Literature DB >> 2309453

Transcription of orthopoxvirus telomeres at late times during infection.

B L Parsons1, D J Pickup.   

Abstract

The telomeres of orthopoxvirus DNAs consists largely of short repeated sequences organized into at least two separate sets. Although the sequence composition of the orthopoxvirus telomeres is highly conserved, these regions do not appear to encode any proteins. At late times during infection, the telomeres of vaccinia virus are transcribed. A promoter in the region between the two sets of repeats directs transcription towards the hairpin-loop end of the viral DNA. This promoter resembles the promoters of other poxvirus late genes, and directs the synthesis of RNAs whose structure is consistent with the presence of 5' poly(A) sequences typical of late RNAs. The lengths of these late transcripts suggest that some transcription extends through the hairpin-loop region. This might occur either when the genome is in a monomeric form or when the genome is in the concatemeric form of the DNA replication intermediate. The function of late transcription of the telomeres is unclear, but similar transcription of the telomeres of vaccinia virus, cowpox virus, and raccoonpox virus suggests that such transcription may have a role in viral replication.

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Year:  1990        PMID: 2309453     DOI: 10.1016/0042-6822(90)90187-v

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


  13 in total

1.  Site-specific RNA cleavage generates the 3' end of a poxvirus late mRNA.

Authors:  J B Antczak; D D Patel; C A Ray; B S Ink; D J Pickup
Journal:  Proc Natl Acad Sci U S A       Date:  1992-12-15       Impact factor: 11.205

2.  A temperature-sensitive lesion in the small subunit of the vaccinia virus-encoded mRNA capping enzyme causes a defect in viral telomere resolution.

Authors:  M S Carpenter; A M DeLange
Journal:  J Virol       Date:  1991-08       Impact factor: 5.103

3.  The target DNA sequence for resolution of poxvirus replicative intermediates is an active late promoter.

Authors:  D Stuart; K Graham; M Schreiber; C Macaulay; G McFadden
Journal:  J Virol       Date:  1991-01       Impact factor: 5.103

4.  Mutational analysis of the resolution sequence of vaccinia virus DNA: essential sequence consists of two separate AT-rich regions highly conserved among poxviruses.

Authors:  M Merchlinsky
Journal:  J Virol       Date:  1990-10       Impact factor: 5.103

5.  Vaccinia virus DNA replication: two hundred base pairs of telomeric sequence confer optimal replication efficiency on minichromosome templates.

Authors:  S Du; P Traktman
Journal:  Proc Natl Acad Sci U S A       Date:  1996-09-03       Impact factor: 11.205

6.  Pervasive initiation and 3'-end formation of poxvirus postreplicative RNAs.

Authors:  Zhilong Yang; Craig A Martens; Daniel P Bruno; Stephen F Porcella; Bernard Moss
Journal:  J Biol Chem       Date:  2012-07-24       Impact factor: 5.157

7.  Magnesium-induced conformational change of packaging RNA for procapsid recognition and binding during phage phi29 DNA encapsidation.

Authors:  C Chen; P Guo
Journal:  J Virol       Date:  1997-01       Impact factor: 5.103

8.  Characterization of small nontranslated polyadenylylated RNAs in vaccinia virus-infected cells.

Authors:  C Lu; R Bablanian
Journal:  Proc Natl Acad Sci U S A       Date:  1996-03-05       Impact factor: 11.205

9.  Biochemical and biophysical properties of a putative hub protein expressed by vaccinia virus.

Authors:  Nicole E Kay; Travis W Bainbridge; Richard C Condit; Michael R Bubb; Reuben E Judd; Balasubramanian Venkatakrishnan; Robert McKenna; Susan M D'Costa
Journal:  J Biol Chem       Date:  2013-03-08       Impact factor: 5.157

10.  Complete inhibition of virion assembly in vivo with mutant procapsid RNA essential for phage phi 29 DNA packaging.

Authors:  M Trottier; C Zhang; P Guo
Journal:  J Virol       Date:  1996-01       Impact factor: 5.103

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