Ancient DNA reveals reason for high MS and Alzheimer’s rates in Europe – ScienceBlog.com

Researchers have created the worlds largest ancient human gene bank by analysing the bones and teeth of almost 5,000 humans who lived across western Europe and Asia up to 34,000 years ago.

By sequencing ancient human DNA and comparing it to modern-day samples, the international team of experts mapped the historical spread of genes and diseases over time as populations migrated.

The astounding results have been revealed in four trailblazing papers published in the journal Nature and provide new biological understanding of debilitating disorders.

The study involved a large international team led byProfessor Eske Willerslevat the Universities of Cambridge and Copenhagen,Professor Thomas Wergeat the University of Copenhagen, andProfessor Rasmus Nielsenat University of California, Berkeley, with contributions from 175 researchers from around the globe. They found:

Future analysis is hoped to reveal more about the genetic markers of autism, ADHD, schizophrenia, bipolar disorder, and depression.

Northern Europe has the highest prevalence of multiple sclerosis in the world.

The new study foundthe genes that significantly increase a persons risk of developing multiple sclerosis (MS) were introduced into north-western Europe around 5,000 years ago by sheep and cattle herders migrating from the east.

By analysing the DNA of ancient human bones and teeth, found at documented locations across Eurasia, researchers traced the geographical spread of MS from its origins on the Pontic Steppe (a region spanning parts of what are now Ukraine, South-West Russia and the West Kazakhstan Region).

They found that the genetic variants associated with a risk of developing MS travelled with the Yamnaya people livestock herders who migrated over the Pontic Steppe into North-Western Europe.

These genetic variants provided a survival advantage to the Yamnaya people, most likely by protecting them from catching infections from their sheep and cattle. But they also increased the risk of developing MS.

It must have been a distinct advantage for the Yamnaya people to carry the MS risk genes, even after arriving in Europe, despite the fact that these genes undeniably increased their risk of developing MS. These results change our view of the causes of multiple sclerosis and have implications for the way it is treated.

Professor Eske Willerslev, jointly at the Universities of Cambridge and Copenhagen, Fellow of St Johns College, expert in analysis of ancient DNA and Director of the project.

The age of specimens ranges from the Mesolithic and Neolithic through the Bronze Age, Iron Age and Viking period into the Middle Ages. The oldest genome in the data set is from an individual who lived approximately 34,000years ago.

The findings provide an explanation for the North-South Gradient, in which there are around twice as many modern-day cases of MS in northern Europe than southern Europe, which has long been a mystery to researchers.

From a genetic perspective, the Yamnaya people are thought to be the ancestors of the present-day inhabitants of much of North-Western Europe. Their genetic influence on todays population of southern Europe is much weaker.

Previous studies have identified 233 genetic variants that increase the risk of developing MS. These variants, also affected by environmental and lifestyle factors, increase disease risk by around 30 percent. The new research found that this modern-day genetic risk profile for MS is also present in bones and teeth that are thousands of years old.

These results astounded us all. They provide a huge leap forward in our understanding of the evolution of MS and other autoimmune diseases. Showing how the lifestyles of our ancestors impacted modern disease risk just highlights how much we are the recipients of ancient immune systems in a modern world.

Dr William Barrie, postdoc in the University of Cambridges Department of Zoology and first author of the MS study.

Multiple sclerosis is a neurodegenerative disease in which the bodys immune system mistakenly attacks the insulation surrounding the nerve fibres of the brain and spinal cord. This causes symptom flares known as relapses as well as longer-term degeneration, known as progression.

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