Difference between revisions of "Kevinmcgee Week 11"
From LMU BioDB 2013
				
								
				
				
																
				
				
								
				| Kevinmcgee  (Talk | contribs)  (Added unknown terms) | Kevinmcgee  (Talk | contribs)   (Added Database Answers) | ||
| (6 intermediate revisions by one user not shown) | |||
| Line 9: | Line 9: | ||
| glycoinositol-phospholipids | glycoinositol-phospholipids | ||
| prenylation | prenylation | ||
| + | |||
| + | |||
| + | =Leishmania Background= | ||
| + | #Leishmania Major is a tropical parasite | ||
| + | #Sepctrum of disease, “Leishmaniases” | ||
| + | #*broad term describing a flesh eating virus specific to Leishmania | ||
| + | #*2 million infections in 88 countries annually | ||
| + | #Have adapted to avoid host destruction | ||
| + | #*curing is very hard and doesn’t always work | ||
| + | =Genome Structure and Content= | ||
| + | #32,816,678 base pairs obtained | ||
| + | #36 chromosomes | ||
| + | #*single continuous sequence generated for each chromosome | ||
| + | #911 RNA genes | ||
| + | #*Organized differently in Tritryp genomes from L. Major | ||
| + | #8272 protein coding genes | ||
| + | #663 related families | ||
| + | #*Smaller gene families arose from gene duplication | ||
| + | #*Larger families have single genes at multiple locations on the gene | ||
| + | =Genome Comparison= | ||
| + | #Leishmania is compared with other organisms | ||
| + | #*Trypanosoma Brucei | ||
| + | #*Trypanosoma Cruzi | ||
| + | #*Leishmania has many orthologs under in these genomes | ||
| + | #910 genes not orthologs | ||
| + | #*“Leishmania Restricted genes” | ||
| + | #**responsible for key metabolic differences | ||
| + | #LmjF33.1740 and LmjF33.1750  | ||
| + | #*Macrophage migration inhibition factor | ||
| + | #**Similar to that in humans that deals with immunity from macrophage | ||
| + | =Significant Genetic Findings= | ||
| + | ==Transcription== | ||
| + | #L. major genome is organized into 133 clusters of tens to hundreds of protein-coding genes on same DNA strand | ||
| + | #Pollycistronic transcription initiates in both directions:  | ||
| + | #*In divergent strand-switch regions | ||
| + | #*terminates within the convergent strand-switch regions | ||
| + | #RNAP I, II and III were found in Trytrip | ||
| + | #*Very different from other eukaryotes | ||
| + | #Not many other homologs of RNAP were found  | ||
| + | #These findings, along with the polycistronic gene organization, are consistent with posttranscriptional control mechanisms being the primary determinants of Tritryp gene expression  | ||
| + | ==RNA Processing== | ||
| + | #Polyadenylation is determined by trans-splicing of downstream mRNA | ||
| + | #Tritryp Poly (A) polymerases | ||
| + | #*two distinct ones with different functional roles | ||
| + | #**Homologs of CPF are present | ||
| + | #**No homologs of CstF are present except for CstF50 | ||
| + | #***CstF50 deals with poyadenylation and transcription initiation/termination | ||
| + | #***reflects polycistronic transcription | ||
| + | #Degredation of mRNA is important in gene expression | ||
| + | #*Exonucleases involved in decapping of mRNA were found. | ||
| + | # All of these imply reliance on posttranscriptional control of gene expression | ||
| + | ==Translation and co-/postranslational modification== | ||
| + | #Translation machinery are found withing the tritryps | ||
| + | #*large amount of elF-4A gene | ||
| + | #**Implies nucleic acid binding | ||
| + | #Protein Modification steps | ||
| + | #*phosphorylation | ||
| + | #*glycosylation | ||
| + | #*lipidation | ||
| + | #Essential modifications | ||
| + | #*glycosylphosphatidylinositol anchor addition | ||
| + | #*acytlation | ||
| + | #*protein-protein interaction | ||
| + | #*Enzymes that catalyze these modifications are potential drug targets | ||
| + | ==Surface molecules== | ||
| + | #Surface molecules are very important in the infection process | ||
| + | #*lipophosphoglycan (LPG) | ||
| + | #**assembled in the lumen of the golgi apparatus | ||
| + | #**entire synthetic pathway has not been fully mapped | ||
| + | #*glycoinositol-phospholipids (GIPLs) | ||
| + | #*membrane proteophosphoglycan (PPG) | ||
| + | #*glycosylated GPI-anchored proteins | ||
| + | #Sphingolipids are essential membrane componenets of eukaryotes | ||
| + | #*good drug targets | ||
| + | ==Proteolysis== | ||
| + | #Peptidases have already been identified as virulence factors and vaccine candidates | ||
| + | =Implications= | ||
| + | #Tritryp genomes help show unique biology of Leishmania and give insight to Eukaryote evolution | ||
| + | #*Leishmania branched off from other eukaryotes very early on | ||
| + | #*Differences arose after branching off of Leishmania | ||
| + | #Differences from other eukaryotes: posttranslational modification | ||
| + | #*polycistronic gene clusters | ||
| + | #*mRNA trans-splicing coupled with polyadenylation | ||
| + | #Full genome provides crucial information for new therapies of Leishmaniasis | ||
| + | #*analysis of virulence factors | ||
| + | #*enzymes in metabolic pathways | ||
| + | #*potential vaccine candidates | ||
| + | |||
| + | =TritrypDB= | ||
| + | #Contains mostly sequences that are manually added by the community. It is a meta database. | ||
| + | #It is held under the EuPathDB Bioinformatics Resource Center | ||
| + | #Funded by the Bill and Melinda Gates Foundation and the Welcome Trust | ||
| + | #Database is free and open to the public as long as proper citation is included | ||
| + | #Updated as new information comes in. Last update was in September of this year | ||
| + | #Yes. There are links to other databases on every organism that is on the site. | ||
| + | #Files can be downloaded in FAFSTA and gff. | ||
| + | #The database was somewhat friendly. It is organized well enough and there is a help section, but things are very clearly defined to me and I got lost easily. The eample querry gave me what I was looking for, but when I typed into Leishmania Major the actual data for L. Major was far down the page. | ||
| + | #LmjF.##.### | ||
| + | |||
| + | [[Leishmania major]]  | ||
| + | |||
| + | [[User:Kevinmcgee|Kevinmcgee]] ([[User talk:Kevinmcgee|talk]]) 22:07, 11 November 2013 (PST) | ||
Latest revision as of 06:07, 12 November 2013
trypanosomatid Ecotins chymotrypsin amastins Sphingolipids PG-galactosyltransferases pseudogenes ribonuclease glycoinositol-phospholipids prenylation
| Contents | 
[edit] Leishmania Background
- Leishmania Major is a tropical parasite
- Sepctrum of disease, “Leishmaniases”
- broad term describing a flesh eating virus specific to Leishmania
- 2 million infections in 88 countries annually
 
- Have adapted to avoid host destruction
- curing is very hard and doesn’t always work
 
[edit] Genome Structure and Content
- 32,816,678 base pairs obtained
- 36 chromosomes
- single continuous sequence generated for each chromosome
 
- 911 RNA genes
- Organized differently in Tritryp genomes from L. Major
 
- 8272 protein coding genes
- 663 related families
- Smaller gene families arose from gene duplication
- Larger families have single genes at multiple locations on the gene
 
[edit] Genome Comparison
- Leishmania is compared with other organisms
- Trypanosoma Brucei
- Trypanosoma Cruzi
- Leishmania has many orthologs under in these genomes
 
- 910 genes not orthologs
- “Leishmania Restricted genes”
- responsible for key metabolic differences
 
 
- “Leishmania Restricted genes”
- LmjF33.1740 and LmjF33.1750 
- Macrophage migration inhibition factor
- Similar to that in humans that deals with immunity from macrophage
 
 
- Macrophage migration inhibition factor
[edit] Significant Genetic Findings
[edit] Transcription
- L. major genome is organized into 133 clusters of tens to hundreds of protein-coding genes on same DNA strand
- Pollycistronic transcription initiates in both directions: 
- In divergent strand-switch regions
- terminates within the convergent strand-switch regions
 
- RNAP I, II and III were found in Trytrip
- Very different from other eukaryotes
 
- Not many other homologs of RNAP were found
- These findings, along with the polycistronic gene organization, are consistent with posttranscriptional control mechanisms being the primary determinants of Tritryp gene expression
[edit] RNA Processing
- Polyadenylation is determined by trans-splicing of downstream mRNA
- Tritryp Poly (A) polymerases
- two distinct ones with different functional roles
- Homologs of CPF are present
- No homologs of CstF are present except for CstF50
- CstF50 deals with poyadenylation and transcription initiation/termination
- reflects polycistronic transcription
 
 
 
- two distinct ones with different functional roles
- Degredation of mRNA is important in gene expression
- Exonucleases involved in decapping of mRNA were found.
 
- All of these imply reliance on posttranscriptional control of gene expression
[edit] Translation and co-/postranslational modification
- Translation machinery are found withing the tritryps
- large amount of elF-4A gene
- Implies nucleic acid binding
 
 
- large amount of elF-4A gene
- Protein Modification steps
- phosphorylation
- glycosylation
- lipidation
 
- Essential modifications
- glycosylphosphatidylinositol anchor addition
- acytlation
- protein-protein interaction
- Enzymes that catalyze these modifications are potential drug targets
 
[edit] Surface molecules
- Surface molecules are very important in the infection process
- lipophosphoglycan (LPG)
- assembled in the lumen of the golgi apparatus
- entire synthetic pathway has not been fully mapped
 
- glycoinositol-phospholipids (GIPLs)
- membrane proteophosphoglycan (PPG)
- glycosylated GPI-anchored proteins
 
- lipophosphoglycan (LPG)
- Sphingolipids are essential membrane componenets of eukaryotes
- good drug targets
 
[edit] Proteolysis
- Peptidases have already been identified as virulence factors and vaccine candidates
[edit] Implications
- Tritryp genomes help show unique biology of Leishmania and give insight to Eukaryote evolution
- Leishmania branched off from other eukaryotes very early on
- Differences arose after branching off of Leishmania
 
- Differences from other eukaryotes: posttranslational modification
- polycistronic gene clusters
- mRNA trans-splicing coupled with polyadenylation
 
- Full genome provides crucial information for new therapies of Leishmaniasis
- analysis of virulence factors
- enzymes in metabolic pathways
- potential vaccine candidates
 
[edit] TritrypDB
- Contains mostly sequences that are manually added by the community. It is a meta database.
- It is held under the EuPathDB Bioinformatics Resource Center
- Funded by the Bill and Melinda Gates Foundation and the Welcome Trust
- Database is free and open to the public as long as proper citation is included
- Updated as new information comes in. Last update was in September of this year
- Yes. There are links to other databases on every organism that is on the site.
- Files can be downloaded in FAFSTA and gff.
- The database was somewhat friendly. It is organized well enough and there is a help section, but things are very clearly defined to me and I got lost easily. The eample querry gave me what I was looking for, but when I typed into Leishmania Major the actual data for L. Major was far down the page.
- LmjF.##.###
Kevinmcgee (talk) 22:07, 11 November 2013 (PST)

