Characterisation of gene expression profiles of yeast cells expressing BRCA1 missense variants

2009 ◽  
Vol 45 (12) ◽  
pp. 2187-2196 ◽  
Author(s):  
Leontina Di Cecco ◽  
Erika Melissari ◽  
Veronica Mariotti ◽  
Caterina Iofrida ◽  
Alvaro Galli ◽  
...  
Keyword(s):  
Gene Expression ◽  
Expression Profiles ◽  
Gene Expression Profiles ◽  
Yeast Cells ◽  
Missense Variants

722 Characterisation of gene expression profiles in HeLa cells expressing BRCA1 missense variants

2010 ◽  
Vol 8 (5) ◽  
pp. 182
Author(s):  
M. Caligo ◽  
V. Mariotti ◽  
E. Melissari ◽  
L. Guidugli ◽  
C. Iofrida ◽  
...  
Keyword(s):  
Gene Expression ◽  
Hela Cells ◽  
Expression Profiles ◽  
Gene Expression Profiles ◽  
Missense Variants

scholarly journals Transcriptional Repression by the Pho4 Transcription Factor Controls the Timing of SNZ1 Expression

2008 ◽  
Vol 7 (6) ◽  
pp. 949-957 ◽  
Author(s):  
Masafumi Nishizawa ◽  
Tae Komai ◽  
Nobuyuki Morohashi ◽  
Mitsuhiro Shimizu ◽  
Akio Toh-e
Keyword(s):  
Gene Expression ◽  
Transcription Factor ◽  
Transcriptional Repression ◽  
Structural Changes ◽  
Expression Profiles ◽  
Gene Expression Profiles ◽  
Nutrient Sensing ◽  
Yeast Cells ◽  
Diauxic Shift

ABSTRACT Nutrient-sensing kinases play important roles for the yeast Saccharomyces cerevisiae to adapt to new nutrient conditions when the nutrient status changes. Our previous global gene expression analysis revealed that the Pho85 kinase, one of the yeast nutrient-sensing kinases, is involved in the changes in gene expression profiles when yeast cells undergo a diauxic shift. We also found that the stationary phase-specific genes SNZ1 and SNO1, whch share a common promoter, are not properly induced when Pho85 is absent. To examine the role of the kinase in SNZ1/SNO1 regulation, we analyzed their expression during the growth of various yeast mutants, including those affecting Pho85 function or lacking the Pho4 transcription factor, an in vivo substrate of Pho85, and tested Pho4 binding by chromatin immunoprecipitation. Pho4 exhibits temporal binding to the SNZ1/SNO1 promoter to down-regulate the promoter activity, and a Δpho4 mutation advances the timing of SNZ1/SNO1 expression. SNZ2, another member of the SNZ/SNO family, is expressed at an earlier growth stage than SNZ1, and Pho4 does not affect this timing, although Pho85 is required for SNZ2 expression. Thus, Pho4 appears to regulate the different timing of the expression of the SNZ/SNO family members. Pho4 binding to the SNZ1/SNO1 promoter is accompanied by alterations in chromatin structure, and Rpd3 histone deacetylase is required for the proper timing of SNZ1/SNO1 expression, while Asf1 histone chaperone is indispensable for their expression. These results imply that Pho4 plays positive and negative roles in transcriptional regulation, with both cases involving structural changes in its target chromatin.

scholarly journals Global Gene Expression Analysis of Yeast Cells during Sake Brewing

2006 ◽  
Vol 72 (11) ◽  
pp. 7353-7358 ◽  
Author(s):  
Hong Wu ◽  
Xiaohong Zheng ◽  
Yoshio Araki ◽  
Hiroshi Sahara ◽  
Hiroshi Takagi ◽  
...  
Keyword(s):  
Gene Expression ◽  
Gene Expression Analysis ◽  
Expression Profiles ◽  
Gene Expression Profiles ◽  
Global Gene Expression ◽  
Yeast Cells ◽  
Yeast Gene ◽  
High Concentration ◽  
Brewing Process ◽  
Global Gene Expression Analysis

ABSTRACT During the brewing of Japanese sake, Saccharomyces cerevisiae cells produce a high concentration of ethanol compared with other ethanol fermentation methods. We analyzed the gene expression profiles of yeast cells during sake brewing using DNA microarray analysis. This analysis revealed some characteristics of yeast gene expression during sake brewing and provided a scaffold for a molecular level understanding of the sake brewing process.

scholarly journals Data mining of Gene expression profiles of Saccharomyces cerevisiae in response to mild heat stress response

2014 ◽  
Author(s):  
Kaiyuan Ji ◽  
Wenli Ma ◽  
Wenling Zheng
Keyword(s):  
Gene Expression ◽  
Heat Stress ◽  
Expression Profiles ◽  
Model Organism ◽  
Gene Expression Profiles ◽  
Time Frame ◽  
Yeast Cells ◽  
Nucleic Acid Metabolism ◽  
Biological Processes ◽  
Heat Stress Response

We chose yeast as a model organism to explore how eukaryotic cells respond to heat stress. This study provides details on the way yeast responds to temperature changes and is therefore an empirical reference for basic cell research and industrial fermentation of yeast. We use the Qlucore Omics Explorer (QOE) bioinformatics software to analyze the gene expression profiles of the heat stress from Gene Expression Omnibus (GEO). Genes and their expression are listed in heat maps, and the gene function is analyzed against the biological processes and pathways. We can find that the expression of genes changed over time after heat stress. Gene expression changed rapidly from 0 min to 60 min after heat shock, and gene expression stabilized between 60 min to 360 min. The yeast cells begin to adjust themselves to the high temperatures in terms of the level of gene expression at about 60 min. In all of the involved pathways and biological processes, those related to ribosome and nucleic acid metabolism declined in about 15?30 min and those related to starch and sucrose increased in the same time frame. Temperature can be a simple way to control the biological processes and pathways of cell.

1327: Gene Expression Profiles in Benign Prostatic Hyperplasia

2004 ◽  
Vol 171 (4S) ◽  
pp. 349-350
Author(s):  
Gaelle Fromont ◽  
Michel Vidaud ◽  
Alain Latil ◽  
Guy Vallancien ◽  
Pierre Validire ◽  
...  
Keyword(s):  
Gene Expression ◽  
Benign Prostatic Hyperplasia ◽  
Expression Profiles ◽  
Gene Expression Profiles ◽  
Prostatic Hyperplasia
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