Biotechnology - Linn–Benton Community...

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Biotechnology Chapter 17 section 1 (only) 5-16-16

Transcript of Biotechnology - Linn–Benton Community...

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Biotechnology

Chapter 17 section 1 (only)

5-16-16

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Learning Goals for Today:

• Explain how DNA profiling can identify individuals

• Interpret data from DNA electrophoresis

• Discuss genetically modified organisms

• Explain some ways DNA can be recombined in nature

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What Is Biotechnology?

• Biotechnology is the use of organisms, cells, or biological molecules to produce food, drugs, or other goods – Yeast: fermentation (10,000 years ago)– Selective breeding of animals/plants (between 6

and 15,000 years ago)– cloning– genetic engineering– Finger-printing– Genome sequencing– Diagnosing and treating diseases

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• Merriam Webster’s definition of natural: “being in accordance with or determined by nature”

Is all this natural?

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According to nature

Lemon

Corn

Banana

PigDog

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Things that we assume com straight from nature, do not!

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ALL dogs come from the wolf!

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All these veggies come from wild mustard!

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Genetically Modified Organism (GMO):

– an organism that contains foreign DNA

– w/ altered characteristic(s)

– does not occur naturally because the selection pressure in for human benefit

– obtained via cloning technology

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Genetic engineering

• Recombinant DNA - combining DNA molecules not found together in nature; via cloning

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How Does DNA Recombine in Nature?

• Bacteria and yeast: can take in DNA from the environment– Transformation

• DNA piece can come from a the same or a different species

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plasmid

plasmid

bacterial

chromosome

(a) Bacterium

DNA

fragments

bacterial

chromosome

(b) Transformation with a DNA fragment

(c) Transformation with a plasmid

A DNA fragment is

incorporated into

the chromosome

bacterial

chromosome

The plasmid replicates

in the cytoplasm

1 micrometer

Transformation in Bacteria

Fig. 13-1

Bacteria can take in DNA from their environment

New DNA might code for anything

Big Issue: Genes for antibiotic resistance

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Viruses Also Transfer DNA

Fig. 13-2

The virus releases itsDNA into the host cell; some viral DNA (red) may be incorporated intothe host cell’s DNA (blue)

The virus enters the host cell

Viral genes encode the synthesis of viral proteins and viral gene replication; some host cell DNA may attach to the replicated viral DNA (red/blue combination)New viruses assemble;

some host cell DNA is carried by recombinant viruses

The host cell bursts open, releasing newly assembled viruses; if recombinant viruses infect a second cell, they may transfer genes from the first cell to the second cell

viral proteinsrecombinant virus

virus

viral DNA

viral DNA

A virus attaches to a susceptible host cell

host

cell

host cell DNA

2

3

1

4

5

6

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Types of Cloning

• Molecular cloning (DNA cloning)

– Manipulating a small piece of DNA, typically using bacteria as host

• Therapeutic cloning

– Creating stem cell lines with same DNA as a patient, used for treating diseases and disorders

• Reproductive cloning

– Technique used to generate an animal with exact genetic makeup (DNA) as another animal

Genetic Engineering

Recombinant DNA - combining DNA molecules not found together in nature; via cloning

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DNA Cloning –

– Molecular cloning

– Inserting foreign DNA from one organism into another

what is it?

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Bacteria can transfer DNA into plants

• Agrobacterium infects plants

• Physically injects part of its own DNA into the plant cell

• Plant will grow a gall at the infection site– Bacteria live in the gall

– Plant synthesizes nutrients for the bacteria

• Similar process with Rhizogenes bacteria but the end result benefits the plant

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Agrobacterium is a natural, and

commonly used, plant genetic engineer

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The “gene gun” is also used to introduce

DNA into cells

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After cells are

modified, they

are induced to

regenerate into

whole plants

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Where are GM foods?

The Marketplace

– 60 to 70% of processed food contains GMO

In the US:

– Corn ~45% is GM

– Soybean ~85% is GM

– Cotton ~76% is GM

– Canola ~60% is GM

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Biotech crops widespread, rapidly

adopted: Grown on >10% arable land on planet,

extensive uptake in developing world

http://www.isaaa.org/resources/publications/briefs/46/pptslides/Brief46slides.pdf

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Four crops dominate,

8+ crops in USA

http://www.isaaa.org/resources/publications/briefs/46/pptslides/Brief46slides.pdf

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Two traits dominate worldwide

http://www.isaaa.org/resources/publications/briefs/46/pptslides/Brief46slides.pdf

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Newly approved GE crop varieties in

USA • Soybean – insect resistant (Apr. 2014)

• Alfalfa – reduced lignin (Nov. 2014)

• Potato – reduced black spot bruise and low acrylamide production (Nov. 2014), reduced browning and disease resistant as well (August 2015)

• Soybean and cotton – new herbicide tolerances (Jul. 2014 – Jan. 2015)

• Apple – non-browning (Feb. 2015)

• Plum – virus resistant (2014)

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Non-browning “Arctic Apple” Reduced spoilage/waste, improved quality – USDA

approved

Courtesy of Jennifer Armen, Okanagan Specialty Fruits, Canada

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Non-browning “Arctic Apple” Time lapse video

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“Innate” potato approved – reduced browning

and acrylamide (↓waste, ↑safety)

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“Innate” potato in my hands for teaching

One hour after cutting – Control vs. Innate

Two days after cutting – Innate vs. Control

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“Innate” potato 2.0 – late blight resistant,

reduced acrylamide, reduced sprouting and

browning (↓ waste, ↑ safety, ↓ pesticide, ↑ yield)

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Dramatic change in color of chips,

highly prized by consumers

Provided by Walter De Jong, Cornell University

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Scientific AmericanMarch, 2013

Resistance transgenes promising solution/s to devastating ‘citrus greening’

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Face the “wall of opposition” ?

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Defensin-like proteins from spinach

for citrus greening disease resistance

Courtesy of Eric Mirkov, Texas A & M

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Helping forests: American Chestnut

restoration by genetic modification

March 2014 issue - Scientific American

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Forest health a major and growing

concern

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Diverse pipeline of biofortification

products = enhancement of critical

vitamins or nutrients

Many more examples funded by Gates Foundation / other sources

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• Rice

• Cassava

• Sorghum

• Banana

Biotech methods useful where breeding is

ineffective or slow

RiceCassava

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Management of monocultures

• Mismanagement promotes the proliferation of weeds resistant to herbicides and bugs resistant to pesticide– Many weeds have developed resistance to glyphosate

(RoundUp)

– Rootworms have also developed resistance to Bt

• Herbicide can kills plants that are not weeds– Milkweed supplies Monarch butterflies eat

• Rotating crops, eliminate volunteers, and creating havens with no pesticide

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Cloned Stem Cells• Immune system will recognize & destroy cells with different DNA

• Therefore, stem cells need to contain same DNA as patient

• Cloned Stem Cells -

• Somatic Cell Nuclear Transfer

“Therapeutic Cloning”

Somatic cells = all body cells

Nucleus = region of cell containing DNA

Transfer = remove and replace

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Somatic Cell Nuclear Transfer

https://www.youtube.com/watch?v=tELZEPcgKkE

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Induced Pluripotent Stem cells

(iPScells)

• Reprogramming somatic cells (skin) so they

behave as stem cells

• Can replace embryo harvesting

• Human cloning not needed

• Used for therapeutic cloning

• Must add new proteins (transcription factors)

to reprogram

https://www.youtube.com/watch?v=Q9-

4SMGiKnE

https://www.youtube.com/watch?v=Q6U5kf5By

NE

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How Is Biotechnology Used in Forensic Science?

• DNA identification: huge role in criminal investigations

• Individual have unique DNA sequences

– DNA “fingerprint”

• How to we figure out a person’s DNA “fingerprint”?

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Differences in short tandem repeats (STRs) can identify individuals by their DNA

• STRs: noncoding DNA

– STRs are not transcribed into mRNA

– Short sequence of 2-5 nucleotides

– Repeated many times (up to 50)

– All in a row (in tandem)

• Number of repeats varies (different alleles)

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Example of a STR

Fig. 13-4

Eight side-by-side (tandem) repeats

of the same four-nucleotide sequence

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Using STRs to Identify Individuals

• Different people may have different alleles of the STRs – Allele: number of repeats

• U.S. Department of Justice – 13 standard STRs tested

• Over a trillion possible combinations of alleles

– Exact match needed for conviction

https://www.youtube.com/watch?v=9bEAJYnVVBA

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Question for Thought:

• DNA fingerprinting is very useful– Paternity/mate

rnity testing– Criminal

investigations

• Should there be a national database of everyone’s DNA?

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How do we figure out someone’s DNA “fingerprint?”

• DNA sequence cannot be read directly

• Sequencing entire genomes is expensive and takes time

• Sometimes there isn’t much DNA in the sample

• PCR: a technique for making lots of DNA copies of specified pieces of DNA

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PCR: the Polymerase Chain Reaction• Modern version developed by Kary Mullis

• Only need a tiny amount of starting DNA

• Makes lots of copies of DNA of interest

DNA Learning Center, Cold Spring Harbor Laboratory

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Gel electrophoresis: a method to examine PCR results

• After PCR: a lot of pieces of DNA

– Often alleles are different sizes

• Gel electrophoresis: a method to separate DNA based on size

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Example of DNA Profiling for one STR

DNA samples from

13 different people

15

14

13

12

11

10

9

8

D16: An STR on chromosome 16

Nu

mb

er

of

rep

eat

s

Why do some people have 1 band and some people have 2 bands?

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DNA Profiling

Fig. 13-7

STR name

Penta D

CSF

D16

D7

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Mutations

• Substitutions or point mutations

• Insertions

• Deletions

• Inversions

• Translocations

Due to errors during replication (1 in 100,000, but proof-reading fixes 99%) or external factors like toxins and radiation

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Mutations in STRs

• STRs: Sequence Tandem Repeats (forensics)

• Errors are due to replication slippage

• Slippage occurs in STRs about 1 per 1000 generations

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Replication slippage

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Other uses for gene sequencing

• Genes other than the STRs are often sequenced

– Health-related tests

– Studying gene function