Telomeres cap ends of eukaryotic
chromosomes prevent them from degradation and ensure genomic
stability. Cdc13 is an essential telomere recruitment and maintenance protein. A temperature-sensitive point mutation in cdc13
gene leads to telomere impairment, giving rise to cdc13-1 mutants that
suffer lethality at enhanced temperatures. Deleting Exo1 gene from these mutants,
however, leads to the emergence of temperature-tolerant mutants called survivors.
Yeasts are known to exist as either diploids or haploids. These yeastgenotypes
generate survivors. The frequency of survivorship inthe haploid genotype is one cell in 104 cells/generation
at 36°C, however,
the frequency at which they emerge in their diploid counterparts at the same temperature is not known. In this study, we investigated the frequency
of Survivorship in heterozygous diploids of cdc13-1exo1Δmutants of S. cerevisiae at 36°C. Diploids were constructed by mating haploid strains of opposite mating type
cdc13-1 exo1:LEU strains with strains of cdc13-1 exo1:HIS. The crosses were 1296×3181, 2561×3182, 1296×3182 and
References
[1]
Markiewicz-Potoczny, M., Lobanova, A., Loeb, A.M., Ruiz, S. and Lazzerini Denchi, E. (2021) TRF2-Mediated Telomere Protection Is Dispensable in Pluripotent Stem Cells. Nature, 589, 110-115. https://doi.org/10.1038/s41586-020-2959-4
[2]
Lundblad, V. and Blackburn, E.H. (1993) An Alternative Pathway for Yeast Telomere Maintenance Rescues est1-Senescence. Cell, 73, 347-360.
https://doi.org/10.1016/0092-8674(93)90234-H
[3]
Dewhurst, S.M., Yao, X., Rosiene, J., De Lange, T. and Imieliński, M. (2021) Structural Variant Evolution after Telomere Crisis. Nature Communications, 12, Article No. 2093. https://doi.org/10.1038/s41467-021-21933-7
[4]
Zubko, M.K. and Lydall, D. (2006) Linear Chromosome Maintenance in the Absence of Essential Telomere-Capping Proteins. Nature Cell Biology, 8, 734-740.
https://doi.org/10.1038/ncb1428
[5]
Ayra-Plasencia, J., Ramos-Pérez, C., Santana-Sosa, S., Lisby, M. and Machín, F. (2021) Topoisomerase II Deficiency Leads to a Postreplicative Structural Shift in All Saccharomyces cerevisiae Chromosomes. Scientific Reports, 11, Article No. 14940.
https://doi.org/10.1038/s41598-021-93875-5
[6]
Ferreira, M.G. and Cooper, J.P. (2004) Two Modes of DNA Double-Strand Break Repair Are Reciprocally Regulated through the Fission Yeast Cell Cycle. Genes Development, 18, 2249-2254. https://doi.org/10.1101/gad.315804
[7]
Lim, H. and Surana, U. (1996) Cdc20, β-Transducin Homolog, Links RAD9-Mediated G2/M Checkpoint Control to Mitosis in Saccharomyces cerevisiae. Molecular Genetics and Genomics, 253, 138-148. https://doi.org/10.1007/s004380050306
[8]
Foster, S.S., Zubko, M.K., Guillard, S. and Lydall, D. (2006) MRX Protects Telomeric DNA at Uncapped Telomeres of Budding Yeast Cdc13-1 Mutants. DNA Repair (Amst), 135, 840-851. https://doi.org/10.1016/j.dnarep.2006.04.005
[9]
Charifi, F., Churikov, D., Eckert-Boulet, N., Simon, M.-N. and Géli, V. (2021) Rad52 SUMOylation Functions as a Molecular Switch That Determines a Balance between the Rad51- and Rad59-Dependent Survivors. iScience, 24, Article ID: 102231.
https://doi.org/10.1016/j.isci.2021.102231
[10]
Charrier-Savournin, F.B., Chateau, M., Gire, V., Sedivy, J., Piette, J. and Dulić, V. (2004) p21-Mediated Nuclear Retention of Cyclin B1-Cdk1 in Response to Genotoxic Stress. Molecular Biology of the Cell, 15, 3965-3976.
https://doi.org/10.1091/mbc.e03-12-0871
[11]
Roy, U., Kwon, Y., Marie, L., Lisby, M. and Greene, E.C. (2021) The Rad51 Paralog Complex Rad55-Rad57 Acts as a Molecular Chaperone during Homologous Recombination. Molecular Cell, 81, 1043-1057.e8.
https://doi.org/10.1016/j.molcel.2020.12.019
[12]
Ambjørn, S.M., Duxin, J.P., Hertz, E.P.T., Lisby, M. and Nilsson, J. (2021) A Complex of BRCA2 and PP2A-B56 Is Required for DNA Repair by Homologous Recombination. Nature Communications, 12, Article No. 5748.
https://doi.org/10.1038/s41467-021-26079-0
[13]
Teixeira-Silva, A., Ait Saada, A., Hardy, J., Iraqui, I., Nocente, M.C., Fréon, K. and Lambert, S. (2017) The End-Joining Factor Ku Acts in the End-Resection of Double Strand Break-Free Arrested Replication Forks. Nature Communications, 8, Article No. 1982. https://doi.org/10.1038/s41467-017-02144-5
[14]
Bowen, N. and Kolodner, R. (2017) Reconstitution of Saccharomyces cerevisiae DNA Polymerase Epsilon-Dependent Mismatch Repair with Purified Proteins. Proceedings of the National Academy of Sciences of the United States of America, 114, 3607-3612.
https://doi.org/10.1073/pnas.1701753114
[15]
Craig, E.A. and Kurt, J. (1984) Mutations of the Heat Inducible 70 Kilodaiton Genes of Yeast Confer Temperature Sensitive Growth. Cell, 38, 841-849.
https://doi.org/10.1016/0092-8674(84)90279-4
[16]
Olbrich, T., Vega-Sendino, M., Tillo, D., Nussenzweig, A. and Ruiz, S. (2021) CTCF Is a Barrier for 2C-Like Reprogramming. Nature Communications, 12, Article No. 4856. https://doi.org/10.1038/s41467-021-25072-x
[17]
Blackburn, E.H. (2000) Telomere States and Cell Fates. Nature, 408, 53-56.
https://doi.org/10.1038/35040500
[18]
Lie, S., Banks, P., Lawless, C., Lydall, D. and Petersen, J. (2018) The Contribution of Non-Essential Schizosaccharomyces Pombe Genes to Fitness in Response to Altered Nutrient Supply and Target of Rapamycin Activity. Open Biology, 8, Article ID: 180015.
https://doi.org/10.1098/rsob.180015
[19]
Shi, Y., Hellinga, H. and Beese, L. (2017) Interplay of Catalysis, Fidelity, Threading, and Processivity in the Exo- and Endonucleolytic Reactions of Human Exonuclease I. Proceedings of the National Academy of Sciences of the United States of America, 114, 6010-6015. https://doi.org/10.1073/pnas.1704845114
[20]
Hao, L.Y., Armanios, M., Strong, M.A., Karim, B., Feldser, D.M., Huso, D. and Greider, C.W. (2005) Short Telomeres, Even in the Presence of Telomerase, Limit Tissue Renewal Capacity. Cell, 123, 1121-1131. https://doi.org/10.1016/j.cell.2005.11.020
[21]
Garcia, L.E., Zubko, M.K., Zubko, E.I. and Sanchez-Puerta, M.V. (2019) Elucidating Genomic Patterns and Recombination Events in Plant Cybrid Mitochondria. Plant Molecular Biology, 100, 433-450. https://doi.org/10.1007/s11103-019-00869-z
[22]
Morafraile, E.C., Hänni, C., Allen, G., Lydall, D. and Zegerman, P. (2019) Checkpoint Inhibition of Origin Firing Prevents DNA Topological Stress. Genes & Development, 33, 1539-1554. https://doi.org/10.1101/gad.328682.119
[23]
Rodrigues, J. and Lydall, D. (2018) Paf1 and Ctr9, Core Components of the PAF1 Complex, Maintain Low Levels of Telomeric Repeat Containing RNA. Nucleic Acids Research, 46, 621-634. https://doi.org/10.1093/nar/gkx1131
[24]
Strucko, T., Lisby, M. and Mortensen, U.H. (2021) DNA Double-Strand Break-Induced Gene Amplification in Yeast. Methods in Molecular Biology, 2153, 239-252.
https://doi.org/10.1007/978-1-0716-0644-5_17
[25]
Rodrigues, J. and Lydall, D. (2018) Cis and Trans Interactions between Genes Encoding PAF1 Complex and ESCRT Machinery Components in Yeast. Current Genetics, 64, 1105-1116. https://doi.org/10.1007/s00294-018-0828-6
[26]
Torrance, V. and Lydall, D. (2018) Overlapping Open Reading Frames Strongly Reduce Human and Yeast STN1 Gene Expression and Affect Telomere Function. PLoS Genetics, 14, e1007523. https://doi.org/10.1371/journal.pgen.1007523
[27]
Betlem, K., Hoksbergen, S., Mansouri, N., Banks, C. and Peeters, M. (2018) Real-Time Analysis of Microbial Growth by Means of the Heat-Transfer Method (HTM) Using Saccharomyces cerevisiae as Model Organism. Physics in Medicine, 6, 1-8.
https://doi.org/10.1016/j.phmed.2018.05.001
[28]
Rodrigues, J., Banks, P. and Lydall, D. (2018) Vps74 Connects the Golgi Apparatus and Telomeres in Saccharomyces cerevisiae. G3: Genes, Genomes, Genetics, 8, 1807-1816. https://doi.org/10.1534/g3.118.200172
[29]
LeBel, C., Rosonina, E., Sealey, D.C., Pryde, F., Lydall, D., Maringele, L. and Harrington, L.A. (2009) Telomere Maintenance and Survival in Saccharomyces cerevisiae in the Absence of Telomerase and RAD52. Genetics, 176, 1659-1665.
https://doi.org/10.1534/genetics.109.102939
[30]
Makovets, S., Williams, T.L. and Blackburn, E.H. (2008) The Telotype Defines the Telomere State in Saccharomyces cerevisiae and Is Inherited as a Dominant Non-Mendelian Characteristic in Cells Lacking Telomerase. Genetics, 178, 245-257.
https://doi.org/10.1534/genetics.107.083030
[31]
Okafor, S.A., Okey-Mbata, C.C., Daniel, J.A., Arukalam, F.M., Daniel-Nwosu, E.I. and Okafor, A.L. (2021) Miscellany of Hospital Contact Surfaces Microbiome: A Case Study of Selected Hospitals in Owerri South Eastern Nigeria. African Journal of Medical Physics, Biomedical Engineering and Sciences, 2, 48-57.