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Ume6 is required for the MATa/MATα cellular identity and transcriptional silencing in Kluyveromyces lactis
Stockholm University, Faculty of Science, The Wenner-Gren Institute , Developmental Biology. (Stefan Åström)
Stockholm University, Faculty of Science, The Wenner-Gren Institute , Developmental Biology. (Stefan Åström)
Stockholm University, Faculty of Science, The Wenner-Gren Institute , Developmental Biology.
2010 (English)In: Genetics, ISSN 0016-6731, E-ISSN 1943-2631, Vol. 184, no 4, 999-1011 p.Article in journal (Refereed) Published
Abstract [en]

To explore the similarities and differences of regulatory circuits among budding yeasts, we characterized the role of the unscheduled meiotic gene expression 6 (UME6) gene in Kluyveromyces lactis. We found that Ume6 was required for transcriptional silencing of the cryptic mating-type loci HMLα and HMRa. Chromatin immunoprecipitation (ChIP) suggested that Ume6 acted directly by binding the cis-regulatory silencers of these loci. Unexpectedly, a MATa ume6 strain was mating proficient, whereas a MATα ume6 strain was sterile. This observation was explained by the fact that ume6 derepressed HMLα2 only weakly, but derepressed HMRa1 strongly. Consistently, two a/α-repressed genes (MTS1 and STE4) were repressed in the MATα ume6 strain, but were expressed in the MATa ume6 strain. Surprisingly, ume6 partially suppressed the mating defect of a MATa sir2 strain. MTS1 and STE4 were repressed in the MATa sir2 ume6 double-mutant strain, indicating that the suppression acted downstream of the a1/α2-repressor. We show that both STE12 and the MATa2/HMRa2 genes were overexpressed in the MATa sir2 ume6 strain. Consistent with the idea that this deregulation suppressed the mating defect, ectopic overexpression of Ste12 and a2 in a MATa sir2 strain resulted in efficient mating. In addition, Ume6 served as a block to polyploidy, since ume6/ume6 diploids mated as pseudo a-strains. Finally, Ume6 was required for repression of three meiotic genes, independently of the Rpd3 and Sin3 corepressors.

Place, publisher, year, edition, pages
The Genetics Society of America , 2010. Vol. 184, no 4, 999-1011 p.
Keyword [en]
Ume6, transcriptional scilencing, K. lactis, Mts1, Ste4, Sir2
National Category
Developmental Biology
Research subject
Zoological Developmental Biology
Identifiers
URN: urn:nbn:se:su:diva-42002DOI: 10.1534/genetics.110.114678ISI: 000281889000010PubMedID: 20139343OAI: oai:DiVA.org:su-42002DiVA: diva2:343505
Available from: 2010-08-13 Created: 2010-08-13 Last updated: 2017-12-12Bibliographically approved
In thesis
1. Mating type switching and transcriptional silencing in Kluyveromyces lactis
Open this publication in new window or tab >>Mating type switching and transcriptional silencing in Kluyveromyces lactis
2010 (English)Doctoral thesis, comprehensive summary (Other academic)
Abstract [en]

To explore the similarities and differences of regulatory circuits among budding yeasts, we characterized the role of unscheduled meiotic gene expression 6 (UME6) and a novel mating type switching pathway in Kluyveromyces lactis. We found that Ume6 was required for transcriptional silencing of the cryptic mating-type loci HMLα and HMRa. Ume6 acted directly at these loci by binding to the cis-regulatory silencers. Ume6 also served as a block to polyploidy and was required for repression of three meiotic genes, independently of the Rpd3 and Sin3 corepressors.

Mating type switching from MATα to MATa required the α3 protein. The α3 protein was similar to transposases of the mutator like elements (MULEs). Mutational analysis showed that the DDE-motif in α3, which is conserved in MULEs was necessary for switching. During switching α3 mobilizes from the genome in the form of a DNA circle. The sequences encompassing the α3 gene circle junctions in the MATα locus were essential for switching from MATα to MATa. Switching also required a DNA binding protein, Mating type switch 1 (Mts1), whose binding sites in MATα were important. Expression of Mts1 was repressed in MATa/MATα diploids and by nutrients, limiting switching to haploids in low nutrient conditions.

In a genetic selection for strains with increased switching rates we found a mutation in the RAS1 gene. By measuring the levels of the MTS1 mRNA and switching rates in ras1, pde2 and msn2 mutant strains we show that mating type switching in K. lactis was regulated by the RAS/cAMP pathway and the transcription factor Msn2. ras1 mutants contained 20-fold higher levels of MTS1 mRNA compared to wild type whereas pde2 and msn2 expressed less MTS1 mRNA and had decreased switching rates. Furthermore we found that MTS1 contained several potential Msn2 binding sites upstream of its ORF. We suggest that these observations explain the nutrient regulation of switching.

Place, publisher, year, edition, pages
Stockholm: The Wenner-Gren Institute, Stockholm University, 2010. 61 p.
Keyword
Mating type switch, transcriptional silencing, alpha3, transposase, Ume6, Mts1, Ras, cAMP, K. lactis
National Category
Developmental Biology
Research subject
Developmental Biology
Identifiers
urn:nbn:se:su:diva-41969 (URN)978-91-7447-105-2 (ISBN)
Public defence
2010-09-21, Magnélisalen, Kemiska övningslaboratoriet, Svante Arrhenius väg 16 B, Stockholm, 10:00 (English)
Opponent
Supervisors
Note
At the time of the doctoral defense, the following papers were unpublished and had a status as follows: Paper 3: Manuscript.Available from: 2010-08-30 Created: 2010-08-12 Last updated: 2010-08-19Bibliographically approved

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