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      Creation of Stable Heterothallic Strains of Komagataella phaffii Enables Dissection of Mating Gene Regulation

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          ABSTRACT

          The methylotrophic yeast Komagataella phaffii ( Pichia pastoris) is homothallic and has been reported to switch mating type by an ancient inversion mechanism. Two mating-type ( MAT) loci include homologs of the MAT a and MATα transcription factor genes, with the expression from one locus downregulated by telomere position effects. However, not much is known about mating gene regulation, since the mixture of mating types complicates detailed investigations. In this study, we developed K. phaffii strains with stable mating types by deletion of the inverted-repeat region required for mating-type switching. These heterothallic strains retain their ability to mate with cells of the opposite mating type and were used to further elucidate mating gene regulation. Functional analysis of MAT mutant strains revealed the essential role of MAT a 2 and MATα 1 in diploid cell formation. Disruption of MAT a 1 or MATα 2 did not affect mating; however, in diploid cells, both genes are required for sporulation and the repression of shmoo formation. The heterothallic strains generated in this study allowed the first detailed characterization of mating gene regulation in K. phaffii. They will be a valuable tool for further studies investigating cell-type-specific behavior and will enable in-depth genetic analyses and strain hybridization in this industrially relevant yeast species.

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          Most cited references45

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          Self-processing of ribozyme-flanked RNAs into guide RNAs in vitro and in vivo for CRISPR-mediated genome editing.

          CRISPR/Cas9 uses a guide RNA (gRNA) molecule to execute sequence-specific DNA cleavage and it has been widely used for genome editing in many organisms. Modifications at either end of the gRNAs often render Cas9/gRNA inactive. So far, production of gRNA in vivo has only been achieved by using the U6 and U3 snRNA promoters. However, the U6 and U3 promoters have major limitations such as a lack of cell specificity and unsuitability for in vitro transcription. Here, we present a versatile method for efficiently producing gRNAs both in vitro and in vivo. We design an artificial gene named RGR that, once transcribed, generates an RNA molecule with ribozyme sequences at both ends of the designed gRNA. We show that the primary transcripts of RGR undergo self-catalyzed cleavage to generate the desired gRNA, which can efficiently guide sequence-specific cleavage of DNA targets both in vitro and in yeast. RGR can be transcribed from any promoters and thus allows for cell- and tissue-specific genome editing if appropriate promoters are chosen. Detecting mutations generated by CRISPR is often achieved by enzyme digestions, which are not very compatible with high-throughput analysis. Our system allows for the use of universal primers to produce any gRNAs in vitro, which can then be used with Cas9 protein to detect mutations caused by the gRNAs/CRISPR. In conclusion, we provide a versatile method for generating targeted mutations in specific cells and tissues, and for efficiently detecting the mutations generated. © 2013 Institute of Botany, Chinese Academy of Sciences.
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            Position effect at S. cerevisiae telomeres: reversible repression of Pol II transcription.

            S. cerevisiae chromosomes end with the telomeric repeat (TG1-3)n. When any of four Pol II genes was placed immediately adjacent to the telomeric repeats, expression of the gene was reversibly repressed as demonstrated by phenotype and mRNA analyses. For example, cells bearing a telomere-linked copy of ADE2 produced predominantly red colonies (a phenotype characteristic of ade2- cells) containing white sectors (characteristic of ADE2+ cells). Repression was due to proximity to the telomere itself since an 81 bp tract of (TG1-3)n positioned downstream of URA3 when URA3 was approximately 20 kb from the end of chromosome VII did not alter expression of the gene. However, this internal tract of (TG1-3)n could spontaneously become telomeric, in which case expression of the URA3 gene was repressed. These data demonstrate that yeast telomeres exert a position effect on the transcription of nearby genes, an effect that is under epigenetic control.
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              Mating-type genes and MAT switching in Saccharomyces cerevisiae.

              Mating type in Saccharomyces cerevisiae is determined by two nonhomologous alleles, MATa and MATα. These sequences encode regulators of the two different haploid mating types and of the diploids formed by their conjugation. Analysis of the MATa1, MATα1, and MATα2 alleles provided one of the earliest models of cell-type specification by transcriptional activators and repressors. Remarkably, homothallic yeast cells can switch their mating type as often as every generation by a highly choreographed, site-specific homologous recombination event that replaces one MAT allele with different DNA sequences encoding the opposite MAT allele. This replacement process involves the participation of two intact but unexpressed copies of mating-type information at the heterochromatic loci, HMLα and HMRa, which are located at opposite ends of the same chromosome-encoding MAT. The study of MAT switching has yielded important insights into the control of cell lineage, the silencing of gene expression, the formation of heterochromatin, and the regulation of accessibility of the donor sequences. Real-time analysis of MAT switching has provided the most detailed description of the molecular events that occur during the homologous recombinational repair of a programmed double-strand chromosome break.
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                Author and article information

                Journal
                Mol Cell Biol
                Mol. Cell. Biol
                mcb
                mcb
                MCB
                Molecular and Cellular Biology
                American Society for Microbiology (1752 N St., N.W., Washington, DC )
                0270-7306
                1098-5549
                23 October 2017
                29 December 2017
                15 January 2018
                29 December 2017
                : 38
                : 2
                : e00398-17
                Affiliations
                [a ]Christian Doppler Laboratory for Innovative Immunotherapeutics at Department of Biotechnology, BOKU-University of Natural Resources and Life Sciences Vienna, Vienna, Austria
                [b ]Department of Biotechnology, BOKU-University of Natural Resources and Life Sciences Vienna, Vienna, Austria
                Author notes
                Address correspondence to Diethard Mattanovich, diethard.mattanovich@ 123456boku.ac.at .

                Citation Heistinger L, Gasser B, Mattanovich D. 2018. Creation of stable heterothallic strains of Komagataella phaffii enables dissection of mating gene regulation. Mol Cell Biol 38:e00398-17. https://doi.org/10.1128/MCB.00398-17.

                Author information
                http://orcid.org/0000-0002-0907-4167
                Article
                00398-17
                10.1128/MCB.00398-17
                5748462
                29061733
                1d64a8cf-b695-4b6f-b5ef-ef705a355ea7
                Copyright © 2017 Heistinger et al.

                This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license.

                History
                : 25 July 2017
                : 21 August 2017
                : 16 October 2017
                Page count
                supplementary-material: 1, Figures: 7, Tables: 1, Equations: 0, References: 47, Pages: 16, Words: 9850
                Funding
                Funded by: Austrian Science Fund (FWF), https://doi.org/10.13039/501100002428;
                Award ID: W1224
                Award Recipient : Award Recipient :
                Funded by: Christian Doppler Forschungsgesellschaft (CDG), https://doi.org/10.13039/501100006012;
                Award Recipient :
                Funded by: Merck KGaA, https://doi.org/10.13039/100009945;
                Award Recipient : Award Recipient : Award Recipient :
                Categories
                Research Article
                Custom metadata
                January 2018

                Molecular biology
                komagataella phaffii,mat genes,mat locus,pichia pastoris,heterothallic strains,mating,mating type,pheromone receptor,sporulation,yeasts

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