Monthly Archives: February 2015

Three-Parent IVF Deserves a Chance in the U.S.

Posted: February 4, 2015 at 8:44 pm

TIME Ideas health Three-Parent IVF Deserves a Chance in the U.S. All new fertility methods sound crazy at first

In a historic vote that rocked the world of fertility medicine Tuesday, British lawmakers approved the use of a controversial IVF practice that would take genetic material from three people to create a single embryo.

The promising technique, which involves replacing the defective cellular material of a womans eggs with that from a healthy donor, aims to prevent patients from passing down crippling genetic diseases to their offspring. It also might hold the key to other groundbreaking applications, such as extending womens fertility by rehabilitating old eggs.

The decision is inspiring because members of Parliament chose science over a firestorm of often ill-informed debate questioning whether weve gone too far in experimenting with genetic engineering. Hopefully, they will motivate the U.S. Food and Drug Administration, which held public hearings on the topic last year but declined to move forward with human trials citing lack of safety data, to follow suit. New research published in the New England Journal of Medicine estimated that more than 12,000 women in the U. S. of childbearing age risk passing down such mitochondrial diseases, which have been linked to everything from poor growth, blindness, neurological problems and heart and kidney problems.

The world is right to be cautious about this latest mind-boggling advance in reproductive medicine. It does sound like science fiction: If youre a woman who suffers from a mutation in her mitochondrial DNAthe part of our cells that generate energyscientists can take your egg, extract the nucleusthe part containing your most important genetic instructions, such as hair and eye colorand insert it into a new egg that has been provided by another woman. (The nucleus would have already been removed from the donor egg.) This newly renovated egg is then fertilized by your partners sperm and implanted into your uterus. You carry on with your pregnancy, just like billions of women before you. (Another version of the technique switches out the nucleus of a newly fertilized egg.)

Have we pushed the boundaries too far in innovative baby-making? Think back to when critics charged that the inventors of in-vitro fertilization recklessly played God by daring to combine a sperm and an egg in a lab to create Louise Brown in 1978. Now some 5 million of the worlds babies have been conceived via IVF. But its one thing to get used to combining reproductive parts in a lab; its a lot less comfortable to imagine tinkering with those parts beforehand. In an open letter to the U.K. Parliament, Paul Knoepfler, stem cell and developmental biology researcher at the University of California Davis School of Medicine, warned that supporters could well find themselves on the wrong side of history with horrible consequences.

Yet its important to understand that mitochondrial replacement isnt genetic engineering run amok, cautions Debra Mathews of the Berman Institute of Bioethics at Johns Hopkins University. The mitochondrial energy-making material of an egg accounts for a mere 37 genes, compared to the nucleus, which contains about 23,000 genes. No one is messing directly with genes, she says. Scientists are replacing damaged mitochondria with healthy mitochondria. Its a specific technology for a specific application. Were modifying eggs to avoid serious diseases. So far, researchers havent attempted a pregnancy using the technique, but a study published in 2012 in Nature found that resulting embryos appeared to develop normally with the nucleus intact and did not contain any of the mutated mitochondria from patients previous eggs. And scientists at Oregon Health and Science University transferred the mitochondria between rhesus-monkey eggs and created four healthy monkey babies.

Yet determining when a technology is safe is especially challenging in fertility medicine because the only way to find out is to create another human. The FDAs prudence is a welcome change from the early wild west days of reproductive medicine when many scientists implanted and prayed that their experiments wouldnt lead to the horrible consequences Knoepfler is warning against. So far, weve been incredibly lucky.

We dont want to risk holding up progress by being too cautious, especially when some 1,000 to 4,000 babies are estimated to be born every year with mitochondrial disease, according to the United Mitochondrial Disease Foundation.

Yet what should the threshold be? The FDA shut down other such research being done more than a decade ago. Scientists at several fertility clinics were responsible for 30 pregnancies from eggs that had been injected with donor cytoplasm that contained mitochondria. The kids havent been tracked over the long term, and its unknown whether the procedure contributed to two cases of chromosomal abnormalities that resulted in one miscarriage and one abortion. And researchers at New York Universitys Langone Medical Center tried a similar mitochondrial transfer technique using younger eggs for three women in their 40s suffering from age-related infertility. Although the embryos developed naturally, none got pregnant. A Chinese team later used the NYU method to achieve a triplet pregnancy, but the patient lost the entire pregnancy after she tried to abort one fetus to give the other two a better chance of survival.

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23andMe Finds Genes for Motion Sickness

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The personal genomics company 23andMe has identified 35 genetic factors tied to motion sickness, according to a new study published in the journal Human Molecular Genetics.

In what the company says is the first ever genome-wide study looking at motion sickness, 23andMe was able to determine several genes that may be tied to the nausea associated with movement in a car or on a boat. Motion sickness affects around one in three people, and prior research has suggested that it could be hereditary.

The researchers, who are employed by 23andMe (or have been in the past) and own stock options in the company, used genetic data from more than 80,000 23andMe customers. They found that many of these genetic factors were involved in balance, eye and ear development and the nervous system. Overall, the effect appeared to be stronger in women.

Read more: Genetic Testing Company 23andMe Finds New Revenue With Big Pharma

The study also found links between risk for motion sickness and a greater likelihood of having migraines, morning sickness and vertigo.

Its still unclear what the actual drivers are, and even if a person has the gene variants linked to motion sickness, it doesnt mean they will definitely have the condition. Genome-wide association studies like the one performed by 23andMe can only find correlations, but theyre still useful strategies for finding at-risk genes.

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The Scientist: Professor Amy Williams Maps Genes, Tracks Risk of Disease

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By SHIRA POLAN

Prof. Amy Williams, computational biology, is most likely not your relative, at least within the last 10 generations. But the newly instated Cornell professor spends much of her time studying your family tree or rather, the genetic tree of all modern humans in order to better understand the complex history of human demographics.

Williams, a graduate of the University of Utah, first became interested in population genetics and parent-to-child genetic transmission during her Ph.D. work at the Massachusetts Institute of Technology.

I went to grad school expecting to do very traditional computer science but ended up taking a genetics class for my minor [and] really just fell in love with it, she said. For my Ph.D., I ended up developing an algorithm for inferring the way in which DNA gets transmitted from parents to children in single families. I then got a postdoc in a human population genetics lab and have continued to fall in love with the discipline.

Following graduate school, Williams pursued postdoctoral positions at Harvard Medical School and Columbia University before beginning research as an assistant professor in the Department of Computational Biology and Population Genetics last April.

Next fall, Williams will teach a course that will serve as an introduction to computational biology.

[The class] will likely be aimed at individuals who have a little bit of computational background. Well talk about the ways of analyzing genetic data and will begin by asking, What is the human genome? she said. This is something you can download off the Internet and read off all those letters, but how was it actually generated?

Williams said she considers her field of computational biology to be very broad, referring to the many applications computers have in the realm of biology.

Its anything from trying to predict how a protein will fold using computers, to trying to infer relationships between individuals on the basis of their genetic makeup, to comparing the genetic makeup of different species in order to learn about evolution, to methodologies for performing genome-wide association studies that attempt to identify genetic variants that affect a given trait or disease, she said.

One specific application of Williams work is the characterization of haplotypes, a series of genes that occur on a single chromosome and are likely to be inherited together.

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The Scientist: Professor Amy Williams Maps Genes, Tracks Risk of Disease

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Aw: Live! DNA With ‘Ak 12’ – Video

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COD AW Ps4 Gameplay DNA / Nuklear 47-5 – Video

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COD AW DNA BOMB #12 11 – Video

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"92-4 DNA BOMB w/ KF5" ( What I have been up to recently ) – Video

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DNA: Never said I will not travel business class, says Kejriwal – Video

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Call of Duty: Advanced Warfare First DNA Gameplay on Comeback Domination – Video

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