Humans carry an average of one to two mutations per person that can cause severe genetic disorders or prenatal death when two copies of the same mutation are inherited, revealed a large global study spanning over two decades.
Most genetic disorders that result in sterility or childhood death are caused by recessive mutations -- DNA sequence variants that are harmless when a person carries only one copy. But if such mutations are present at both copies (where one copy was inherited from each parent), they can cause devastating diseases like cystic fibrosis.
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"These records offered a fantastic opportunity to estimate disease mutation carrier rates in a new way that disentangles the effects of genetic and socioeconomic factors," said Dr. Ziyue Gao, lead author from the University of Chicago.
For the study, the team studied genetic contributions to disease using a large 13-generation family tree that traces the ancestry of more than 1,500 living people. Using this information, the team estimated that there were around three mutations of this type for every five people among the original founders.
But that only counted mutations that allow children carrying two copies to survive at least until birth.
Based on estimates of the proportion of recessive mutations that cause death during fetal development, the team concluded that each founder carried approximately one to two recessive mutations that cause sterility or death before adolescence.
"This number is probably lower than the real average for most populations. Most importantly, unlike previous estimates, it is unaffected by socioeconomic factors," Gao noted.
The number of recessive disease mutations will vary from person to person and the new number does not necessarily help predict a specific couple's risk for passing on a genetic disorder.
Gao also pointed out that most infant mortality worldwide is caused by non-genetic factors like nutrition and infectious disease, rather than inherited disorders. It is an interesting evolutionary question for further research, the authors concluded.
The results were published in the journal Genetics.