Download - Genomics of cold-adapted microorganisms
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Some like it cold
What can microbial genomes tell us about life's extremes?
Neil SaundersSchool of Molecular and Microbial Sciences, UQ
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We live on a cold planet
80% of the biosphere is permanently < 5 °C
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Microbial diversity in cold environments
Karl et al. (2001). Nature 409: 507-510
● Estimates 1.3 x 1028 archaeal cells, 3.1 x 1028 bacterial cells in the oceans
● Other cold environments: polar and alpine regions, permafrost, subsurface
● Non-terrestrial environments?
● Ecological significance: carbon cycle, methane
● Biotechnological potential: enzymes
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Archaea and extremophiles
● Archaea are the third domain of life, distinct from Bacteria and Eukarya
● Many (but not all) Archaea are extremophiles
Temperature extremes
psychrophile < 20 °Cmesophile 20 - 45 °Cthermophile > 45 °Chyperthermophile > 80 °C
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Archaeal isolates from Antarctica
Isolates Topt
Tmin
● Methanogenium frigidum 15 °C < 0 °C● Methanococcoides burtonii 23 °C < 0 °C● Halorubrum lacusprofundi
Ace Lake, Vestfold Hills, Antarctica
● Moderately saline
● Perennially 1-2 °C
● Methane-saturated
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Shotgun sequencing of archaeal genomes
Sequencing centres● Joint Genome Institute● Molecular Dynamics/Genome Applications● AGRF
StatisticsM. frigidum ~ 2x coverage, 10 000 readsM. burtonii ~ 12x coverage, 50 000 reads
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Computational infrastructure for genomics
"So what new skills will postdocs need to ensure that they don't become science relics? The answer is math,statistics, and knowledge of a scripting language for computers."
-The Scientist, "Bioinformatics Knowledge Vital to Careers"Volume 16 | Issue 17 | 53 | Sep. 2, 2002www.the-scientist.com
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Computational infrastructure for genomics
Key points● Linux!● Perl/BioPerl● Free, open-source● Many tools + “glue”● Never-ending...
Genome
Assembly
Gene sequence
Protein sequence
Protein structure
Pathway
Computationalobjects
Hardware● Workstation?● Cluster?
Software● Linux● Databases● Web servers● Toolkits/libraries● Scripts/compiled● Open source
Biologicalobjects
Analysis(limitless)
Comparative genomics
Pathway reconstruction
Phylogeny
Structural modeling
Sequence analysis
Regulatory motifs
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“Global” genomic features of cold-adapted prokaryotes
Is there anything “obviously different” about genes and proteins from psychrophilic prokaryotes?
● Amino acid composition and protein structure
● Novel gene products
● Structural RNA features
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Amino acid composition of the proteome
Archaea27 organisms62 338 ORFs
Bacteria52 organisms165 192 ORFs
Amino acid frequency(bioperl)
PCAprincipal components
(R stats package)
data matrixorganisms (rows) x
composition (columns)
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Statistical analysis of amino acid composition
Archaea Amino acid composition v. PC2
27 organisms Asp 0.66His 0.53
PC1 v. GC -0.95 Leu -0.91PC2 v. OGT -0.94 Gln 0.61
Ser 0.57Thr 0.72Trp -0.68
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Statistical analysis of amino acid composition
Bacteria Amino acid composition v. PC2
52 organisms Asp 0.71Glu -0.74
PC1 v. GC 0.96 His 0.56PC2 v. OGT -0.81 Leu -0.41
Met 0.55Gln 0.55Ser 0.67Thr 0.74
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Protein structure homology modeling
Archaea27 organisms62 338 ORFs
Bacteria52 organisms165 192 ORFs
BLAST v. PDBselect templates
PROSPECTmodeller script
MODELLER5 513 raw models 20 785 raw models
ProCheckg-factor > -0.53 383 models 13 966 models
DSSP3 207 models 13 035 models
For the set of models from each organism, calculatefraction of each residue that is solvent-accessible
Analyse using LDA
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Analysis of homology models
Archaea Bacteria
LD1 v. OGT 0.89 LD1 v. OGT 0.84
Ala -0.78 Ala -0.41Asp -0.63 Asp -0.73Ser -0.62 His -0.41Thr -0.85 Ser -0.38
Thr -0.46Trp 0.40Tyr 0.39
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Proteins: summary
● Psychrophiles, mesophiles and thermophiles can be distinguished by the amino acid composition of the proteome
CompositionIn the direction thermophile psychrophile we see:
● increase in non-charged polar (Gln, Ser, Thr), His and Asp● decrease in hydrophobic (Leu, Trp) and Glu
Accessible surface● The 3 thermal classes of organism can also be distinguished by the
degree to which certain residues are solvent-accessible● In general, Asp, Ala, Ser and Thr are more exposed in proteins from
psychrophiles versus thermophiles
Biological rationales● Thermal denaturation: Gln (deamidation), Thr (peptide cleavage)● Thermostability: Glu (surface salt bridges), hydrophobic core● Low temperature function: increased global/local flexibility?
surface destabilisation (hydrophobic) ?avoid aggregation (polar non-charged) ?
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Analysis of structural RNA
OGT (°C)%
GC
Is tRNA GC content related to OGT?
● Use tRNAScan to find tRNA in archaeal genomes
● Calculate mean GC content for each organism
stems
all bases
GC content becomes significant only above ~ 60 °C
Flexibility and nucleoside modificationM. burtonii tRNA contains > 1 dihydrouridine/molecule(Noon et al. 2003, J. Bact. 185: 5483)
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Cold shock protein in M. frigidum
● First CSP identified in a psychrophilic archaeon
● Contains all conserved residues for RNA binding
● Is being functionally and structurally characterised
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CSD-like proteins in M. burtonii● No CSP homologue identified in M. burtonii
● csp mutants of E. coli can be complemented by proteins with a CSD-fold
● Does M. burtonii express novel CSD-like proteins?
d1sro__ M. burtonii YP_564958
Protein sequences
PROSPECTthread v. CSD folds
MODELLERstructural model
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Proteomic studies of M. burtonii
● What's expressed at 4 °C ?
● What's different at 4 °C versus 23 °C ?
● Protein identification is easy witha genome sequence!
● Work performed by Amber Goodchild at the BMSF, UNSW
● 2D-PAGE and LC MS/MS both employed
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What's different between 4 °C and 23 °C?
● 237 spots analysed● 21 spots more intense at 4 °C● 33 spots more intense at 23 °C● 19/21 and 24/33 identified
Upregulated 4 °C● RNAP subunit E● Methanogenesis● Acetate -> amino acid biosynthesis● CheY-like response regulator● Peptidyl prolyl cis/trans isomerase
Upregulated 23 °C● DnaK/HSP70
Goodchild et al. (2004b). Mol. Microbiol. 53: 309
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Protein modifications and new amino acids● Several spot patterns indicate PTM● Trimethylamine methyltransferase
(TMA-MT) maps to 2 ORFs● This results from read-through of an
in-frame amber UAG codon
● The amino acid incorporated at the UAGis pyrrolysine - the 22nd genetically-encodedamino acid.
Hao et al. (2002). Science 296: 1459.
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What's expressed at 4 °C? LC MS/MS
Goodchild et al. (2004a). J. Prot. Res. 3: 1164
● 528 proteins identified● ~ 23% of the proteome● Proteins annotated and classified
by (1) biological process, (2) genome organisation
● 135 hypothetical/conserved hypothetical proteins analysed separately
DNA replication/processing
Transposases
Cell division/chromosome partitioningDefense mechanisms
RNA synthesis/processingSignal transduction
Motility
Protein synthesis/processingProtein PTM/degradation/folding
Cell envelopeTransport
Methanogenesis
Energy production/conversion
Carbon fixation/carbohydrate metabolism
Nucleotide metabolismAmino acid metabolism
Coenzyme metabolismUnassigned
Some key processes● Expression of 2 transposases● Protein folding (chaperones,
chaperonins, isomerases)● RNA and protein processing
(exosome/proteasome superoperon)● Our predicted CSD-like proteins are
part of the putative exosome
Goodchild et al. (2004a). J. Prot. Res. 3: 1164
Putative exosome/proteasome components
Koonin et al. (2001). Genome Res. 11: 240
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Conclusions: the biology● Cold physiology is a complex process; no “gene for cold adaptation”
● Features of psychrophilic archaea include:
➢ Higher proportion of polar non-charged amino acids
➢ More hydrophobic, less charged solvent-accessible surface
➢ Modified structural RNAs for increased flexibility
➢ Membrane lipid unsaturation
➢ Complex transcriptional and translational regulatory networks
➢ Metabolic regulation: energy production v. biosynthesis
➢ Mechanisms to promote proper protein folding
➢ Coupled regulation of RNA/protein synthesis and turnover
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Conclusions: the computers
Biological system Biological objects
Computational objects
AnalysesBiological inferences
Generic approach to biological problems
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Future directions
● M. burtonii Genome closed, released April 2006
● M. frigidum High coverage draft planned (JCVI)
● H. lacusprofundi Scheduled for sequencing (JGI)
Other UNSW projects
● Sphingopyxis alaskensis Genome closed, due for release
● Marine and environmental microbiology
Pseudoalteromonas tunicata JCVI Vibrio angustum JCVI Roseobacter gallaeciensis JCVI LAS-degrading consortium (3 organisms) JGI
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Acknowledgements
UNSW BABS UNSW BMSF UNSW PhysicsRick Cavicchioli Mark Raftery Paul CurmiSohail Siddiqui Mike GuilhausTorsten ThomasAmber GoodchildLaura GiaquintoDominic BurgLily TingDavide de FrancisciCharmaine NgMarilyn Katrib
Sequencing Centres CSIROJoint Genome Institute, CA, USA Peter FranzmannGenomics Applications, CA, USAVenter Institute/Moore Foundation, MD, USAAGRF, Brisbane
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Methanogenesis(CH
3)
3NH+
MttP
(CH3)
3NH+
MttB
MtbB
MtmB
MttC
MtbC
MtmC
CoM-SH
CoM-S-CH3
CoB-SHMcr
CH4
CoM-S-S-CoB
(CH3)
2HNH+
Hdr
A1AO
CH3H
2NH+
Fpo
MP
MPH2
CoM-SH + CoB-SH
F420H2
F420
2H+ 2H+
MtrCoM-SH H4-MPT
H4-MPT-CH3
NH4
+
Mer
H4-MPT=CH2
Mtd
H4-MPT≡CH
Fol/Ftr
H+
ADP + Pi
ATP
Na+
MF
H4-MPT
CHO-MF
Fwd
CO2 + 2H+ + MF
F420
F420
F420H2
F420H2
FrhF420
F420H2
2H+ H2
Na+
MtbA
CH3