<scp>DDX60</scp> selectively reduces translation off viral type <scp>II</scp> internal ribosome entry sites-Reference-Cited by-同舟云学术

DDX60 selectively reduces translation off viral type II internal ribosome entry sites

Published:2022-10-18 Issue:12 Volume:23 Page:
ISSN:1469-221X
Container-title:EMBO reports
language:en
Short-container-title:EMBO Reports

Author:

Sadic Mohammad¹^ORCID,Schneider William M²,Katsara Olga¹,Medina Gisselle N³⁴,Fisher Ashley¹,Mogulothu Aishwarya³⁵,Yu Yingpu²,Gu Meigang²,de los Santos Teresa³^ORCID,Schneider Robert J¹^ORCID,Dittmann Meike¹^ORCID

Affiliation:

1. NYU Grossman School of Medicine New York NY USA

2. The Rockefeller University New York NY USA

3. Plum Island Animal Disease Center, ARS USDA Greenport NY USA

4. National Bio and Agro‐Defense Facility (NBAF), ARS USDA Manhattan KS USA

5. Department of Pathobiology and Veterinary Science University of Connecticut Storrs CT USA

Funder

National Institute of Allergy and Infectious Diseases

U.S. Department of Agriculture

Publisher

EMBO

Subject

Genetics,Molecular Biology,Biochemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.15252/embr.202255218

Reference123 articles.

1. DDX21, a Host Restriction Factor of FMDV IRES-Dependent Translation and Replication

2. Polioviruses containing picornavirus type 1 and/or type 2 internal ribosomal entry site elements: genetic hybrids and the expression of a foreign gene.

3. The 3' to 5' degradation of yeast mRNAs is a general mechanism for mRNA turnover that requires the SKI2 DEVH box protein and 3' to 5' exonucleases of the exosome complex

4. Differential factor requirement to assemble translation initiation complexes at the alternative start codons of foot-and-mouth disease virus RNA

5. Glycyl-tRNA synthetase specifically binds to the poliovirus IRES to activate translation initiation

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