By Jenifer Goodwin
WEDNESDAY, June 6 (HealthDay News) -- Researchers report they have decoded the entire genome of a fetus using only a blood sample from the mother and a saliva sample from the father.
The scientists said prenatal genome sequencing using the noninvasive method could one day be used to determine if a fetus has any of the thousands of genetic disorders that are caused by a single, often devastating, mutation on one gene.
In pregnant women, bits of fetal DNA move through the mother's body in the plasma, a component of blood. Unlike a sample of DNA taken directly from fetal tissue or from amniotic fluid -- such as when expectant mothers undergo amniocentesis to look for chromosomal disorders such as Down syndrome -- the DNA in plasma is in fragments.
That makes analyzing it complex, but increasingly possible given the latest generation of gene-sequencing technology, explained study author Jay Shendure, an associate professor of genome sciences at the University of Washington.
"The chromosomes are shattered, but all the information is there, represented in small fragments," Shendure said.
In the current study, researchers used plasma from a woman who was 18 weeks pregnant and saliva from the dad to tease out which was fetal DNA. Researchers confirmed the accuracy of their conclusions by mapping the baby's DNA using umbilical cord blood after birth.
Testing for genetic problems using a blood sample and saliva would be an improvement over more-invasive tests such as amniocentesis, which can pose risks to the fetus, Shendure said.
"This fits in quite well with what we do today, which is to provide expectant mothers with as much information as we can," Shendure said. "It would simply be more comprehensive."
Still, he noted, the paper should be viewed as a "proof of concept," or showing that noninvasive whole fetal genome sequencing was possible. More research is needed before the technique is ready to be used in doctor's offices, he said.
The study is published in the June 6 issue of Science Translational Medicine.
Until the last few years, whole genome sequencing has been extraordinarily expensive. That began to change after the Human Genome Project produced the first whole human genome in 2001 at a cost of about $3 billion. By 2010, sequencing an entire genome cost around $50,000, while experts now put the cost at a few thousand dollars and dropping.
"The study is the next logical step in beginning to figure out how to use this amazing new technology we have that allows very robust sequencing of the genome. We now are in a situation [where], for relatively affordable and dropping prices, one can evaluate an individual's whole genome," said Dr. James Evans, editor-in-chief of Genetics in Medicine, the journal of the American College of Medical Genetics and Genomics.
Already there are several commercial companies that sift through the fetal DNA in plasma to look for an extra copy of chromosome 21 that indicates Down syndrome, Evans said.
But there are some 3,000 other single-gene genetic disorders that individually are rare, but collectively affect up to about 1 percent of births, Shendure said. Those diseases include Tay-Sachs, Marfan syndrome, cystic fibrosis, Huntington's disease and Kabuki syndrome.
The fetal genome sequencing could tell parents before the baby is born if the child has the mutation that causes the disease, informing their decisions and helping them to prepare, Shendure said -- not unlike what amniocentesis and other prenatal tests such as ultrasound offer today.
But significant questions remain, including how early in the pregnancy whole genome sequencing could be done. Research has found that there is fetal DNA in the mother's plasma between four and seven weeks, but researchers have not yet determined if the technique would give an accurate picture of a fetal genetic profile that early, Shendure said. (Their analysis of maternal plasma at 8.2 weeks gestation turned up fetal DNA in the mother's blood.)