Literature DB >> 6689230

Multiple origins of the complementary defective genomes of RF and origin proximal sequences of GS, two human papovavirus isolates.

A Pater, M M Pater, L S Chang, K Slawin, G Di Mayorca.   

Abstract

It has previously been shown that the genome of RF virus, a variant of the human papovavirus, BK, consists of two DNA species, one (R1a) with a deletion corresponding to the early and the other (R2) with a deletion corresponding to the late region of BKV (A. Pater, M.M. Pater, and G. di Mayorca (1980). J. Virol. 36, 480-487; A. Pater, M. M. Pater, R. M. Dougherty, and G. di Mayorca (1981a). Virology 113, 86-94). In this report transfection experiments are used to show that these DNA species are individually defective for infection and that both DNA molecules are required simultaneously for the infection of human embryonic kidney (HEK) cells. DNA fragments containing the origin of replication in each of the DNA species are analyzed to show that R1a contains three and R2 contains two origins of replication. In addition, several changes in the repeat region proximal to the origin of replication are observed. The changes involve deletions and insertions. Examination of the deleted junctions most often reveals involvement of short stretches of repeated sequences (hot spots) in recombination. Another observed change is the insertion into R2 of a 63-bp sequence which contains no homology to either BK or SV40 DNA. This insertion is into the late-promoter region of this late-region coding DNA and appears to replace a poor "TATA" box in BK wild type with a better TATA box with the correct spacing from the "CAAT" box. A 304-bp fragment containing the origin of replication, early and late promoters, and the repeat units proximal to the origin of replication of GS, another variant of human BKV papovaviruses has also been sequenced. Several rearrangements, including deletions and insertions in the repeat region, are observed. Moreover, when homologous regions of this virus are compared to that of BKV, five base changes are detected, one of which is in the 23-bp origin region. This base change gives this 23-bp palindrome of GS a perfect two-fold rotational symmetry.

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Year:  1983        PMID: 6689230     DOI: 10.1016/0042-6822(83)90509-3

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


  13 in total

1.  Recurring theme of changes in the transcriptional control region of BK virus during adaptation to cell culture.

Authors:  R Rubinstein; B C Schoonakker; E H Harley
Journal:  J Virol       Date:  1991-03       Impact factor: 5.103

2.  Nucleotide sequence of the human polyomavirus AS virus, an antigenic variant of BK virus.

Authors:  J E Tavis; D L Walker; S D Gardner; R J Frisque
Journal:  J Virol       Date:  1989-02       Impact factor: 5.103

3.  Structure and function of the transcriptional control region of nonpassaged BK virus.

Authors:  R Rubinstein; N Pare; E H Harley
Journal:  J Virol       Date:  1987-05       Impact factor: 5.103

4.  DNA rearrangement in the control region for early transcription in a human polyomavirus JC host range mutant capable of growing in human embryonic kidney cells.

Authors:  T Miyamura; A Furuno; K Yoshiike
Journal:  J Virol       Date:  1985-06       Impact factor: 5.103

5.  Naturally occurring BK virus variants (JL and Dik) with deletions in the putative early enhancer-promoter sequences.

Authors:  J ter Schegget; C J Sol; E W Baan; J van der Noordaa; H van Ormondt
Journal:  J Virol       Date:  1985-01       Impact factor: 5.103

6.  Differences in regulatory sequences of naturally occurring JC virus variants.

Authors:  J D Martin; D M King; J M Slauch; R J Frisque
Journal:  J Virol       Date:  1985-01       Impact factor: 5.103

7.  Transformation of primary human embryonic kidney cells to anchorage independence by a combination of BK virus DNA and the Harvey-ras oncogene.

Authors:  A Pater; M M Pater
Journal:  J Virol       Date:  1986-05       Impact factor: 5.103

8.  Regulatory DNA sequence conserved in the course of BK virus evolution.

Authors:  C Sugimoto; K Hara; F Taguchi; Y Yogo
Journal:  J Mol Evol       Date:  1990-12       Impact factor: 2.395

9.  Identification of HeLa cell nuclear factors that bind to and activate the early promoter of human polyomavirus BK in vitro.

Authors:  T Chakraborty; G C Das
Journal:  Mol Cell Biol       Date:  1989-09       Impact factor: 4.272

10.  Prevalence of the archetypal regulatory region and sequence polymorphisms in nonpassaged BK virus variants.

Authors:  M Negrini; S Sabbioni; R R Arthur; A Castagnoli; G Barbanti-Brodano
Journal:  J Virol       Date:  1991-09       Impact factor: 5.103

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