Literature DB >> 378617

Yeast chromosomal DNA molecules have strands which are cross-linked at their termini.

M A Forte, W L Fangman.   

Abstract

The microbial eukaryote Saccharomyces cerevisiae has 18 chromosomes, each consisting of a DNA molecule of 1 x 15 x 10(8) daltons (150 to 2,300 kilobase pairs). Interstand cross-links have now been found in molecules of all sizes by examining the ability of high molecular weight DNA to snap back, i.e., to rapidly renature after denaturation. Experiments in which snap back was assessed for molecules broken by shearing indicate that there are probably two cross-links in each chromosome. Evidence that the cross-links occur at specific sites in the genome was obtained by treating total chromosomal DNA with the endonuclease EcoRI which cleaves the yeast genome into approximately 2,000 discrete fragments. Cross-link containing fragments were separated from fragments without cross-links. This purification resulted in enrichment for about 18 specific fragments. To determine whether the cross-links are terminal or at internal sites in chromosomal DNA, large shear-produced fragments were examined by electron microsopy. With complete denaturation few fragments exhibit the X-shaped single strand configuration expected for internal cross-links. When partially denatured fragments were examined some ends had single strand loops as expected for (AT-rich) cross-linked termini. We propose that a duplex chromosomal DNA molecules have cross-linked termini. We propose that a duplex chromosomal DNA molecule in this eukaryote consists of a continuous, single, self-complementary strand of DNA. This structure has implications for the mechanism of chromosome replication and may be the basis of telomere behavior.

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Year:  1979        PMID: 378617     DOI: 10.1007/bf00293230

Source DB:  PubMed          Journal:  Chromosoma        ISSN: 0009-5915            Impact factor:   4.316


  29 in total

1.  Electron microscopic observations on the meiotic karyotype of diploid and tetraploid Saccharomyces cerevisiae.

Authors:  B Byers; L Goetsch
Journal:  Proc Natl Acad Sci U S A       Date:  1975-12       Impact factor: 11.205

2.  Structure and replication of mitochondrial DNA from Paramecium aurelia.

Authors:  J M Goddard; D J Cummings
Journal:  J Mol Biol       Date:  1975-10-05       Impact factor: 5.469

3.  Electron microscopy of DNA crosslinked with trimethylpsoralen: test of the secondary structure of eukaryotic inverted repeat sequences.

Authors:  T R Cech; M L Pardue
Journal:  Proc Natl Acad Sci U S A       Date:  1976-08       Impact factor: 11.205

4.  The Stability of Broken Ends of Chromosomes in Zea Mays.

Authors:  B McClintock
Journal:  Genetics       Date:  1941-03       Impact factor: 4.562

5.  A model for replication of the ends of linear chromosomes.

Authors:  J M Heumann
Journal:  Nucleic Acids Res       Date:  1976-11       Impact factor: 16.971

6.  Origin and termination of adeno-associated virus DNA replication.

Authors:  W W Hauswirth; K I Berns
Journal:  Virology       Date:  1977-05-15       Impact factor: 3.616

7.  Size and structure of yeast chromosomal DNA.

Authors:  T D Petes; B Byers; W L Fangman
Journal:  Proc Natl Acad Sci U S A       Date:  1973-11       Impact factor: 11.205

8.  Characterization and localization of the naturally occurring cross-links in vaccinia virus DNA.

Authors:  P Geshelin; K I Berns
Journal:  J Mol Biol       Date:  1974-10-05       Impact factor: 5.469

9.  Origin of concatemeric T7 DNA.

Authors:  J D Watson
Journal:  Nat New Biol       Date:  1972-10-18

10.  Periodic density fluctuation during the yeast cell cycle and the selection of synchronous cultures.

Authors:  L H Hartwell
Journal:  J Bacteriol       Date:  1970-12       Impact factor: 3.490

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  9 in total

1.  Linear plasmid DNAs of the plant pathogenic fungus Rhizoctonia solani with unique terminal structures.

Authors:  S Miyashita; H Hirochika; J E Ikeda; T Hashiba
Journal:  Mol Gen Genet       Date:  1990-01

2.  A vaccinia virus DNase preparation which cross-links superhelical DNA.

Authors:  N Lakritz; P D Foglesong; M Reddy; S Baum; J Hurwitz; W R Bauer
Journal:  J Virol       Date:  1985-03       Impact factor: 5.103

3.  Occurrence and evolution of homogeneously staining regions may be due to breakage-fusion-bridge cycles following telomere loss.

Authors:  J K Cowell; O J Miller
Journal:  Chromosoma       Date:  1983       Impact factor: 4.316

4.  Replication of linear mitochondrial DNA from Paramecium: sequence and structure of the initiation-end crosslink.

Authors:  A E Pritchard; D J Cummings
Journal:  Proc Natl Acad Sci U S A       Date:  1981-12       Impact factor: 11.205

5.  The terminal organization of macronuclear DNA in Oxytricha fallax.

Authors:  A F Pluta; B P Kaine; B B Spear
Journal:  Nucleic Acids Res       Date:  1982-12-20       Impact factor: 16.971

6.  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

7.  Characterization of the terminal inverted repeats and their neighboring tandem repeats in the Chlorella CVK1 virus genome.

Authors:  T Yamada; T Higashiyama
Journal:  Mol Gen Genet       Date:  1993-12

8.  Mitotic chromosome loss in a radiation-sensitive strain of the yeast Saccharomyces cerevisiae.

Authors:  R K Mortimer; R Contopoulou; D Schild
Journal:  Proc Natl Acad Sci U S A       Date:  1981-09       Impact factor: 11.205

9.  Repair of interstrand cross-links in DNA of Saccharomyces cerevisiae requires two systems for DNA repair: the RAD3 system and the RAD51 system.

Authors:  W J Jachymczyk; R C von Borstel; M R Mowat; P J Hastings
Journal:  Mol Gen Genet       Date:  1981
  9 in total

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