Literature DB >> 1850931

The 5' and 3' limits of transcription in the pseudorabies virus latency associated transcription unit.

S A Priola1, J G Stevens.   

Abstract

While latent in sensory neurons of infected pigs, pseudorabies virus expresses transcripts from a limited genomic area. These RNAs are transcribed from the strand opposite to that which encodes the pseudorabies immediate-early protein. Using a combination of in situ nucleic acid hybridization performed on latently infected pig trigeminal ganglia and DNA sequencing, 5' and 3' limits of transcription for the pseudorabies LAT transcription unit have been defined. The 5' limit of transcription has been localized to a NarI-BamHI subfragment of the BamHI-6 fragment. Several promoter elements in the correct orientation for the transcript are present including consensus TATA and CAAT boxes and an SP1 site. The 3' limit of transcription has been localized to a HindIII-KpnI subfragment of the BamHI-5 fragment which contains a consensus polyadenylation signal and two termination codones in the correct orientation. From these results we conclude that the region of pseudorabies virus DNA which is active during latency can be no longer than 12.6 kb and completely overlaps the gene encoding the pseudorabies immediate-early protein.

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Year:  1991        PMID: 1850931     DOI: 10.1016/0042-6822(91)90628-o

Source DB:  PubMed          Journal:  Virology        ISSN: 0042-6822            Impact factor:   3.616


  23 in total

1.  A 348-base-pair region in the latency-associated transcript facilitates herpes simplex virus type 1 reactivation.

Authors:  D C Bloom; J M Hill; G Devi-Rao; E K Wagner; L T Feldman; J G Stevens
Journal:  J Virol       Date:  1996-04       Impact factor: 5.103

Review 2.  Experimental investigation of herpes simplex virus latency.

Authors:  E K Wagner; D C Bloom
Journal:  Clin Microbiol Rev       Date:  1997-07       Impact factor: 26.132

Review 3.  Molecular biology of pseudorabies virus: impact on neurovirology and veterinary medicine.

Authors:  Lisa E Pomeranz; Ashley E Reynolds; Christoph J Hengartner
Journal:  Microbiol Mol Biol Rev       Date:  2005-09       Impact factor: 11.056

4.  Detection of pseudorabies virus antibody in swine oral fluid using a serum whole-virus indirect ELISA.

Authors:  Ting-Yu Cheng; Alexandra Buckley; Albert Van Geelen; Kelly Lager; Alexandra Henao-Díaz; Korakrit Poonsuk; Pablo Piñeyro; David Baum; Ju Ji; Chong Wang; Rodger Main; Jeffrey Zimmerman; Luis Giménez-Lirola
Journal:  J Vet Diagn Invest       Date:  2020-05-25       Impact factor: 1.279

5.  Expression of the pseudorabies virus latency-associated transcript gene during productive infection of cultured cells.

Authors:  L Jin; G Scherba
Journal:  J Virol       Date:  1999-12       Impact factor: 5.103

6.  Expression of pseudorabies virus-encoded long noncoding RNAs in epithelial cells and neurons.

Authors:  Xiang Guan; Jie Liu; Hui Jiang; Chang-Xian Wu; Huan-Chun Chen; Zheng-Fei Liu
Journal:  J Neurovirol       Date:  2018-07-09       Impact factor: 2.643

7.  Identification and characterization of a novel structural glycoprotein in pseudorabies virus, gL.

Authors:  B G Klupp; J Baumeister; A Karger; N Visser; T C Mettenleiter
Journal:  J Virol       Date:  1994-06       Impact factor: 5.103

8.  Correlation between precolonization of trigeminal ganglia by attenuated strains of pseudorabies virus and resistance to wild-type virus latency.

Authors:  L M Schang; G F Kutish; F A Osorio
Journal:  J Virol       Date:  1994-12       Impact factor: 5.103

9.  The activity of the pseudorabies virus latency-associated transcript promoter is dependent on its genomic location in herpes simplex virus recombinants as well as on the type of cell infected.

Authors:  C J Huang; M K Rice; G B Devi-Rao; E K Wagner
Journal:  J Virol       Date:  1994-03       Impact factor: 5.103

10.  Suppression of promoter activity of the LAT gene by IE180 of pseudorabies virus.

Authors:  Chia-Jen Ou; Min-Liang Wong; Chienjin Huang; Tien-Jye Chang
Journal:  Virus Genes       Date:  2002-12       Impact factor: 2.332

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