDX3's newly identified function in innate antiviral signalling. This review discusses the role of DDX3 in antiviral immunity and its inhibition or exploitation by different viruses.


mBio ◽  
2018 ◽  
Vol 9 (2) ◽  
pp. e02071-17 ◽  
Author(s):  
Lamya El Mortaji ◽  
Sylvie Aubert ◽  
Eloïse Galtier ◽  
Christine Schmitt ◽  
Karine Anger ◽  
...  

ABSTRACTPresent in every kingdom of life, generally in multiple copies, DEAD-box RNA helicases are specialized enzymes that unwind RNA secondary structures. They play major roles in mRNA decay, ribosome biogenesis, and adaptation to cold temperatures. Most bacteria have multiple DEAD-box helicases that present both specialized and partially redundant functions. By using phylogenomics, we revealed that theHelicobactergenus, including the major gastric pathogenH. pylori, is among the exceptions, as it encodes a sole DEAD-box RNA helicase. InH. pylori, this helicase, designated RhpA, forms a minimal RNA degradosome together with the essential RNase, RNase J, a major player in the control of RNA decay. Here, we usedH. pylorias a model organism with a sole DEAD-box helicase and investigated the role of this helicase inH. pyloriphysiology, ribosome assembly, and duringin vivocolonization. Our data showed that RhpA is dispensable for growth at 37°C but crucial at 33°C, suggesting an essential role of the helicase in cold adaptation. Moreover, we found that a ΔrhpAmutant was impaired in motility and deficient in colonization of the mouse model. RhpA is involved in the maturation of 16S rRNA at 37°C and is associated with translating ribosomes. At 33°C, RhpA is, in addition, recruited to individual ribosomal subunits. Finally, via its role in the RNA degradosome, RhpA directs the regulation of the expression of its partner, RNase J. RhpA is thus a multifunctional enzyme that, inH. pylori, plays a central role in gene regulation and in the control of virulence.IMPORTANCEWe present the results of our study on the role of RhpA, the sole DEAD-box RNA helicase encoded by the major gastric pathogenHelicobacter pylori. We observed that all theHelicobacterspecies possess such a sole helicase, in contrast to most free-living bacteria. RhpA is not essential for growth ofH. pyloriunder normal conditions. However, deletion ofrhpAleads to a motility defect and to total inhibition of the ability ofH. pylorito colonize a mouse model. We also demonstrated that this helicase encompasses most of the functions of its specialized orthologs described so far. We found that RhpA is a key element of the bacterial adaptation to colder temperatures and plays a minor role in ribosome biogenesis. Finally, RhpA regulates transcription of thernjgene encoding RNase J, its essential partner in the minimalH. pyloriRNA degradosome, and thus plays a crucial role in the control of RNA decay.


2016 ◽  
Vol 90 (10) ◽  
pp. 5200-5204 ◽  
Author(s):  
Myra Hosmillo ◽  
Trevor R. Sweeney ◽  
Yasmin Chaudhry ◽  
Eoin Leen ◽  
Stephen Curry ◽  
...  

The eukaryotic initiation factor 4A (eIF4A) is a DEAD box helicase that unwinds RNA structure in the 5′ untranslated region (UTR) of mRNAs. Here, we investigated the role of eIF4A in porcine sapovirus VPg-dependent translation. Using inhibitors and dominant-negative mutants, we found that eIF4A is required for viral translation and infectivity, suggesting that despite the presence of a very short 5′ UTR, eIF4A is required to unwind RNA structure in the sapovirus genome to facilitate virus translation.


2020 ◽  
Vol 43 (7) ◽  
pp. 1722-1739 ◽  
Author(s):  
Carmen Capel ◽  
Irene Albaladejo ◽  
Isabel Egea ◽  
Isabel L. Massaretto ◽  
Fernando J. Yuste‐Lisbona ◽  
...  

Cell Cycle ◽  
2008 ◽  
Vol 7 (6) ◽  
pp. 830-832 ◽  
Author(s):  
Volker M. Stucke ◽  
Delphine Gorses ◽  
Francesco Hofmann

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