Molecular Markers DNA & PROTEINS –mtDNA = often used in systematics; in general, no recombination = uniparental inheritance –cpDNA = often used in systematics;

Slides:



Advertisements
Similar presentations
Applications of genome sequencing projects 1) Molecular Medicine 2) Energy sources and environmental applications 3) Risk assessment 4) Bioarchaeology,
Advertisements

applications of genome sequencing projects
RAPD Randomly Amplified Polymorphic DNA
DNA Typing bsapp.com. bsapp.com DNA strands come from the nucleus or the mitochondria bsapp.com.
Summary of 8th lesson Exotic microbes have a reduced level of genetic variability If genotypes fall on clades separated by long branches, it may be an.
DNA fingerprinting Every human carries a unique set of genes (except twins!) The order of the base pairs in the sequence of every human varies In a single.
Molecular Tools for Aiding and Breeding of Aquaculture Species Masters in Aquaculture and Fisheries Genetic and Selection 2014 Tamara Moedas nº 47853;
Using DNA sequences Obtain sequence Align sequences, number of parsimony informative sites Gap handling Picking sequences (order) Analyze sequences (similarity/parsimony/exhaustive/bayesian.
Cloning lab results Cloning the human genome Physical map of the chromosomes Genome sequencing Integrating physical and recombination maps Polymorphic.
Summary of sixth lesson Janzen-Connol hypothesis; explanation of why diseases lead to spatial heterogeneity Diseases also lead to heterogeneity or changes.
Genetic analysis requires variation at loci, variation of markers (polymorphisms) How the variation is structured will tell us –Does the microbe reproduce.
Physical Mapping I CIS 667 February 26, Physical Mapping A physical map of a piece of DNA tells us the location of certain markers  A marker is.
Overview Armillaria bulbosa (gallica) Known as the Humungous Fungus, or honey mushroom Form rhizomorphs, which make up much of the “humungous” part Basidiocarp:
Introduction to Linkage Analysis March Stages of Genetic Mapping Are there genes influencing this trait? Epidemiological studies Where are those.
Generation and Analysis of AFLP Data
Quiz What were the two most significant consequences of geographic isolation of some mangrove stand in Panama? In the Hogberg et al paper on Fomitopsis.
Three Clonal Lineages of Phytophthora cinnamomi in Australia Revealed by Microsatellites M.P Dobrowolski et al., Phytopathology 2002.
What is Population Genetics?  About microevolution (evolution within species)  The study of the change of allele frequencies, genotype frequencies, and.
PLANT BIOTECHNOLOGY & GENETIC ENGINEERING (3 CREDIT HOURS)
Constant Allele Frequencies Hardy-Weinberg Equilibrium.
Molecular Markers DNA & PROTEINS –mtDNA = often used in systematics; in general, no recombination = uniparental inheritance –cpDNA = often used in systematics;
Restriction Fragment Length Polymorphisms (RFLPs) By Amr S. Moustafa, M.D.; Ph.D. Assistant Prof. & Consultant, Medical Biochemistry Dept. College of.
RFLP DNA molecular testing and DNA Typing
Population Genetics of Puccinia coronata f. sp. avenae Hattie Dambroski and Martin Carson USDA-ARS Cereal Disease Laboratory Saint Paul, MN.
DNA Fingerprinting Sotheavy Vann. What is DNA Fingerprinting?  “The generation of a set of distinct DNA fragments from a single DNA sample”  Aka DNA.
Plant Molecular Systematics Michael G. Simpson
CHAPTER 20 BIOTECHNOLOGY: PART I. BIOTECHNOLOGY Biotechnology – the manipulation of organisms or their components to make useful products Biotechnology.
Maria Eugenia D’Amato Slide 1
Maria Eugenia D’Amato. Molecular genetics techniques Types and properties of molecular makers Factors that determine the patterns of genetic variation.
Additive genetic variance and heritability One of the most important questions we can ask to understand evolutionary change is how the phenotypes of parents.
PLANT GENETIC MARKERS Plant Biotechnology Dr.Ir. Sukendah, MSc.
DNA fingerprinting. DNA fingerprinting is used to determine paternity Look at the DNA of the mother, father and child Could these parents produce this.
14 Population Genetics and Evolution. Population Genetics Population genetics involves the application of genetic principles to entire populations of.
Manipulation of DNA. Restriction enzymes are used to cut DNA into smaller fragments. Different restriction enzymes recognize and cut different DNA sequences.
Objective 1 - Describe how restriction enzymes are used to manipulate DNA. Run the virtual gel electrophoresis at this web site
Molecular identification of living things. Molecular Markers Single locus marker Multi-locus marker RFLP Microsatellite DNA Fingerprinting AFLP RAPD.
1 Gene Therapy Gene therapy: the attempt to cure an underlying genetic problem by insertion of a correct copy of a gene. –Tantalizingly simple and profound.
Announcements: Proposal resubmission deadline 4/23 (Thursday).
Summary AFLP, RAPDs, RFLPs, microsatellites Repeatability Test for power (PID and test progeny) Have we sampled enough? Rarefaction curves, resampling,
Experimental Design and Data Structure Supplement to Lecture 8 Fall
 DNA Fingerprinting. Variation in Human DNA  Of 3 billion nucleotides in human DNA more than 99% are identical  Of 1% that are different  significant.
Genes in human populations n Population genetics: focus on allele frequencies (the “gene pool” = all the gametes in a big pot!) n Hardy-Weinberg calculations.
Unit 4, Topic 5 - Genetic Engineering
Molecular Basis for Relationship between Genotype and Phenotype DNA RNA protein genotype function organism phenotype DNA sequence amino acid sequence transcription.
Chapter 5 The Content of the Genome 5.1 Introduction genome – The complete set of sequences in the genetic material of an organism. –It includes the.
ABC for the AEA Basic biological concepts for genetic epidemiology Martin Kennedy Department of Pathology Christchurch School of Medicine.
1 DNA Polymorphisms: DNA markers a useful tool in biotechnology Any section of DNA that varies among individuals in a population, “many forms”. Examples.
Molecular markers Non-PCR based 1courtesy of Carol Ritland.
In The Name of GOD Genetic Polymorphism M.Dianatpour MLD,PHD.
Simple-Sequence Length Polymorphisms SSLPs Short tandemly repeated DNA sequences that are present in variable copy numbers at a given locus. Scattered.
Plant Breeding Shree Krishna Adhikari ©Shree Krishna Adhikari.
Types of genome maps Physical – based on bp Genetic/ linkage – based on recombination from Thomas Hunt Morgan's 1916 ''A Critique of the Theory of Evolution'',
All rights Reserved Cengage/NGL/South-Western © 2016.
Restriction Fragment Length Polymorphism. Definition The variation in the length of DNA fragments produced by a restriction endonuclease that cuts at.
Arun Kumar. B M.Sc 1st Year Biotechnology SSBS
GENETIC MARKERS (RFLP, AFLP, RAPD, MICROSATELLITES, MINISATELLITES)
Molecular Marker Characterization of plant genotypes
All rights Reserved Cengage/NGL/South-Western © 2016.
Genetic markers and their detection
All rights Reserved Cengage/NGL/South-Western © 2016.
DNA Marker Lecture 10 BY Ms. Shumaila Azam
Relationship between Genotype and Phenotype
With Genetic Analyzers from Applied Biosystems
Are my haplotypes sensitive enough?
DNA Polymorphisms: DNA markers a useful tool in biotechnology
MUTATIONS.
THE EVOLUTION OF POPULATIONS
Restriction Fragment Length Polymorphism (RFLP)
The Indispensable Forensic Tool
9-3 DNA Typing with Tandem Repeats
Presentation transcript:

Molecular Markers DNA & PROTEINS –mtDNA = often used in systematics; in general, no recombination = uniparental inheritance –cpDNA = often used in systematics; in general, no recombination = uniparental inheritance –Microsatellites = tandem repeats; genotyping & population structure –Allozymes = variations of proteins; population structure –RAPDs = short segments of arbitrary sequences; genotyping –RFLPs = variants in DNA exposed by cutting with restriction enzymes; genotyping, population structure –AFLPs = after digest with restriction enzymes, a subset of DNA fragments are selected for PCR amplification; genotyping

Genetic analysis requires variation at loci, variation of markers (polymorphisms) How the variation is structured will tell us –Does the microbe reproduce sexually or clonally –Is infection primary or secondary –Is contagion caused by local infectious spreaders or by a long-disance moving spreaders –How far can individuals move: how large are populations –Is there inbreeding or are individuals freely outcrossing

CASE STUDY A grou A stand of adjacent trees is infected by a disease: How can we determine the way trees are infected?

CASE STUDY A grou A stand of adjacent trees is infected by a disease: How can we determine the way trees are infected? BY ANALYSING THE GENOTYPE OF THE MICROBES: if the genotype is the same then we have local secondary tree-to-tree contagion. If all genotypes are different then primary infection caused by airborne spores is the likely cause of Contagion.

CASE STUDY A grou WE HAVE DETERMINED AIRBORNE SPORES (PRIMARY INFECTION ) IS THE MOST COMMON FORM OF INFECTION QUESTION: Are the infectious spores produced by a local spreader, or is there a general airborne population of spores that may come from far away ? HOW CAN WE ANSWER THIS QUESTION?

If spores are produced by a local spreader.. Even if each tree is infected by different genotypes (each representing the result of meiosis like us here in this class)….these genotypes will be related HOW CAN WE DETERMINE IF THEY ARE RELATED?

By using random genetic markers we find out the genetic similarity among these genotypes infecting adjacent trees is high If all spores are generated by one individual –They should have the same mitochondrial genome –They should have one of two mating alleles

WE DETERMINE INFECTIOUS SPORES ARE NOT RELATED QUESTION: HOW FAR ARE THEY COMING FROM? ….or…… HOW LARGE IS A POPULATION? Very important question: if we decide we want to wipe out an infectious disease we need to wipe out at least the areas corresponding to the population size, otherwise we will achieve no result.

HOW TO DETERMINE WHETHER DIFFERENT SITES BELONG TO THE SAME POP OR NOT? Sample the sites and run the genetic markers If sites are very different: –All individuals from each site will be in their own exclusive clade, if two sites are in the same clade maybe those two populations actually are linked (within reach) –In AMOVA analysis, amount of genetic variance among populations will be significant (if organism is sexual portion of variance among individuals will also be significant) –F statistics: Fst will be over ) 0.10 (suggesting stongt structuring) –There will be isolation by distance