Showing posts with label CRISPR. Show all posts
Showing posts with label CRISPR. Show all posts

Thursday, November 16, 2017

US Scientists Made a Genetically Modified Human Embryo

US Scientists Made a Genetically Modified Human Embryo | genetically-modified-human | General Health GMOs Medical & Health Science & Technology Sleuth Journal Special Interests


By The Daily Sheeple | 


This is the first confirmed case of the gene editing of human embryos in the US and it gets scientists one step closer to the ability to create genetically engineered humans. Researchers in Portland, Oregon have used a powerful gene editing tool called CRISPR to create genetically modified human embryos, MIT Technology Review reported in an exclusive.


CRISPR, which is often compared to the cut-and-paste function on a word processor, is a powerful and comparatively new genetic engineering technique that allows scientists to make specific, targeted changes to the DNA of a plant, animal, or human. It’s relatively cheap and easy to use and has the potential to cure a wide range of diseases, such as muscular dystrophy or HIV (Human Immunodeficiency Virus). But scientists seem to be using it to create designer humans and animals instead leading to ethics questions.


In 2015, Chinese scientists used CRISPR to make muscled beagles. But even beyond the often-stated fear that gene editing will lead to a world of designer babies and “genetic have-nots,” CRISPR is still new and may have consequences we don’t understand.


Several countries have a ban or at least some type of regulation on gene editing in human embryos, although as the use of CRISPR speeds up in the lab, regulations, and viewpoints continue to evolve as well. Earlier this year, the US National Academy of Sciences said that editing the DNA of human embryos could be allowed in order to cure disease, with certain safeguards in place; and scientists are going ahead.


According to Motherboard, teams in China have edited human embryos at least three times, and earlier this year, a Chinese team reported another first: using CRISPR to correct genetic mutations in three normal human embryos. (Previous tests were done on non-viable embryos that couldn’t have produced children. According toTechnology Review, the US experiment destroyed embryos after a few days, with no intention to implant them.) Scientists in the US watched developments in China “with a combination of awe, envy, and some alarm,” Technology Review reported.


It looks like Americans were more than eager to try CRISPR for themselves. And the creation of a gene-modified human could happen anytime. Hopefully, scientists will use the technology for the greater good and actually cure viruses and illnesses rather than to create perfect humans in jars.



Contributed by The Daily Sheeple of www.TheDailySheeple.com.


The post US Scientists Made a Genetically Modified Human Embryo appeared first on The Sleuth Journal.

US Scientists Made a Genetically Modified Human Embryo

US Scientists Made a Genetically Modified Human Embryo | genetically-modified-human | General Health GMOs Medical & Health Science & Technology Sleuth Journal Special Interests


By The Daily Sheeple | 


This is the first confirmed case of the gene editing of human embryos in the US and it gets scientists one step closer to the ability to create genetically engineered humans. Researchers in Portland, Oregon have used a powerful gene editing tool called CRISPR to create genetically modified human embryos, MIT Technology Review reported in an exclusive.


CRISPR, which is often compared to the cut-and-paste function on a word processor, is a powerful and comparatively new genetic engineering technique that allows scientists to make specific, targeted changes to the DNA of a plant, animal, or human. It’s relatively cheap and easy to use and has the potential to cure a wide range of diseases, such as muscular dystrophy or HIV (Human Immunodeficiency Virus). But scientists seem to be using it to create designer humans and animals instead leading to ethics questions.


In 2015, Chinese scientists used CRISPR to make muscled beagles. But even beyond the often-stated fear that gene editing will lead to a world of designer babies and “genetic have-nots,” CRISPR is still new and may have consequences we don’t understand.


Several countries have a ban or at least some type of regulation on gene editing in human embryos, although as the use of CRISPR speeds up in the lab, regulations, and viewpoints continue to evolve as well. Earlier this year, the US National Academy of Sciences said that editing the DNA of human embryos could be allowed in order to cure disease, with certain safeguards in place; and scientists are going ahead.


According to Motherboard, teams in China have edited human embryos at least three times, and earlier this year, a Chinese team reported another first: using CRISPR to correct genetic mutations in three normal human embryos. (Previous tests were done on non-viable embryos that couldn’t have produced children. According toTechnology Review, the US experiment destroyed embryos after a few days, with no intention to implant them.) Scientists in the US watched developments in China “with a combination of awe, envy, and some alarm,” Technology Review reported.


It looks like Americans were more than eager to try CRISPR for themselves. And the creation of a gene-modified human could happen anytime. Hopefully, scientists will use the technology for the greater good and actually cure viruses and illnesses rather than to create perfect humans in jars.



Contributed by The Daily Sheeple of www.TheDailySheeple.com.


The post US Scientists Made a Genetically Modified Human Embryo appeared first on The Sleuth Journal.

Saturday, September 16, 2017

A CRISPR Future New Form of Eugenics?

By Dr. Mercola


Gene editing was once a very imprecise and expensive process, but today, thanks to the development of CRISPR, or Clustered Regularly Interspaced Short Palindromic Repeat, scientists can go into your DNA and essentially cut and paste it at specified places. Progress is being made in tackling genetic diseases such as sickle-cell anemia and certain forms of blindness and muscular dystrophy.


A CRISPR clinical trial in people with cancer is already underway in China, and the technology has been used to edit human embryos made from sperm from men carrying inherited disease mutations. The researchers successfully altered the DNA in a way that would eliminate or correct the genes causing the inherited disease.1



If the embryos were implanted into a womb and allowed to grow, the process, which is known as germline engineering, would result in the first genetically modified children — and any engineered changes would be passed on to their own children. The technology is moving so fast that innovations like this are occurring before their full implications are known or fully understood.


“Some critics say germline experiments could open the floodgates to a brave new world of ‘designer babies’ engineered with genetic enhancements,” Technology Review reported, bringing up questions of ethics and eugenics.2


Does the Elimination of Down Syndrome in Iceland Point to a Dark Future for CRISPR?


It’s recently been reported that, in Iceland, Down syndrome births are becoming increasingly rare, with just one or two children born with the condition each year. In essence, Down syndrome is disappearing, but not by nature or happenstance. In Iceland, up to 85 percent of pregnant women receive prenatal screening tests to detect chromosome abnormalities, including Down syndrome. Close to 100 percent of women who receive a positive result end up terminating their pregnancy, CBS News reported.3


Other countries also have high termination rates for fetuses with Down syndrome: 67 percent in the U.S.; 77 percent in France; and 98 percent in Denmark, for instance. As for why so many women terminate their Down syndrome pregnancies in Iceland, geneticist Kari Stefansson told CBS News, “It reflects a relatively heavy-handed genetic counseling. And I don’t think that heavy-handed genetic counseling is desirable … You’re having impact on decisions that are not medical, in a way.”4


Writing in The Nation, journalist and historian — and father to a young son with Down syndrome — David Perry noted that “we’re failing our test run for the age of CRISPR.”5 He points out that today children with Down syndrome can lead long, happy and productive lives, but many expectant parents aren’t informed of this reality.


Prenatal testing companies market heavily to physicians but provide little information on the conditions being tested for. As a result, some parents are receiving wrong information about their would-be child’s prognosis. Perry writes:6



“What does all this have to do with CRISPR? Right now, we’re still in a liminal state when it comes to predicting genetic outcomes for fetuses. Our tools, from amniocentesis (developed in the 1950s and ’60s) to contemporary screenings that locate fetal blood cells in the mother’s bloodstream, are reactive and postconception.




Soon, they’ll shift to preconception and proactive. What will the tens of thousands of clinicians tell would-be parents as they get flooded with messaging from companies eager to sell their high-tech CRISPR product lines?”



As it stands, access to information, or lack thereof, may result in physicians providing outdated or biased genetic counseling to patients. As CRISPR moves ahead, access to accurate and neutral data will be essential. Difficult questions — such as, “When does abortion become eugenics?” as posed by The Atlantic7 — must be asked, and answered. The time has come when parents can choose to abort a fetus based on a disability, but soon this may extend into sex, race or even, one day, sexual orientation.


Even now, Miami-based radiologist Dr. Grazie Pozo Christie pointed out that “eugenics and equality can’t mix,” explaining in U.S. News & World Report, “When we do everything in our power to detect the existence of a baby with a special need with the sole purpose of terminating him or her, we create a discriminatory culture, where only perfect humans may apply for entrance.


This is a powerful obstacle against equality and acceptance of the disabled, which a just society must set as its first goal.”8 Perry also notes that access to unbiased, up-to-date information is crucial in an age of genetic testing and CRISPR:9



“Preventing this potentially dystopian future where altered genes separate the haves from the have-nots starts by shifting discourse. A pro-information approach demands that everyone involved in genetic counseling have access to the best data and presents it in a value-neutral way. We must build systems now that grow as our tools evolve. If we do not, genetic diversity will gradually become code for poverty, and new stigmas will run all the way to the DNA.”



Many Countries Have Already Banned Genetic Engineering of Human Embryos, Germ-Line Modification


Whether or not the creation of “designer babies” with a certain eye color or increased intelligence is inevitable remains to be seen, but some regions are not willing to take a wait-and-see approach. About 40 countries have already banned the genetic engineering of human embryos and 15 of 22 European countries prohibit germ line modification.10 Time reported:11



“Using CRISPR on humans is still hugely controversial, in part because it’s so easy. The fact that it allows scientists to efficiently edit any gene — for some cancers, but also potentially for a predisposition for red hair, for being overweight, for being good at math — worries ethicists because of what could happen if it gets into the wrong hands.




… As CRISPR goes mainstream in medicine and agriculture, profound moral and ethical questions will arise. Few would argue against using CRISPR to treat terminal cancer patients, but what about treating chronic diseases? Or disabilities? If sickle-cell anemia can be corrected with CRISPR, should obesity, which drives so many life-threatening illnesses? Who decides where that line ought to be drawn?”



Correcting embryonic DNA to eliminate genetic defects associated with inheritable diseases currently has the greatest support, but some scientists argue that using germ-line gene editing to eliminate genetic disease is unnecessary, since the technology to test and choose embryos free of genetic disease already exists and is regularly used in IVF clinics.


The alteration of genes to protect a person against future disease or diseases is another area of ongoing research, while genetic enhancement, in which genes are installed or modified to change a person’s appearance, or physical or mental potential is most controversial. A top U.S. intelligence official even added gene-editing to a list of potential weapons of mass destruction that pose a threat to national safety.12


As complex and futuristic as it seems, gene editing is inexpensive and easy to do. Killer mosquitoes, agricultural plagues and DNA-targeting viruses have all been suggested as potential bioweapons should CRISPR or other gene-editing tools fall into the wrong hands.13


Gene editing has become so mainstream there are classes on the topic available at community colleges and DIY kits you can order online. Even middle school students may learn the basics of gene editing in science class, with some comparing the new technology to computer coding a few decades ago.


CRISPR May Cause Unexpected Mutations


Gene-editing technology has gotten much more precise over the years, particularly with the invention of CRISPR-Cas9.14 By modifying an enzyme called Cas9, the gene-editing capabilities are significantly improved, in some cases reducing the error rate to “undetectable levels.” It’s not perfect, however, and may accidently hit other parts of the genome.


A recent study searched for unintended mutations, based on a separate study that used CRISPR-Cas9 to restore sight in blind mice by correcting a genetic mutation. The researchers sequenced the entire genome of the CRISPR-edited mice to search for mutations. In addition to the intended genetic edit, they found more than 100 additional deletions and insertions along with more than 1,500 single-nucleotide mutations. Study co-author Dr. Stephen Tsang, of Columbia University Medical Center, told Scienmag:15



“We feel it’s critical that the scientific community consider the potential hazards of all off-target mutations caused by CRISPR, including single nucleotide mutations and mutations in non-coding regions of the genome … Researchers who aren’t using whole genome sequencing to find off-target effects may be missing potentially important mutations. Even a single nucleotide change can have a huge impact.”



It’s too soon to say whether the mutations are a cause for alarm. However, in the recent study in which researchers used CRISPR to edit human embryos, altering the DNA to prevent inherited disease, they claim to have developed a better technique that avoids off-target effects, as well as mosaicism, in which the DNA changes are taken up by some of the embryo’s cells instead of all of them.16


Meanwhile, a February 2017 report issued by the U.S. National Academies of Sciences (NAS) basically set the stage for allowing research on germline modification and CRISPR, but only for the purpose of eliminating serious diseases — not for “enhancing traits or abilities beyond ordinary health.” The latter would raise concerns “about whether the benefits can outweigh the risks, and about fairness if available only to some people,” NAS noted.17


According to Technology Review, however, “Despite such barriers, the creation of a gene-edited person could be attempted at any moment, including by IVF clinics operating facilities in countries where there are no such legal restrictions.”18


With the technology becoming increasingly accessible to anyone with an interest, it’s probably going to be a matter of when, not if, this boundary is crossed, with unknown consequences. While gene-editing technology has the potential to be great, it could also be easily, and seriously, misused and abused.


– Sources and References

A CRISPR Future New Form of Eugenics?

By Dr. Mercola


Gene editing was once a very imprecise and expensive process, but today, thanks to the development of CRISPR, or Clustered Regularly Interspaced Short Palindromic Repeat, scientists can go into your DNA and essentially cut and paste it at specified places. Progress is being made in tackling genetic diseases such as sickle-cell anemia and certain forms of blindness and muscular dystrophy.


A CRISPR clinical trial in people with cancer is already underway in China, and the technology has been used to edit human embryos made from sperm from men carrying inherited disease mutations. The researchers successfully altered the DNA in a way that would eliminate or correct the genes causing the inherited disease.1



If the embryos were implanted into a womb and allowed to grow, the process, which is known as germline engineering, would result in the first genetically modified children — and any engineered changes would be passed on to their own children. The technology is moving so fast that innovations like this are occurring before their full implications are known or fully understood.


“Some critics say germline experiments could open the floodgates to a brave new world of ‘designer babies’ engineered with genetic enhancements,” Technology Review reported, bringing up questions of ethics and eugenics.2


Does the Elimination of Down Syndrome in Iceland Point to a Dark Future for CRISPR?


It’s recently been reported that, in Iceland, Down syndrome births are becoming increasingly rare, with just one or two children born with the condition each year. In essence, Down syndrome is disappearing, but not by nature or happenstance. In Iceland, up to 85 percent of pregnant women receive prenatal screening tests to detect chromosome abnormalities, including Down syndrome. Close to 100 percent of women who receive a positive result end up terminating their pregnancy, CBS News reported.3


Other countries also have high termination rates for fetuses with Down syndrome: 67 percent in the U.S.; 77 percent in France; and 98 percent in Denmark, for instance. As for why so many women terminate their Down syndrome pregnancies in Iceland, geneticist Kari Stefansson told CBS News, “It reflects a relatively heavy-handed genetic counseling. And I don’t think that heavy-handed genetic counseling is desirable … You’re having impact on decisions that are not medical, in a way.”4


Writing in The Nation, journalist and historian — and father to a young son with Down syndrome — David Perry noted that “we’re failing our test run for the age of CRISPR.”5 He points out that today children with Down syndrome can lead long, happy and productive lives, but many expectant parents aren’t informed of this reality.


Prenatal testing companies market heavily to physicians but provide little information on the conditions being tested for. As a result, some parents are receiving wrong information about their would-be child’s prognosis. Perry writes:6



“What does all this have to do with CRISPR? Right now, we’re still in a liminal state when it comes to predicting genetic outcomes for fetuses. Our tools, from amniocentesis (developed in the 1950s and ’60s) to contemporary screenings that locate fetal blood cells in the mother’s bloodstream, are reactive and postconception.




Soon, they’ll shift to preconception and proactive. What will the tens of thousands of clinicians tell would-be parents as they get flooded with messaging from companies eager to sell their high-tech CRISPR product lines?”



As it stands, access to information, or lack thereof, may result in physicians providing outdated or biased genetic counseling to patients. As CRISPR moves ahead, access to accurate and neutral data will be essential. Difficult questions — such as, “When does abortion become eugenics?” as posed by The Atlantic7 — must be asked, and answered. The time has come when parents can choose to abort a fetus based on a disability, but soon this may extend into sex, race or even, one day, sexual orientation.


Even now, Miami-based radiologist Dr. Grazie Pozo Christie pointed out that “eugenics and equality can’t mix,” explaining in U.S. News & World Report, “When we do everything in our power to detect the existence of a baby with a special need with the sole purpose of terminating him or her, we create a discriminatory culture, where only perfect humans may apply for entrance.


This is a powerful obstacle against equality and acceptance of the disabled, which a just society must set as its first goal.”8 Perry also notes that access to unbiased, up-to-date information is crucial in an age of genetic testing and CRISPR:9



“Preventing this potentially dystopian future where altered genes separate the haves from the have-nots starts by shifting discourse. A pro-information approach demands that everyone involved in genetic counseling have access to the best data and presents it in a value-neutral way. We must build systems now that grow as our tools evolve. If we do not, genetic diversity will gradually become code for poverty, and new stigmas will run all the way to the DNA.”



Many Countries Have Already Banned Genetic Engineering of Human Embryos, Germ-Line Modification


Whether or not the creation of “designer babies” with a certain eye color or increased intelligence is inevitable remains to be seen, but some regions are not willing to take a wait-and-see approach. About 40 countries have already banned the genetic engineering of human embryos and 15 of 22 European countries prohibit germ line modification.10 Time reported:11



“Using CRISPR on humans is still hugely controversial, in part because it’s so easy. The fact that it allows scientists to efficiently edit any gene — for some cancers, but also potentially for a predisposition for red hair, for being overweight, for being good at math — worries ethicists because of what could happen if it gets into the wrong hands.




… As CRISPR goes mainstream in medicine and agriculture, profound moral and ethical questions will arise. Few would argue against using CRISPR to treat terminal cancer patients, but what about treating chronic diseases? Or disabilities? If sickle-cell anemia can be corrected with CRISPR, should obesity, which drives so many life-threatening illnesses? Who decides where that line ought to be drawn?”



Correcting embryonic DNA to eliminate genetic defects associated with inheritable diseases currently has the greatest support, but some scientists argue that using germ-line gene editing to eliminate genetic disease is unnecessary, since the technology to test and choose embryos free of genetic disease already exists and is regularly used in IVF clinics.


The alteration of genes to protect a person against future disease or diseases is another area of ongoing research, while genetic enhancement, in which genes are installed or modified to change a person’s appearance, or physical or mental potential is most controversial. A top U.S. intelligence official even added gene-editing to a list of potential weapons of mass destruction that pose a threat to national safety.12


As complex and futuristic as it seems, gene editing is inexpensive and easy to do. Killer mosquitoes, agricultural plagues and DNA-targeting viruses have all been suggested as potential bioweapons should CRISPR or other gene-editing tools fall into the wrong hands.13


Gene editing has become so mainstream there are classes on the topic available at community colleges and DIY kits you can order online. Even middle school students may learn the basics of gene editing in science class, with some comparing the new technology to computer coding a few decades ago.


CRISPR May Cause Unexpected Mutations


Gene-editing technology has gotten much more precise over the years, particularly with the invention of CRISPR-Cas9.14 By modifying an enzyme called Cas9, the gene-editing capabilities are significantly improved, in some cases reducing the error rate to “undetectable levels.” It’s not perfect, however, and may accidently hit other parts of the genome.


A recent study searched for unintended mutations, based on a separate study that used CRISPR-Cas9 to restore sight in blind mice by correcting a genetic mutation. The researchers sequenced the entire genome of the CRISPR-edited mice to search for mutations. In addition to the intended genetic edit, they found more than 100 additional deletions and insertions along with more than 1,500 single-nucleotide mutations. Study co-author Dr. Stephen Tsang, of Columbia University Medical Center, told Scienmag:15



“We feel it’s critical that the scientific community consider the potential hazards of all off-target mutations caused by CRISPR, including single nucleotide mutations and mutations in non-coding regions of the genome … Researchers who aren’t using whole genome sequencing to find off-target effects may be missing potentially important mutations. Even a single nucleotide change can have a huge impact.”



It’s too soon to say whether the mutations are a cause for alarm. However, in the recent study in which researchers used CRISPR to edit human embryos, altering the DNA to prevent inherited disease, they claim to have developed a better technique that avoids off-target effects, as well as mosaicism, in which the DNA changes are taken up by some of the embryo’s cells instead of all of them.16


Meanwhile, a February 2017 report issued by the U.S. National Academies of Sciences (NAS) basically set the stage for allowing research on germline modification and CRISPR, but only for the purpose of eliminating serious diseases — not for “enhancing traits or abilities beyond ordinary health.” The latter would raise concerns “about whether the benefits can outweigh the risks, and about fairness if available only to some people,” NAS noted.17


According to Technology Review, however, “Despite such barriers, the creation of a gene-edited person could be attempted at any moment, including by IVF clinics operating facilities in countries where there are no such legal restrictions.”18


With the technology becoming increasingly accessible to anyone with an interest, it’s probably going to be a matter of when, not if, this boundary is crossed, with unknown consequences. While gene-editing technology has the potential to be great, it could also be easily, and seriously, misused and abused.


– Sources and References

Friday, August 11, 2017

Scientists Cross Hurdle in Growing Pig Organs for Human Transplant

For many years, some members of the scientific community have been absolutely engrossed in trying to solve one of the biggest health conundrums in the United States: how to get more people to donate their organs. And if that can’t happen on a grand scale, well, scientists are turning to cloned pigs for organs.


In 2016, there were just 33,600 organ transplants, while there were 116,800 patients on transplant waiting lists. Since you can’t force people to become organ donors, scientists figure the only other option is to look elsewhere for organs. Now, through gene-editing and cloned some pigs, scientists have come a step closer to solving the problem, but the process is risky. [1]


You can’t transplant pig organs into humans because the body would assuredly reject them. There is also a concern that pig retroviruses could spread to human cells. With the help of pig cloning and CRISPR-Cas9 gene-editing technology, researchers have been able to solve the latter problem. [2]



The CRISPR-Cas9 is a medical and scientific advancement like no other that holds the potential to eradicate genetic diseases and create transplantable organs for humans. However, the technology is still relatively new and hasn’t been around long enough for scientists to know if gene-editing could cause serious, irreversible damage to animals and the environment.


(One recent study by researchers at Columbia University found that while CRISPR-Cas9 did correct blindness in mice, using the technique also resulted in unintentional mutations in more than 1,000 other genes.)


Humans, Organs, and Pigs


Researchers took cells from the pigs, then snipped the viral DNA from their genomes using CRISPR technology. [1]


Each pig cell was restored to its earliest developmental stage and then placed in an egg, giving it the genetic material to allow the egg to develop into an embryo. The embryos, now genetically identical to the pig that supplied the initial cell, were implanted in sows, who eventually gave birth to the piglets.


Read: Scientists Create Human-Pig Embryo for Transplant Research


Most of the cloned piglets died shortly after birth, but 15 of them lived, and the oldest is now 4 months old. Scientists will monitor the genetically-modified piglets throughout their lives looking for any long-term adverse effects from the procedure.


Pigs are considered one of the “best” viable sources for organ transplants for humans because their organs are similar in size. Studies have looked specifically at the possibility of transplanting swine hearts, kidneys, livers, and lungs into human patients. [2]



Dixon Kaufman, president-elect of the American Society of Transplant Surgeons and a transplant surgeon at the University of Wisconsin School of Medicine and Public Health, believes kidneys and pancreases will be the first animal organs to be transplanted into humans.

Humans can live without a pancreas and can survive with only 1 working kidney, so if the body were to reject the organs, someone who needs a kidney could still receive dialysis, and someone who needed a pancreas could still receive insulin. [3]


Read: Mouse Pancreas Grown in GMO Rats Reverses Diabetes in Mice


To many patients facing suffering and death, receiving a genetically-modified pig organ probably doesn’t sound much more life-threatening than not finding a human donor.


But it could be.


Kaufman said:



“The field is inherently sort of risky to begin with, and I think a lot of patients have already processed that. I tell patients in the grand design we were not meant to swap body parts between ourselves.”



The pig experiments were conducted by scientists from eGenesis, a company based in Cambridge, Massachusetts, and is detailed in the journal Science.



Sources:


[1] The New York Times


[2] Reuters


[3] Newsweek



Storable Food





About Julie Fidler:
Author Image
Julie Fidler is a freelance writer, legal blogger, and the author of Adventures in Holy Matrimony: For Better or the Absolute Worst. She lives in Pennsylvania with her husband and two ridiculously spoiled cats. She occasionally pontificates on her blog.

Wednesday, August 2, 2017

Scientists Use CRISPR to Edit Human Embryos in U.S. for First Time

A group of scientists in Oregon have edited the genes of human embryos for the first time in the United States, using CRISPR-Cas9, a cut-and-paste gene-editing tool. [1]


The experiments were conducted by Shoukhrat Mitalipov and colleagues at Oregon Health & Science University in Portland. The single-celled embryos Mitalipov edited were discarded after the experiments to ensure they could not become too developed.


Live Science explains how the CRISPR/Cas9 gene-editing tool works:




“The CRISPR/Cas9 gene-editing system is a simple “cut and replace” method for editing precise spots on the genome. CRISPRS are long stretches of DNA that are recognized by molecular “scissors” called Cas9; by inserting CRISPR DNA near target DNA, scientists can theoretically tell Cas9 to cut anywhere in the genome. Scientists can then swap a replacement gene sequence in the place of the snipped sequence. The replacement sequence then gets automatically incorporated into the genome by natural DNA repair mechanisms.”


Source: Daily Mail

CRISPR was used by scientists in China in 2015 to edit several human embryos that had severe defects. Like the scientists in Oregon, the team in China discarded the embryos before they could become too developed.


The Chinese technique led to genetic changes in a few of the embryos, and in a few cases, CRISPR sometimes snipped out the wrong place in the DNA.


Mitalipov’s experiments were reportedly successful in that they edited far more embryos than scientists did in past research. Additionally, Mitalipov and his colleagues claim they managed to do so without causing as many errors as previous scientists. [2]


Someday – perhaps much sooner than we realize – scientists could use this technique to edit not just the offspring of people with genetic diseases, but their offspring, as well. Theoretically, this could eradicate diseases caused by mutated genes, such as Huntington’s, sickle-cell anemia, Tay-Sachs, and many others.


But it’s risky…


Gene-editing is rife with controversy and ethical concerns. While many say CRISPR-Cas9 will help reduce the occurrence of genetic diseases, Marcy Darnovsky, Executive Director of the Center for Genetics and Society, says there are ways to do that which don’t involve editing the human genome.


“This is just not needed for preventing inheritable disease. There are [other techniques that] can already be used safely to prevent the births of children with serious genetic diseases in almost every case.”


For example, preimplantation diagnosis (PGD) allows parents to screen embryos for certain disease-causing genes before implanting them via in-vitro fertilization (IVF). However, in cases where someone carries 2 copies of a defective gene, PGD won’t work because all their embryos would also carry that gene.


Read: Study: CRISPR Gene-Editing Ignites Tons Of Unintentional Genetic Mutations


Darnovsky is also greatly worried about the safety of CRISPR gene-editing. He said:


“Despite whatever the claims are about safety, [like] no mosaicism, we still don’t know if that would mean it’s safe to create a new human being and anyone who tried it would be taking an enormous and unacceptable risk with that future person’s life.”


Right now, scientists are supposed to focus their efforts on editing disease-causing genes. But CRISPR could potentially open the door to the creation of “designer babies,” in which parents are permitted to edit their children to be better at sports or math, for example, or to be more physically attractive.


Source: Metro news

Darnovsky explained:


“That would be layering new forms of inequality and discrimination onto the ones we already live with.”


He’s not alone in his concerns.




In 2016, the U.S. intelligence community called CRISPR a potential “weapon of mass destruction.” [3]


Sources:


[1] Live Science


[2] Mother Jones


[3] MIT Technology Review


Daily Mail


Metro News



Storable Food


About Julie Fidler:


Author Image
Julie Fidler is a freelance writer, legal blogger, and the author of Adventures in Holy Matrimony: For Better or the Absolute Worst. She lives in Pennsylvania with her husband and two ridiculously spoiled cats. She occasionally pontificates on her blog.

Sunday, June 4, 2017

Study: CRISPR Gene-Editing Ignites Tons of Unintentional Genetic Mutations (VIDEO)

Study: CRISPR Gene-Editing Ignites Tons of Unintentional Genetic Mutations (VIDEO) | dna-gene-editing-crispr | Multimedia Science & Technology Special Interests


By: Julie Fidler, Natural Society | 


CRISPR-Cas9 gene-editing has been hailed as one of the biggest scientific breakthroughs of our lifetime. The technology is often called “molecular scissors” for its ability to “cut and paste” pieces of DNA, thereby removing unwanted traits and replacing them with more desirable ones. CRISPR is being celebrated for its accuracy, but a recent study sheds light on some imperfections surrounding the technology that we should be aware of.


When researchers at Columbia University used CRISPR-Cas9 to correct blindness in mice, they found that the process did successfully edit the gene responsible for blindness. However, it also caused unintentional mutations to more than 1,000 other genes. It’s exactly what critics of the technology have been warning about – that in the process of “fixing” part of the human genome, scientists could actually wind up doing irreparable damage. [1]



Study co-author Stephen Tsang, M.D., Ph.D., associate professor of ophthalmology, pathology, and cell biology at CUMC, Columbia’s Institute of Genomic Medicine, and the Institute of Human Nutrition, said:



“We feel it’s critical that the scientific community consider the potential hazards of all off-target mutations caused by CRISPR, including single-nucleotide mutations and mutations in noncoding regions of the genome.” [2]



CRISPR alters specific DNA sequences, but fails to correct the side effects that occur as a result.


There are currently 2 clinical trials involving humans underway in China, and a U.S. trial is slated to begin sometime next year. As many as 20 trials are in the works. One of the trials is aimed at preventing cervical cancers by using CRISPR to target and destroy the genes of the human papillomavirus (HPV) that cause tumors. [1] [3]


Here is a video talking a little bit about CRISPR.



Scientists identify areas likely to be affected by off-target DNA mutations with the assistance of predictive computer algorithms. Refinements to the technology suggested that in those trials off-target effects would be few. But nobody knows for certain how many side effects will result, or how serious they will be, and many experts are convinced the technology is simply not safe for use in humans at this point in time. [2]

Alexander Bassuk, M.D., Ph.D., the study’s co-author and professor of pediatrics at the University of Iowa, said:



“These predictive algorithms seem to do a good job when CRISPR is performed in cells or tissues in a dish, but whole-genome sequencing (WGS) has not been employed to look for all off-target effects in living animals.”



In the experiment in mice, researchers learned that success in the lab doesn’t always translate into success in the real world. The team looked at mice that they had previously corrected a blindness-associated gene in and sequenced their entire genome to find changes.


Though the mice’s vision was restored, 2 of them were left with over 1,500 unintended mutations, and more than 100 deletions and insertions of genes the researchers never intended to touch. What’s more, the computer algorithm failed to predict any of them. [1]


Outwardly, the mice didn’t look any different or develop any superpowers. But how the mutations will impact the mice in the future, or in subtle ways, remains an unanswered question for now. The vast majority of genetic mutations are not good. They’re exactly what CRISRP is intended to treat.


One scientist warned in January 2017 that gene-editing has the potential to “ruin human evolution.” Obviously, others see it as a promising advancement for the future.


The researchers concluded:



“This finding warns that CRISPR technology must be further tailored, particularly before it is used for human gene therapy.”



Sources:



[1] Gizmodo


[2] GEN Genetic Engineering & Biotechnology News


[3] New Scientist

Thursday, June 1, 2017

Study: CRISPR Gene-Editing Ignites Tons of Unintentional Genetic Mutations

CRISPR-Cas9 gene-editing has been hailed as one of the biggest scientific breakthroughs of our lifetime. The technology is often called “molecular scissors” for its ability to “cut and paste” pieces of DNA, thereby removing unwanted traits and replacing them with more desirable ones. CRISPR is being celebrated for its accuracy, but a recent study sheds light on some imperfections surrounding the technology that we should be aware of.


When researchers at Columbia University used CRISPR-Cas9 to correct blindness in mice, they found that the process did successfully edit the gene responsible for blindness. However, it also caused unintentional mutations to more than 1,000 other genes. It’s exactly what critics of the technology have been warning about – that in the process of “fixing” part of the human genome, scientists could actually wind up doing irreparable damage. [1]


Read: British Research Gets Green Light to Edit Human Embryos




Study co-author Stephen Tsang, M.D., Ph.D., associate professor of ophthalmology, pathology, and cell biology at CUMC, Columbia’s Institute of Genomic Medicine, and the Institute of Human Nutrition, said:


“We feel it’s critical that the scientific community consider the potential hazards of all off-target mutations caused by CRISPR, including single-nucleotide mutations and mutations in noncoding regions of the genome.” [2]


CRISPR alters specific DNA sequences, but fails to correct the side effects that occur as a result.


There are currently 2 clinical trials involving humans underway in China, and a U.S. trial is slated to begin sometime next year. As many as 20 trials are in the works. One of the trials is aimed at preventing cervical cancers by using CRISPR to target and destroy the genes of the human papillomavirus (HPV) that cause tumors. [1] [3]


Here is a video talking a little bit about CRISPR.


Read: First Human Injected with Controversial Genetically Modified Genes

Scientists identify areas likely to be affected by off-target DNA mutations with the assistance of predictive computer algorithms. Refinements to the technology suggested that in those trials off-target effects would be few. But nobody knows for certain how many side effects will result, or how serious they will be, and many experts are convinced the technology is simply not safe for use in humans at this point in time. [2]


Alexander Bassuk, M.D., Ph.D., the study’s co-author and professor of pediatrics at the University of Iowa, said:


“These predictive algorithms seem to do a good job when CRISPR is performed in cells or tissues in a dish, but whole-genome sequencing (WGS) has not been employed to look for all off-target effects in living animals.”


In the experiment in mice, researchers learned that success in the lab doesn’t always translate into success in the real world. The team looked at mice that they had previously corrected a blindness-associated gene in and sequenced their entire genome to find changes.


Though the mice’s vision was restored, 2 of them were left with over 1,500 unintended mutations, and more than 100 deletions and insertions of genes the researchers never intended to touch. What’s more, the computer algorithm failed to predict any of them. [1]


Outwardly, the mice didn’t look any different or develop any superpowers. But how the mutations will impact the mice in the future, or in subtle ways, remains an unanswered question for now. The vast majority of genetic mutations are not good. They’re exactly what CRISRP is intended to treat.


One scientist warned in January 2017 that gene-editing has the potential to “ruin human evolution.” Obviously, others see it as a promising advancement for the future.


The researchers concluded:


“This finding warns that CRISPR technology must be further tailored, particularly before it is used for human gene therapy.”





Sources:


[1] Gizmodo


[2] GEN Genetic Engineering & Biotechnology News


[3] New Scientist



Storable Food


About Julie Fidler:


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Julie Fidler is a freelance writer, legal blogger, and the author of Adventures in Holy Matrimony: For Better or the Absolute Worst. She lives in Pennsylvania with her husband and two ridiculously spoiled cats. She occasionally pontificates on her blog.

Thursday, May 25, 2017

Gene-Editing Technology may Replace Antibiotics in the Future

Doctors and researchers are in a race against the clock to find new antibiotics and alternatives to antibiotics as the problem of drug-resistance worsens and spreads. One bacterial superbug in particular which has researchers especially worried is Clostridium difficile, or C. difficile – a bacterium which can cause fatal infections in hospitals and nursing homes. Scientists are now working on a “pill” that uses CRISPR gene-editing technology to kill the harmful bacteria. [1]


Considered a probiotic, the technology is still in its infancy and is yet to be tested on animals. Jan-Peter van Pijkeren, a food scientist from the University of Wisconsin-Madison who is the creator of the CRISPR pill (which could also be given in liquid form), says:


“The downside of antibiotics is they are a sledgehammer that depletes and destroys the gut microbial community. You want to instead use a scalpel in order to specifically eradicate the microbe of interest.”





The idea behind using CRISPR to defeat antibiotic-resistant bacteria is that it could kill a single species of germ while leaving the beneficial bacteria unharmed.


Herbert DuPont, director of the Center for Infectious Diseases at the University of Texas, says:


“As long as we house patients together in a hospital or in a nursing home and we give a lot of them antibiotics we’re going to have a problem with C. difficile.”


Here’s how it works:


  • Van Pijkeren plans to create a virus that can carry a customized CRISPR message into the body via the probiotic liquid or pill.

  • When it passes into the intestinal tract, the virus would exit and infect the C. difficile.

  • The “message” in the pill then causes the bacteria to self-destruct. [2]

The Technology Doesn’t Come Without Worry


Though some are excited about such advancements, there are some inherent risks in using CRISPR-Cas9 technology to edit the human genome, or other living organisms that interact with the human body and our ecosystems at large. Gang Bao, a professor of bioengineering at Rice University, explains that unwanted gene edits, called off-target effects, “could influence the function of many genes, possibly posing serious health problems.”


Bao adds:


“In the germline, off-target effects might persist for generations and could lead to long-term changes in the genome.”


The so-called CRISPR pill that researchers are now championing would be designed to leave “good” bacteria untouched. So far, there has been no mention of the risks associated with the technology but that doesn’t mean scientists aren’t concerned.


Unless (or until) we encounter serious issues concerning CRISPR technology on a larger scale, it seems that this advancement in science is continuing at full speed, so it is essential that we consider all the possibilities and weigh the risks and potential benefits properly. Hopefully we’ll take more precautions than we did with speedily approving genetically modified foods, as any change of this scale requires in-depth controlled research, analysis, and most of all, time.


Sources:


[1] Futurism


[2] Digital Trends



Storable Food


About Mike Barrett:


Author Image
Mike is the co-founder, editor, and researcher behind Natural Society. Studying the work of top natural health activists, and writing special reports for top 10 alternative health websites, Mike has written hundreds of articles and pages on how to obtain optimum wellness through natural health.