lecture one: foundation course genetics tools of human molecular genetics i
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Lecture ONE: Foundation Course Genetics Tools of Human Molecular Genetics I. Discuss the following:. Genetic engineering Molecular Genetics Genetic Screening Recombinant DNA Stem cells. Recombinant DNA methods Restriction enzymes Enzymes from bacteria - PowerPoint PPT PresentationTRANSCRIPT
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Lecture ONE: Lecture ONE: Foundation Course GeneticsFoundation Course Genetics
Tools of Human Molecular Genetics ITools of Human Molecular Genetics I
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Discuss the following:Discuss the following:
• Genetic engineering
• Molecular Genetics
• Genetic Screening
• Recombinant DNA
• Stem cells
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Copyright © 2005 Brooks/Cole — Thomson Learning
Biology, Seventh Edition CHAPTER 14 DNA Technologies
Recombinant DNA methods• Restriction enzymes
–Enzymes from bacteria–Used to cut DNA molecules in specific places
• cut DNA is placed in a Vector carrier • DNA ligase joins cut pieces of DNA
• Transformation: uptake of foreign DNA into cells
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Cloning Vectors
Vector Maximum Insert size
Approx. No. of clones required in library
plasmid 10 kb 10 x 105
lambda 20 kb 5 x 105
cosmid 45 kb 2 x 105
YAC 1 Mb 104
BAC > 500 kb 5 x 104
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Biology, Seventh Edition CHAPTER 14 DNA Technologies
Plasmids
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Biology, Seventh Edition CHAPTER 14 DNA Technologies
Cutting DNA with a restriction enzyme
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• Restriction enzymes are molecular scissors which cut DNA at specific base sequences.
E.g. HindIII and EcoR1 are restriction enzymes
• Hind III cuts DNA at the recognition sequence 5’-AAGCTT-3’
• EcoR1 cuts DNA at the recognition sequence 5’- GAATTC-3’
Restriction Enzymes fig 14.2Restriction Enzymes fig 14.2
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Restriction Enzymes: (Fig 14-1)Restriction Enzymes: (Fig 14-1)
• Many of the sites in DNA which restriction enzymes recognize are
PALINDROMIC
• Palindromic: means that the sequence reads the same 5’-3’ in both directions
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Copyright © 2005 Brooks/Cole — Thomson Learning
Biology, Seventh Edition CHAPTER 14 DNA Technologies
Cutting DNA with a restriction enzyme
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Copyright © 2005 Brooks/Cole — Thomson Learning
Biology, Seventh Edition CHAPTER 14 DNA Technologies
• Splicing foreign DNA into a vector• Foreign DNA and plasmid DNA cut with
same restriction enzyme• Produces linear molecules with
complementary single-stranded ends• Recombinant DNA created by mixing so
sticky ends pair• DNA ligase forms covalent bonds, linking
the two fragments
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Biology, Seventh Edition CHAPTER 14 DNA Technologies
Producing a genomic or chromosome library
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• Genomic library• Collection of DNA fragments that
represent all the DNA in the genome
• Chromosome library• All the DNA fragments in that specific
chromosome
• cDNA library• Produced using reverse transcriptase• Makes DNA copies of mature mRNA
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Biology, Seventh Edition CHAPTER 14 DNA Technologies
Cloning DNACloning DNA: :
• The recombinant DNA can be put back into bacteria and the bacteria allowed to grow
• This will produce many genetically identical copies of the piece of DNA. This is called cloning
• A clone is a genetically identical individual or cell
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Biology, Seventh Edition CHAPTER 14 DNA Technologies
• Genetic probes• Segments of single-stranded DNA that
can hybridize to complementary base sequences in target gene
• Southern blot technique
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Southern Northern, and Western Southern Northern, and Western BlottingBlotting
•Southern Blotting: DNA
•Northern Blotting: RNA
•Western Blotting : Protein
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Biology, Seventh Edition CHAPTER 14 DNA Technologies
Using a geneticprobe to find bacterial cellswith a specificrecombinant DNA molecule
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Biology, Seventh Edition CHAPTER 14 DNA Technologies
• Amplifying DNA in vitro by PCR–Small amount of double-stranded DNA–DNA precursors–Specific nucleic acid primers–Taq DNA polymerase
• DNA is denatured• Primers attach to primer-binding site on
each DNA strand• Each strand acts as template for DNA
synthesis
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Copyright © 2005 Brooks/Cole — Thomson Learning
Biology, Seventh Edition CHAPTER 14 DNA Technologies
Amplification of DNA by PCR
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Types of PCR ITypes of PCR I
RT PCR Reverses transcriptase PCR. DNA is amplified
from mRNA.
QRT PCR Quantitative Real Time PCR the amplified product is linked to a fluorescent
reporter molecule, the fluorescence is measured at each cycle. This allows the amplification to be monitored to optimize the efficiency of amplification.
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Types of PCR IITypes of PCR II
Multiplex PCR two or more sets of primers are used in
the same reaction mix.
Nested PCR (also nested RT-PCR) There are two amplifications made: the:
The first amplifying a large product which, in the second amplification is used as the template.
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Gel ElectrophoresisGel Electrophoresis
• A method of separation pieces of DNA
• Horizontal gel (Agarose)
• Vertical (Polyacrylamide)
• Many variations on the methods exist
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The DNA is negatively charged and migrates towards the positive pole
The smallest fragments move the fastest through the gel and therefore move the furthestThe largest fragments move the least By comparing the fragments in the sample with standards of known sizethe size of the sample fragments can be estimated
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Links to virtual labsLinks to virtual labs
• DNA extractionhttp://learn.genetics.utah.edu/units/biotech/extraction
/
• Making a gelhttp://learn.genetics.utah.edu
/units/biotech/gel
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Stem Cells are undifferentiated cellsStem Cells are undifferentiated cells
Type of Stem Cell Developmental Potential
Early Embryonic Totipotent
Blastocyst Embryonic Pluripotent
Fetal Pluripotent
Umbilical Multipotent
Adult Multipotenthttp://learn.genetics.utah.edu/units/stemcells
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Biology, Seventh Edition CHAPTER 14 DNA Technologies
Possible therapeutic uses of stem cellsPossible therapeutic uses of stem cells
• Treatment of disease • Diabetes
• Parkinsons disease
• Treatment of spinal injury
• Culture of differentiated tissues
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