Translational control of gene expression mediated by the 3' untranslated region of Barley yellow dwarf virus

Thumbnail Image
Date
2005-01-01
Authors
Pettit, Elizabeth
Major Professor
Advisor
W. Allen Miller
Committee Member
Journal Title
Journal ISSN
Volume Title
Publisher
Altmetrics
Authors
Research Projects
Organizational Units
Organizational Unit
Plant Pathology and Microbiology
The Department of Plant Pathology and Microbiology and the Department of Entomology officially merged as of September 1, 2022. The new department is known as the Department of Plant Pathology, Entomology, and Microbiology (PPEM). The overall mission of the Department is to benefit society through research, teaching, and extension activities that improve pest management and prevent disease. Collectively, the Department consists of about 100 faculty, staff, and students who are engaged in research, teaching, and extension activities that are central to the mission of the College of Agriculture and Life Sciences. The Department possesses state-of-the-art research and teaching facilities in the Advanced Research and Teaching Building and in Science II. In addition, research and extension activities are performed off-campus at the Field Extension Education Laboratory, the Horticulture Station, the Agriculture Engineering/Agronomy Farm, and several Research and Demonstration Farms located around the state. Furthermore, the Department houses the Plant and Insect Diagnostic Clinic, the Iowa Soybean Research Center, the Insect Zoo, and BugGuide. Several USDA-ARS scientists are also affiliated with the Department.
Journal Issue
Is Version Of
Versions
Series
Abstract

The 869 nt 3' untranslated region (3' UTR) of Barley yellow dwarf luteovirus (BYDV) RNA facilitates cap-independent and poly(A) tail-independent translation. A 105 nt cap-independent translation element (BTE, or BYDV TE) within the 3' UTR was previously defined using wheat germ translation extracts (Guo et al., 2000), but additional 3' UTR sequence is required for translation in plant cells. One domain, nt 4918--5008, confers cap-independent translation in vivo in a discrete and strong manner. Some of this extra sequence places the BTE on a phylogenetically conserved, long double-stranded "stalk", making it more accessible to cellular translational machinery. Another sequence in the 3' UTR, nt 5089--5142, downstream of the cap-mimic is functionally replaceable by a poly(A) tail on the 3' end of the mRNA. The influence of this sequence on translation is somewhat weaker than that of the cap-mimic sequence, and may be correlated with length. The requirement for these elements suggests that at least 250 nt of BYDV 3' UTR are necessary for the virus to compete effectively with host cell mRNAs in recruiting the translation apparatus in vivo.;The BTE recruits wheat translation initiation factors, including eukaryotic initiation factor 4E (eIF4E), the cap-binding protein, and its isoform eIFiso4E. Together with eIF4G and eIFiso4G respectively, these proteins complex to form eIF4F and eIFiso4F. Pulldown experiments using BTE RNA as bait showed that both eIF4E and eIF4G are associated with the BTE RNA. UV-crosslinking followed by immunoprecipitation with antisera to eIF4F and eIFiso4F shows that wild type BTE RNA associates with these factors while a nonfunctional mutant BTE does not. Depletion of cap-binding factors resulted in a substantial loss of translation of viral RNA in vitro which was recovered by adding back recombinant eIF4F and eIFiso4F. Thus, cap-binding proteins facilitate cap-independent translation of BYDV RNA. Finally, m7GTP added in trans inhibits translation in vitro of both uncapped and capped full-length infectious RNA, suggesting that the cap-binding site of eIF4E or eIFiso4E enables recruitment of the factor for BYDV translation.

Comments
Description
Keywords
Citation
Source
Copyright
Sat Jan 01 00:00:00 UTC 2005