Heterogeneity among the 2 microns plasmids in Saccharomyces cerevisiae: a new sequence for the REP1 gene

P Neuville1, M Bonneu, M Aigle

  • 1Laboratoire de Génétique, CNRS URA 542, Université de Bordeaux II, Talence, France.

Gene
|April 30, 1990
PubMed

Insights

The 2-micron plasmid REP1 gene in Saccharomyces cerevisiae shows significant nucleotide differences between Scp1 and Scp3 variants. These variations suggest intraspecific evolution and conserved selection pressures on REP1 protein domains.

Area of Science:

  • Molecular Biology
  • Yeast Genetics

Background:

  • Naturally occurring circular DNA plasmids exist in some yeast species.
  • The 2-micron circle of Saccharomyces cerevisiae is the most studied yeast plasmid.
  • Three variants (Scp1, Scp2, Scp3) of the 2-micron plasmid are known, differentiated by restriction maps.

Purpose of the Study:

  • To determine the nucleotide sequence of the 2-micron plasmid REP1 gene from S. cerevisiae strain SKQ2n.
  • To compare the Scp3 variant sequence with the previously published Scp1 variant sequence.
  • To analyze the genetic differences and their potential impact on the encoded REP1 protein.

Main Methods:

  • Nucleotide sequencing of the REP1 gene from the Scp3 variant of the 2-micron plasmid.
  • Restriction analysis to confirm the plasmid variant.
  • Comparative sequence analysis between Scp1 and Scp3 variants.

Main Results:

  • The 2-micron plasmid from S. cerevisiae strain SKQ2n was identified as the Scp3 variant.
  • Significant nucleotide differences (128 nt, ~8.5%) were found between the Scp1 and Scp3 variants.
  • These differences affected both coding (8%) and noncoding (9.7%) regions, leading to modifications in the putative REP1 protein (38 aa modified/deleted, 11 aa added).

Conclusions:

  • The nucleotide sequence of the Scp3 variant's REP1 gene differs substantially from the published Scp1 variant.
  • Observed genetic variations indicate significant intraspecific evolution between 2-micron plasmid variants.
  • Conserved selection pressures appear to act on specific domains of the REP1 protein.