Using molecular marker technology in

studies on plant genetic diversity

DNA-based technologies

PCR-based technologies
Latest strategies
(DNA sequencing, ESTs, microarrays, DArT, SNPs)

Copyright: IPGRI and Cornell University, 2002 Latest strategies 1

Contents

! DNA sequencing

! Expressed sequence tags (ESTs)

! Microarray technology

! Diversity array technology (DArT)

! Single nucleotide polymorphisms (SNPs)

Copyright: IPGRI and Cornell University, 2003 Latest strategies 2

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 DNA sequencing

! DNA sequencing is the most fundamental

measure of diversity because it detects
polymorphisms within the DNA's building blocks
themselves

! Data collection can be automated

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DNA sequencing provides the most fundamental measure of diversity, because all
markers are derived from polymorphisms in the DNA's building blocks, that is, the
nucleotide sequence of a particular DNA segment. Sequencing technology has vastly
improved in recent years, and now PCR products (a DNA region amplified in sufficient
quantity) can be sequenced directly and targeted to any genomic location of interest.
Data collection can be automated.

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 DNA sequencing: methods

Two main methods exist:

! Maxam-Gilbert

! Sanger (dideoxy sequencing or chain

termination)

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The two methods differ slightly, with the Sanger method (described in slide 6) being
easier to automate and, thus, more widely used.

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DNA sequencing: procedures
! The DNA is broken up into fragments, which are
then subcloned
! Each short piece is used as a template to
generate a set of fragments that differ in length
from each other by a single base
! Fragments are separated by gel electrophoresis
! The base at the end of each fragment is
identified ('base-calling'). The original sequence
of As, Ts, Cs and Gs is recreated for each short
piece generated in the first step
! The short sequences are assembled into one
long sequence
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 A diagram of the Sanger method
5’ 3’
C A T A G C T G T T T C C T G T G A A A
C T T T Label
Polymerase + dNTPs
C A T A G C T G T T T C C T G T G A A A
+
A G G A C A C T T T
+
G C A A A G G A C A C T T T
+
ddATP ddTTP ddCTP ddGTP
C A C T T T
+
G T A T C G A C A A A G G A C A T T T

Adapted from Griffiths et al. 1996

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Differently coloured fluorescent dyes can be used, permitting the separation of all four
fragments in a single lane on the gel and greatly increasing efficiency. Automated sequencers
can analyse the resulting electropherograms to produce a four-colour chromatogram that
shows peaks representing each of the four DNA bases.

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 DNA sequencing: advantages and disadvantages

! Advantages:

• Results are highly reproducible

• Maximum amount of information content

! Disadvantages:

• Costs are still high

• Technically demanding

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The results are, of course, highly reproducible and informative. Costs are high, however,
and a high level of technical expertise is needed, making this technology unavailable to
many researchers. The use of PCR for targeting particular regions of DNA and the
availability of automated sequencing machines have reduced the technical difficulties, but
the process is still expensive, particularly to set up.

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 Applications

! Evolutionary studies

! Calculations of genetic variation

! Comparative genomics

! Creating PCR assays (making primers to convert

any marker to a PCR-based marker)

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Although marker technology is, in general, based on DNA sequence variation,

fortunately, a researcher does not necessarily need to know the entire DNA sequence to
use molecular markers. Of course, DNA sequencing has many useful applications, but a
major drawback, particularly for diversity measurements, is that different genes evolve
at different rates. Extrapolating information from particular genes to the species level
must therefore be done with care (Brown and Kresovich, 1996).

Reference

Brown, S.M. and S. Kresovich. 1996. Molecular characterization for plant genetic
resources conservation. Pp. 85-93 in Genome Mapping in Plants (H. Paterson, ed.).
R.G. Landes Company, Georgetown, TX.

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Basic references

Maxam, A.M. and W. Gilbert. 1977. A new method for sequencing DNA. Proc. Natl Acad.
Sci. U.S.A. 74:560-564.

Sanger, F. 1988. Sequences, sequences and sequences. Annu. Rev. Biochem. 57:1-28.

Sanger, F., S. Nicklen and A.R. Coulson. 1977. DNA sequencing with chain-terminating
inhibitors. Proc. Natl Acad. Sci. U.S.A. 74:5463-5468.

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 Expressed sequence tags (ESTs)

! Expressed sequence tags are small pieces of

DNA sequence, usually 200 to 500 nucleotides
long

! Generated by sequencing either one or both

ends of an expressed gene from a cDNA library

! This strategy is an extremely efficient way to find

new genes

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The number of publicly available plant EST sequences has increased dramatically in the
last few years to more than 1,000,000 as of writing (National Plant Genome Initiative
Progress Report, December 2001). A list of databases of ESTs for many plants can be
found at http://www.ostp.gov/NSTC/html/mpgi2001/building.htm

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Designing EST primers
mRNA
A C U G Reverse transcriptase

RNA
A C U G

T G A C
cDNA
Ribonuclease degradation of RNA
Synthesis of second strand of DNA

A C T G
Double-stranded DNA
T G A C
Primer Primer

5’ EST 3’ EST

http://www.ostp.gov/NSTC/html/mpgi2001/building.htm

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ESTs: advantages and disadvantages

! Advantages:
• Extremely good as genetic markers
• Codominant
• Sequences can be generated rapidly
• Efficient source of sequences to derive
primers for SSRs

! Disadvantages:
• Isolation of mRNA may be difficult
• Introns, which may contain important
information, are not part of cDNA

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 ESTs: applications

EST applications are all based on the fact that

ESTs originate from segments of gene sequences:

! Comparing gene diversity in different organisms

! Gene evolution studies

! Searching databases for putative orthologues

! Probes for gene expression studies

! Detection of SNPs*

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*See section beginning slide 29

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Basic reference
National Center for Biotechnology Information (NCBI). 2001. ESTs: gene discovery made
easier. http://www.ncbi.nlm.nih.gov/About/primer/est.html

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 Microarray, or ‘chip’, technology

! Microarrays are arrangements of small spots

of DNA fixed to glass slides or nylon membranes
! The technology allows monitoring of the
whole genome at once
! The underlying principle of chips is base-pairing
or hybridisation between short probes and
complementary DNA sequences
! Microarrays are constructed using cDNAs
(cDNA arrays), genomic sequences or
oligonucleotides synthesised in silico (‘DNA
chips’)

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Genomes can now be analysed on a whole-genome scale, using microarray (also called
'chip') technology. This technology is based on hybridisation between short
oligonucleotide probes and complementary DNA sequences. Tens of thousands of
samples can be immobilised on a tiny glass (more typically) or nylon slide (chip), and
can be hybridised more than once with different probes or targets (the terminology is
inconsistent on whether the immobilised DNA on the chip should be called the target or
probe). More than one probe can be hybridised at a time, for example, to compare
differences in expression, by labelling them with different-coloured fluorescent dyes.

Special software programs generate the data automatically. Microarrays can be used for
diagnostics, studying gene expression and gene mapping, among other things. However,
the technology is still relatively expensive, especially to set up, and the amount of data
generated can be daunting.

For useful references, see Richmond and Somerville (2000) and Brown and Botstein
(1999) at the end of this submodule (slide 19).

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 A hybridised chip

http://bti.cornell.edu/CGEP/CGEP.html

Copyright: IPGRI and Cornell University, 2003 Latest strategies 16

Image courtesy of Mark D'Ascenzo, Boyce Thompson Institute for Plant Research,
Center for Gene Expression Profiling, Cornell University.

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Microarrays: advantages and disadavantages

! Advantages:
• High-throughput technology
• Whole genome scanning
• Allow the discovery of genotype-phenotype
relationship
! Disadvantages:
• Gene sequence data must be available
• Expensive
• Technically demanding
• Amount and type of data produced requires
high-level computing expertise and equipment

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Microarrays: applications

! Identification of sequence (gene or gene mutation)

! Determination of expression level of genes
• Assay of specific genomic DNA sequence
abundances
• Analysis of expression of very large
numbers of genes (cDNA arrays)
• Identification of large numbers of specific DNA
markers (e.g. single nucleotide
polymorphisms or SNPs) by molecular
hybridisation (synthetic oligonucleotide arrays)

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Basic references
Alscher, R. 2001. Grid it: resources for microarray research. http://www.bsi.vt.edu/
ralscher/gridit/

Brown, P.O. and D. Botstein. 1999. Exploring the new world of the genome with DNA
microarrays. Nature Genet. 21(supp):33-37.

Richmond, T. and S. Somerville. 2000. Chasing the dream: plant EST microarrays.
Current Opinion Plant Biol. 3(2):108-116.

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 Diversity array technology (DArT)

Two steps are involved:

! Generating the array

! Genotyping a sample

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Diversity arrays, also called DArT, was developed by CAMBIA. It involves a new use of
microarrays that does not require sequence knowledge, and thus may become very
useful to crop researchers.

All the following slides on DArT have been taken, with the Centre's previous
authorisation, from CAMBIA's Web site: http://www.cambia.org.au/

References

CAMBIA. 2000. Enabling innovation. http://www.cambia.org/

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DArTs: preparing the array (1)

! Restriction generated fragments representing

the diversity of a genepool are cloned. The
outcome is called a 'representation' (typically
0.1% to 10% of the genome)

! Polymorphic clones in the library are identified

by arraying inserts from a random set of clones
and hybridising the array to different samples

! The inserts from polymorphic clones are

immobilised on a chip

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DArTs: preparing the array (2)
Gx Gy Gn DNAs of interest

Use complexity reduction

method, e.g. RE digest,
adaptor ligation, PCR
Pool genomes
amplification

Pick individual clones

and PCR amplification
Clone fragments from
the representation Library

Array-purified PCR products

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DArTs: genotyping a sample (1)

! Label the representation (DNA) of the sample

with fluorescence and hybridise against the array

! Scan the array and measure, for each array spot,

the amount of hybridisation signal

! By using multiple labels, contrast a representation

from one sample with a representation from
another or with a control probe

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DArTs: genotyping a sample (2)
Gx Gy
Choose 2 genomes to analyse

Same complexity
reduction as used to make
the diversity panel

Cut, ligate adaptors

and PCR amplify

Label each genomic

subset: red...
Label each genomic
subset … green

Hybridise to chip

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A hybridised DArT chip

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DArTs: advantages and disadvantages
! Advantages:
• Do not require sequence information
• High throughput
• Fast data acquisition and analysis
• Detects single-base changes as well as insertions and
or deletions
• Detects differences in DNA methylation, depending
on the enzyme used to generate the fragments
• Sequence-ready clones are generated
• Small DNA sample required
• Good transferability of markers among breeding
populations
• Full automation possible
! Disadvantages:
• Dominance of markers
• Technically demanding
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 DArTs: applications

! Rapid germplasm characterisation

! Genetic mapping

! Marker-assisted breeding

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Reference

Jaccoud, D., K. Peng, D. Feinstein and A. Kilian. 2001. Diversity arrays: a solid-state
technology for sequence information independent genotyping. Nucleic Acids Res.
29(4):E25.

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Basic References

CAMBIA. 2000. Enabling innovation. http://www.cambia.org/

Jaccoud, D., K. Peng, D. Feinstein and A. Kilian. 2001. Diversity arrays: a solid-state
technology for sequence information independent genotyping. Nucleic Acids
Research 29 (4): E25.

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 Single nucleotide polymorphisms (SNPs)

! Single-base substitutions between

homologous sequences

! SNPs occur more frequently than any

other type of polymorphism

! Can be identified on using microarrays and

DHPLC equipment

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A newer type of marker that has now been made available through new sequencing
technologies is single nucleotide polymorphisms (SNPs). These polymorphisms are
single-base substitutions between sequences. SNPs occur more frequently than any
other type of marker, and are very near to or even within the gene of interest.

SNPs can be identified by either using microarrays or DHPLC machines.

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 DHPLC equipment

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DHPLC refers to denaturing high-performance liquid chromatography, which is used to

visualise SNPs.

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 Interpreting SNPs (1)

http://bldg6.arsusda.gov/pberkum/Public/sarl/cregan/snps.htm

Copyright: IPGRI and Cornell University, 2003 Latest strategies 31

The schematic drawing of a single nucleotide polymorphism shows two DNA fragments
(top and bottom) sharing the same sequence for 31 base pairs, except one. In position
28, an A-T (top) has changed to a C-G (bottom).

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 Interpreting SNPs (2)

SNP #1

SNP #2

From Patil et al., 2001. Science 294:1719-1723.

Copyright: IPGRI and Cornell University, 2003 Latest strategies 32

The height of the block represents a stretch of DNA in a chromosome. Each column of
small boxes represents the same section of DNA in a different individual per genotype.
Each row of yellow or blue boxes represents a single SNP. The blue boxes in each row
represent the major allele for that SNP, and the yellow boxes represent the minor allele.
The absence of a box at any position in a row indicates missing data.

In this block, 26 common SNPs may be identified. They may be arranged in seven
different haplotype patterns (5, 4, 4, 3, 2, 1 and 1 genotypes). The four most common
patterns include 16 of the 20 chromosomes sampled. The blue and yellow circles
indicate the allele patterns of two SNPs (surrounded by a line), which unambiguously
distinguish the four common haplotypes in the block.

Reference

Patil, N., A.J. Berno, D.A. Hinds, W.A. Barret, J.M. Doshi, C.R. Hacker, and others. 2001.
Blocks of limited haplotype diversity revealed by high-resolution scanning of human
chromosome 21. Science 294:1719-1723.

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In summary
! Strategies are continuously being developed to improve
the detection of polymorphisms
! DNA sequencing allows the detection of variation at even
the nucleotide level
! ESTs are powerful tools for detecting diversity within
coding regions
! Microarrays and DArT make the simultaneous analysis of
many loci possible
! SNPs are single-base substitutions between sequences,
and represent the most frequent DNA variant

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By now you should know

! The different types of DNA variation that can be

detected by sequencing, ESTs and SNPs

! The underlying principle of microarrays and DArT

! The advantages and disadvantages of the newest

technologies for analysing genetic diversity

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Basic references

Griffiths, A.J.F., J.H. Miller, D.T. Suzuki, R.C. Lewontin and W.M. Gelbart. 1996. An
introduction to genetic analysis (6th edn.). W.H. Freeman and Co., NY.

Hajeer, A., J. Worthington and S. John (eds.). 2000. SNP and Microsatellite Genotyping:
Markers for Genetic Analysis. Biotechniques Molecular Laboratory Methods Series.
Eaton Publishing, Manchester, UK.

USDA-ARS. 1999. The Cregan lab. http://bldg6.arsusda.gov/pberkum/Public/sarl/cregan/

snps.htm

Wang, D.G., J.B. Fan, C.J. Siao, A. Berno, P. Young, R. Sapolsky, and others. 1998.
Large-scale identification, mapping, and genotyping of single-nucleotide
polymorphisms in the human genome. Science 280(5366):1077-1082.

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Next

Complementary technologies

! Final considerations

! Glossary

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