Analysis of immediate-early transcripts of equine cytomegalovirus.
Abstract: Equine cytomegalovirus (ECMV) contains a linear, double-stranded DNA genome composed of a 146-kbp unique region flanked by a pair of 18-kbp direct repeat (DR) sequences at the termini. Cycloheximide, actinomycin D, and phosphonoacetic acid were applied to infected cell cultures to divide viral transcription into immediate-early (IE), early, and late phases. Eight IE transcripts were identified and mapped to two regions (I and II) of the viral genome. Two of these IE RNAs (13.0 and 5.5 kb in size) were transcribed from region I, which is located within the DR regions; these IE genes are diploid. The other IE transcripts (17.0, 9.0, 7.2, 6.8, 4.5, and 4.2 kb) originated from region II. IE region II is adjacent to region I and spans both unique and DR sequences at the left terminus of the genome. Region II IE transcripts are spliced and transcribed in the opposite direction from region I IE transcripts. IE transcripts from region I were present throughout the replication cycle, whereas those from region II were more abundant during the IE stage than at the early and late stages of infection. These studies demonstrate that ECMV differs from other herpesviruses in the organization and unusually large transcription units of its IE genes.
Publication Date: 1992-02-01 PubMed ID: 1310181DOI: 10.1016/0042-6822(92)90015-hGoogle Scholar: Lookup
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- Journal Article
- Research Support
- Non-U.S. Gov't
- Research Support
- U.S. Gov't
- P.H.S.
Summary
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This research examines the genetic structure and replication process of Equine Cytomegalovirus (ECMV), identifying and mapping eight initial immediate-early (IE) transcripts to two regions in the viral genome, each with its own unique attributes and contribution to the infection cycle.
Genetic Structure of ECMV
- Equine Cytomegalovirus (ECMV) has a linear, double-stranded DNA genome, basically composed of a unique 146-kilo base pair (kbp) region.
- This unique region is flanked by two 18-kbp direct repeat (DR) sequences customarily situated on both ends.
Dividing Viral Transcription into Phases
- Viral transcription was divided into immediate-early (IE), early, and late phases using cycloheximide, actinomycin D, and phosphonoacetic acid.
- These substances were applied to the infected cell cultures to manipulate the transcription phases.
Identification and Mapping of IE Transcripts
- Eight IE transcripts were identified and mapped onto two specific regions, namely region I and region II, of the viral genome.
- Region I yielded two IE RNAs of 13.0kb and 5.5kb sizes. These genes are diploid and are transcribed from within the DR regions.
- The other six IE transcripts (17.0, 9.0, 7.2, 6.8, 4.5, and 4.2 kb) were found to originate from region II. This region spans both unique and DR sequences and is located at the left terminus of the genome.
- Significantly, region II IE transcripts are spliced and transcribed in the opposite direction from region I IE transcripts.
Differences in IE Transcript Presence
- IE transcripts from region I were present throughout the replication cycle.
- In contrast, IE transcripts from region II were more abundant during the IE stage than in the early and late stages of infection.
Significance of the Study
- This research highlights that ECMV differs significantly from other herpesviruses in terms of its IE gene organization and the unusually large transcription units.
- The findings could potentially enhance the understanding of the ECMV virus replication process and can contribute to the development of more efficient treatment strategies.
Cite This Article
APA
Raengsakulrach B, Staczek J.
(1992).
Analysis of immediate-early transcripts of equine cytomegalovirus.
Virology, 186(2), 496-506.
https://doi.org/10.1016/0042-6822(92)90015-h Publication
Researcher Affiliations
- Department of Microbiology and Immunology, Louisiana State University Medical Center, Shreveport 71130-3932.
MeSH Terms
- Antigens, Viral / genetics
- Blotting, Northern
- Cell Line
- Cytomegalovirus / genetics
- Cytomegalovirus / immunology
- Genes, Viral
- Immediate-Early Proteins
- Protein Precursors / genetics
- Restriction Mapping
- Transcription, Genetic
Grant Funding
- 2S07RR05882-05 / NCRR NIH HHS
- AI21996 / NIAID NIH HHS
Citations
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