α2p controls donor preference during mating type interconversion in yeast by inactivating a recombinational enhancer of chromosome III

Lisa Szeto, Maria K. Fafalios, Hualin Zhong, Andrew K. Vershon, James Broach

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Abstract

Homothallic strains of Saccharomyces cerevisiae can change mating type as often as every generation by replacing the allele at the MAT locus with a copy of mating type information present at one of two storage loci, HML and HMR, located on either end of chromosome III. Selection of the appropriate donor locus is dictated by a mating type-specific repressor protein, α2p: Cells containing α2p select HMR, whereas those lacking α2p select HML. As a repressor protein, α2p binds to DNA cooperatively with the transcriptional activator Mcm1p. Here we show that two α2p/Mcm1p-binding sites, DPS1 and DPS2, control donor selection. DPS1 and DPS2 are located ~30 kb from the left arm of chromosome III, well removed from HML, HMR, and MAT. Precise deletion of only DPS1 and DPS2 results in random selection of donor loci and in a cells without affecting selection in α cells. Reciprocally, deletion of only the α2p binding segments in each of these two sites results in selection of the wrong donor loci in α cells without affecting preference in a cells. These results suggest that Mcm1p, bound to these two sites in the absence of α2p, activates HML as donor. Binding of α2p blocks the ability of Mcm1p bound to DPS1 and DPS2 to activate HML, resulting in default selection of HMR as donor. DPS1 and DPS2 also regulate expression of several noncoding RNAs, although deletion of at least one of these RNA loci does not affect donor preference. This suggests that transcriptional activation, rather than transcription of a specific product, is the initiating event in activating the left arm of chromosome III for donor selection.

Original languageEnglish (US)
Pages (from-to)1899-1911
Number of pages13
JournalGenes and Development
Volume11
Issue number15
DOIs
StatePublished - Aug 1 1997

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Donor Selection
Chromosomes
Yeasts
Repressor Proteins
Untranslated RNA
Transcriptional Activation
Saccharomyces cerevisiae
Alleles
Binding Sites
RNA
DNA

All Science Journal Classification (ASJC) codes

  • Genetics
  • Developmental Biology

Cite this

Szeto, Lisa ; Fafalios, Maria K. ; Zhong, Hualin ; Vershon, Andrew K. ; Broach, James. / α2p controls donor preference during mating type interconversion in yeast by inactivating a recombinational enhancer of chromosome III. In: Genes and Development. 1997 ; Vol. 11, No. 15. pp. 1899-1911.
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abstract = "Homothallic strains of Saccharomyces cerevisiae can change mating type as often as every generation by replacing the allele at the MAT locus with a copy of mating type information present at one of two storage loci, HML and HMR, located on either end of chromosome III. Selection of the appropriate donor locus is dictated by a mating type-specific repressor protein, α2p: Cells containing α2p select HMR, whereas those lacking α2p select HML. As a repressor protein, α2p binds to DNA cooperatively with the transcriptional activator Mcm1p. Here we show that two α2p/Mcm1p-binding sites, DPS1 and DPS2, control donor selection. DPS1 and DPS2 are located ~30 kb from the left arm of chromosome III, well removed from HML, HMR, and MAT. Precise deletion of only DPS1 and DPS2 results in random selection of donor loci and in a cells without affecting selection in α cells. Reciprocally, deletion of only the α2p binding segments in each of these two sites results in selection of the wrong donor loci in α cells without affecting preference in a cells. These results suggest that Mcm1p, bound to these two sites in the absence of α2p, activates HML as donor. Binding of α2p blocks the ability of Mcm1p bound to DPS1 and DPS2 to activate HML, resulting in default selection of HMR as donor. DPS1 and DPS2 also regulate expression of several noncoding RNAs, although deletion of at least one of these RNA loci does not affect donor preference. This suggests that transcriptional activation, rather than transcription of a specific product, is the initiating event in activating the left arm of chromosome III for donor selection.",
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α2p controls donor preference during mating type interconversion in yeast by inactivating a recombinational enhancer of chromosome III. / Szeto, Lisa; Fafalios, Maria K.; Zhong, Hualin; Vershon, Andrew K.; Broach, James.

In: Genes and Development, Vol. 11, No. 15, 01.08.1997, p. 1899-1911.

Research output: Contribution to journalArticle

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T1 - α2p controls donor preference during mating type interconversion in yeast by inactivating a recombinational enhancer of chromosome III

AU - Szeto, Lisa

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AB - Homothallic strains of Saccharomyces cerevisiae can change mating type as often as every generation by replacing the allele at the MAT locus with a copy of mating type information present at one of two storage loci, HML and HMR, located on either end of chromosome III. Selection of the appropriate donor locus is dictated by a mating type-specific repressor protein, α2p: Cells containing α2p select HMR, whereas those lacking α2p select HML. As a repressor protein, α2p binds to DNA cooperatively with the transcriptional activator Mcm1p. Here we show that two α2p/Mcm1p-binding sites, DPS1 and DPS2, control donor selection. DPS1 and DPS2 are located ~30 kb from the left arm of chromosome III, well removed from HML, HMR, and MAT. Precise deletion of only DPS1 and DPS2 results in random selection of donor loci and in a cells without affecting selection in α cells. Reciprocally, deletion of only the α2p binding segments in each of these two sites results in selection of the wrong donor loci in α cells without affecting preference in a cells. These results suggest that Mcm1p, bound to these two sites in the absence of α2p, activates HML as donor. Binding of α2p blocks the ability of Mcm1p bound to DPS1 and DPS2 to activate HML, resulting in default selection of HMR as donor. DPS1 and DPS2 also regulate expression of several noncoding RNAs, although deletion of at least one of these RNA loci does not affect donor preference. This suggests that transcriptional activation, rather than transcription of a specific product, is the initiating event in activating the left arm of chromosome III for donor selection.

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