Literature DB >> 6250716

Tandem repeats within the inverted terminal repetition of vaccinia virus DNA.

R Wittek, B Moss.   

Abstract

A tandemly repeated sequence within the genome of vaccinia virus is cut to fragments of approximately 70 bp by Hinf I, Taq I or Mbo II. The 70 bp repetition was localized within the much larger (10,300 bp) inverted terminal repetition by restriction analysis of cloned DNA fragments and by hybridization of the purified 70 bp repeat to vaccinia virus DNA restriction fragments. The molar abundance of the 70 bp fragment corresponds to a 30 fold repetition at each end of the genome. The repeating restriction endonuclease sites were mapped by agarose gel electrophoresis of partial Hinf I digests of the terminally labeled cloned DNA fragment. The first of 13 repetitive Hinf I sites occurred approximately 150 bp from the end of the cloned DNA. After an intervening sequence of approximately 435 bp, a second series of 17 repetitive Hinf I sites occurred. The DNA between the two blocks of repetitions has a unique sequence containing single Dde I, Alu I and Sau 3A sites. Tandem repeats within the inverted terminal repetition could serve to accelerate self-annealing of single strands of DNA to form circular structures during replication.

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Year:  1980        PMID: 6250716     DOI: 10.1016/0092-8674(80)90135-x

Source DB:  PubMed          Journal:  Cell        ISSN: 0092-8674            Impact factor:   41.582


  36 in total

Review 1.  Poxvirus DNA replication.

Authors:  Bernard Moss
Journal:  Cold Spring Harb Perspect Biol       Date:  2013-09-01       Impact factor: 10.005

Review 2.  The vaccinia virus DNA polymerase and its processivity factor.

Authors:  Maciej W Czarnecki; Paula Traktman
Journal:  Virus Res       Date:  2017-02-01       Impact factor: 3.303

Review 3.  Viruses and viruslike particles of eukaryotic algae.

Authors:  J L Van Etten; L C Lane; R H Meints
Journal:  Microbiol Rev       Date:  1991-12

4.  Vaccinia virus encodes two proteins that are structurally related to members of the plasma serine protease inhibitor superfamily.

Authors:  G J Kotwal; B Moss
Journal:  J Virol       Date:  1989-02       Impact factor: 5.103

Review 5.  Genetically engineered poxviruses for recombinant gene expression, vaccination, and safety.

Authors:  B Moss
Journal:  Proc Natl Acad Sci U S A       Date:  1996-10-15       Impact factor: 11.205

6.  Mapping of the vaccinia virus DNA polymerase gene by marker rescue and cell-free translation of selected RNA.

Authors:  E V Jones; B Moss
Journal:  J Virol       Date:  1984-01       Impact factor: 5.103

7.  Mapping of the vaccinia virus thymidine kinase gene by marker rescue and by cell-free translation of selected mRNA.

Authors:  J P Weir; G Bajszár; B Moss
Journal:  Proc Natl Acad Sci U S A       Date:  1982-02       Impact factor: 11.205

Review 8.  Organization and expression of the poxvirus genome.

Authors:  R Wittek
Journal:  Experientia       Date:  1982-03-15

9.  Organization and closing of mitochondrial deoxyribonucleic acid from Paramecium tetraaurelia and Paramecium primaurelia.

Authors:  D J Cummings; J L Laping
Journal:  Mol Cell Biol       Date:  1981-11       Impact factor: 4.272

10.  Interferon prevents the generation of spontaneous deletions at the left terminus of vaccinia virus DNA.

Authors:  E Paez; M Esteban
Journal:  J Virol       Date:  1985-10       Impact factor: 5.103

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