Sunday, April 10, 2016

Chinese researchers have genetically modified human embryos—yet again

Less than a year ago, when a group of leading researchers was calling for a moratorium on the use of a revolutionary technology, Chinese researchers shocked the world by using it to genetically modify human embryos. The worry was that unfettered access to the technology might enable such embryos to become fully grown humans, who will then pass on mutations to all their offspring. The risk of unintended consequences seemed too great.
Now a different group of Chinese researchers have again wielded the technology to genetically modify human embryos. This time, however, the reaction from some scientists is just an annoyed shrug. Clearly a lot happened in the last year for perceptions to change so drastically.
The technology in question is called CRISPR, and it allows researchers to make genetic modifications with greater precision than ever before. In 2015, Chinese researchers used CRISPR to target genes responsible for a blood disorder called β-thalassaemia. They were only able to replace the defective gene in 28 out 71 embryos. Worse still, it left a slew of unintended changes in other parts of the genome.
In the latest attempt, researchers at Guangzhou Medical University have gone a step ahead. Instead of trying to correct mutations that could cause disease, they used CRISPR technology to insert a genetic mutation which might offer resistance against HIV.
The mutation was targeted in the CCR5 gene, which is responsible for producing a protein that HIV uses to latch on, enter, and infect a human immune cell. If the CCR5 gene were mutated, the logic goes, the HIV virus would not be able to infect—and thus the mutation would confer resistance to the disease.
The researchers report in the Journal of Assisted Reproduction and Genetics that they were successfully inserted the mutated gene in four out of 26 embryos. And, even in the successful cases, not all copies of the CCR5 gene were modified. In other cases mutations were caused that weren’t intended.
The experiment had been approved by a local ethics committee, which ensured that the study followed Chinese government guidelines. All the experimental human embryos were “non-viable,” which means they would have been unable to become fully grown humans. Such abnormal embryos are an inevitable part of in-vitro fertilization therapy, where sometimes two sperms insert their DNA into a single egg.
“The results are both comforting and disturbing,” says Peter Donovan of the University of California at Irvine. “The good news is that the technique worked for this group in the same way that it did for the first group… an important part of the scientific process showing it wasn’t a fluke the first time. The salutary lesson is that there is still much to be learned about gene editing in human embryos before it is ready for prime time.”
The rate of failure has made some bioethicists and scientists question the motives of Chinese researchers who continue to test CRISPR in human embryos. They argue that, while CRISPR offers greater precision, it still isn’t ready for testing in human embryos. Others, like Donovan, maintain that it will be studies using donated human embryos that will give us the most understanding.
Despite the divided opinion, there is definitely a change in perception. The first study reporting the genetic modification of human embryos resulted in a summit held in November between the science academies of China, the US and the UK. After days of deliberation, the world’s leading geneticists agreed that, while no CRISPR-modified embryos should become full human beings, research using human embryos can continue.
The Chinese group that did the latest work insists that their “proof-of-concept” may provide solutions to improving human health. They write, “Despite the significant scientific and ethical issues involved, however, we believe that it is necessary to keep developing and improving the technologies for precise genetic modifications in humans.

2015 was the year it became OK to genetically engineer babies

December 22, 2015
In April of this year, researchers in China published the results of an experiment in modifying the DNA of human embryos. Though the embryos they worked on were damaged ones that could not have grown into living babies, it sent a tremor through the scientific establishment.
Just a month earlier, a group of leading geneticists had called for a moratorium on gene-editing in embryos. Since any genetic changes would get passed on to future generations, they argued, the risk of unintended consequences was too great. And in November, at a summit in Washington DC, scientists from across the world agreed that, while research should continue, it’s still too risky to allow any altered embryos to grow into full human beings.
And, yet, when historians of science look back decades from now, they may well mark 2015 as the year genetically engineering humans became acceptable. That’s because, while the world was paying attention to the gene-editing summit, a more momentous decision had been made just a month earlier in the UK. There, a governmental body got ready to hand out licenses for creating a particular kind of genetically engineered human—using a technique the US tried and then banned 13 years ago.
This technique won’t create the fabled “designer babies” just yet. But the changes made to an embryo will be hereditary, and thus alter the genetic makeup of all the offspring to follow. The story of how we got here, and what will come next, is why 2015 will be remembered as a turning-point.

Just getting better

Our ability to do some form of genetic engineering goes back 40,000 years. Selective breeding created a tamer and more likable version of a wolf, the common ancestor of all today’s dogs.
Our desire to design better humans is also old. In Plato’s Republic, Socrates calls for a state-run program to get the best citizens to mate so that the population could be improved.
By the 19th century, the ideology of eugenics—a word not invented by Plato, but coined much later from the Greek for “good breeding”—had taken such a hold that countries were passing laws for such programs. Before World War II, 30 states in the US had passed some form of eugenics laws that mandated sexual sterilization of those deemed unfit (typically the mentally ill).
Only after the horror of Hitler’s genocide did the world recoil from eugenics. Most geneticists never returned to the idea that biological intervention would build a better society than social intervention. As Nathaniel Comfort, a professor of history of medicine, writes in Aeon, eugenics survived only in the form of “preventive medicine for genetic diseases”—such as screening people for them and, occasionally, treating them with gene therapy.
Not everyone stopped trying. Taking inspiration from Aldous Huxley’s Brave New World, eugenicist Robert Graham created the Repository for Germinal Choice, a sperm bank for the super-intelligent. The bank existed from 1980 to 1999 and had some 19 high-IQ donors, including at least one Nobel laureate (William Shockley).
The resulting “Genius Babies ”—some 200 of them—are no different from normal people. One of those conceived through Graham’s sperm bank told CNN, “There’s only so much you can control when it comes to genetics. It all has to do with what you give to your family.”

Beyond our control

That comment defines the limits of science today. In the 1970s, we finally understood how to tweak the genes of microbes, plants and animals to achieve certain traits. But in humans, with the exception of a few things such as color blindness or tasting certain foods, “designer baby” traits, such as greater intelligence, taller stature, stronger muscles, or better memory, are controlled by hundreds of genes, each of which also perform many other critical functions. Tools that can deal with such complexity are still a long way off.
For now, then, the only foreseeable use for gene-editing is to prevent disease. And the goal is to make genetic tools good enough to do that without any unintended consequences.
Since 1989, thousands of people have received experimental gene therapies. Typically these involve the use of a “vector”—a biological vehicle, such as a virus, that can deliver the correct copy of a faulty gene to the specific cells in the body affected by the genetic disorder, such as cancer cells or faulty cells in the eye.
While most of these treatments have been safe, only a few have been effective. China approved the world’s first gene therapy in 2003 to treat certain kinds of cancers. Europe got its first in 2012 that treats a rare inherited disorder (pdf) affecting the pancreas. The US is likely to get its first gene therapy approved in 2016 to treat a form of blindness.
None of these therapies, however, have used the latest advance in gene-editing: CRISPR-Cas9, a highly precise copy-and-paste tool that allows for the removal and replacement of individual genes. Since its development in 2012, it has become an instant favorite among scientists.
CRISPR-Cas9’s immediate potential lies in curing single-gene disorders in embryos. Changes made at that stage would affect every cell in the body and could cure many diseases. We know some 4,000 such disorders, and, though each is rare, put together they could change the lives of millions in the next generation, and keep many more free from those diseases for all the generations to follow.
However, the Chinese study earlier this year showed that we might need something even more precise than CRISPR-Cas9 currently is. Only in one-third of the 86 embryos was the faulty gene erased as predicted, and even in those cases, CRISPR-Cas9 had also modified things it wasn’t meant to—the unintended consequences scientists worry about.
There is, however, another form of genetic engineering of human embryos. This is the one that the US tried and then banned, and that the British government recently opened licensing applications for. And what’s probably more important for the future of the debate is how Britain decided the technology works and is safe.

Three-parent child

Alana Saarinen was born in the US with three biological parents. Two of them contribute more than 99% of her genetic material and the third provides the rest. She is one of only 30 or so people in the world who grew from a genetically engineered embryo into a healthy adult.
Sharon and Paul Saarinen had attempted in-vitro fertilization (IVF) four times, but without success. A likely reason was that Sharon’s egg cells had faulty mitochondria. These are like biological batteries within a cell—they play an essential role in converting your food into the energy that powers your body. Uniquely, they also have their own DNA (though it’s only some 37 of the 20,000 or so genes that make up the human genome).
During reproduction, when an egg cell fuses with a sperm cell, creating the first cell of an embryo, it’s only the DNA in its nucleus that is a mix of both parents’ DNA. Mitochondria and their DNA are passed on directly from mother to offspring. Because Sharon Saarinen’s mitochondria were faulty, she basically needed a mitochondria transplant in order to conceive.
That was where the third parent came in. A donor provided an egg cell, whose nucleus was removed and healthy mitochondria along with other bits of the cell were transferred to Sharon’s egg. The egg cell was then mixed with Paul’s sperm cells in a normal IVF procedure, and the resulting embryo would become Alana Saarinen.
This technique won’t only help women like Sharon conceive. In a lot of cases with faulty mitochondria, pregnancies proceed normally, but the child then turns out to have one of several mitochondrial diseases, which can lead to all sorts of problems, from poor growth to autism to diabetes. One in every 5,000 children suffers from one of them.
Mitochondrial replacement therapy like the Saarinens had is currently the only known way of preventing mitochondrial diseases. But since they conceived Alana in 2000, only some 30 or so children have been born using the technique. In 2002, the US Food and Drug Administration (FDA) banned its use. Apart from ethical concerns about scientists “playing God,” there was a scientific worry too. We had never attempted to edit the “germ line”—the DNA that is transferred from one generation to another—and the risks were unknown. (About 10% of the pregnancies that resulted from this treatment had complications, but it wasn’t clear whether the procedure was to blame.)

Selfish genes

The FDA ban meant that US women with faulty mitochondria were left with difficult choices (pdf). They could choose not to have children, or undergo IVF and pick the fertilized embryo with the fewest defective mitochondria—taking a gamble on whether their child would develop mitochondrial disease.
But nearly a decade later the UK government’s Human Fertilization and Embryology Agency (HFEA) took up the case. In 2012, after taking a detailed look at the results of studies on animals and humans, it deemed that mitochondrial replacement therapy was “not unsafe”—meaning that the benefits of curing mitochondrial disease would outweigh the risks of the procedure.
The interesting thing was what the HFEA did next. In Sept. 2012, it launched a public consultation, creating a website that explained both the risks and benefits, and holding public events to do the same. Then it conducted a survey and asked people to send in their comments online. After the public had shown broad support for the therapy—and despite stiff opposition from scholarly groups and religious groups alike—the HFEA spent two years taking the necessary steps to get the regulations discussed in parliament. In February, MPs agreed to allow the use of the therapy under strict guidelines. In October, the process for handing out licenses began.
We already use genetic engineering to create climate-resistant crops and drug-producing bacteria. Now one of the world’s most scientifically advanced countries—and, fittingly, the birthplace of IVF—has agreed that genetically modified humans, too, are sometimes not just OK, but desirable. This is what makes 2015 an historic year.
Based on past progress, it is likely that genetic enhancements to humans will become a reality step by step. Just like mitochondrial replacement therapy, they will first appear for a very narrow purpose, such as curing single-gene disorders, and then, likely over many decades, we might reach the stage of creating those fabled designer babies.
That gives us enough time to deliberate the implications of each step. When our decisions will affect generations of humans to come, it is important we use that time well. The process that HFEA designed to win public and political support is a model worth emulating. If each step were to get the same scrutiny that mitochondrial replacement therapy got, genetically modified humans could become as normal as genetically modified crops and bacteria are today—and, barring the occasional controversy, as widely accepted.
Corrected Dec. 23: An earlier version of this post incorrectly said that Sharon Saarinen’s nucleus was implanted in a donor’s egg. It also said that HFEA began handing out licenses in October, but in fact it then began the process of handing them out.

The pros and cons of genetically engineering your children

December 03, 2015
From time to time, science troubles philosophers with difficult ethical questions. But none has been as difficult as considering permanently altering the genetic code of future generations. At a meeting that began on Dec. 1 in Washington DC, the world’s leading gene-editing experts met with ethicists, lawyers, and interested members of the public to decide whether it should be done.
Gene-editing tools have existed since 1975, when a meeting of a similar kind was held to discuss the future of genetic technology. But recent developments have made the technology safe enough to consider turning science fiction into reality. In fact, in April, Chinese researchers announced that they had conducted experiments to remove genes of an inheritable disease in human embryos (embryos that were alive but damaged, so they could not have become babies).
So the stakes are high. By eliminating “bad” genes from sperm and egg cells—called the “germline”—these tools have the potential to permanently wipe out diseases caused by single mutations in genes, such as cystic fibrosis, Huntington’s disease, or Tay-Sachs.
At the same time, there is huge uncertainty about what could go wrong if seemingly troubling genes are eliminated.
One of the key researchers in the field is Jennifer Doudna at the University of California, Berkeley. She has been touted for a Nobel Prize for the development of CRISPR-Cas9, a highly precise copy-paste genetic tool. In the build-up to the meeting, Doudna made her concerns clear in Nature:
“Human-germline editing for the purposes of creating genome-modified humans should not proceed at this time, partly because of the unknown social consequences, but also because the technology and our knowledge of the human genome are simply not ready to do so safely.”
Her sentiments were echoed in a report released before the meeting by the Center for Genetics and Society. They believe that research in genetic tools must advance, but only through therapy for adults (where genetic modifications are targeted at some cells in the body but not passed on to kids, such as in curing a form of inherited blindness). The report continues:
“But using the same techniques to modify embryos in order to make permanent, irreversible changes to future generations and to our common genetic heritage—the human germline, as it is known—is far more problematic.”
Consider sickle-cell anemia, an occasionally fatal genetic disorder. Its genes, though clearly harmful, have persisted and spread because, while having two copies of the sickle-cell gene causes anemia, having just one copy happens to provide protection against malaria, one of the most deadly diseases in human history. Had we not known about their benefits, eliminating sickle-cell genes would have proved to be a bad idea.
More importantly, there is a worry that once you allow for designer babies you go down a slippery slope. Emily Smith Beitiks, disability researcher at the University of California, San Francisco, said recently:
“These proposed applications raise social justice questions and put us at risk of reviving eugenics—controlled breeding to increase the occurrence of ‘desirable’ heritable characteristics. Who gets to decide what diversity looks like and who is valued?”
But the history of science shows that it is hard to keep such a cat in the bag. Once developed, technologies have a way of finding their way into the hands of those who desire to use them. That worries George Church, a geneticist at Harvard Medical School, who has been a strong voice in this debate since the beginning. In Nature, he writes:
“Banning human-germlined editing could put a damper on the best medical research and instead drive the practice underground to black markets and uncontrolled medical tourism, which are fraught with much greater risk and misapplication.”
And many believe that the risks of gene-editing are not that high anyway. Nathaniel Comfort, a historian of medicine at Johns Hopkins University in Baltimore, writes in Aeon:
“The dishes do not come à la carte. If you believe that made-to-order babies are possible, you oversimplify how genes work.”
That is because abilities, such as intelligence, height, or personality traits, involve thousands of genes. So there may be some things that you cannot genetically enhance much, and certainly not safely. And even knowingly changing the human genome is not as big a deal as some make it out to be, Church notes:
“Offspring do not consent to their parents’ intentional exposure to mutagenic sources that alter the germ line, including chemotherapy, high altitude, and alcohol—nor to decisions that reduce the prospects for future generations, such as misdirected economic investment and environmental mismanagement.”
The meeting ended on Dec. 3, and the committee of organizers—10 scientists and two bioethicists—came to a conclusion on the debate. They believe that the promises of germline editing are too great to scupper future developments. They endorse that research should continue in non-human embryos and “if, in the process of research, early human embryos … undergo gene editing, the modified cells should not be used to establish a pregnancy.” That is because the committee believes that we neither know enough about safety issues to allow any clinical application, nor enough about how society will respond to the use of this technology in humans.
And, yet, perhaps the the last word on the debate should go to a woman in the audience at the meeting. Her child died only six days old after torturous seizures caused by a genetic ailment. She implored the research community, “If you have the skills and the knowledge to eliminate these diseases, then freakin’ do it!”

Scientists have synthesized a 'minimal genome' with only genes necessary for life

A pioneering accomplishment in the field of genetic research could help scientists gain new insights into the very definition of life. The new research, published Thursday in the journal Science, describes the synthetic creation of a “minimal genome” — a cell containing only the genes absolutely required to keep itself alive.
With just 473 genes, it’s the smallest genome of any living, dividing cell found in nature and may provide important insights into the fundamental genetic requirements for life.
The idea of designing and studying a “minimal genome” is a concept that’s fascinated scientists for decades. In fact, unlocking the secrets of the genome has been a preoccupation of genetic researchers since the first genome sequencing was performed on a bacterium in 1995 — the event that ultimately led to this week’s breakthrough, according to the new study’s authors.
Researchers have designed and synthesized a minimal bacterial
genome, containing only the genes necessary for life.
Image: C. Bickel/Science
“This is a study that had its origins a little over 20 years ago in 1995, when this institute sequenced the very first genome in history, Haemophilus influenzae,” said the new paper’s senior author J. Craig Venter, founder of the J. Craig Venter Institute, which specializes in genomic research, during a Wednesday teleconference.
Later that same year, the institute also sequenced the genome of a second type of bacteria, Mycoplasma genitalium. These breakthroughs allowed for the first genomic comparisons between two different species, Venter said.
Venter is most famous for his role as a leader of the team that first sequenced the human genome in 2000.
“[My colleagues] and myself were discussing the philosophy of these differences in the genomes and decided the only way to answer basic questions about life would be to get to a minimal genome, and probably the only way to do that would be by trying to synthesize a genome,” Venter said.

Image: Giphy
“And that started our 20-year quest to do this.”
The reason that researchers must synthesize, or essentially design their own, minimal genome is because just about every living organism we know of contains more genes than are actually necessary for its basic survival. Even the simplest bacteria contain extra, nonessential genes that are related to its growth, development and ability to react to its environment, but that aren’t technically required to keep the cell alive.
So in order to get down to a truly minimal genome, scientists must take an existing genetic sequence and pare it down themselves, cutting away all the nonessential genes until they end up with only the ones that are absolutely essential

They do this by creating synthetic genomes — genomes that are designed and chemically built from the ground up using our existing knowledge of an organism’s genetic information.
Along the way, scientists can add or delete genetic information as they see fit. It’s the same basic principle that’s used in genetic engineering research. But in the case of a minimal genome, the goal is to slice off as much unnecessary genetic information as possible without changing or adding anything else to the organism’s genome.
And that’s just what Venter and his colleagues set out to do.

DNA minimalism

They started with the genome of a type of bacteria known as Mycoplasma mycoides, a parasite normally found in cows and goats. In 2010, the group succeeded in building the complete M. mycoides genome from scratch and transplanting it into another cell.
J. Craig Venter receives the National Medal of Science on
October 7, 2009 in Washington, DC.
Image: Getty Images
This time around, they used a variety of methods to whittle the genome down before transplanting it.
To start, the researchers divided the bacterium’s genome into eight different segments that could be individually altered and tested — just to make the experiments a little more manageable. They then applied a handful of techniques to peel away the nonessential genes.
They call this their “design-build-test” approach.
First, they applied their basic knowledge of genetics and biochemistry to infer which genes might be safe to remove — but this technique did not produce viable cells.
The researchers then conducted a series of experiments in which they inserted bits of foreign genetic information — called transposons — into the genome in order to disrupt the functions of certain genes and figure out which ones the cell could do without. This process helped them whittle down the genome until no more genes could be removed.
Along the way, the researchers were able to divide the bacterium’s genes into three major categories: essential, nonessential and quasi-essential, meaning they weren’t absolutely required for life but were necessary to help the cell grow at a healthy pace.
It allowed them to discover how much we don’t know, even about the core sections of the genome
Venter and his colleagues also discovered that the genome contained a number of redundant genes — pairs of genes that performed the same function in the cell. These genes made the whittling process a little confusing at first — if one of the redundant genes was removed (but not the other), the cell would continue functioning, tricking the researchers into believing it was a nonessential gene.
A great deal of trial and error was required in order for the researchers to classify all the genes.
Finally, though, they reached a point where no more genes could be removed without killing the cell.
The result is the smallest genome ever recorded in a self-replicating — that means alive and able to divide — cell. It contains just 473 genes, all of which are either directly required to keep the cell alive or to enable it to grow and divide fast enough to be practical for the researchers’ experiments.
J. Craig Venter poses before a gene map of a flu-causing
bacterium in his Rockville, Md., office, March 12, 1997.
Image: Ruth Fremson/AP
Interestingly, about a third of the resulting genome consists of genes with unknown biological functions. Most of the known essential genes perform functions related to expressing genes, passing down genetic information from one generation to the next, or performing essential functions in the cell’s membrane and cytosol, so the scientists predict that the unknown genes will have similar jobs — we just don’t know what yet.
“One of the great findings but also the great caveats of this work is that it allowed them to discover how much we don’t know, even about the core sections of the genome,” said Adam Arkin, director of the Synthetic Biology Institute at the University of California Berkeley, in a statement.
That said, Venter also noted that the concept of a minimal cell is context-dependent.
The specific genes that an organism requires to survive — even an organism as simple as a bacterial cell — depend on what kind of environment the cell is living in and what kinds of nutrients are available to it.
And, of course, one species’ minimal genome would likely differ significantly from that of another species.
With that in mind, exploring different forms of minimal genomes could have important industrial applications, said Daniel Gibson, another of the study’s authors and another scientist at the J. Craig Venter Institute, during the same teleconference.
Because these cells are so simple, devote all their energy to essential functions and are subject to very few genetic mutations, they are “straightforward to engineer” and could provide helpful insights into more complex types of biosynthesis in the future, he said.
Still, there’s plenty of work left to be done before the study of minimal genomes may yield practical applications.
“The major limitation is that this is the beginning of a very long road,” said Sriram Kosuri, an assistant professor of biochemistry at UCLA, in a statement.
“It's not as if this new minimal genome will automatically lead to either fundamental insights or industrial applications immediately. That said, they've created a self-replicating biological organism that might be a better starting point for such scientific and engineering goals than continuing to study natural systems."

Scientists May Have Found the Key to Curing Autism, Cancer and HIV

Gene editing tool CRISPR-Cas9 has made it possible to isolate RNA in living cells for the first time.


Mutations in RNA are linked to autism, cancer, and fragile X syndrome.
By + More

The cures for some of the world's most perplexing diseases might be closer than we think.
According to a study published in Cell, researchers have determined how to isolate and edit messenger RNA that carries genetic instructions from the cell's nucleus to make new proteins for the first time using gene-editing tool Clustered Regularly Interspaced Short Palindromic Repeats, also known as CRISPR-Cas9.

They have previously used this tool to remove HIV from human immune cells and shut down HIV replication permanently, according to a study published in Nature in March.
“It opens up a new area of thinking about manipulating genes and disease,” Gene Yeo, associate professor of molecular medicine at UCSD and a senior author of the study, told Discovery. “In many diseases you cannot edit the genome, you can break the genome into pieces. But here we are doing transcription engineering or editing. That’s quite exciting.”
The gene-editing technique could lead to treatments for diseases that are linked to defective RNA and have previously been untreatable. These include certain cancers, fragile X syndrome and autism.
[READ: FDA Orders Warning Labels on Prescription Narcotic Painkillers]
CRISPR-Cas9 can also potentially be used to edit genes that determine our physical features and maybe even our personality, leading to ethical questions about how to responsibly use the technology.
Discovery reports that the National Academy of Sciences is working on a set of ethical rules for this burgeoning field.

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