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dc.contributor.authorTarhan, Çağatay
dc.contributor.authorÇakır, Özgür
dc.date.accessioned2021-12-10T09:38:12Z
dc.date.available2021-12-10T09:38:12Z
dc.date.issued2021
dc.identifier.citationTarhan Ç., Çakır Ö., "Transcriptome sequencing and screening of genes related to glucose availability in Schizosaccharomyces pombe by RNA-seq analysis", GENETICS AND MOLECULAR BIOLOGY, cilt.44, sa.3, 2021
dc.identifier.issn1415-4757
dc.identifier.otherav_090abb64-1deb-49ac-a561-f42abc691f90
dc.identifier.othervv_1032021
dc.identifier.urihttp://hdl.handle.net/20.500.12627/168154
dc.identifier.urihttps://doi.org/10.1590/1678-4685-gmb-2020-0245
dc.identifier.urihttps://avesis.istanbul.edu.tr/api/publication/090abb64-1deb-49ac-a561-f42abc691f90/file
dc.description.abstractWhile calorie restriction is the most used experimental intervention to increase lifespan in numerous model organisms, increasing evidence suggests that excess glucose leads to decreased lifespan in various organisms. To fully understand the molecular basis of the pro-aging effect of glucose, it is still important to discover genetic interactions, gene expression patterns, and molecular responses depending on glucose availability. Here, we compared the gene expression profiles in Schizosaccharomyces pombe mid-log-phase cells grown in three different Synthetic Dextrose media with 3%, 5%, and 8% glucose, using the RNA sequencing method. Expression patterns of genes that function in carbohydrate metabolism were downregulated as expected, and these genes were downregulated in line with the increase in glucose content. Significant and consistent changes in the expression were observed such as genes that encoding retrotransposable elements, heat shock proteins, glutathione S-transferase, cell agglutination protein, and conserved fungal proteins. We group some genes that function together in the transcription process and mitotic regulation, which have recently been associated with glucose availability. Our results shed light on the relationship between excess glucose, diverse cellular processes, and aging.
dc.language.isoeng
dc.subjectCancer Research
dc.subjectMolecular Biology
dc.subjectDrug Discovery
dc.subjectAging
dc.subjectGeneral Biochemistry, Genetics and Molecular Biology
dc.subjectBiochemistry
dc.subjectStructural Biology
dc.subjectGenetics (clinical)
dc.subjectHealth Sciences
dc.subjectLife Sciences
dc.subjectBİYOKİMYA VE MOLEKÜLER BİYOLOJİ
dc.subjectMoleküler Biyoloji ve Genetik
dc.subjectYaşam Bilimleri (LIFE)
dc.subjectGENETİK VE HAYAT
dc.subjectTıp
dc.subjectSağlık Bilimleri
dc.subjectDahili Tıp Bilimleri
dc.subjectTıbbi Genetik
dc.subjectYaşam Bilimleri
dc.subjectMoleküler Biyoloji ve Genetik
dc.subjectSitogenetik
dc.subjectTemel Bilimler
dc.subjectBiochemistry, Genetics and Molecular Biology (miscellaneous)
dc.subjectGenetics
dc.subjectClinical Biochemistry
dc.titleTranscriptome sequencing and screening of genes related to glucose availability in Schizosaccharomyces pombe by RNA-seq analysis
dc.typeMakale
dc.relation.journalGENETICS AND MOLECULAR BIOLOGY
dc.contributor.departmentİstanbul Üniversitesi , Fen Fakültesi , Moleküler Biyoloji ve Genetik Bölümü
dc.identifier.volume44
dc.identifier.issue3
dc.contributor.firstauthorID2717584


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