Difference between revisions of "Individual hw week 8"
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I looked up the genes associated with VC0647 and chose the gene DSBA_VIBCH. This gene encodes for Thiol:Disulfate interchange protein. This gene's expression increased during this experiment. This protein is responsible for the formation of disulfide bonds.This protein is useful for its involvement in the secretion of virulence factors. | I looked up the genes associated with VC0647 and chose the gene DSBA_VIBCH. This gene encodes for Thiol:Disulfate interchange protein. This gene's expression increased during this experiment. This protein is responsible for the formation of disulfide bonds.This protein is useful for its involvement in the secretion of virulence factors. | ||
[[Media:VC0467_MPM.zip]] | [[Media:VC0467_MPM.zip]] | ||
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| + | ===Data Analysis=== | ||
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| + | It appears that the increased amount of cellular activity in the pathogenic strain compared to the normal strain is all geared towards cell growth and division. There is an increase in the carbohydrate transporters which means an increased up take of glucose for metabolism. There is also a lot of membrane activity going on in the pathogenic strain which would make sense if the bacterium is growing and dividing because membranes are essential for the cellular envelope. The increase in hydrogen symporter activity could have to do with creating some sort of electro-chemical concentration gradient. Most of the other increased activity has to do with some aspect of DNA replication or protein synthesis. | ||
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[[Media:Increased_MPM-Criterion1-GO.txt]]<br> | [[Media:Increased_MPM-Criterion1-GO.txt]]<br> | ||
Revision as of 17:31, 17 October 2013
part 1 text file
Media:Merrell Compiled Raw Data Vibrio MPM.txt
Part 1 excel file
Media:Merrell_Compiled_Raw_Data_Vibrio_MPM.xls
948 results
During this lab I mapped the increased expression on the 2009 gene database. For some reason in the beginning of this assignment my .txt file did not want to load so I used my partner's
the top 10 gene ontology terms were
1.Protein folding
2.Chorismate metabolic process
3.aromatic amino acid biosynthesis process
4. cytoplasm
5.protein-N(PI)-phosphohistidine-sugar phosphotransferase activity
6.solute:hydrogen symporter activity
7.sugar:hydrogen symporter activity
8.cation:sugar symporter activity
9.phosphoenolpyruvate-dependent sugar phosphotransferase system
10.zinc ion binding
When I compared my list to stephen's it was apparent that they were different. I believe that this difference arises from the different versions of the data that we used. Mine was from 2009 and his was from 2010.
GO Search
VC0647- 3'-5' exoribonuclease activity VCA0583- outer membrane-bounded periplasmic space
I looked up the genes associated with VC0647 and chose the gene DSBA_VIBCH. This gene encodes for Thiol:Disulfate interchange protein. This gene's expression increased during this experiment. This protein is responsible for the formation of disulfide bonds.This protein is useful for its involvement in the secretion of virulence factors. Media:VC0467_MPM.zip
Data Analysis
It appears that the increased amount of cellular activity in the pathogenic strain compared to the normal strain is all geared towards cell growth and division. There is an increase in the carbohydrate transporters which means an increased up take of glucose for metabolism. There is also a lot of membrane activity going on in the pathogenic strain which would make sense if the bacterium is growing and dividing because membranes are essential for the cellular envelope. The increase in hydrogen symporter activity could have to do with creating some sort of electro-chemical concentration gradient. Most of the other increased activity has to do with some aspect of DNA replication or protein synthesis.
Media:Increased_MPM-Criterion1-GO.txt
Media:Merrell_Compiled_Raw_Data_Vibrio_SL_10102013.gex
Media:MAPPFinder_GO.txt_excel_file_MPM.xls
Media:Merrell_Compiled_Raw_Data_Vibrio_SL_10102013.EX.txt
Media:Merrell_Compiled_Raw_Data_Vibrio_SL_10102013.gmf
