Literature DB >> 2539485

Interactions between the termini of adeno-associated virus DNA.

R A Bohenzky1, K I Berns.   

Abstract

The adeno-associated virus (AAV) genome is a linear, single polynucleotide chain with inverted terminal repeats of 145 bases. In order to test whether the terminal repeats at opposite ends of the genome have to be able to completely base-pair during DNA replication, we have created chimeric genomes in which an 11 base symmetrical sequence has been deleted from the terminal repeat at one end of the genome and replaced by a different 12 base symmetrical sequence. We have used these chimeric constructs either as a duplex insert in pBR322 or as purified duplex virion DNA to transfect adenovirus-infected HeLa cells. When chimeric duplex virion DNA was used, all of the progeny virions obtained after two cell passages contained DNA with wild-type sequences in both terminal repeats. When plasmid clones were used, the structure of virion DNA depended on the original orientation. If the mutant terminal repeat was originally at the right end of the genome (terminus of genetic map), all progeny terminal repeat sequences were again wild-type. However, if the original construct contained the mutant sequence in the left terminal repeat, the majority of progeny molecules were parental in type (i.e. mutant left and wild-type right terminal repeat). We conclude (1) although the terminal repeats at opposite ends of the genome may interact during DNA replication, it is not necessary that they be perfectly complementary. (2) In direct competition, the wild-type sequence displays an advantage over the mutant allele. (3) In a plasmid clone, the terminal repeat on the left end of the genome is at an advantage in a competitive situation. We note that the left terminal repeat is adjacent to a transcriptional promoter.

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Year:  1989        PMID: 2539485     DOI: 10.1016/0022-2836(89)90526-3

Source DB:  PubMed          Journal:  J Mol Biol        ISSN: 0022-2836            Impact factor:   5.469


  11 in total

Review 1.  Parvovirus replication.

Authors:  K I Berns
Journal:  Microbiol Rev       Date:  1990-09

2.  Sequence requirements for binding of Rep68 to the adeno-associated virus terminal repeats.

Authors:  J H Ryan; S Zolotukhin; N Muzyczka
Journal:  J Virol       Date:  1996-03       Impact factor: 5.103

3.  Determination of adeno-associated virus Rep68 and Rep78 binding sites by random sequence oligonucleotide selection.

Authors:  J A Chiorini; L Yang; B Safer; R M Kotin
Journal:  J Virol       Date:  1995-11       Impact factor: 5.103

4.  Sequence requirements for stable binding and function of Rep68 on the adeno-associated virus type 2 inverted terminal repeats.

Authors:  J A Chiorini; S M Wiener; R A Owens; S R Kyöstió; R M Kotin; B Safer
Journal:  J Virol       Date:  1994-11       Impact factor: 5.103

5.  Adenoviruses with nonidentical terminal sequences are viable.

Authors:  R Lippé; F L Graham
Journal:  J Virol       Date:  1989-12       Impact factor: 5.103

6.  Infectious clones and vectors derived from adeno-associated virus (AAV) serotypes other than AAV type 2.

Authors:  E A Rutledge; C L Halbert; D W Russell
Journal:  J Virol       Date:  1998-01       Impact factor: 5.103

7.  Rescue of the adeno-associated virus genome from a plasmid vector: evidence for rescue by replication.

Authors:  Peter Ward; Per Elias; R Michael Linden
Journal:  J Virol       Date:  2003-11       Impact factor: 5.103

8.  Features of the adeno-associated virus origin involved in substrate recognition by the viral Rep protein.

Authors:  R O Snyder; D S Im; T Ni; X Xiao; R J Samulski; N Muzyczka
Journal:  J Virol       Date:  1993-10       Impact factor: 5.103

9.  Adeno-associated virus DNA replication in vitro: activation by a maltose binding protein/Rep 68 fusion protein.

Authors:  P Ward; E Urcelay; R Kotin; B Safer; K I Berns
Journal:  J Virol       Date:  1994-09       Impact factor: 5.103

10.  Detection of template strand switching during initiation and termination of DNA replication of porcine circovirus.

Authors:  Andrew K Cheung
Journal:  J Virol       Date:  2004-04       Impact factor: 5.103

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