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Status |
Public on Sep 12, 2017 |
Title |
RNA Seq analysis of WT haploid and Disome 10 in Saccharomyces cerevisiae |
Organism |
Saccharomyces cerevisiae |
Experiment type |
Expression profiling by high throughput sequencing
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Summary |
Aneuploidy and epigenetic alterations have long been associated with carcinogenesis, but it was unknown whether aneuploidy could disrupt the epigenetic states required for cellular differentiation. In this study, we found that ~3% of random aneuploid karyotypes in yeast disrupt the stable inheritance of silenced chromatin during cell proliferation. Karyotype analysis revealed that this phenotype was significantly correlated with gains of chromosomes III and X. Chromosome X disomy alone was sufficient to disrupt chromatin silencing and yeast mating-type identity as indicated by a lack of growth response to pheromone. The silencing defect was not limited to the cryptic mating type loci but was associated with global changes in histone modifications and chromatin localization of Sir2 histone deacetylase. The chromatin-silencing defect of disome X can be partially recapitulated by increasing the copy number of several genes on chromosome X. These results suggest that aneuploidy can directly cause epigenetic instability and disrupt cellular differentiation.
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Overall design |
WT haploid vs Disome 10 in triplicates
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Contributor(s) |
Mulla W, Seidel C |
Citation missing |
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Submission date |
May 02, 2017 |
Last update date |
May 15, 2019 |
Contact name |
Wahid A Mulla |
E-mail(s) |
mwahid1@jhmi.edu
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Organization name |
Johns Hopkins University
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Street address |
855 North Wolfe Street
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City |
Baltimore |
State/province |
MD |
ZIP/Postal code |
21205 |
Country |
USA |
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Platforms (1) |
GPL17342 |
Illumina HiSeq 2500 (Saccharomyces cerevisiae) |
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Samples (6)
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Relations |
BioProject |
PRJNA385090 |
SRA |
SRP106028 |