frontiers of biotechnology

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FRONTIERS OF BIOTECHNOLOGY

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Frontiers of Biotechnology. Manipulating DNA. Scientists use several techniques to manipulate DNA. Restriction Enzymes cut DNA. Why cut DNA? To study specific genes instead of ALL the genes on a chromosome Restriction enzymes act as molecular scissors Recognize specific sequences - PowerPoint PPT Presentation

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Page 1: Frontiers of Biotechnology

FRONTIERS OF BIOTECHNOLOGY

Page 2: Frontiers of Biotechnology

MANIPULATING DNA• Scientists use several techniques to

manipulate DNA

Page 3: Frontiers of Biotechnology

RESTRICTION ENZYMES CUT DNA• Why cut DNA?– To study specific genes

instead of ALL the genes on a chromosome

• Restriction enzymes act as molecular scissors– Recognize specific

sequences• Some leave “blunt ends”• Some leave “sticky ends”

Page 4: Frontiers of Biotechnology

RESTRICTION MAPS SHOW THE LENGTHS OF DNA FRAGMENTS

• Gel Electrophoresis: a technique that uses an electrical field within a gel to separate molecules by their size

• DNA is negatively charged and moves toward the positive pole when the electrical field is applied

• Smallest DNA fragments move the fastest

• A pattern of bands is formed

Page 5: Frontiers of Biotechnology

GEL ELECTROPHORESIS

Page 6: Frontiers of Biotechnology

POLYMERASE CHAIN REACTION• PCR: technique

that produces millions of copies of a specific DNA sequence in just a few hours

• Invented by Kary Mullis in 1983

Page 7: Frontiers of Biotechnology

PCR• Uses: – DNA to be copied– DNA polymerase– Plenty of nucleotides A, T, C, and G– Two primers

• 3 Step Process:– Separating– Binding– Copying

Page 8: Frontiers of Biotechnology

RFLPs• Restriction Fragment Length Polymorphisms

• No two individuals have the same genetic material except identical twins

• Restriction enzymes cut at different places, depending on the DNA sequence

• The lengths of DNA restriction fragments are different between two individuals

Page 9: Frontiers of Biotechnology

DNA FINGERPRINTING• A DNA fingerprint is a type of

restriction map

• Representation of parts of a individual’s DNA that can be used to identify a person at the molecular level

• Focuses on noncoding regions of DNA, or DNA sequences outside genes

Page 10: Frontiers of Biotechnology

DNA FINGERPRINTING• DNA sample from:

– Blood– Semen– Bone – Hair

• …Useful in forensics!

Page 11: Frontiers of Biotechnology

DNA FINGERPRINTING IS USED FOR IDENTIFICATION

• DNA fingerprints and probability– Compare at least 5 regions of the

genome

Page 12: Frontiers of Biotechnology

GENETIC ENGINEERING• Entire organisms can be cloned

• Clone: genetically identical copy of a gene or of an organism

• New genes can be added to an organism’s DNA

Page 13: Frontiers of Biotechnology

4 BASIC STEPS TO GENETIC ENGINEERING

• 1. Cutting DNA

• 2. Making recombinant DNA

• 3. Cloning

• 4. Screening

Page 14: Frontiers of Biotechnology

STEP 1: CUTTING DNA

• The DNA from the original organism containing the gene of interest is cut by restriction enzymes

• Restriction Enzymes: bacterial enzymes that destroys foreign DNA molecules by cutting them at specific sites

Page 15: Frontiers of Biotechnology

STEP 1: CUTTING DNA

• Vector: Any agent, such as a plasmid, that carries the gene of interest into another cell

• Plasmid: A circular DNA molecule that is usually found in bacteria and that can replicate independent of the main chromosome

Page 16: Frontiers of Biotechnology

RECOMBINANT DNA

• DNA molecules that are artificially created

• HOW?????

• Created by combining DNA from different sources

Page 17: Frontiers of Biotechnology

EXAMPLE: INSULIN• A protein hormone that controls sugar

metabolism

• Diabetics cannot produce enough

• Must take doses of insulin daily

• Before genetic engineering, insulin was extracted from the pancreases of slaughtered cows and pigs and then purified

• Today the human insulin gene is transferred to bacteria through genetic engineering

• Because the genetic code is universal, bacteria can transcribe and translate the human insulin gene

Page 18: Frontiers of Biotechnology

STEP 2: MAKING RECOMBINANT DNA

• DNA fragments from the gene of interest are combined with the DNA fragments from the vector

• DNA ligase: an enzyme that bonds the DNA fragments together

• The host cell then takes up the recombinant DNA

Page 19: Frontiers of Biotechnology

STEP 3: CLONING

• Gene Cloning: many copies of the gene of interest are made each time the host cell reproduces

• Remember: bacteria reproduce by binary fission, producing identical offspring with the plasmid DNA!

Page 20: Frontiers of Biotechnology

STEP 4: SCREENING• Cells that have received the particular gene

are separated from the cells that did not take up the vector with the gene of interest

• The cells can transcribe and translate the gene of interest to make the protein coded for the gene

Page 21: Frontiers of Biotechnology

CONFIRMATION OF A CLONED GENE

• Southern Blot: a technique used to test for the presence of a specific gene

Page 22: Frontiers of Biotechnology

NORTHERN BLOT• Similar to a

Southern Blot

• Uses RNA instead of DNA

Page 23: Frontiers of Biotechnology

GENETIC ENGINEERING PRODUCES ORGANISMS WITH

NEW TRAITS

Page 24: Frontiers of Biotechnology

SELECTIVE BREEDING• Allowing only those animals with

desired characteristics to produce the next generation

• Horses, cats, farm animals, crops

Page 25: Frontiers of Biotechnology

HYBRIDIZATION

• Crossing dissimilar individuals to bring together the best of both organisms

• Hybrids: the individuals produced from such crosses

• For example, a disease resistant plant and the food producing capacity of another

Page 26: Frontiers of Biotechnology

INBREEDING• The continued breeding of individuals with

similar characteristics

• Often seen in dogs

• Retains characteristics but has risks

• Genetically similar individuals could bring together two recessive alleles for a genetic defect

Page 27: Frontiers of Biotechnology

TODAY…GENETIC ENGINEERING

Page 28: Frontiers of Biotechnology

GENETICALLY ENGINEERED CROPS• More tolerant to

drought

• Plants that can adapt to different soils, climates, and environmental stresses

Page 29: Frontiers of Biotechnology

GENETICALLY ENGINEERED CROPS• Resistant to

biodegradable weedkiller Glyphosate (kills weeds but now doesn’t kill the crop)

• Resistant to insects (gene injures the gut of chewing insects)-therefore plant doesn’t need to be sprayed with pesticides

Page 30: Frontiers of Biotechnology

MORE NUTRITIOUS CROPS• Improve the nutritious value

of many crops

• Asia: rice is a staple food

• Low in iron an beta carotene

• Iron deficient and poor vision

• Genetic engineers have added genes to rice from other plants to overcome this deficiency

Page 31: Frontiers of Biotechnology

POTENTIAL PROBLEMS TO GM CROPS

• Concern that some weeds will become resistant to the weed killer Glyphosate

• New weed-control alternatives will have to be implemented

Page 32: Frontiers of Biotechnology

POTENTIAL PROBLEMS TO GM CROPS

• Nutritional value has been increased in many crops

• Crops must be tested to make sure consumers are not allergic to the GM product

Page 33: Frontiers of Biotechnology

GENE TECHNOLOGY: ANIMAL FARMING

• Farmers added growth hormones to the diet of cows to increase milk production

• Growth hormone was extracted from the brains of dead cows

• The hormone was introduced into bacteria and added as a supplement to a cow’s diet

Page 34: Frontiers of Biotechnology

TRANSGENIC ANIMALS• Animals that have

foreign DNA in their cells

• Human genes have been added to farm animals in order to get the farm animals to produce human proteins in their milk

Page 35: Frontiers of Biotechnology

TRANSGENIC ANIMALS• This is complex and cannot be made by

bacteria through gene technology

• Human proteins are extracted from the animal’s milk and sold for pharmaceutical purposes

• Cloning animals: creating herds of identical animals that can make medically useful proteins

Page 36: Frontiers of Biotechnology

CLONING FROM ADULT ANIMALS• The intact nucleus of an embryonic or fetal

cell (whose DNA has been recombined with a human gene) is placed into an egg whose nucleus has been removed

• The egg with the new nucleus is put in the uterus of a surrogate, or substitute mother and allowed to develop

Page 37: Frontiers of Biotechnology

CLONING FROM ADULT ANIMALS

• 1997 Ian Wilmut first successful cloning using differentiated cells from an adult animal

• Dolly the sheep

Page 38: Frontiers of Biotechnology

CLONING FROM ADULT ANIMALS• Differentiated cells: cells that

have become specialized to become specific cell types

• Scientists had thought that embryonic or fetal cells were the only way…wrong!

Page 39: Frontiers of Biotechnology

CLONING FROM ADULT ANIMALS• Mammary cells from one sheep were fused

with egg cells without nuclei form a different sheep

• The fused cells divided to form embryos, implanted into surrogate mothers

• Only one survived the cloning process

• Dolly, identical to the sheep that provided the mammary cell

Page 40: Frontiers of Biotechnology
Page 41: Frontiers of Biotechnology

PROBLEMS WITH CLONING

• Only a few of the cloned offspring survive for long

• Many become fatally oversized

• Problems in development

Page 42: Frontiers of Biotechnology

GENOMIC IMPRINTING• The right combination of genes are

turned “on” and “off” during early development

• The egg takes years to develop the genomic imprint

• In cloning, the egg divides within minutes

Page 43: Frontiers of Biotechnology

GENOMIC IMPRINTING

• Reprogramming is not possible in such a short time

• Critical errors in development can occur

• Because of these technical problems and ethical problems, cloning humans is illegal in most countries

Page 44: Frontiers of Biotechnology

CONCERNS ABOUT GENETIC ENGINEERING

• Ethical?

• GM crops

– Not enough research had been done to see if added genes might cause allergic reactions or have other unknown side effects

– Interbreeding with natural plants…what does it mean?

Page 45: Frontiers of Biotechnology

GENOMICS INVOLVES THE STUDY OF GENES, GENE FUNCTIONS, AND ENTIRE

GENOMES

• Genomics: The study of genomes, which can include the sequencing of all of an organism’s DNA

• Gene sequencing: determining the order of DNA nucleotides in genes or in genomes

Page 46: Frontiers of Biotechnology

THE GEOGRAPHY OF THE GENOME

• Only 1-1.5% of the human genome codes for proteins

• Each human cell contains about 6 feet of DNA

• Less than 1 inch are exons

Page 47: Frontiers of Biotechnology

THE GEOGRAPHY OF THE GENOME

• Human cells contain about 25,000 genes (scientists had expected 120,000!)

• Only 2x the number of genes in a fruit fly!

• Many human genes are identical to those of other species

• All humans are genetically close (DNA of any 2 people is 99.9% identical)

Page 48: Frontiers of Biotechnology

THE HUMAN GENOME PROJECT• Our genome is relatively small! 3 billion base

pairs, but only between 30,000-40,000 genes

• Project started in 1990 with 2 main goals:

– Map and sequence all of the DNA base pairs of the human chromosomes (accomplished in 2003)

– Identify all of the genes within the sequence (still be worked on)

Page 49: Frontiers of Biotechnology

THE HUMAN MICROBIOME PROJECT• 200 scientists at 80 institutions

sequenced the genetic material of bacteria taken from nearly 250 healthy people

• As many as a thousand bacterial strains on each person.

• Each person’s collection of microbes, the “microbiome”, was unique

Page 50: Frontiers of Biotechnology

TECHNOLOGY ALLOWS THE STUDY AND COMPARISON OF BOTH GENES AND

PROTEINS• Bioinformatics: the use of computer databases

to organize and analyze biological data

• DNA microarrays: tools that allow scientists to study many genes, and their expression at once; a small chip dotted with the genes being studied

• Proteomics: the study and comparison of all the proteins that result from an organism’s genome

Page 51: Frontiers of Biotechnology

GENETIC SCREENING AND GENE THERAPY

• Genetic screening: the process of testing DNA to determine a person’s risk of having or passing on a genetic disorder

• Gene therapy: the replacement of a defective of missing gene, or the addition of a new gene, into a person’s genome to treat a gene

Page 52: Frontiers of Biotechnology

GENETICALLY ENGINEERED DRUGS & VACCINES

• Possibilities for the applications of genetic engineering are endless!

Page 53: Frontiers of Biotechnology

DRUGS• Many genetic disorders and other human

illnesses occur when the body fails to make critical proteins

• Example: juvenile diabetes– Body is unable to control levels of sugar in the blood

because the protein insulin cannot be made

• Example: Hemophilia– Factor VIII, a protein that promotes blood clotting– Donated blood was sometimes infected with HIV

and hepatitis B– Genetically engineered factor VIII eliminates these

risks

Page 54: Frontiers of Biotechnology

VACCINESTraditional Vaccines

• Many viral diseases, such as smallpox and polio, cannot be treated effectively by existing drugs

• Vaccine: a solution containing all or part of a harmless version of a pathogen (disease-causing microorganism)

• When the vaccine is injected, the immune system recognizes the pathogen’s surface proteins and responds by making defensive proteins called antibodies

Genetically Engineered Vaccines• Avoid the danger of giving a

patient a disease

• The genes that encode the pathogen’s surface proteins can be inserted into the DNA of harmless viruses, such as cowpox

• The modified, harmless cowpox virus becomes an effective, safe vaccine