Literature DB >> 2249252

Detection of length heterogeneity in the ribosomal DNA of Pythium ultimum by PCR amplification of the intergenic region.

J Buchko1, G R Klassen.   

Abstract

About one-half of the ribosomal repeat unit of two isolates of Pythium ultimum was amplified by means of the polymerase chain reaction using one primer pair. The amplified region includes a small part of the large subunit ribosomal RNA gene, about half of the small subunit ribosomal RNA gene, and the entire intergenic region. The intergenic region of both isolates of P. ultimum has length heterogeneity due to the presence of subrepeat arrays (Klassen and Buchko 1990). PCR amplification of the heterogeneous target DNA resulted in sets of fragments which accurately reflect the heterogeneity in the target DNA, although there is a preferential amplification of the smaller targets. PCR product sizes ranged from 4.6 to 5.8 kb.

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Year:  1990        PMID: 2249252     DOI: 10.1007/bf00318381

Source DB:  PubMed          Journal:  Curr Genet        ISSN: 0172-8083            Impact factor:   3.886


  7 in total

1.  Arrangement of the genes coding for ribosomal ribonucleic acids in Neurospora crassa.

Authors:  S J Free; P W Rice; R L Metzenberg
Journal:  J Bacteriol       Date:  1979-03       Impact factor: 3.490

2.  Correlations between development rates, enzyme activities, ribosomal DNA spacer-length phenotypes, and adaptation in Drosophila melanogaster.

Authors:  P D Cluster; D Marinković; R W Allard; F J Ayala
Journal:  Proc Natl Acad Sci U S A       Date:  1987-01       Impact factor: 11.205

3.  A compilation of large subunit RNA sequences presented in a structural format.

Authors:  R R Gutell; G E Fox
Journal:  Nucleic Acids Res       Date:  1988       Impact factor: 16.971

4.  Primer-directed enzymatic amplification of DNA with a thermostable DNA polymerase.

Authors:  R K Saiki; D H Gelfand; S Stoffel; S J Scharf; R Higuchi; G T Horn; K B Mullis; H A Erlich
Journal:  Science       Date:  1988-01-29       Impact factor: 47.728

5.  Specific enzymatic amplification of DNA in vitro: the polymerase chain reaction.

Authors:  K Mullis; F Faloona; S Scharf; R Saiki; G Horn; H Erlich
Journal:  Cold Spring Harb Symp Quant Biol       Date:  1986

6.  Amplification of human minisatellites by the polymerase chain reaction: towards DNA fingerprinting of single cells.

Authors:  A J Jeffreys; V Wilson; R Neumann; J Keyte
Journal:  Nucleic Acids Res       Date:  1988-12-09       Impact factor: 16.971

7.  Enhancers and ribosomal gene spacers.

Authors:  R H Reeder
Journal:  Cell       Date:  1984-09       Impact factor: 41.582

  7 in total
  5 in total

1.  Primers ITS1, ITS2 and ITS4 detect the intraspecies variability in the internal transcribed spacers and 5.8S rRNA gene region in clinical isolates of fungi.

Authors:  M Korabecná; V Liska; K Fajfrlík
Journal:  Folia Microbiol (Praha)       Date:  2003       Impact factor: 2.099

2.  The 5S ribosomal RNA gene is linked to large and small subunit ribosomal RNA genes in the oomycetes, Phytophthora vignae, P. cinnamomi, P. megasperma f.sp. glycinea and Saprolegnia ferax.

Authors:  B J Howlett; A G Brownlee; D I Guest; G J Adcock; G I McFadden
Journal:  Curr Genet       Date:  1992-12       Impact factor: 3.886

3.  Outcrossing in the homothallic oomycete, Pythium ultimum, detected with molecular markers.

Authors:  D M Francis; D A St Clair
Journal:  Curr Genet       Date:  1993 Jul-Aug       Impact factor: 3.886

4.  Molecular epidemiology of Pseudomonas cepacia determined by polymerase chain reaction ribotyping.

Authors:  J R Kostman; T D Edlind; J J LiPuma; T L Stull
Journal:  J Clin Microbiol       Date:  1992-08       Impact factor: 5.948

5.  Heterogeneity in intergenic regions of the ribosomal repeat of the pine-blister rusts Cronartium flaccidum and Peridermium pini.

Authors:  S Moricca; T Kasuga; K Mitchelson; A Ragazzi; S Diamandis
Journal:  Curr Genet       Date:  1996-03       Impact factor: 3.886

  5 in total

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