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Life Science I 83.101.201 Dr. Ekaterina (Kate) Vorotnikova Office: Olsen 413b E-mail: [email protected] Lecture 26 Genetically modified organisms. DNA profiling. (Page 231; 236-243)

Life Science I 83.101.201 Dr. Ekaterina (Kate) Vorotnikova Office: Olsen 413b E-mail: [email protected][email protected] Lecture

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Page 1: Life Science I 83.101.201 Dr. Ekaterina (Kate) Vorotnikova Office: Olsen 413b E-mail: Ekaterina_Vorotnikova@uml.eduEkaterina_Vorotnikova@uml.edu Lecture

Life Science I83.101.201

Dr. Ekaterina (Kate) VorotnikovaOffice: Olsen 413b

E-mail: [email protected]

Lecture 26Genetically modified organisms.

DNA profiling.

(Page 231; 236-243)

Page 2: Life Science I 83.101.201 Dr. Ekaterina (Kate) Vorotnikova Office: Olsen 413b E-mail: Ekaterina_Vorotnikova@uml.eduEkaterina_Vorotnikova@uml.edu Lecture

GENETICALLY MODIFIED ORGANISMS:

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Genetically Modified Bacteria

Genetically Modified Plants

Genetically Modified Animals

Page 3: Life Science I 83.101.201 Dr. Ekaterina (Kate) Vorotnikova Office: Olsen 413b E-mail: Ekaterina_Vorotnikova@uml.eduEkaterina_Vorotnikova@uml.edu Lecture

Recombinant cells and organisms can

mass-produce gene products – Cells and organisms containing cloned

genes are used to manufacture large quantities of gene products

– Capabilities of the host cell are matched to the characteristics of the desired product

– Prokaryotic host: E. coli– Can produce eukaryotic proteins that do not require post-

translational modification

– Has many advantages in gene transfer, cell growth, and quantity of protein production

– Can be engineered to secrete proteins

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Page 4: Life Science I 83.101.201 Dr. Ekaterina (Kate) Vorotnikova Office: Olsen 413b E-mail: Ekaterina_Vorotnikova@uml.eduEkaterina_Vorotnikova@uml.edu Lecture

– Eukaryotic hosts

– Yeast: Saccharomyces cerevisiae

– Can produce and secrete complex eukaryotic proteins

– Mammalian cells in culture

– Can attach sugars to form glycoproteins

– “Pharm” animals

– Will secrete gene product in milk

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Page 5: Life Science I 83.101.201 Dr. Ekaterina (Kate) Vorotnikova Office: Olsen 413b E-mail: Ekaterina_Vorotnikova@uml.eduEkaterina_Vorotnikova@uml.edu Lecture

Media_26\12_08ATransgenics_DV.mpg

Page 6: Life Science I 83.101.201 Dr. Ekaterina (Kate) Vorotnikova Office: Olsen 413b E-mail: Ekaterina_Vorotnikova@uml.eduEkaterina_Vorotnikova@uml.edu Lecture

“Pharm” animals that produce a human protein.Examples of products from “pharm” animals include: goats producing tissue plasminogen activator (TPA) for heart attack victims, sheep producing alpha-1-antitrypsin to treat emphysema, and pigs producing hemoglobin as a blood substitute.

Page 7: Life Science I 83.101.201 Dr. Ekaterina (Kate) Vorotnikova Office: Olsen 413b E-mail: Ekaterina_Vorotnikova@uml.eduEkaterina_Vorotnikova@uml.edu Lecture

DNA technology has changed the

pharmaceutical industry and medicine

– Products of DNA technology– Therapeutic hormones

– Insulin to treat diabetes

– Human growth hormone to treat dwarfism

– Diagnosis and treatment of disease– Testing for inherited diseases

– Detecting infectious agents such as HIV

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Page 8: Life Science I 83.101.201 Dr. Ekaterina (Kate) Vorotnikova Office: Olsen 413b E-mail: Ekaterina_Vorotnikova@uml.eduEkaterina_Vorotnikova@uml.edu Lecture

– Products of DNA technology– Vaccines

– Stimulate an immune response by injecting

– Protein from the surface of an infectious agent

– A harmless version of the infectious agent

– A harmless version of the smallpox virus containing genes from other infectious agents

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Page 9: Life Science I 83.101.201 Dr. Ekaterina (Kate) Vorotnikova Office: Olsen 413b E-mail: Ekaterina_Vorotnikova@uml.eduEkaterina_Vorotnikova@uml.edu Lecture

Equipment used in the production of a vaccine against hepatitis B.

Page 10: Life Science I 83.101.201 Dr. Ekaterina (Kate) Vorotnikova Office: Olsen 413b E-mail: Ekaterina_Vorotnikova@uml.eduEkaterina_Vorotnikova@uml.edu Lecture

– Advantages of recombinant DNA products– Identity to human protein

– Purity

– Quantity

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Page 11: Life Science I 83.101.201 Dr. Ekaterina (Kate) Vorotnikova Office: Olsen 413b E-mail: Ekaterina_Vorotnikova@uml.eduEkaterina_Vorotnikova@uml.edu Lecture

Genetically modified organisms are transforming

agriculture – Genetically modified (GM) organisms contain one or

more genes introduced by artificial means– Transgenic organisms contain at least one gene from

another species – GM plants

– Resistance to herbicides– Resistance to pests– Improved nutritional profile

– GM animals– Improved qualities– Production of proteins or therapeutics

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Page 12: Life Science I 83.101.201 Dr. Ekaterina (Kate) Vorotnikova Office: Olsen 413b E-mail: Ekaterina_Vorotnikova@uml.eduEkaterina_Vorotnikova@uml.edu Lecture

Agrobacterium tumefaciens

DNA containinggene for desired trait

Tiplasmid Insertion of gene

into plasmid

RecombinantTi plasmid

1

Restriction site

A modified form of the Ti (tumor inducing) plasmid is used in plant genetic engineering. The tumor inducing genes have been removed from the plasmid but genes required for insertion into plant chromosomes have been retained. The gene of interest has been inserted into the plasmid under the control of a bacterial promoter.

Using the Ti plasmid as a vector for genetically engineering plants.

Page 13: Life Science I 83.101.201 Dr. Ekaterina (Kate) Vorotnikova Office: Olsen 413b E-mail: Ekaterina_Vorotnikova@uml.eduEkaterina_Vorotnikova@uml.edu Lecture

Agrobacterium tumefaciens

DNA containinggene for desired trait

Tiplasmid Insertion of gene

into plasmid

RecombinantTi plasmid

1

Restriction site

Plant cell

Introductioninto plantcells

2

DNA carrying new gene

Page 14: Life Science I 83.101.201 Dr. Ekaterina (Kate) Vorotnikova Office: Olsen 413b E-mail: Ekaterina_Vorotnikova@uml.eduEkaterina_Vorotnikova@uml.edu Lecture

Agrobacterium tumefaciens

DNA containinggene for desired trait

Tiplasmid Insertion of gene

into plasmid

RecombinantTi plasmid

1

Restriction site

Plant cell

Introductioninto plantcells

2

DNA carrying new gene

Regenerationof plant

3

Plant with new trait

Page 15: Life Science I 83.101.201 Dr. Ekaterina (Kate) Vorotnikova Office: Olsen 413b E-mail: Ekaterina_Vorotnikova@uml.eduEkaterina_Vorotnikova@uml.edu Lecture

A mix of “golden rice” and standard rice.

Page 16: Life Science I 83.101.201 Dr. Ekaterina (Kate) Vorotnikova Office: Olsen 413b E-mail: Ekaterina_Vorotnikova@uml.eduEkaterina_Vorotnikova@uml.edu Lecture

Gene therapy aims to treat a disease by supplying a functional allele

One possible procedure – Clone the functional allele and

insert it in a retroviral vector

– Use the virus to deliver the gene to an affected cell type from the patient, such as a bone marrow cell

– Viral DNA will insert the functional allele into the patient’s chromosome

– Return the cells to the patient for growth and division

Gene therapy may someday help treat a variety of diseases

Page 17: Life Science I 83.101.201 Dr. Ekaterina (Kate) Vorotnikova Office: Olsen 413b E-mail: Ekaterina_Vorotnikova@uml.eduEkaterina_Vorotnikova@uml.edu Lecture

– SCID (severe combined immune deficiency) was the first disease treated by gene therapy

– First trial in 1990 was inconclusive

– Second trial in 2000 led to the development of leukemia in some patients due to the site of gene insertion

– Challenges– Safe delivery to the area of the body affected

by the disease

– Achieving a long-lasting therapeutic effect

– Addressing ethical questions

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Page 18: Life Science I 83.101.201 Dr. Ekaterina (Kate) Vorotnikova Office: Olsen 413b E-mail: Ekaterina_Vorotnikova@uml.eduEkaterina_Vorotnikova@uml.edu Lecture

DNA PROFILING

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Page 19: Life Science I 83.101.201 Dr. Ekaterina (Kate) Vorotnikova Office: Olsen 413b E-mail: Ekaterina_Vorotnikova@uml.eduEkaterina_Vorotnikova@uml.edu Lecture

– DNA evidence was used to solve a double murder in England

– Showed that two murders could have been committed by the same person

– Showed the innocence of someone who confessed to one of the murders

– Showed the absence of a match in 5,000 men tested when the murderer persuaded another man to donate blood in his name

– Showed a match with the murderer and DNA found with both victims Media_26\12_15ADNAForensics_DV.mpg

DNA and Crime Scene Investigations

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Page 20: Life Science I 83.101.201 Dr. Ekaterina (Kate) Vorotnikova Office: Olsen 413b E-mail: Ekaterina_Vorotnikova@uml.eduEkaterina_Vorotnikova@uml.edu Lecture

DNA profiling is the analysis of DNA fragments to determine whether they come from a particular individual

– Compares genetic markers from noncoding regions that show variation between individuals

– Involves amplification (copying) of markers for analysis

– Sizes of amplified fragments are compared

Page 21: Life Science I 83.101.201 Dr. Ekaterina (Kate) Vorotnikova Office: Olsen 413b E-mail: Ekaterina_Vorotnikova@uml.eduEkaterina_Vorotnikova@uml.edu Lecture

Polymerase chain reaction (PCR) is a method of amplifying a specific segment of a DNA molecule

Relies upon a pair of primers– Short DNA molecules that bind to sequences at each end of the

sequence to be copied– Used as a starting point for DNA replication

Repeated cycle of steps for PCR– Sample is heated to separate DNA strands– Sample is cooled and primer binds to specific target sequence– Target sequence is copied with heat-stable DNA polymerase

The PCR method is used to amplify DNA sequences

Page 22: Life Science I 83.101.201 Dr. Ekaterina (Kate) Vorotnikova Office: Olsen 413b E-mail: Ekaterina_Vorotnikova@uml.eduEkaterina_Vorotnikova@uml.edu Lecture

– Advantages of PCR– Can amplify DNA from a small sample

– Results are obtained rapidly

– Reaction is highly sensitive, copying only the target sequence

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Page 23: Life Science I 83.101.201 Dr. Ekaterina (Kate) Vorotnikova Office: Olsen 413b E-mail: Ekaterina_Vorotnikova@uml.eduEkaterina_Vorotnikova@uml.edu Lecture

Compare STR (short tandem repeats) from individuals.

Page 24: Life Science I 83.101.201 Dr. Ekaterina (Kate) Vorotnikova Office: Olsen 413b E-mail: Ekaterina_Vorotnikova@uml.eduEkaterina_Vorotnikova@uml.edu Lecture

Gel electrophoresis separates DNA molecules based on size– DNA sample is placed at one end of a porous gel– Current is applied and DNA molecules move from the negative electrode

toward the positive electrode– Shorter DNA fragments move through the gel pores more quickly and

travel farther through the gel – DNA fragments appear as bands, visualized through staining or detecting

radioactivity or fluorescence– Each band is a collection of DNA molecules of the same length

Page 25: Life Science I 83.101.201 Dr. Ekaterina (Kate) Vorotnikova Office: Olsen 413b E-mail: Ekaterina_Vorotnikova@uml.eduEkaterina_Vorotnikova@uml.edu Lecture

DNA profiling has provided evidence in many

forensic investigations – Forensics

– Evidence to show guilt or innocence

– Establishing family relationships– Paternity analysis

– Identification of human remains– After tragedies such as the September 11, 2001,

attack on the World Trade Center

– Species identification– Evidence for sale of products from endangered

species

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