Genetic engineering techniques allow scientists to modify the DNA of living organisms. This includes selective breeding, cloning, and gene splicing. Selective breeding involves choosing which organisms to mate to produce offspring with desired traits, but does not allow control over specific gene transfer. Cloning creates an exact genetic copy of an organism. Gene splicing cuts DNA from one organism and inserts it into another, transferring traits between them. These techniques have led to genetically modified organisms that can benefit agriculture and medicine by increasing crop yields, producing human proteins like insulin in other organisms, and potentially curing genetic diseases.
Genetic engineering (also called genetic modification) is a process that uses laboratory-based technologies to alter the DNA makeup of an organism. This may involve changing a single base pair (A-T or C-G), deleting a region of DNA or adding a new segment of DNA. For example, genetic engineering may involve adding a gene from one species to an organism from a different species to produce a desired trait. Used in research and industry, genetic engineering has been applied to the production of cancer therapies, brewing yeasts, genetically modified plants and livestock, and more.
Genetic engineering techniques allow scientists to modify the DNA of living organisms. Some key techniques include selective breeding to concentrate desirable traits, hybridization to combine traits from different organisms, cloning to create genetically identical copies, and gene splicing to transfer individual genes between unrelated species. Genetic engineering has applications in medicine, agriculture, and research, but also raises ethical concerns about unintended consequences for human health and the environment.
Selective breeding, cloning, and genetic engineering are methods for developing organisms with desirable traits. Selective breeding involves selecting organisms with desired traits to breed the next generation. Inbreeding, breeding genetically related parents, can increase recessive or deleterious traits in offspring. Hybridization crosses genetically different individuals to produce offspring with the best traits of both parents. Cloning produces genetically identical organisms, which has been done with plants, sheep, and pigs. Genetic engineering transfers genes between organisms to produce desired traits and is used to develop medicines and improve crops, though some are concerned about long term effects.
Cloning is the process of creating a genetically identical copy of an organism. The document outlines the history of cloning experiments from sea urchins in 1894 to Dolly the sheep in 1996. It describes the main types as DNA cloning, reproductive cloning, and therapeutic cloning. Reproductive cloning aims to create copies of existing organisms while therapeutic cloning produces stem cells for medical research. The document discusses advantages like maintaining good genetics in animals, risks like low success rates and health issues in clones, and applications in biomedical research and livestock breeding.
Cloning is the process of creating a genetically identical copy of an organism. The document outlines the history of cloning experiments from sea urchins in 1894 to Dolly the sheep in 1996. It describes the main types as DNA cloning, reproductive cloning, and therapeutic cloning. Reproductive cloning aims to create copies of existing organisms while therapeutic cloning produces stem cells for medical research. The document discusses advantages like maintaining good genetics in animals, risks like low success rates and health issues in clones, and applications in biomedical research and livestock breeding.
This document discusses several advances in genetics including genetic engineering, the human genome project, and transgenic organisms. It describes techniques like selective breeding, recombinant DNA, cloning, and how genetically modified plants and animals are created. Recombinant DNA technology involves using restriction enzymes to cut and combine DNA from different organisms, which can then be inserted into bacteria or plant cells. The human genome project mapped the entire human genome to identify all human genes. Transgenic organisms have DNA from other species inserted into their genomes, and are used in research and to produce human proteins.
BIOLOGY FORM 5 CHAPTER 5 - 5.3 B (Genetics Application)Nirmala Josephine
油
The document discusses various applications of genetics including DNA technologies that allow studying and modifying genes, cloning which reproduces identical copies of organisms, and the cloning of Dolly the sheep in 1997. It also covers cloning of other animals, the high failure rate of cloning, human cloning using stem cells from embryos, gene therapy techniques, genetic diseases that can be treated, selective breeding of plants and animals to produce desirable traits, and examples of hybridization.
The document discusses different types of genetic mutations including point mutations, frame shift mutations, and chromosomal inversions. It also discusses genetic engineering techniques like genetic modification of organisms, gene therapy, cloning, and the potential benefits and concerns of transgenic engineering including creating more productive plants and animals or addressing human diseases. The Human Genome Project aims to map all human genes to better understand genetic diseases.
DNA recombinant technology on insulin modificationaulia624292
油
This document provides information on various biotechnology tools and techniques, including:
- Restriction enzymes, gel electrophoresis, PCR, vectors, gene libraries, and DNA sequencing which were used in the Human Genome Project to map the human genome.
- Genetic engineering techniques like DNA cloning, transformation, and applications like disease diagnosis, gene therapy, and GMOs.
- Stem cell types and their potential medical uses.
- Genome sizes of various organisms and comparisons.
- Advantages and disadvantages of genetic modification in plants, animals, and medicine.
The document provides information on genetic engineering techniques including selective breeding, hybridization, inbreeding, inducing mutations, polyploidy, DNA extraction, restriction enzymes, recombinant DNA, polymerase chain reaction, cell transformation, transgenic organisms, cloning, and applications of genetic engineering such as glowing plants and animals, disease resistance, and producing human proteins.
Genetic engineering techniques allow scientists to directly manipulate DNA. Restriction enzymes cut DNA at specific sequences, which can then be fused together from different organisms through recombinant DNA techniques. Genetically modified organisms have been created, including bacteria that produce human insulin, transgenic plants with pest resistance, and animals cloned from donor cells. While these techniques hold promise for applications like producing pharmaceuticals, genetically modified crops, and preserving endangered species, they also raise moral issues that warrant consideration.
Genetic engineering involves artificially manipulating or altering genes by removing a gene from one organism and inserting it into the DNA of another organism. This process involves using restriction enzymes to cut out the gene of interest and using vectors to splice the gene fragment into the recipient organism's DNA, creating a genetically modified organism. Some examples of genetic engineering applications include using E. coli bacteria to produce synthetic insulin for diabetes treatment and genetically modifying rice to produce beta-carotene to address vitamin A deficiencies. However, some genetic engineering techniques like reproductive cloning and stem cell research involving human embryos remain ethically controversial.
This document discusses various techniques in genetic engineering including selective breeding, recombinant DNA, PCR, gel electrophoresis, and transgenic organisms. Selective breeding has been used for thousands of years to develop crops and livestock. Recombinant DNA allows combining DNA from different organisms and was first used in the 1970s with bacteria. PCR and gel electrophoresis are used to copy and analyze DNA fragments. Transgenic plants and animals have been genetically modified to have desirable traits like disease resistance.
genetic engineering, principles, b pharma 6th sem, biotechnology
What is a gene ?
Definition
History
Process
Molecular tools of genetic engineering
Restriction enzymes
History of restriction enzyme
Mechanism of action
Types of restriction enzymes
Application of restriction enzymes
Blunt ends
Sticky ends
transgenic
cisgenic.
knockout organism.
Host organism vector
TRANSGENIC PLANTS
DOLLY THE SHIP
TRANSGENIC ANIMALS
Here are some potential implications of selective breeding for each area of concern:
1. Ecosystems - Domesticated species may become invasive if they escape and outcompete native species. Monocultures may lack resilience.
2. Genetic biodiversity - Narrowing of gene pool over time from focusing on few traits. Increased inbreeding depression. Loss of genetic variation makes populations more vulnerable.
3. Health/survival of individuals - Some breeds may experience health/welfare issues from being bred for extreme traits. Requires intervention like C-sections.
4. Survival of populations - Reliance on humans for care/breeding. Loss of ability to survive without human intervention if reintroduced to wild
There are three main types of cloning: 1) DNA cloning which clones genes for uses like protein production and vaccine development, 2) reproductive cloning which produces genetically identical animals but risks are high inefficiency and potential harm, and 3) therapeutic cloning which produces stem cells for research on treating diseases but risks include killing embryos.
Chromosomes contain genes and carry genetic information in a linear sequence. Genes dictate traits by controlling protein synthesis through DNA's sequence of nitrogenous bases. DNA is a double helix of polynucleotides with four bases - A, T, G, C. Genetic technologies like the Human Genome Project, DNA fingerprinting, stem cell research and genetic engineering can help understand and manipulate genes to treat diseases. However, some techniques raise ethical concerns about safety, consent and commercialization.
This document discusses genetic engineering techniques such as selective breeding, recombinant DNA, polymerase chain reaction (PCR), gel electrophoresis, and transgenic organisms. Recombinant DNA allows combining DNA from different organisms and was first used in the 1970s with bacteria. Genetically modified plants and animals are created through insertion of foreign DNA and have applications such as producing human proteins and increasing disease resistance. PCR and gel electrophoresis are techniques used to analyze and identify DNA.
Cloning is the process of producing genetically identical individuals of an organism either naturally or artificially. Natural cloning occurs through asexual reproduction in bacteria, insects, and plants. Artificial cloning involves techniques used to clone DNA fragments, cells, or whole organisms. The first animal cloned was a frog in 1952. In 1996, Dolly the sheep was the first mammal cloned from an adult cell. Cloning works by transferring the nucleus of a donor adult cell into an egg cell with its nucleus removed. Potential benefits include species preservation and medical research applications like organ transplants. However, cloning faces ethical concerns and technical challenges like low success rates and premature aging.
Mutations and genetic engineering can alter genes. There are different types of mutations like point mutations, frameshift mutations, and chromosomal inversions that can cause genetic disorders. The Human Genome Project mapped gene sequences to aid in diagnosing and treating diseases. Genetic engineering techniques allow manipulating genes and include gene therapy, transgenic organisms, cloning, and other applications that could help cure diseases but also raise safety concerns if not properly addressed.
Introduction
Definition
History
Why are the transgenic animals being produced
Transgenic mice
Mice: as model organism
Methods of creation of transgenic mice
knock-out mice
Application of transgenic mice
Conclusion
References
Genetic engineering techniques allow scientists to alter the DNA of living organisms. Selective breeding has been used for thousands of years to develop desirable traits in crops and livestock. Recombinant DNA technology developed in the 1970s allows genes from one organism to be inserted into another, such as inserting human genes into bacteria to produce human insulin. Transgenic organisms result from inserting genes from one species into another, producing benefits like disease-resistant crops and goats that produce human proteins in their milk.
Epigenetics refers to heritable changes in gene expression that occur without changes to DNA sequences. This chapter discusses several molecular processes that lead to epigenetic changes, including DNA methylation, histone modifications, and RNA molecules. These epigenetic processes produce diverse effects, such as paramutation, behavioral influences, environmental impacts, and cell differentiation. The epigenome represents the overall pattern of chromatin modifications in an organism and can be detected using techniques like bisulfate sequencing and ChIP.
This document discusses several advances in genetics including genetic engineering, the human genome project, and transgenic organisms. It describes techniques like selective breeding, recombinant DNA, cloning, and how genetically modified plants and animals are created. Recombinant DNA technology involves using restriction enzymes to cut and combine DNA from different organisms, which can then be inserted into bacteria or plant cells. The human genome project mapped the entire human genome to identify all human genes. Transgenic organisms have DNA from other species inserted into their genomes, and are used in research and to produce human proteins.
BIOLOGY FORM 5 CHAPTER 5 - 5.3 B (Genetics Application)Nirmala Josephine
油
The document discusses various applications of genetics including DNA technologies that allow studying and modifying genes, cloning which reproduces identical copies of organisms, and the cloning of Dolly the sheep in 1997. It also covers cloning of other animals, the high failure rate of cloning, human cloning using stem cells from embryos, gene therapy techniques, genetic diseases that can be treated, selective breeding of plants and animals to produce desirable traits, and examples of hybridization.
The document discusses different types of genetic mutations including point mutations, frame shift mutations, and chromosomal inversions. It also discusses genetic engineering techniques like genetic modification of organisms, gene therapy, cloning, and the potential benefits and concerns of transgenic engineering including creating more productive plants and animals or addressing human diseases. The Human Genome Project aims to map all human genes to better understand genetic diseases.
DNA recombinant technology on insulin modificationaulia624292
油
This document provides information on various biotechnology tools and techniques, including:
- Restriction enzymes, gel electrophoresis, PCR, vectors, gene libraries, and DNA sequencing which were used in the Human Genome Project to map the human genome.
- Genetic engineering techniques like DNA cloning, transformation, and applications like disease diagnosis, gene therapy, and GMOs.
- Stem cell types and their potential medical uses.
- Genome sizes of various organisms and comparisons.
- Advantages and disadvantages of genetic modification in plants, animals, and medicine.
The document provides information on genetic engineering techniques including selective breeding, hybridization, inbreeding, inducing mutations, polyploidy, DNA extraction, restriction enzymes, recombinant DNA, polymerase chain reaction, cell transformation, transgenic organisms, cloning, and applications of genetic engineering such as glowing plants and animals, disease resistance, and producing human proteins.
Genetic engineering techniques allow scientists to directly manipulate DNA. Restriction enzymes cut DNA at specific sequences, which can then be fused together from different organisms through recombinant DNA techniques. Genetically modified organisms have been created, including bacteria that produce human insulin, transgenic plants with pest resistance, and animals cloned from donor cells. While these techniques hold promise for applications like producing pharmaceuticals, genetically modified crops, and preserving endangered species, they also raise moral issues that warrant consideration.
Genetic engineering involves artificially manipulating or altering genes by removing a gene from one organism and inserting it into the DNA of another organism. This process involves using restriction enzymes to cut out the gene of interest and using vectors to splice the gene fragment into the recipient organism's DNA, creating a genetically modified organism. Some examples of genetic engineering applications include using E. coli bacteria to produce synthetic insulin for diabetes treatment and genetically modifying rice to produce beta-carotene to address vitamin A deficiencies. However, some genetic engineering techniques like reproductive cloning and stem cell research involving human embryos remain ethically controversial.
This document discusses various techniques in genetic engineering including selective breeding, recombinant DNA, PCR, gel electrophoresis, and transgenic organisms. Selective breeding has been used for thousands of years to develop crops and livestock. Recombinant DNA allows combining DNA from different organisms and was first used in the 1970s with bacteria. PCR and gel electrophoresis are used to copy and analyze DNA fragments. Transgenic plants and animals have been genetically modified to have desirable traits like disease resistance.
genetic engineering, principles, b pharma 6th sem, biotechnology
What is a gene ?
Definition
History
Process
Molecular tools of genetic engineering
Restriction enzymes
History of restriction enzyme
Mechanism of action
Types of restriction enzymes
Application of restriction enzymes
Blunt ends
Sticky ends
transgenic
cisgenic.
knockout organism.
Host organism vector
TRANSGENIC PLANTS
DOLLY THE SHIP
TRANSGENIC ANIMALS
Here are some potential implications of selective breeding for each area of concern:
1. Ecosystems - Domesticated species may become invasive if they escape and outcompete native species. Monocultures may lack resilience.
2. Genetic biodiversity - Narrowing of gene pool over time from focusing on few traits. Increased inbreeding depression. Loss of genetic variation makes populations more vulnerable.
3. Health/survival of individuals - Some breeds may experience health/welfare issues from being bred for extreme traits. Requires intervention like C-sections.
4. Survival of populations - Reliance on humans for care/breeding. Loss of ability to survive without human intervention if reintroduced to wild
There are three main types of cloning: 1) DNA cloning which clones genes for uses like protein production and vaccine development, 2) reproductive cloning which produces genetically identical animals but risks are high inefficiency and potential harm, and 3) therapeutic cloning which produces stem cells for research on treating diseases but risks include killing embryos.
Chromosomes contain genes and carry genetic information in a linear sequence. Genes dictate traits by controlling protein synthesis through DNA's sequence of nitrogenous bases. DNA is a double helix of polynucleotides with four bases - A, T, G, C. Genetic technologies like the Human Genome Project, DNA fingerprinting, stem cell research and genetic engineering can help understand and manipulate genes to treat diseases. However, some techniques raise ethical concerns about safety, consent and commercialization.
This document discusses genetic engineering techniques such as selective breeding, recombinant DNA, polymerase chain reaction (PCR), gel electrophoresis, and transgenic organisms. Recombinant DNA allows combining DNA from different organisms and was first used in the 1970s with bacteria. Genetically modified plants and animals are created through insertion of foreign DNA and have applications such as producing human proteins and increasing disease resistance. PCR and gel electrophoresis are techniques used to analyze and identify DNA.
Cloning is the process of producing genetically identical individuals of an organism either naturally or artificially. Natural cloning occurs through asexual reproduction in bacteria, insects, and plants. Artificial cloning involves techniques used to clone DNA fragments, cells, or whole organisms. The first animal cloned was a frog in 1952. In 1996, Dolly the sheep was the first mammal cloned from an adult cell. Cloning works by transferring the nucleus of a donor adult cell into an egg cell with its nucleus removed. Potential benefits include species preservation and medical research applications like organ transplants. However, cloning faces ethical concerns and technical challenges like low success rates and premature aging.
Mutations and genetic engineering can alter genes. There are different types of mutations like point mutations, frameshift mutations, and chromosomal inversions that can cause genetic disorders. The Human Genome Project mapped gene sequences to aid in diagnosing and treating diseases. Genetic engineering techniques allow manipulating genes and include gene therapy, transgenic organisms, cloning, and other applications that could help cure diseases but also raise safety concerns if not properly addressed.
Introduction
Definition
History
Why are the transgenic animals being produced
Transgenic mice
Mice: as model organism
Methods of creation of transgenic mice
knock-out mice
Application of transgenic mice
Conclusion
References
Genetic engineering techniques allow scientists to alter the DNA of living organisms. Selective breeding has been used for thousands of years to develop desirable traits in crops and livestock. Recombinant DNA technology developed in the 1970s allows genes from one organism to be inserted into another, such as inserting human genes into bacteria to produce human insulin. Transgenic organisms result from inserting genes from one species into another, producing benefits like disease-resistant crops and goats that produce human proteins in their milk.
Epigenetics refers to heritable changes in gene expression that occur without changes to DNA sequences. This chapter discusses several molecular processes that lead to epigenetic changes, including DNA methylation, histone modifications, and RNA molecules. These epigenetic processes produce diverse effects, such as paramutation, behavioral influences, environmental impacts, and cell differentiation. The epigenome represents the overall pattern of chromatin modifications in an organism and can be detected using techniques like bisulfate sequencing and ChIP.
Epigenetic phenomena involve changes in gene expression and chromatin configuration that are independent of DNA sequence. Epigenetics includes DNA methylation and histone post-translational modifications. While monozygotic twins share an identical genotype, there can be significant phenotypic discordance due to epigenetic differences. The epigenome is influenced by environmental factors and changes with age, leading to epigenetic differences even between identical twins. Epigenetic mechanisms stably maintain gene expression states and are essential for cell differentiation.
Nucleic acid hybridization uses labeled probes to identify related DNA or RNA molecules in a complex mixture. It relies on base complementarity between the probe and target molecules to form double-stranded hybrids. Probes can be radioactively or nonradioactively labeled. Hybridization is affected by factors like temperature, salt concentration, and mismatches. Southern blotting uses hybridization to detect specific DNA sequences separated by gel electrophoresis and transferred to membranes.
C.H. Waddington coined the term "epigenetics" to describe mechanisms above genetics that explain cell differentiation. Epigenetics refers to non-sequence dependent inheritance, such as how stem cells determine cell fate and how identical twins can have different traits despite identical DNA. DNA methylation and histone modifications form an epigenetic code that regulates gene expression and chromatin structure in a heritable, but potentially reversible manner independent of DNA sequence.
The document describes the bacteriophage lambda and its ability to enter either the lytic or lysogenic life cycle in an infected bacterial cell. It discusses how the phage regulatory proteins CI (repressor) and Cro control transcription and determine whether the phage follows the lytic pathway of viral replication and host cell lysis, or the lysogenic pathway of integrating into the host genome. The repressor binds DNA operators and represses transcription from lytic promoters, while Cro competes with repressor binding to instead activate lytic transcription and inhibit lysogeny.
Regulation of gene expression allows organisms to benefit from efficiency, conserving energy and cell size. In prokaryotes, operons regulate groups of genes, turned on or off by repressors, activators, or inducers. Eukaryotes separate transcription and translation, introducing many regulatory mechanisms. These include epigenetic modifications, transcription factors, RNA processing, stability, and translation factors. Cancer arises from dysregulation of genes controlling cell growth, especially tumor suppressors and oncogenes.
Agarose gel electrophoresis is a technique used to separate DNA fragments by size. It involves pouring agarose gel containing DNA samples into a chamber, applying an electric current which causes the negatively charged DNA to migrate through the gel at rates depending on their size. Larger DNA fragments move slower through the gel matrix than smaller fragments. Restriction enzymes are used to cut DNA into fragments at specific recognition sites. The fragments can then be visualized on an agarose gel to produce a restriction map. Polymerase chain reaction (PCR) is used to amplify specific DNA regions using primers and repeated heating/cooling cycles.
The document provides an overview of unit 2.4 which introduces students to basic concepts in bioinformatics and databases. The objectives are to understand relational databases, major online biological databases, and how to extract data from databases. It also discusses challenges with large genomic data sets and how bioinformatics can help make sense of such data through databases, algorithms, and computational approaches.
1) Primary databases contain original experimental data directly submitted by researchers, such as sequence data in GenBank, EMBL, and DDBJ.
2) Secondary databases contain derived or analyzed data from primary databases to make the information more useful, such as protein family databases like PROSITE and BLOCKS.
3) Biological databases serve important purposes like organizing and providing computational support for analyzing biological data, enabling researchers to retrieve information through various search criteria.
Presentation A - Using Restriction Enzymes.pptxBlackHunt1
油
This document provides information about using restriction enzymes to analyze DNA through gel electrophoresis. It describes how restriction enzymes cut DNA at specific recognition sequences, producing restriction fragments that can be separated by size using gel electrophoresis. The document explains that restriction enzymes are used in research and medicine to create recombinant DNA by producing complementary sticky ends on DNA fragments, and in DNA profiling for various applications. It provides examples of specific restriction enzymes and their recognition sequences.
This document discusses the properties and production of recombinant vaccines. It notes that recombinant vaccines are produced using recombinant DNA technology by inserting DNA encoding an antigen into cells to express and purify the antigen. The first approved recombinant vaccine was for hepatitis B. The document outlines the types of recombinant vaccines and the process of recombinant DNA technology, including isolating genetic material, amplifying genes of interest, and inserting recombinant DNA into host cells to produce the foreign gene product. It lists some advantages as being able to more quickly produce recombinant vaccines in larger quantities without infectious particles, making them safer for immunosuppressed individuals.
Blind Spots in AI and Formulation Science Knowledge Pyramid (Updated Perspect...Ajaz Hussain
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This presentation delves into the systemic blind spots within pharmaceutical science and regulatory systems, emphasizing the significance of "inactive ingredients" and their influence on therapeutic equivalence. These blind spots, indicative of normalized systemic failures, go beyond mere chance occurrences and are ingrained deeply enough to compromise decision-making processes and erode trust.
Historical instances like the 1938 FD&C Act and the Generic Drug Scandals underscore how crisis-triggered reforms often fail to address the fundamental issues, perpetuating inefficiencies and hazards.
The narrative advocates a shift from reactive crisis management to proactive, adaptable systems prioritizing continuous enhancement. Key hurdles involve challenging outdated assumptions regarding bioavailability, inadequately funded research ventures, and the impact of vague language in regulatory frameworks.
The rise of large language models (LLMs) presents promising solutions, albeit with accompanying risks necessitating thorough validation and seamless integration.
Tackling these blind spots demands a holistic approach, embracing adaptive learning and a steadfast commitment to self-improvement. By nurturing curiosity, refining regulatory terminology, and judiciously harnessing new technologies, the pharmaceutical sector can progress towards better public health service delivery and ensure the safety, efficacy, and real-world impact of drug products.
How to Modify Existing Web Pages in Odoo 18Celine George
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In this slide, well discuss on how to modify existing web pages in Odoo 18. Web pages in Odoo 18 can also gather user data through user-friendly forms, encourage interaction through engaging features.
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In this slide, well discuss on how to attach file using upload button Odoo 18. Odoo features a dedicated model, 'ir.attachments,' designed for storing attachments submitted by end users. We can see the process of utilizing the 'ir.attachments' model to enable file uploads through web forms in this slide.
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2. Genetic engineering: Changing the DNA in
living organisms to create something new.
This organisms are called Genetically
Modified Organism (GMO)
Example:
Bacteria that produce human insulin
Genetically Modified organism are called
transgenic organism; since genes are
transferred from one organism to another.
3. Some genetic engineering techniques are
as follows:
1. Artificial selection
A. selective breeding
B. hybridization
C. inbreeding
2. Cloning
3. Gene splicing
4. Gel electrophoresis: analyzing DNA
4. 1. artificial selection: breeders choose which
organism to mate to produce offspring with
desired traits.
They cannot control what genes are passed.
When they get offspring with the desired traits,
the maintain them.
Three types of artificial selection:
A. selective breeding
B. hybridization
C. inbreeding
5. A. Selective breeding: when animals with
desired characteristics are mated to
produce offspring with those desired traits.
Passing of important genes to next
generation.
Example: Champion race horses, cows
with tender meat, large juicy oranges on a
tree.
6. For example people breed dogs for specific
purposes.
Dachshund were once bred to hunt badgers
and other burrowing animals.
They must be small to fit into the animals hole
in the ground.
7. Selective breeding occurs when you choose the
best male and female to breed.
This allows you to fine tune and control the
traits
The offspring or babies will then have the best
traits.
Then you continue to breed those organism
with the best traits, those traits will be
maintained.
8. Examples of
selective breeding:
Angus cows are bred to
increase muscle mass so
that we get more meat,
Egg-Laying Hen-
produces more eggs
than the average hen
9. B. Hybridizations: two individuals with unlike
characteristics are crossed to produce the best in both
organisms.
Example: Luther Burbank created a disease resistant
potato called the Burbank potato.
He crossed a disease resistant plant with one that had
a large food producing capacity.
Result: disease resistant plant that makes a lot of
potatoes.
11. 2. Grape + apple= grapple. The fruit
tastes like grapes and looks like apple.
12. C. Inbreeding breeding of organism that
genetically similar to maintain desired
traits.
Dogs breeds are kept pure this way.
Its how a Doberman remains a Doberman.
It keeps each breed unique from others.
Risk: since both have the same genes,
the chance that a baby will get a recessive
genetic disorder is high.
13. Variation: difference between
individuals of a species.
The differences are in the
genes but we see the
physical differences.
For example: Some humans
have blond hair and some
have brown. This is a
variation among humans.
Some finches have short
beaks, some have long
beaks.
Inbreeding decreases
variations.
14. 2. Cloning: creating an organism that is an
exact genetic copy of another.
There are human clones in our school.
identical twins are naturally created
clones.
Clone: group of cells or organisms that
are genetically identical as a result of
asexual reproduction
They will have the same exact DNA as the
parent.
15. How is cloning done?
A single cell is removed from a
parent organism.
An entire individual is grown from
that cell.
Remember one cell has all the DNA
needed to make an entire organism.
Each cell in the body has the same
16. Dolly:
Dolly was the first
mammal cloned.
She had the same exact
DNA as her mother and
had no father.
Cloning is a form of
asexual reproduction.
Only one genetic parent.
http://content.tutorvista.com/biology_11/content/media/cloning.swf
17. Since Dolly, cats and other organisms have
been cloned.
The cat that was cloned had the same
exact DNA but different color fur than the
mother.
How can this be?
Environment plays a huge part in the way
organisms develop.
18. Eggs are haploid
Haploid: half the
chromosomes, 23 in
humans
Body cells are diploid:
Diploid: two sets of
chromosomes, one from
mom and one set from
dad 46 in humans.
19. How could you clone
a human?
Step 1: An egg is
removed from a female
human
Eggs are haploid: 23
chromosomes.
The nucleus of the egg
is removed and is
thrown away.
23
EGG CELL
20. Step 2: A body cell is
removed from another
person.
The nucleus of the
body cell is removed
Body cells are diploid:
46 chromosomes.
46
Body Cell
21. Step 3:
The nucleus of the
diploid body cell is put
into the egg.
This egg no longer
needs to be fertilized
since it has all 46
chromosomes.
46
EGG CELL
22. Step 4: The egg is then
charged with electricity to
start mitosis.
Step 5: Its then put into a
surrogate mother so it can
grow.
Its going to be genetically
identical to the parent of the
body cell.
But it will be a baby.
Plants and animals can be
cloned.
24. Click and clone
http://learn.genetics.utah.edu/content/tech/cloni
ng/clickandclone/
25. Benefits of cloning:
1. you can make exact
copies of organisms
with strong traits.
2. Increase food supply
3. Medical purposes:
clone organs for
transplants.
4. Bring back or Stop
species from going
extinct.
Saber Tooth Tiger extinct
26. Risks of cloning:
1. Decreases genetic
diversity
2. If one of your clones
gets a disease, they all
get it: same immune
system.
3. Inefficient: high failure
rate: 90%+
4. Expensive
27. 3. Gene splicing: DNA is cut
out of one organism and put
into another organism
A trait will be transferred from
one organism to another.
For example: the human
insulin gene can be removed
from a human cell.
It can be put into a bacterial
cell.
The bacterial will now make
human insulin.
28. This picture represents gene splicing.
However, DNA is much smaller.
Its done with high tech lab equipment since
DNA, is too small to hold or see without a
microscope.
The red piece the woman
is holding is an insulin
gene from a human
being. It is being
combined with DNA from
a bacteria.
Creates recombinant
DNA, something that has
never existed before.
29. Benefits:
insulin is cheaper
There are no side
effects because it
is human insulin.
We once used pig
insulin but there
are side effects
and it more
expensive.
30. How are genes cut for gene
splicing?
A bacterial plasmid is used.
Plasmid: circular DNA in a bacteria
cell.
It is very simple and easy to
manipulate.
31. A restriction enzyme: enzyme that cuts the
DNA at a specific code.
There are thousands of restriction enzymes.
Each cuts DNA at a different sequence.
Some look for GGCC and cut in between the G
and C.
Every time GGCC is found in the DNA it is cut
by the restriction enzyme
DNA Code:
TTATGGCCATACGGCCTT
AATACCGGTATGCCGGAA
32. TTATGGCCATACGGCCTT
AATACCGGTATGCCGGAA
TTATGG CCATACGG CCTT
AATACC GGTATGCC GGAA
This DNA segment was cut twice creating three
fragments.
Since every one is different, we all have a
different amount of times GGCC is found.
My DNA may be cut seven times
Yours may be cut ten times.
34. How is gene
splicing done?
1. A restriction
enzyme cuts the
insulin gene out of
the human DNA.
2. A plasmid is
removed from a
bacteria and cut
with a restriction
enzyme
35. 3. The human gene is place into the bacteria
plasmid
4. The plasmid is placed back into the bacteria.
The cell now has directions (DNA) to make
insulin.
That's exactly what it does.
Its human insulin, bacteria do not make insulin
on their own.
Plasmid with
insulin gene
36. This is called transformation: when a gene
from one organism is transferred to different
organism.
The organisms that have DNA transferred to
them are called transgenic organisms.
trans: means different,
genic: refers to genes
Genetic engineering has given rise to a new
technological field called biotechnology
(technology of life).
37. 1. Transgenic (GMO) animals: genes
inserted into animals so they produce what
humans need.
Why?: A way to improve the food supply:
A. Transgenic cows: gene inserted to
increase milk production.
38. B. Spider goat: gene from spider inserted
into goat.
Goats makes silk of the spider web in their
milk.
Flexible, stronger than steel. Used in
bullet proof jackets.
39. C. Glow-in-the-dark
cats
Scientist used a
virus to insert DNA
from jellyfish
The gene made the
cat produce a
fluorescent protein
in its fur.
40. 2. Transgenic bacteria: gene inserted
into bacteria so they produce things
humans need.
For example: insulin and clotting factors
in blood are now made by bacteria.
41. 3. Transgenic plants: plants are given
genes so they meet human needs.
A. Transgenic corn: given a gene so corn
produces a natural pesticide.
Now they dont have to be sprayed with
cancer causing pesticides.
25% of all corn is like this.
42. B. Venomous cabbage
gene from a scorpion tails
inserted into cabbage.
Cabbage now produces
that chemical.
Why? Limit pesticide use
while still preventing
insects from damaging
crops.
Corporations state the
toxin is modified so it isnt
harmful to humans.
43. C. Banana vaccines
virus is injected into a banana,
the virus DNA becomes part of
the plant.
As the plant grows, it produces
the virus proteins but not the
disease part of the virus.
When people eat a bite, their
immune systems creates
antibodies to fight the disease
just like a traditional vaccine
Vaccines for hepatitis and
cholera
44. A virus is often used to deliver DNA.
In the movie I Am Legend, A healthy gene was
inserted into a virus.
The virus invaded the cancer cells and inserts the
healthy gene to cure cancer.
Worked at first but the virus mutated and became
deadly.
This is being attempted in real life.
45. Gene therapy: when disease causing
genes are cut out and good gene are
inserted.
Restriction enzymes are used to cut out
bad genes.
Viruses are used to insert good genes.
Not approved for human use yet.
Some possible side effects.
46. 4. Gel electrophoresis: a
technique used to compare
DNA from two or more
organisms.
Why compare DNA:
1. Find your babys daddy
2. Who committed a crime.
3. How closely species are
related.
47. How is
electrophoresis
done?
A. The DNA is cut into
fragments with a
restriction enzyme.
B. The cut DNA is then
put into the wells of a
machine filled with
gel.
The gel is spongy and
the DNA squeezes
through the pores.
48. C. The machine is plugged in and the
fragments get separated based on their size.
The smaller fragments move further than the
large.
50. Electricity provides the energy
Why does DNA move?
DNA has a negative charge.
When the machine is plugged it, its moves towards
the positive pole created by the electricity
52. Your DNA is so unique its considered to be a
DNA fingerprint.
Gel electrophoresis will separate your DNA
differently from anyone else.
Nova: who done it
http://www.pbs.org/wgbh/nova/sheppard/analyze.html
http://www.teachersdomain.org/asset/tdc02_i
nt_creatednafp2/
53. Genetic engineering creates organisms with
recombinant DNA.
Recombinant DNA: when DNA is combined
from at least two organisms.
Which techniques create recombinant DNA
1. Sexual reproduction: natural
2. selective breeding
3. Hybridization
4. Gene splicing
54. Does cloning create organisms with
recombinant DNA?
No, the DNA from one organism is
copied.
DNA is not recombined.