The document describes several classes of molecular markers used in genetic analysis, including isozymes, RFLPs, RAPDs, AFLPs, microsatellites, and SNPs. Isozymes analyze differences in protein mobility on a gel, while RFLPs, RAPDs, AFLPs detect DNA fragment length polymorphisms. Microsatellites analyze differences in repeat number, and SNPs detect single nucleotide differences. The techniques vary in their genetic nature, use of radioactivity, cost, reproducibility, and number of loci analyzed. Choosing a marker system depends on these factors and the research question.
Comparative sequence studies of the repeat elements in diverse insect species can provide useful information on how to make use of them for developing abundant markers that can be used in those species;
$ At the moment, a total of 8 species are in genome assembly stages and another 35 are in progress for genome sequencing;
$ Different molecular marker systems in the field of entomology are expected to provide new directions to study insect genomes in an unprecedented way in the years to come
Site directed mutgenesis, OLIGONUCLEOTIDE DIRECTED MUTAGENESIS Vipin Shukla
INTRODUCTION, HISTORY, MUTATION, DIRECTED MUTAGENESIS,BASIC MECHANISM OF SITE DIRECTED MUTAGENESIS,METHOD FOR SITE DIRECTED MUTATIONS,THE SINGLE PRIMER METHOD, CASETTEE MUTAGENESIS, PCR-SITED DIRECTED MUTAGENESIS, APPLICATION OF SITE DIRECTED MUTAGENESIS.
A genetic marker is a gene or DNA sequence with a known location on a chromosome and associated with a particular gene or trait. It can be described as a variation, which may arise due to mutation or alteration in the genomic loci that can be observed. A genetic marker may be a short DNA sequence, such as a sequence surrounding a single base-pair change (single nucleotide polymorphism, SNP), or a long one, like mini & microsatellites.
Comparative sequence studies of the repeat elements in diverse insect species can provide useful information on how to make use of them for developing abundant markers that can be used in those species;
$ At the moment, a total of 8 species are in genome assembly stages and another 35 are in progress for genome sequencing;
$ Different molecular marker systems in the field of entomology are expected to provide new directions to study insect genomes in an unprecedented way in the years to come
Site directed mutgenesis, OLIGONUCLEOTIDE DIRECTED MUTAGENESIS Vipin Shukla
INTRODUCTION, HISTORY, MUTATION, DIRECTED MUTAGENESIS,BASIC MECHANISM OF SITE DIRECTED MUTAGENESIS,METHOD FOR SITE DIRECTED MUTATIONS,THE SINGLE PRIMER METHOD, CASETTEE MUTAGENESIS, PCR-SITED DIRECTED MUTAGENESIS, APPLICATION OF SITE DIRECTED MUTAGENESIS.
A genetic marker is a gene or DNA sequence with a known location on a chromosome and associated with a particular gene or trait. It can be described as a variation, which may arise due to mutation or alteration in the genomic loci that can be observed. A genetic marker may be a short DNA sequence, such as a sequence surrounding a single base-pair change (single nucleotide polymorphism, SNP), or a long one, like mini & microsatellites.
A new effector pathway links ATM kinase with the DNA damage responseCostas Demonacos
The related kinases ATM (ataxia-telangiectasia mutated) and ATR (ataxia-telangiectasia and Rad3-related) phosphorylate a limited number of downstream protein targets in response to DNA damage. Here we report a new pathway in which ATM kinase signals the DNA damage response by targeting the transcriptional cofactor Strap. ATM phosphorylates Strap at a serine residue, stabilizing nuclear Strap and facilitating formation of a stress-responsive co-activator complex. Strap activity enhances p53 acetylation, and augments the response to DNA damage. Strap remains localized in the cytoplasm in cells derived from ataxia telangiectasia individuals with defective ATM, as well as in cells expressing a Strap mutant that cannot be phosphorylated by ATM. Targeting Strap to the nucleus reinstates protein stabilization and activates the DNA damage response. These results indicate that the nuclear accumulation of Strap is a critical regulator in the damage response, and argue that this function can be assigned to ATM through the DNA damage-dependent phosphorylation of Strap.
High-resolution melt analysis for semen discriminationJoana Antunes, PhD
Brief presentation about the most relevant discoveries on the article. Full article available https://www.researchgate.net/publication/282911197_High_Resolution_Melt_analysis_of_DNA_methylation_to_discriminate_semen_in_biological_stains
Epigenetic silencing of MGMT (O6-methylguanine DNA methyltransferase) gene in...arman170701
O6–methylgunine-DNA methyltransferace (MGMT) is a DNA binding protein that is involved in repairing mutations.
MGMT gene - a tumor suppressor gene that codes MGMT (O6-methylguanine DNA methyltransferase) protein.
The MGMT protein removes mutagenic methyl groups from guanines through the methyltransferase activity.
DNA damage repair Neil3 gene Knockout in MOLT-4iosrjce
RNAi is superannuated cellular mechanism that protect organism against viruses that replicate
through double- stranded RNA. RNAi can be used to diminish gene expression from plasmid expressing and
inserted sequence repeat. A stable harpin would be expressed after the vector was integrated into the genome.
In this paper a shiRNA expressing vector for Neil3 was designed and developed which is capable of replication
in MOLT-4. This shiRNA vector had the ability to arose the RNAi pathway, and reduce the gene expression of
Neil3. This was assessed by using pSilence 4.1CMV as a vector, and Gapdh as positive control.
A new effector pathway links ATM kinase with the DNA damage responseCostas Demonacos
The related kinases ATM (ataxia-telangiectasia mutated) and ATR (ataxia-telangiectasia and Rad3-related) phosphorylate a limited number of downstream protein targets in response to DNA damage. Here we report a new pathway in which ATM kinase signals the DNA damage response by targeting the transcriptional cofactor Strap. ATM phosphorylates Strap at a serine residue, stabilizing nuclear Strap and facilitating formation of a stress-responsive co-activator complex. Strap activity enhances p53 acetylation, and augments the response to DNA damage. Strap remains localized in the cytoplasm in cells derived from ataxia telangiectasia individuals with defective ATM, as well as in cells expressing a Strap mutant that cannot be phosphorylated by ATM. Targeting Strap to the nucleus reinstates protein stabilization and activates the DNA damage response. These results indicate that the nuclear accumulation of Strap is a critical regulator in the damage response, and argue that this function can be assigned to ATM through the DNA damage-dependent phosphorylation of Strap.
High-resolution melt analysis for semen discriminationJoana Antunes, PhD
Brief presentation about the most relevant discoveries on the article. Full article available https://www.researchgate.net/publication/282911197_High_Resolution_Melt_analysis_of_DNA_methylation_to_discriminate_semen_in_biological_stains
Epigenetic silencing of MGMT (O6-methylguanine DNA methyltransferase) gene in...arman170701
O6–methylgunine-DNA methyltransferace (MGMT) is a DNA binding protein that is involved in repairing mutations.
MGMT gene - a tumor suppressor gene that codes MGMT (O6-methylguanine DNA methyltransferase) protein.
The MGMT protein removes mutagenic methyl groups from guanines through the methyltransferase activity.
DNA damage repair Neil3 gene Knockout in MOLT-4iosrjce
RNAi is superannuated cellular mechanism that protect organism against viruses that replicate
through double- stranded RNA. RNAi can be used to diminish gene expression from plasmid expressing and
inserted sequence repeat. A stable harpin would be expressed after the vector was integrated into the genome.
In this paper a shiRNA expressing vector for Neil3 was designed and developed which is capable of replication
in MOLT-4. This shiRNA vector had the ability to arose the RNAi pathway, and reduce the gene expression of
Neil3. This was assessed by using pSilence 4.1CMV as a vector, and Gapdh as positive control.
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10 Ways to Win at SlideShare SEO & Presentation OptimizationOneupweb
Thank you, SlideShare, for teaching us that PowerPoint presentations don't have to be a total bore. But in order to tap SlideShare's 60 million global users, you must optimize. Here are 10 quick tips to make your next presentation highly engaging, shareable and well worth the effort.
For more content marketing tips: http://www.oneupweb.com/blog/
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How to Make Awesome SlideShares: Tips & TricksSlideShare
Turbocharge your online presence with SlideShare. We provide the best tips and tricks for succeeding on SlideShare. Get ideas for what to upload, tips for designing your deck and more.
The Matrix metalloproteinase-9 is involved in several pathologies. Its strong presence in ocular pathologies explains our interest for its genetic variation in cataract, glaucoma and retinoblastoma in Senegal. MMP9 is highly polymorphic with cataract and glaucoma. 77 mutations were noted with 21 haplotypes for the entire population. The haplotype diversity Hd is 0.831 and the nucleotide diversity Pi is 0.016; k = 17.395. The polymorphism of the Matrix metalloproteinase-9 gene is associated with all three diseases and SNP 3918249 is found in both cataract and glaucoma.
DNA SEQUENCING METHODS AND STRATEGIES FOR GENOME SEQUENCINGPuneet Kulyana
This presentation will give you a brief idea about the various DNA sequencing methods and various strategies used for genome sequencing and much more vital information related to gene expression and analysis
A powerful non-transgenic reverse genetics method that combines chemical mutagenesis with PCR based screening to identify point mutations in regions of interest.
EcoTILLING is a molecular technique that is similar to TILLING, except that its objective is to uncover natural genetic variation as opposed to induced mutations.
TILLING is a general reverse genetic technique that combines chemical mutagenesis with PCR based screening to identify point mutations in regions of interest.
Microsatellite are powerful DNA markers for quantifying genetic variations within & between populations of a species, also called as STR, SSR, VNTR. Tandemly repeated DNA sequences with the repeat/size of 1 – 6 bases repeated several times
Targeted Induced Local Lesions IN Genome. Mutations (Single base pair substitution) are created by traditionally used chemical mutagens. Identify SNPs and / or INDELS in a gene / genes of interest from a mutagenized population.
ONLY THE LAST QUESTION IS THE POINT OF POST. THE OTHER PAGES ARE B.pdfamzonknr
ONLY THE LAST QUESTION IS THE POINT OF POST. THE OTHER PAGES ARE
BACKGROUND CONTEXT Lab: Differential Expression Differential gene expression provides
the ability for a cell or organism to respond to a constantly changing external environment. The
specific constellation of proteins required for optimal function and growth varies with cellular
age and environmental context. Thus, protein production is carefully regulated by multiple
mechanisms that modulate both transcriptional and translational pathways. Control of
transcription initiation by RNA polymerase is a predominant mechanism for regulating
expression of specific proteins, presumably because it provides maximal conservation of energy
for the cell. We can often observe the consequence of differential transcription due to the
presence or absence of particular proteins or the growth in particular environments. Control can
also occur at translation; the mRNA is synthesized, but only in certain circumstances is it
translated. Control can also occur at the level of protein function; the protein is inactive, or
activity is not observed due to the lack of the substrate. In this lab we will observe differential
expression of two different genes encoded on plasmids. We will analyze transcriptional activity,
translational activity, and protein function. Plasmids are extra-chromosomal DNA. Bacteria often
have plasmids and will replicate the plasmid and pass it to daughter cells (vertical transmission)
and to neighboring cells (horizontal). Plasmids are a mechanism of gene diversity. In order to
stably retain the plasmid, there needs to be some type of metabolic reason for the bacteria to
maintain the plasmid. In other words, the plasmid confers an advantage. Plasmids contain: 1. Ori:
the plasmid may present is low or high copy number. 2. Lab generated plasmids typically also
contain a selectable marker (antibiotic resistance), 3. Additional gene for ease of visual screening
4. Multiple cloning site
pUC19 is one of a series of plasmid cloning vectors created by Joachim Messing and co-workers.
The designation "pUC" is derived from the classical "p" prefix (denoting "plasmid") and the
abbreviation for the University of California, where early work on the plasmid series had been
conducted. It is a circular double stranded DNA and has 2686 base pairs. pUC19 is one of the
most widely used vector molecules as the recombinants, or the cells into which foreign DNA has
been introduced, can be easily distinguished from the non-recombinants based on color
differences of colonies on growth media. pUC18 is similar to pUC19, but the MCS region is
reversed. - pUC 19 has an origin of replication and is maintained at a high copy number. -
pUC19 encodes for an ampicillin resistance gene (amopR), via a -lactamase enzyme that
functions by degrading ampicillin and reducing its toxicity to the host. - It has an N-terminal
fragment of -galactosidase (lacZ) gene of E. coli which allows for visual screening of
recombinant.
ONLY THE LAST QUESTION IS THE POINT OF POST. THE OTHER PAGES ARE BAC.pdfamzonknr
ONLY THE LAST QUESTION IS THE POINT OF POST. THE OTHER PAGES ARE
BACKGROUND CONTEXT Lab: Differential Expression Differential gene expression provides
the ability for a cell or organism to respond to a constantly changing external environment. The
specific constellation of proteins required for optimal function and growth varies with cellular
age and environmental context. Thus, protein production is carefully regulated by multiple
mechanisms that modulate both transcriptional and translational pathways. Control of
transcription initiation by RNA polymerase is a predominant mechanism for regulating
expression of specific proteins, presumably because it provides maximal conservation of energy
for the cell. We can often observe the consequence of differential transcription due to the
presence or absence of particular proteins or the growth in particular environments. Control can
also occur at translation; the mRNA is synthesized, but only in certain circumstances is it
translated. Control can also occur at the level of protein function; the protein is inactive, or
activity is not observed due to the lack of the substrate. In this lab we will observe differential
expression of two different genes encoded on plasmids. We will analyze transcriptional activity,
translational activity, and protein function. Plasmids are extra-chromosomal DNA. Bacteria often
have plasmids and will replicate the plasmid and pass it to daughter cells (vertical transmission)
and to neighboring cells (horizontal). Plasmids are a mechanism of gene diversity. In order to
stably retain the plasmid, there needs to be some type of metabolic reason for the bacteria to
maintain the plasmid. In other words, the plasmid confers an advantage. Plasmids contain: 1. Ori:
the plasmid may present is low or high copy number. 2. Lab generated plasmids typically also
contain a selectable marker (antibiotic resistance), 3. Additional gene for ease of visual screening
4. Multiple cloning site
pUC19 is one of a series of plasmid cloning vectors created by Joachim Messing and co-workers.
The designation "pUC" is derived from the classical "p" prefix (denoting "plasmid") and the
abbreviation for the University of California, where early work on the plasmid series had been
conducted. It is a circular double stranded DNA and has 2686 base pairs. pUC19 is one of the
most widely used vector molecules as the recombinants, or the cells into which foreign DNA has
been introduced, can be easily distinguished from the non-recombinants based on color
differences of colonies on growth media. pUC18 is similar to pUC19, but the MCS region is
reversed. - pUC 19 has an origin of replication and is maintained at a high copy number. -
pUC19 encodes for an ampicillin resistance gene (amopR), via a -lactamase enzyme that
functions by degrading ampicillin and reducing its toxicity to the host. - It has an N-terminal
fragment of -galactosidase (lacZ) gene of E. coli which allows for visual screening of
recombinant.
An honest effort to present molecular marker in easiest way both informative and conceptual. Hybridization based (non-PCR) and PCR based markers are discussed to the point with suitable diagram.
Richard's entangled aventures in wonderlandRichard Gill
Since the loophole-free Bell experiments of 2020 and the Nobel prizes in physics of 2022, critics of Bell's work have retreated to the fortress of super-determinism. Now, super-determinism is a derogatory word - it just means "determinism". Palmer, Hance and Hossenfelder argue that quantum mechanics and determinism are not incompatible, using a sophisticated mathematical construction based on a subtle thinning of allowed states and measurements in quantum mechanics, such that what is left appears to make Bell's argument fail, without altering the empirical predictions of quantum mechanics. I think however that it is a smoke screen, and the slogan "lost in math" comes to my mind. I will discuss some other recent disproofs of Bell's theorem using the language of causality based on causal graphs. Causal thinking is also central to law and justice. I will mention surprising connections to my work on serial killer nurse cases, in particular the Dutch case of Lucia de Berk and the current UK case of Lucy Letby.
Observation of Io’s Resurfacing via Plume Deposition Using Ground-based Adapt...Sérgio Sacani
Since volcanic activity was first discovered on Io from Voyager images in 1979, changes
on Io’s surface have been monitored from both spacecraft and ground-based telescopes.
Here, we present the highest spatial resolution images of Io ever obtained from a groundbased telescope. These images, acquired by the SHARK-VIS instrument on the Large
Binocular Telescope, show evidence of a major resurfacing event on Io’s trailing hemisphere. When compared to the most recent spacecraft images, the SHARK-VIS images
show that a plume deposit from a powerful eruption at Pillan Patera has covered part
of the long-lived Pele plume deposit. Although this type of resurfacing event may be common on Io, few have been detected due to the rarity of spacecraft visits and the previously low spatial resolution available from Earth-based telescopes. The SHARK-VIS instrument ushers in a new era of high resolution imaging of Io’s surface using adaptive
optics at visible wavelengths.
Richard's aventures in two entangled wonderlandsRichard Gill
Since the loophole-free Bell experiments of 2020 and the Nobel prizes in physics of 2022, critics of Bell's work have retreated to the fortress of super-determinism. Now, super-determinism is a derogatory word - it just means "determinism". Palmer, Hance and Hossenfelder argue that quantum mechanics and determinism are not incompatible, using a sophisticated mathematical construction based on a subtle thinning of allowed states and measurements in quantum mechanics, such that what is left appears to make Bell's argument fail, without altering the empirical predictions of quantum mechanics. I think however that it is a smoke screen, and the slogan "lost in math" comes to my mind. I will discuss some other recent disproofs of Bell's theorem using the language of causality based on causal graphs. Causal thinking is also central to law and justice. I will mention surprising connections to my work on serial killer nurse cases, in particular the Dutch case of Lucia de Berk and the current UK case of Lucy Letby.
Multi-source connectivity as the driver of solar wind variability in the heli...Sérgio Sacani
The ambient solar wind that flls the heliosphere originates from multiple
sources in the solar corona and is highly structured. It is often described
as high-speed, relatively homogeneous, plasma streams from coronal
holes and slow-speed, highly variable, streams whose source regions are
under debate. A key goal of ESA/NASA’s Solar Orbiter mission is to identify
solar wind sources and understand what drives the complexity seen in the
heliosphere. By combining magnetic feld modelling and spectroscopic
techniques with high-resolution observations and measurements, we show
that the solar wind variability detected in situ by Solar Orbiter in March
2022 is driven by spatio-temporal changes in the magnetic connectivity to
multiple sources in the solar atmosphere. The magnetic feld footpoints
connected to the spacecraft moved from the boundaries of a coronal hole
to one active region (12961) and then across to another region (12957). This
is refected in the in situ measurements, which show the transition from fast
to highly Alfvénic then to slow solar wind that is disrupted by the arrival of
a coronal mass ejection. Our results describe solar wind variability at 0.5 au
but are applicable to near-Earth observatories.
Cancer cell metabolism: special Reference to Lactate PathwayAADYARAJPANDEY1
Normal Cell Metabolism:
Cellular respiration describes the series of steps that cells use to break down sugar and other chemicals to get the energy we need to function.
Energy is stored in the bonds of glucose and when glucose is broken down, much of that energy is released.
Cell utilize energy in the form of ATP.
The first step of respiration is called glycolysis. In a series of steps, glycolysis breaks glucose into two smaller molecules - a chemical called pyruvate. A small amount of ATP is formed during this process.
Most healthy cells continue the breakdown in a second process, called the Kreb's cycle. The Kreb's cycle allows cells to “burn” the pyruvates made in glycolysis to get more ATP.
The last step in the breakdown of glucose is called oxidative phosphorylation (Ox-Phos).
It takes place in specialized cell structures called mitochondria. This process produces a large amount of ATP. Importantly, cells need oxygen to complete oxidative phosphorylation.
If a cell completes only glycolysis, only 2 molecules of ATP are made per glucose. However, if the cell completes the entire respiration process (glycolysis - Kreb's - oxidative phosphorylation), about 36 molecules of ATP are created, giving it much more energy to use.
IN CANCER CELL:
Unlike healthy cells that "burn" the entire molecule of sugar to capture a large amount of energy as ATP, cancer cells are wasteful.
Cancer cells only partially break down sugar molecules. They overuse the first step of respiration, glycolysis. They frequently do not complete the second step, oxidative phosphorylation.
This results in only 2 molecules of ATP per each glucose molecule instead of the 36 or so ATPs healthy cells gain. As a result, cancer cells need to use a lot more sugar molecules to get enough energy to survive.
Unlike healthy cells that "burn" the entire molecule of sugar to capture a large amount of energy as ATP, cancer cells are wasteful.
Cancer cells only partially break down sugar molecules. They overuse the first step of respiration, glycolysis. They frequently do not complete the second step, oxidative phosphorylation.
This results in only 2 molecules of ATP per each glucose molecule instead of the 36 or so ATPs healthy cells gain. As a result, cancer cells need to use a lot more sugar molecules to get enough energy to survive.
introduction to WARBERG PHENOMENA:
WARBURG EFFECT Usually, cancer cells are highly glycolytic (glucose addiction) and take up more glucose than do normal cells from outside.
Otto Heinrich Warburg (; 8 October 1883 – 1 August 1970) In 1931 was awarded the Nobel Prize in Physiology for his "discovery of the nature and mode of action of the respiratory enzyme.
WARNBURG EFFECT : cancer cells under aerobic (well-oxygenated) conditions to metabolize glucose to lactate (aerobic glycolysis) is known as the Warburg effect. Warburg made the observation that tumor slices consume glucose and secrete lactate at a higher rate than normal tissues.
THE IMPORTANCE OF MARTIAN ATMOSPHERE SAMPLE RETURN.Sérgio Sacani
The return of a sample of near-surface atmosphere from Mars would facilitate answers to several first-order science questions surrounding the formation and evolution of the planet. One of the important aspects of terrestrial planet formation in general is the role that primary atmospheres played in influencing the chemistry and structure of the planets and their antecedents. Studies of the martian atmosphere can be used to investigate the role of a primary atmosphere in its history. Atmosphere samples would also inform our understanding of the near-surface chemistry of the planet, and ultimately the prospects for life. High-precision isotopic analyses of constituent gases are needed to address these questions, requiring that the analyses are made on returned samples rather than in situ.
Comparing Evolved Extractive Text Summary Scores of Bidirectional Encoder Rep...University of Maribor
Slides from:
11th International Conference on Electrical, Electronics and Computer Engineering (IcETRAN), Niš, 3-6 June 2024
Track: Artificial Intelligence
https://www.etran.rs/2024/en/home-english/
This presentation explores a brief idea about the structural and functional attributes of nucleotides, the structure and function of genetic materials along with the impact of UV rays and pH upon them.
Nucleic Acid-its structural and functional complexity.
Classes of-molecular-markers
1. -1-
Classes of Molecular Markers
Isozymes
Gel-based approach
Protein analyzed
Allelic difference detected
o Alleles migrate at different rate in starch gel
Locus-by-locus approach
RFLP – Restriction Fragment Length Polymorphism
Hybridization-based approach
RFLP recognized by specific clone/enzyme combinations
Locus-by-locus approach
RAPD – Randomly Amplified Polymorphic DNA
Gel-based approach
PCR amplification of fragment
10mer oligonucleotides recognize inverted repeats
o Fragment between the inverted repeats is amplified
Genome-wide approach
AFLP – Amplified Fragment Length Polymorphism
2. -2-
Gel- or capillary-based approach
Combines restriction disgestion with PCR amplification
Selectively amplifies a subset of possible genomic fragments
Genome-wide approach
Microsattelites
Gel- or capillary-based approach
Mostly based on differences in number of di- or tri nucleotide
repeats at a specific locus
Locus-by-locus approach
SNP – Single Nucleotide Polymorphism
Multiple detection procedures
Based on nucleotide differences between two alleles
Locus-by-locus approach
3. -3-
Isozymes
Enzyme Systems
Rbcs – Ribulose bisphosphate carboxylase, small subunit
Skdh – Shikimate dehydrogenase
Prx – Peroxidase
Me – Malic enzyme
Mdh – Malate dehyrogenase
Diap – Diaphorase
Lap – Leucine aminopeptidase
Matrix
Starch
Typically five samples per gel
Scoring Protocol
Most frequent allele is given the designation “100”
Other alleles designated by distance in millimeters from the
most frequent allele
Allele nomenclature examples from P. vulgaris
o Me98
– 2 millimeters slower in the gel
o Me100
– most frequent allele
o Me105
– 5 millimeters faster in the gel
4. -4-
RFLP Clones, Enzymes, and
Informative Hybridizations
1. Source of clones
a. Random clones – poor choice because they often contain
repetitive DNA
b. cDNA clones – contain only expressed sequences; often
low copy number
c. PstI clones – based on the concept that expressed (low
copy number) genes are undermethylated; therefore the
methylation sensitive enzyme PstI will only cut in regions
where expressed genes reside
2. Enzymes – need to screen parents by digestions with a series
of enzymes to find polymorphic hybridizations
3. Informative hybridizations – those specific restriction
enzyme/clone combinations that are polymorphic will be
informative for mapping a segregating population
5. -5-
Restriction-modification system
Restriction enzyme - cleaves DNA at a specific sequence
Methylase - protects the host DNA from being cleaved
The E. coli Type RI (EcoRI) restriction enzyme site is:
m
5' - G A A T T C - 3'
3' - C T T A A G - 5'
m
(Remember, the enzyme will not cut
if the 3' A is methylated.)
5' - G - 3' 5' - A A T T C - 3'
3' - C T T A A - 5' 3' - G - 5'
6. -6-
Restriction enzyme = EcoRI cuts between the G and A. in the
sequence GAATTC
Methylase = EcoRI methylase protects the EcoRI by adding a
methyl group to the 3'-adenine
How the system works
1. Growth of foreign DNA (such as virus DNA) is restricted in the
cell by the restriction enzyme
2. The bacterial DNA is modified by the methylase to prevent
cleavage by the restriction enzyme.
7. -7-
Methylation of Plant DNA and its Effect on Restriction
Digestion
Grenbaum et al. Methylation of cytosines in higher plants
Nature 297:86 August 1981
5-methyl cytosine (5mC) is found to be a component of plant DNA
much more frequently than animal DNA
% Cytosine as 5mC
Animals 2-7
Plants >25
Why???
1. 5mC occurs at 70-80% of the 5'-CG-3' dinucleotides. What are
the occurrences of the dinucleotide in the two kingdoms?
% dinucleotides
as 5-'CG-3
Animals 0.5-1.0
Plants 3.4
2. 5mC also occurs at the 5'-CXG-3' sequence in plants but
does not occur in animals. How often are these sequences
methylated in plants?
Sequence % C methylated
5'-CAG-3 80
5'-CCG-3 50
8. -8-
Do Not Use These Enzymes
to Analyze Plant DNA
1. Site has 5'-CXG-3'
PstI 5'-C*TGCAG-3'
PvuII 5'-CAGC*TG-3'
MspI 5'-C*CGG-3
EcoRII 5'-CC*WGG-3'
(W = A or T)
2. C at or near end of site;if
next base in DNA is G, it will
be methylated
BamHI 5'-GGATC*C-3
KpnI 5'-GGTACC*-3
Use These Enzymes Instead
DraI 5'-TTTAAA-3'
EcoRV 5-'GA*TATC-3
EcoRI 5-GAA*TTC*-3'
HindIII 5'-A*AGC*TT-3'
XbaI 5'-TC*TAGA*-3'
9. -9-
RAPD Markers
A PCR-based marker system
Amplifies inverted repeats in the genome
Can generate larger number of markers than RFLP in a
short period of time
Popular because easy to do and does not require
radioisotopes
10. -10-
AFLP Procedure
1. Digest sample DNA with restriction enzymes EcoRI and
MseI.
5'----GAATTCN------------------------NTTAA----3'
3'----CTTAAGN------------------------NAATT----5"
AATTCN------------------------NT
GN------------------------NAAT
2. Anneal EcoRI and MseI adaptors to restriction products.
??????AATTCN-------------------------NTTA??????
??????TTAAGN-------------------------NAAT??????
(?????? = unknown sequences that are unique for the
companies primers)
3. Preselect products by PCR amplification with "EcoRI + A"
and "MseI +C" oligonucleotide primers.
EcoRI Primer+A
????????AATTCN---------------------NTTA????????
????????TTAAGN---------------------NAAT????????
C+MseI Primer
11. -11-
4. Selectively amplify preselect PCR products by using "EcoRI +
3" and "MseI +3" oligonucleotide primers.
EcoRI Primer+AAC
????????AATTCA----------------------GTTA????????
????????TTAAGT----------------------CAAT????????
AAC+MseI Primer
5. Separate fragments by denaturing polyacrylamide gel
electrophoresis
12. -12-
Microsatellites
Also called:
SSR = Simple Sequence Repeats
SSLP = Simple Sequence Length Polymorphisms
STMS = Sequence Tagged Microsatellites)
What are they?
Typically repeated di-, tri or tetranucleotide sequences
Examples:
AG4 (AG AG AG AG)
CGA3 (CGA CGA CGA)
GATA5 (GATA GATA GATA GATA)
13. -13-
How are they discovered?
Sequenced genes in databases searched for repeats
Repeat olignucleotide probes used to screen random clone
library
Rice example [Mol Gen Genet (1996) 252:597]:
Library:
300-600 bp fragments generated by shearing DNA
fragments cloned into plasmid vector
Probes:
GA13
CGG9
ATC9
ATT9
14. -14-
The Microsatellite Application
Primers highly specific to sequences flanking the repeat are
designed
Individual DNA samples are amplified
Products compared by polyacrylamide or agarose gels using
staining producedures
Recently fluorescently labeled primers are used and products
are analyzed with laser technology (gel or capillary)
Differences in two samples are represented by size differences
of amplified fragments
The size difference is the polymorphism
Single-base pair polymorphisms can be detected
15. -15-
Advantages of Microsatellites
Genetic
Many loci in the genome (goal: 30,000 in humans)
Randomly distributed in a genome
Extensive polymorphism within a species
Many act as codominant markers
Technical
Generally reproducible from lab to lab
Small amounts of target DNA needed
Can be automated
Mulitplexing possible
Disdvantages of Microsatellites
Genetic
Null alleles at a specific locus result in a dominant marker
and heterozygotes can not be scored
Technical
Very high development costs
16. -16-
Arabidopsis Microsatellite Summary
Bioinformatics (2004) 20:1081-1086
93% of microsattelites are trinucleotides
Repeats less frequent in coding than non-coding regioins
Microsatellite more abundant in 5’ region of gene
AG and AAG were the most frequent repeats
Studied 1140 full length genes with an AG or AAG repeat in 5”
region
o These repeats often associated with function of gene
o Based on proximity to beginning of first exon
These genes more often performed a molecular
activitythan genes without a repeat
17. -17-
Modern Approach to Microsatellite Discovery
Collect sequence data
EST
Will be in genes that are in the low copy region of the
genome
Random genome reads
May be low copy or high copy regions of the genome
Soybean EST Discovery
Song et al. Crop Science 50:1950 (2010)
Screened
Whole genome sequence
ESTs
Minimum of 5 copies of the repeat
Genome sequence EST sequences
Total 210,990 33,327
Dinucleotide 168,625 20,161
Trinucleotide 38,411 12,440
Tetranucleotide 3,954 636
Most abundant in genome sequence
(AT)n, (ATT)n, (AAAT)n
o 61,458
Testing the approach
1034 primer pairs developed
Screened 7 diverse genotypes
o 94.6% (978) amplified a single PCR product
77.2% (798) were polymorphic
18. -18-
Single Nucleotide Polymorphisms (SNPs)
Single nucleotides are the smallest unit of mutation
Single nucleotides therefore are the smallest polymorphic unit
SNP = single nucleotide polymorphisms
Uses:
Detect level of variation within a species
Follow patterns of evolution
Mark genes
Distinguish alleles of “disease” genes
Create designer pharmaceuticals
The SNP Consortium, Ltd
Goal
Identify 300,000 human SNPs by Dec. 31, 2001
Progress
7,365 (Dec. 31, 1999)
1.2 million detected (Jan 26, 2002) and mapped in one
population
1.1 high quality mapped in three populations; 1 SNP every
5 kilobases
19. -19-
Detecting DNA Polymorphisms
DNA molecules greater than 10 base pairs contains essentially
the same mass-to-charge ratio
Procedure that separates the molecules based on mass alone will
uncover DNA polymorphisms
Current Procedure
Gel electrophoresis
Emerging Procedures
Capillary array electrophoresis
Matrix-assisted laser desorption/ionization time-of-flight
mass spectrometry (MALDI-TOF MS)
New technology in 2002 that has not really caught on
Advantage of New Procedures
SPEEEEEEEED
20. -20-
Gel Electrophoresis
Most widely adapted technique for detecting polymorphism.
Principle
Samples loaded into a gel and allowed to migrate in an
electric field
DNA is positively charged and samples migrate toward
the negative pole
Separation of the molecules is strictly based on size
smallest fragments move farther in the gel
They can navigate through the small pores in the gel
faster than large molecules.
Types of Gel Matrices
Agarose
Polyacrylamide
Separation is function of the polymer concentration
Agarose Polyacrylamide
% Resolution (kb) % Resolution (bp)
0.9 0.5 - 7.0 3.5 1000 - 2000
1.2 0.4 - 6.0 5.0 80 - 500
1.5 0.2 - 3.0 8.0 60 - 400
2.0 0.1 - 2.0 12.0 40 - 200
21. -21-
What polymer do you choose?
Polymer choice is based on the size range of fragment
Agarose
RFLP
RAPD
Polyacrylamide
Microsatellites
AFLPs
Observing the Polymorphisms
Dye Detection
Ethidium bromide (Agarose)
RAPD
Silver nitrate (Polyacrylamide)
Microsatellites
AFLPs
Authoradiography Detection
RFLP (more later)
Microsatellites
AFLP
22. -22-
Laser Technology Detection
Applied to the microsatellites
Procedure
PCR primer is labelled with a fluorescent dye
Samples are separated in a polyacrylamide gel
Fragments are detected by a laser as they flow through
the bottom of the gel
Computer programs output data as size difference
RFLPs and Southern Hybridizations
Restriction digested DNA separated in agarose gel
DNA transferred to a nylon membrane
Membrane contains a faithful representation of the
fragment distribution found in the gel
Probe is hybridized to the membrane
Unbound probe is removed by a series of stringent
washes
Membrane is exposed autoradiographic film
Polymorphisms observed
23. -23-
Capillary Array Electrophoresis
Small DNA fragments are rapidly separated in narrow capillaries.
Heat is lost rapidly from thin capillaries
Thus, molecules can be separated rapidly using high voltage.
High voltage separation greatly speeds sample processing
Capillaries arrays have reached the market
Eight capillary array (Beckman-Coulter)
96 capillary array (Applied Biosystems)
Advantage
Multipe samples simultaneously introduce into each
arrays
Size detected by laser technology
24. -24-
Advantages and Disadvantages of Different
Marker Systems
Marker Advantages Disadvantages
Classical Easily scored; new
equipment not needed;
traits of economic
importance
Time to score;
environmental influences;
limited for most species;
mostly dominant
Isozyme Easy to apply; codominant;
multiple alleles
Limited number of assays
available; scored at only one
developmental stage
RFLP Codominant; highly
repeatable; maps available
for major species
Limited polymorphisms, time
consuming; relatively
expensive; requires
radioactivity
RAPD Easy technique; rapidly
screening; no radioactivity
Low lab-to-lab repeatability;
mostly dominant
AFLP Large number of
polymorphisms per
sample; easy to apply
(once mastered)
Difficult to learn; radioactivity
might be used; expensive;
time-consuming; mostly
dominant
Microsatellites Highly polymorphic; easy
to apply; large number of
loci available; mostly co-
dominant
Slow and expensive
development costs
SNP High accuracy; potentially
a very large number; co-
dominant
Expensive to discover;
assays are currently
expensive
25. -25-
What to consider when choosing a marker
system
Genetic nature of the system
Radioactivity
Cost
Reproducibility
Time (Discovery and application)
Efficiency (Time invested vs. breadth of results)
Is a system in place??? (Map available; technique defined)
Reason for experiments (Marker development vs. application)
Amount of polymorphisms
Technical skill needed
26. -26-
Types of Nucleic Acid Hybridizations
1. Southern hybridization - hybridization of a probe to filter
bound DNA; the DNA is typically transferred to the filter from a
gel
2. Northern hybridization - hybridization of a probe to filter
bound RNA; the RNA is typically transferred to the filter from a
gel
Probe - a single-stranded nucleic acid that has been radiolabelled
and is used to identify a complimentary nucleic acid sequence
that is membrane bound
The following steps describe the Southern transfer procedure.
1. Digest DNA with the restriction enzyme of choice.
2. Load the digestion onto a agarose gel and apply an electrical
current. DNA is negatively charged so it migrates toward the "+"
pole. The distance a specific fragment migrates is inversely
proportional to the fragment size.
3. Stain the gel with EtBr, a fluorescent dye which intercalates into
the DNA molecule. The DNA can be visualized with a UV light
source to assess the completeness of the digestion.
4. Denature the double-stranded fragments by soaking the gel in
alkali (>0.4 M NaOH)
5. Transfer the DNA to a filter membrane (nylon or nitrocellulose)
by capillary action.
27. -27-
Steps in Southern Hybridization Procedure
1. Prepare a probe by nick translation or random, oligo-primed
labelling.
2. Add the probe to a filter (nylon or nitrocellulose) to which
single-stranded nucleic acids are bound. (The filter is
protected with a prehybridization solution which contains
molecules which fill in the spots on the filter where the nucleic
acid has not bound.
3. Hybridize the single-stranded probe to the filter-bound nucleic
acid for 24 hr. The probe will bind to complementary
sequences.
4. Wash the filter to remove non-specifically bound probe.
5. Expose the filter and determine:
a. Did binding occur?
b. If so, what is the size of hybridizing fragment?
28. -28-
Hybridization Stringency
Temperature and salt concentrations of hybridization
conditions directly affect hybridization results
The degree of homology required for binding to occur can be
controlled by these factors
Results are directly related to the “degrees below the Tm” at
which the hybridizations and washes are performed
Tm is the melting temperature of the DNA
29. -29-
Tm = 69.3oC + 0.41(% G + C)oC
From this formula you can see that the GC content has a direct
effect on Tm. The following examples, demonstrate the point.
Tm = 69.3oC + 0.41(45)oC = 87.5oC (for wheat germ)
Tm = 69.3oC + 0.41(40)oC = 85.7oC
Tm = 69.3oC + 0.41(60)oC = 93.9oC
Hybridizations though are always performed with salt. This
requires another formula which considers this fact. This formula
is for the Effective Tm (Eff Tm).
Eff Tm = 81.5 + 16.6(log M [Na+]) + 0.41(%G+C) - 0.72(%
formamide)
30. -30-
Na+ ion concentration of different strengths of SSC
SSC Content [Na+] M
20X 3.3000
10X 1.6500
5X 0.8250
2X 0.3300
1X 0.1650
0.1X 0.0165
Another relevant relationship is a that 1% mismatch of two
DNAs lowers the Tm 1.4oC. So in a hybridization with wheat
germ that is performed at Tm - 20oC (=67.5oC), the two DNAs
must be 85.7% homologous for the hybridization to occur.
100% - (20oC/1.4oC) = 85.7% homology
31. -31-
Let's now look at an actual experiment.
Wheat DNA
Hybridization at 5X SSC at 65o
C
Non-stringent wash: 2X SSC at 65o
C
Stringent wash: 0.1X SSC at 65o
C
The first step is to derive the Eff Tm.
Eff Tm = 81.5 + 16.6(log 0.825) + 18.5 = 98.6
Next figure out hybridization homology
100 - [(98.6-65.0)/1.4] = 100 - (23.6/1.4) = 83.1%.
Next figure out Eff Tm and hybridization homology for non-stringent wash
Eff Tm = 81.5 + 16.6[log(0.33)] + 0.41(45%) = 92.0oC
% Homology = 100 - [(92-65)/1.4] = 80.7%
Next figure out Eff Tm and hybridization homology for stringent wash
Eff Tm = 81.5 + 16.6[log(0.0165)] + 0.41(45%) = 70.4oC
% Homology = 100 -[(70.4-65)/1.4] = 96.1%
Stringency - a term used in hybridization experiments to denote the
degree of homology between the probe and the filter bound nucleic acid;
the higher the stringency, the higher percent homology between the probe
and filter bound nucleic acid
32. -32-
Mapping and Mapping Populations
Types of mapping populations
a. F2
b. Backcross
c. Recombinant Inbred Lines (RILs; F2-derived lines)
Homozygosity of Recombinant Inbred Lines
RI population % within-line homozygosity at each
locus
F23 75.0
F24 87.5
F25 92.25
F26 96.875
F27 98.4375
F28 99.21875
Value of Recombinant Inbred Population
1. Eternal source materials
2. Phenotypic data collection can be replicated to ensure
accuracy
3. Large field trials can be performed to collective quantitative trait
data
4. Problem: dominance and epistasis can not be measured
because no heterozygotes
33. -33-
Segregation Ratio of Mapping Populations
Population Codominant
loci
Dominant
loci
F2 population 1:2:1 3:1
Backcross population 1:1 1:1*
Recombinant inbred population 1:1 1:1
*To score a dominant maker in a backcross population, you must
cross the recessive parent with the F1 plant. Therefore to score
RAPD loci you would need to create two populations, each one
developed by backcrossing to one of the two parents. For this
reason, backcross populations have not been used for mapping
RAPD loci.
34. -34-
Other Mapping Populations
Association Mapping (AM) Population
Limits of traditional bi-parental populations
Limited number of recombination events
o F2: one round of recombination
o RI populations: maximum of two rounds of
recombination
Allele richness
o Poor
Only alleles of parents sampled
Limits discover of all factors controlling a quantitative trait in a
species
But the advantage is:
o With limited recombination
Fewer markers needed to discover relevant
genetic factors
35. -35-
What is an association mapping population?
Collection of genotypes from a species
o Represent the genetic background for which you want
to make inferences
Arabidopsis
o Collection of wild samples from throughout the world
25 regions, four populations each
PLoS Biology (2005) 3:e196
Maize
o 92 inbred
12 stiff stalk, 45 non-stiff stalk, 35 tropical,
semitropical
Nature Genetics (2001) 28:286
Major benefit
o Samples many more recombination events
Great resolution
Resolution depends upon linkage
disequilibrium in sample
But the disadvantage
o Need many markers to find meaningful associations
Size for population used today
o Several hundreds (200-300 individuals)
36. -36-
Nested Association Mapping (NAM) Population
How is a NAM population created?
Developed from crossing
o One common parent to
o Multiple parents of diverse origin
Parents contain relevant diversity specific to the trait(s) of
interest
Often a single populations is developed per species
o High resource cost, so
Choice of parents is important
Maize example
o B73: common parent
Sequenced by maize genome project
o 25 other parents
Represent diversity in maize
200 lines per cross (5,000 total)
o Science (2009) 325:714
Large number of populations give better resolution
o Genetics (2009) 183:1525
Advantages
Like bi-parental population
o Uses current recombination events created by the cross
o Fewer markers than AM will discover the QTL
Like AM population
o Uses many recombination events
o Based on the many crosses used to make the
population members
37. -37-
Diversity or Phylogenetic Populations
Used to determine the relationship among individuals
Define patterns of relatedness
Selection of parents for breeding
Determine ancestral origin
Define gene tree
o Origin of a gene in a lineage
Define a species tree
o What is the relationships of members of a species
Within a species
Within a genera
Within a family
Considerations
Should represent the lineage that is of concern to the study
38. -38-
Specialized Mapping Topics
Bulk Segregant Analysis
Useful for targeting a specific genomic region
Create two DNA bulks
- one contains homozygous dominant individuals
- other contains homozygous recessive individuals
Perform a molecular marker analysis
The bulks are equally random for all regions of the genome
except that which contains your gene of interest
Any difference should be linked to the gene controlling the trait
you bulked upon
39. -39-
Sequence Tagged Sites (STS)
Defined by a pair of PCR sites obtained from DNA sequencing
Each site is usually 18-20 nucleotides long
Amplification is more specific because of the size of the primer
that anneals to one end of the STS
May require subsequent restriction digestion to define a
polymorphism
Reduces lab to lab variability seen with RAPDs
Arabidopsis STS Primers (called CAPS)
- two per chromosome
- allows a rapid mapping of new mutant to a specific
chromosome