This document discusses the history and current state of cloning technology. It begins with early cloning experiments on frogs in 1952 and discovery of DNA structure in 1953. Major milestones include the first IVF baby in 1978, cloning of human embryos in 1993, and Dolly the sheep in 1996. While cloning of animals has potential for preserving endangered species and developing medical treatments, human reproductive cloning raises ethical concerns about genetic harm, altered relationships, and commodification of human life. The document examines debates around therapeutic versus reproductive cloning and regulations in different countries.
its a good type of ppt for understanding cloning and its types. It also enlists the idea of procedure in the lab to initiate initial division of embryo by electric current.
its a good type of ppt for understanding cloning and its types. It also enlists the idea of procedure in the lab to initiate initial division of embryo by electric current.
Cloning, types and challenges
What types of cloning have been successful?
What are the Three Types of Cloning?
Human Cloning: The Good and The Bad
Ethical Issues regarding Human Reproductive Cloning
Challenges
Global and Religious Views
Final Thought
Cloning, types and challenges
What types of cloning have been successful?
What are the Three Types of Cloning?
Human Cloning: The Good and The Bad
Ethical Issues regarding Human Reproductive Cloning
Challenges
Global and Religious Views
Final Thought
This presentation contains various details from history of cloning to what one should expect in the future from cloning and also different cloning methods
What is greenhouse gasses and how many gasses are there to affect the Earth.moosaasad1975
What are greenhouse gasses how they affect the earth and its environment what is the future of the environment and earth how the weather and the climate effects.
Cancer cell metabolism: special Reference to Lactate PathwayAADYARAJPANDEY1
Normal Cell Metabolism:
Cellular respiration describes the series of steps that cells use to break down sugar and other chemicals to get the energy we need to function.
Energy is stored in the bonds of glucose and when glucose is broken down, much of that energy is released.
Cell utilize energy in the form of ATP.
The first step of respiration is called glycolysis. In a series of steps, glycolysis breaks glucose into two smaller molecules - a chemical called pyruvate. A small amount of ATP is formed during this process.
Most healthy cells continue the breakdown in a second process, called the Kreb's cycle. The Kreb's cycle allows cells to “burn” the pyruvates made in glycolysis to get more ATP.
The last step in the breakdown of glucose is called oxidative phosphorylation (Ox-Phos).
It takes place in specialized cell structures called mitochondria. This process produces a large amount of ATP. Importantly, cells need oxygen to complete oxidative phosphorylation.
If a cell completes only glycolysis, only 2 molecules of ATP are made per glucose. However, if the cell completes the entire respiration process (glycolysis - Kreb's - oxidative phosphorylation), about 36 molecules of ATP are created, giving it much more energy to use.
IN CANCER CELL:
Unlike healthy cells that "burn" the entire molecule of sugar to capture a large amount of energy as ATP, cancer cells are wasteful.
Cancer cells only partially break down sugar molecules. They overuse the first step of respiration, glycolysis. They frequently do not complete the second step, oxidative phosphorylation.
This results in only 2 molecules of ATP per each glucose molecule instead of the 36 or so ATPs healthy cells gain. As a result, cancer cells need to use a lot more sugar molecules to get enough energy to survive.
Unlike healthy cells that "burn" the entire molecule of sugar to capture a large amount of energy as ATP, cancer cells are wasteful.
Cancer cells only partially break down sugar molecules. They overuse the first step of respiration, glycolysis. They frequently do not complete the second step, oxidative phosphorylation.
This results in only 2 molecules of ATP per each glucose molecule instead of the 36 or so ATPs healthy cells gain. As a result, cancer cells need to use a lot more sugar molecules to get enough energy to survive.
introduction to WARBERG PHENOMENA:
WARBURG EFFECT Usually, cancer cells are highly glycolytic (glucose addiction) and take up more glucose than do normal cells from outside.
Otto Heinrich Warburg (; 8 October 1883 – 1 August 1970) In 1931 was awarded the Nobel Prize in Physiology for his "discovery of the nature and mode of action of the respiratory enzyme.
WARNBURG EFFECT : cancer cells under aerobic (well-oxygenated) conditions to metabolize glucose to lactate (aerobic glycolysis) is known as the Warburg effect. Warburg made the observation that tumor slices consume glucose and secrete lactate at a higher rate than normal tissues.
This pdf is about the Schizophrenia.
For more details visit on YouTube; @SELF-EXPLANATORY;
https://www.youtube.com/channel/UCAiarMZDNhe1A3Rnpr_WkzA/videos
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THE IMPORTANCE OF MARTIAN ATMOSPHERE SAMPLE RETURN.Sérgio Sacani
The return of a sample of near-surface atmosphere from Mars would facilitate answers to several first-order science questions surrounding the formation and evolution of the planet. One of the important aspects of terrestrial planet formation in general is the role that primary atmospheres played in influencing the chemistry and structure of the planets and their antecedents. Studies of the martian atmosphere can be used to investigate the role of a primary atmosphere in its history. Atmosphere samples would also inform our understanding of the near-surface chemistry of the planet, and ultimately the prospects for life. High-precision isotopic analyses of constituent gases are needed to address these questions, requiring that the analyses are made on returned samples rather than in situ.
Professional air quality monitoring systems provide immediate, on-site data for analysis, compliance, and decision-making.
Monitor common gases, weather parameters, particulates.
2. History of cloning
1952 Northern leopard frogs cloned.
1953 Structure of DNA discovered.
3. History of cloning
1978 Louise, the first child conceived
through in vitro fertilization, was born.
1993 Human embryos were first cloned
(artificial embryo twinning)
July 5, 1996 Dolly was born.
Photo from: www.cnn.com
4. Dolly – the first mammal cloned
using mature cell
• Dolly the Lamb in
1996
• Method: Nuclear
transfer
• Organization: Roslin
Institute at UK and
PPL Therapeutics
Photo from Ming Pao 18th
August 2002
5. Example of cloning
• Cumulina the Mouse in
1998
• Organization:
University of Hawaii
Photo from Ming Pao 28th
December 2002
6. Example of cloning
• Cattle in 1998
• Organization:
Kinki University at
Japan
Photo from Ming Pao 28th
December 2002
7. Example of cloning
• Mille, Christa, Alexis,
Carrel and Dotcom the
Pigs in 2000
• Organization: PPL
Therapeutics of UK
Photo from Ming Pao 28th
December 2002
8. Example of cloning
• Carbon Copy the
Cat in 2002
• Organization: Texas
A & M University,
USA
Photo from Ming Pao 23th
January 2003
9. Example of cloning
• Generation of
Prometea, 2003
• Organization: A
research laboratory in
Italy
Photo from Nature No.6949
10. Examples of cloning
• Cloning of donkey,
2004, USA
• Cloning of dog, 2005,
Korea
• Cloning of rhesus
monkey, 2007, Oregon,
USA
http://jamaica-gleaner.com/gleaner/20050806/mind/mind3.html
http://www.pbs.org/newshour/bb/science/july-dec07/stemcells_11-15.html
11. Two methods of cloning
• Embryo cloning - remove a cell from an
embryo for developing into a separate
embryo.
• Adult cell cloning - replace DNA/nucleus
from a cell by another.
12. How to generate Dolly?
Step 1.
cells were taken
from a donor
sheep. Cells were
then cultured to
switch off their
genes and become
dormant.
Photo from www.bootstrike.com, www.nature.com
13. How to generate Dolly?
Step 2.
Unfertilized egg
cell was taken
from another
sheep. The
nucleus was
removed, leaving
an empty egg.
Photo from www.pbs.org. www.nature.com, www.sciam.com
14. How to generate Dolly?
Step 3.
The egg cell without
nucleus was fused
with the donor cell
using a pulse of
electricity. A second
pulse started the cell
division.
Photo from www.advancedcell.com. www.nature.com
15. How to generate Dolly?
Step 4.
After 6 days, the
resulting embryo
was implanted into
another sheep
(surrogate
mother ).
Photo from www.pbs.org, www.nature.com
16. How to generate Dolly?
Step 5.
After gestation ,
the surrogate
mother gave birth
to Dolly which
was identical to
the udder cell
donor.
Photo from www.pbs.org
17. Advantages of animal cloning
• Can produce animal with a desired trait, for
▫ Protein products, organs
• Proliferate endangered animals
18. Cloning of endangered animal
• Noah the Gaur
( an endangered species)
in 2000
• Organization: Advanced
Cell Technology, USA
Photo from Advanced Cell Technology
(www.advancedcell.com)
19. Cloning of endangered animal
• Cloning of woolly
Mammoth
• Extinct 10,000 years ago
From Mingpao 8/8/2003
20. Cloning of transgenic animal
• Cloning of a cow
containing mad cow
disease resistant gene
• In Shangdong, China
From Mingpao 28/4/2006
21. Concerns in Cloning
• Technology complicated
• Survival rate of cloned embryos low
• Overweighing of calves at birth
• Breeders may want to keep their
animal unique
• Breeders may want to create better
offspring
22. Health of clones
From Ming Pao 27-Mar-2001
• Poor development
of heart, lung and
immune system
• Might have
genetic disorder
23. Photo from MingpaoPhoto from Mingpao
Dolly gave birth to a
female lamb in
1998, but Dolly later
died of premature
aging in 2003.
24. Company for cloning pets
• Genetic Savings & Clone – established in 2000,
produced the cloned cat, CC in 2001
• Delivered the first commercially cloned cat, Little
Nicky in 2004 for US$50,000
• Company closed in 2006
• A new company BioArts International was
established for cloning dogs
25. Commercial pet cloning may not be a
good investment
• Demand not high
• Competition from developing countries
• Outcome is unpredicted – cloning is not a
mature techniques
• Pressure from the society
26. • Ethical attention is focused upon cloning in
the context of the genetic copying of a whole
organism.
• While the cloning of non-mammals has
occurred in research.
• Cloned human embryos have been
produced, but there are no reliable reports
that any have been implanted in a woman’s
uterus, let alone developed to birth.
28. Cloning – two kinds
•Reproductive cloning – an
embryo is created and implanted
into a woman’s womb to bring it
to term.
•Therapeutic cloning – an
embryo is created in order to
obtain cells from it.
29. “Cloning can occur at the level of DNA, at the
level of the single cell, or at the level of the
whole organism.”
“Cloning to birth has come to be called
‘reproductive cloning”
“Cloning embryos whose stem cells may be
extracted for possible research or therapeutic
use has come to be called ‘therapeutic cloning.”
30. Why clone human?
• Just an ‘unconventional’ means of reproduction
▫ In vitro fertilization
▫ Surrogate mother
▫ Adoption
31. Why clone human?
• Study human development
• Produce spare parts
• Test for genetic defect
• Increase chance of pregnancy
• Produce two children at the same
time
32. Why clone human?
• Preserve traits and talents
• Extension of life in unusual
circumstances
▫ One spouse sterile
▫ Homosexual marriage
33. Positive points of
therapeutic cloning
• Cloned embryos provide :
▫ Brain cells for disorders like Parkinson and
Alzheimer’s disease
▫ Pancreatic islet cells for diabetes
34. Positive points of therapeutic
cloning
• Cloned embryos provide :
▫ Nerve cells for spinal cord damage
▫ Blood and bone marrow cells for blood
cell disorder
36. 1. Creating an embryo through
in vitro fertilization,
2. culturing ES cells derived
from it to provide a sufficient
population for the tricky task
of inserting genes
3. extracting the nucleus of a
successfully altered cell to
construct a cloned embryo
4. The resulting offspring would
have developed from a cell
derived from an embryo
created with an egg and a
sperm, and "improved" in the
laboratory.
37. Why not perform reproductive
cloning?
• Eugenic – to maximize certain traits intentionally
• Reduce genetic diversity
• Use as substitute for organ
• Clone may have reduced life expectancy
• Clone may be abnormal
38. Why not perform reproductive
cloning?
• Lack of self-identity
▫ Replaceable
▫ Dominated by the ‘father’ or
‘mother’
39. Why not perform reproductive
cloning?
• Upset traditional family
relationship
▫ Twin of the cell donor?
▫ Relationship with its
brother and sister
▫ Relationship with spouse
of the cell donor
40. Human Reproductive Technology Bill
(2000)
• Not allow the followings:
▫ Replace nucleus of an
embryo with nucleus of
another cell
▫ Clone an embryo
▫ Trading of embryo
41. Ethical issues
• The ethical issues with reproductive cloning
include
1. genetic damage to the clone
2. health risks to the mother
3. very low success rate meaning loss of large
numbers of embryos and fetuses
4. psychological harm to the clone
5. complex altered familial relationships, and
commodification of human life.
42. Human cloning in China
• Prohibits surrogate mother
• Prohibits reproductive human cloning
• Prohibits donation of embryos
• Prohibits trading of eggs
43. • CLONAID™ was founded in February
1997, by Raël, the leader of the RaelianRaelian
MovementMovement, an international religious
organization, which claims that a human
extraterrestrial race, called the ElohimElohim,
used DNA and genetic engineering, to
scientifically create all life on Earth
44. Recent Development in Human Cloning
• Clonaid claimed to give birth to ‘Eve’ on 26
December 2002
• announced a second birth to a Dutch lesbian
woman early in January 2003 and a third to a
Japanese couple who "cloned their dead son
killed in an accident", plus two others in late
January
45. Recent Development in Human Cloning
• Korean Scientists led by Dr. Woo-suk Hwang
produced cloned human embryos (Science, Feb.
12, 2004) – later found to be fabricated
• American scientist Panayiotis Zavos claimed to
have cloned 14 human embryos and transferred
11 of them into the wombs of four women (April,
2009)
46. Recent Development in Human Cloning
• August 2004 - UK granted the first licence for
work toward therapeutic cloning.
• Nov. 2004 - Californians passed a $3 billion
measure to create an Institute for Regenerative
Medicine based on embryonic stem cell research.
Editor's Notes
1952 Using nuclear transfer, Philadelphia scientists attempted to clone frogs with the nuclei of early tadpole embryos. The cells began to divide and grow.
Manually separating a very early embryo into individual cells, and then allowing each cell to divide and develop on its own. The resulting embryos are placed into a surrogate mother, where they are carried to term and delivered. Again, since all the embryos came from the same zygote, they are genetically identical. - in early October 1993, by researchers Robert Stillman and Jerry Hall from George Washington University
US$50,000 for cloning a cat
The company was founded as a result of the efforts to clone Lou Hawthorne's favorite family dog, Missy. The Missyplicity project generated enough interest that Lou Hawthorne decided to build a company devoted to dog and cat cloning.
The company opened for business in February 2000, funded production of the first cloned cat, CC, in 2001, and launched its pet cloning service in February 2004, operating a "petbank", to which pet owners could send tissue samples for later use in cloning. The company delivered the world's first commercially cloned cat, Little Nicky, in December 2004. Little Nicky was sold to a Texas woman for a reported US$50,000. He is a genetic twin of "Nicky," a 17-year-old Maine Coon cat that had been kept as a pet.
As well as their success in cloning cats, the company also made significant advances in dog cloning research, although the technology was not mature enough to sustain the business. The company closed in 2006. Letters to this effect were sent out to clients at the end of September 2006, informing them of this decision and offering to transfer any genetic material to another facility.
Cloning of cat, by Genetic Saving and Clone Ltd. USA, 2004- US50,000
http://www.bioarts.com/
http://www.bioarts.com/press_release/ba09_09_09.htm
Until recently, there was a ban in the USA on the use of embryonic or fetal tissue for therapeutic cloning. On the other hand, adult tissues, including stem cells from adults, can be legally utilized for therapeutic cloning, although there is considerable regulation at both the federal and state levels in order to prevent bioethically questionable phenomena such as organ farms, and medically risky practices such as xenoplantation.
Started with 242 oocytes and cumulus cells from 16 donors, the group achieved a cloning efficiency of about 25%, similar that seen in cattle (25%) and pigs (26%)
Californians passed a $3 billion measure yesterday (November 2, 2004) that will create an Institute for Regenerative Medicine based on embryonic stem cell research. Every year uses $300 million.
In August 2004, the Human Fertilisation and Embryology Authority in UK has granted the first licence for work toward therapeutic cloning. The licence initially lasts for 1 year will be held by Newcastle Centre for Life. This licence allows scientists to create human embryos by inserting the nuclei from human skin or stem cells into human eggs.