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2. Introduction
QUESTION:
is whole genome bisulfite sequencing (WGBS) a viable option
for discovering methylated cytosines in non-model species
with limited genomic resources?
HYPOTHESIS:
With limited reference sequence available, it will be very
difficult to annotate methylated regions of DNA
WHO CARES:
DNA methylation is an epigenetic mechanism with important
regulatory functions. Evidence for regulatory role in oysters,
would like to explore in diff populations / generations but
need to know where to look.
3. Introduction
QUESTION:
is whole genome bisulfite sequencing (WGBS) a viable option
for discovering methylated cytosines in non-model species
with limited genomic resources?
HYPOTHESIS:
With limited reference sequence available, it will be very
difficult to annotate methylated regions of DNA
WHO CARES:
DNA methylation is an epigenetic mechanism with important
regulatory functions. Evidence for regulatory role in oysters,
would like to explore in diff populations / generations but
need to know where to look.
4. Background: bisulfite sequencing
m
C AT G T TA C G AT C G G C T C G
bisulfite
m
U AT G T TA U G AT C G G U T C G
PCR
T AT G T TA T G AT C G G T T C G
ATA C A AT A C TA G C C AT G C
5. Bisulfite-PCR
previous work – use design primers to amplify
specific regions of interest
Kismeth
challenging to design primers with specificity,
limited to known sequences
6. WGBS Challenges:
sequencing issues – sequencers can have problems
w/ low complexity sequence
non-model species genomic resources limited
C.gigas
Most resources are ESTs (coding sequences only)
bioinformatics
assemblies/alignments need to recognize C/T
conversion
bisulfite treatment results in 4 unique strands after PCR
7. Approach:
generate mock bisulfite-seq reads using Atlantic
salmon GSS sequences as surrogate to C.gigas
use CLC to assemble mock bisulfite treated reads
back to non-treated mock sequences
8. Approach:
Atlantic salmon after de novo generate 1 million
GSS: 203,387 assembly: 128,337 random, ~40bp
sequences contigs fragments
create similar convert all C to T,
use the non-treated
fragment library that with exception of
library to assemble
is not converted to ‘ACG’ sequences
bisulfite treated
use as reference (259,750 ‘C’s’
reads
sequence remain)
9. Assembly 1st try:
assemble BLAST non
de novo
non treated fragments bisulfite reads treated contigs
assembly non
to de novo non with matches
treated
treated for ID
1 million 459 contigs 42 contigs Found hits,
short reads (~300bp) (~ 46bp) but many
40 mil bp not
1940 bp annotated
11. Other tools:
Nature Reviews Genetics 11, 191-203 | doi:10.1038/nrg2732
12. Conclusions:
QUESTION:
is whole genome bisulfite sequencing (WGBS) a viable
option for discovering methylated cytosines in non-
model species with limited genomic resources?
HYPOTHESIS:
With limited reference sequence available, it will be very
difficult to map methylated regions of DNA
ANSWER:
Yup
13. Conclusions:
QUESTION:
is whole genome bisulfite sequencing (WGBS) a viable
option for discovering methylated cytosines in non-
model species with limited genomic resources?
HYPOTHESIS:
With limited reference sequence available, it will be very
difficult to map methylated regions of DNA
ANSWER:
Yup
14. Next Steps
Find tool to do ‘customizable’ assembly
e.g. only allow C/T (or G/A mismatches)
new protocol using SOLiD that will only sequence
1 strand (this will make analysis easier)
reduced representation
digest w/ restriction enzymes and size select DNA
prior to making library
DNA methylation enrichment kit – fractionate DNA by
binding to methyl binding domain proteins (only
sequence heavily methylated regions)