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Monday, February 16 2015
Press release

Sex has another benefit: it makes humans less prone to disease over time

Mixing our genes through sex helps purge us of disease mutations

MONTREAL, CANADA, February 16, 2015 – For decades, theories on the genetic advantage of sexual reproduction had been put forward, but none had ever been proven in humans, until now. Researchers at the University of Montreal and the Sainte-Justine University Hospital Research Centre in Montreal, Canada have just shown how humanity’s predispositions to disease gradually decrease the more we mix our genetic material together. This discovery was finally made possible by the availability in recent years of repositories of biological samples and genetic data from different populations around the globe.

What we already knew

As humans procreate, generation after generation, the exchange of genetic material between man and woman causes our species to evolve little by little. Chromosomes from the mother and the father recombine to create the chromosomes of their child (chromosomes are the larger building blocks of genomes). Scientists have known for some time, however, that the parents’ genomes don’t mix together in a uniform way. Chromosomes recombine frequently in some segments of the genome, while recombination is less frequent in others. These segments of low-frequency recombination will eventually recombine like others do but it will take many, many generations.

The findings

More specifically, the team of Canadian researchers led by Dr. Philip Awadalla discovered the following: the segments of the human genome that don’t recombine as often as others also tend to carry a significantly greater proportion of the more disease-enabling genetic mutations*. Until chromosome recombination eventually occurs, these segments accumulate more and more bad mutations. In other words, as far as susceptibility to disease is concerned, our genetic material actually worsens, before it gets better. Thankfully, disease-enabling mutations are eventually shuffled off our genetic code through sexual reproduction. “But since these mutations rest on less dynamic segments of our genome, the process can potentially take many hundreds of generations,” explains Dr. Awadalla.

Why these findings are significant

“This discovery gives us a better understanding of how we, as humans, become more or less at risk of developing or contracting diseases,” says Dr. Awadalla. It also tells scientists more precisely where to look in the human genome to find disease-enabling mutations, he adds, which should speed up the discovery and identification of mutations associated with specific diseases. Researchers and health authorities will in turn be able to apply this new information to develop more effective treatments and prevention programs.

The science behind the findings

Dr. Awadalla and his team studied the sequenced genomes of hundreds of individuals from Canada’s CARTaGENE genetic data repository and the multinational 1000 Genomes Project. They found that the proportion of mutations associated with disease was significantly higher in low recombining segments known as “coldspots” relative to highly recombining regions, and that the bad mutations in these coldspots were generally more damaging than the mutations in the highly recombining segments.

Through the 1000 Genomes and CARTaGENE programs, the team was able to compare this phenomenon across four present-day population basins: Africans, Asians, Europeans and Canadians of French descent. Each of these genetic groups exhibit the above behaviour to varying degrees. African individuals showed the smallest relative proportion of disease-associated mutations on their genome’s coldspots, with Western Europeans showing the largest.

The complete scientific paper was published by Nature Genetics and can be found online at www.nature.com.

Research partners

This study was made possible by the financial support of Fonds de la Recherche en Santé du Québec (FRSQ), Genome Québec, Fonds Québécois de la Recherche sur la Nature et les Technologies (FQRNT) and the Canadian Partnership Against Cancer. The CARTaGENE biobank, of which Dr. Awadalla is also the scientific director, receives funding from the Canadian Partnership Against Cancer, Genome Québec, Genome Canada and the Canadian Institutes of Health Research. Dr. Awadalla is also a Professor of Medical and Population Genetics at the University of Montreal and at the Ontario Institute for Cancer Research.

* Mutations, also called “variations”, happen naturally and are not necessarily a cause for concern. They occur when genes get incorrectly copied from one parent to the child or after many generations’ exposure to certain environmental factors. Some mutations are benign, some beneficial. Bad mutations however can increase our risk of contracting or developing debilitating or life-threatening diseases.

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University of Montreal and Sainte-Justine University Hospital Research Centre
Dr. Philip Awadalla

For information
University of Montreal Eloi Courchesne
Media contact

About the Sainte-Justine University Hospital Research Center
The Sainte-Justine University Hospital Research Center is a leading mother-child research institution affiliated with Université de Montréal. It brings together more than 200 researchers and 350 graduate and post-graduate students focused on finding innovative prevention means, faster and less invasive treatments, as well as personalized approaches to medicine. The Center is part of CHU Sainte-Justine, which is the largest mother-child center in Canada and second most important pediatric center in North America.
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Updated on 2/16/2015
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