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We Are All Mutants: Measurement Of Mutation Rate In Humans By Direct Sequencing

Date:
September 1, 2009
Source:
Wellcome Trust Sanger Institute
Summary:
Researchers have calculated a general rate of one mutation in each 15 to 30 million DNA letters in humans. Using next-generation sequencing, researchers sequenced part of the Y chromosome from two distant male-line relatives. Despite 13 generations of separation -- with a common male ancestor 200 years ago -- they found only four letters that differed. Mutation is the ultimate source of human genetic variation and has implications for both evolutionary and disease genetics.

Locations of the four confirmed mutations in the family. The two sequenced chromosomes are indicated by red highlights. Each mutation is shown by a lightning bolt of a different colour, and multiple lightning bolts of the same colour mean that the mutation could have occurred in any of these positions.
Credit: Image courtesy of Wellcome Trust Sanger Institute

An international team of 16 scientists today reports the first direct measurement of the general rate of genetic mutation at individual DNA letters in humans. The team sequenced the same piece of DNA - 10,000,000 or so letters or 'nucleotides' from the Y chromosome - from two men separated by 13 generations, and counted the number of differences. Among all these nucleotides, they found only four mutations.

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In 1935 one of the founders of modern genetics, J. B. S. Haldane, studied men in London with the blood disease haemophilia and estimated that there would be one in 50,000 incidence of mutations causing haemophilia in the gene affected - the equivalent of a mutation rate of perhaps one in 25 million nucleotides across the genome. Others have measured rates at a few further specific genes or compared DNA from humans and chimpanzees to produce general estimates of the mutation rate expressed more directly in nucleotides of DNA.

Remarkably, the new research, recently published in Current Biology, shows that these early estimates were spot on - in total, we all carry 100-200 new mutations in our DNA. This is equivalent to one mutation in each 15 to 30 million nucleotides. Fortunately, most of these are harmless and have no apparent effect on our health or appearance.

"The amount of data we generated would have been unimaginable just a few years ago," says Dr Yali Xue from the Wellcome Trust Sanger Institute and one of the project's leaders. "But finding this tiny number of mutations was more difficult than finding an ant's egg in the emperor's rice store."

Team member Qiuju Wang recruited a family from China who had lived in the same village for centuries. The team studied two distant male-line relatives - separated by thirteen generations - whose common ancestor lived two hundred years ago.

To establish the rate of mutation, the team examined an area of the Y chromosome. The Y chromosome is unique in that, apart from rare mutations, it is passed unchanged from father to son; so mutations accumulate slowly over the generations.

Despite many generations of separation, researchers found only 12 differences among all the DNA letters examined. The two Y chromosomes were still identical at 10,149,073 of the 10,149,085 letters examined. Of the 12 differences, eight had arisen in the cell lines used for the work. Only four were true mutations that had occurred naturally through the generations.

We have known for a long time that mutations occur occasionally in each of us, but have had to guess exactly how often. Now, thanks to advances in the technology for reading DNA, this new research has been possible.

Understanding mutation rates is key to many aspects of human evolution and medical research: mutation is the ultimate source of all our genetic variation and provides a molecular clock for measuring evolutionary timescales. Mutations can also lead directly to diseases like cancer. With better measurements of mutation rates, we could improve the calibration of the evolutionary clock, or test ways to reduce mutations, for example.

Even with the latest DNA sequencing technology, the researchers had to design a special strategy to search for the vanishingly rare mutations. They used next-generation sequencing to establish the order of letters on the two Y chromosomes and then compared these to the Y chromosome reference sequence.

Having identified 23 candidate SNPs - or single letter changes in the DNA - they amplified the regions containing these candidates and checked the sequences using the standard Sanger method. A total of four naturally occurring mutations were confirmed. Knowing this number of mutations, the length of the area that they had searched and the number of generations separating the individuals, the team were able to calculate the rate of mutation.

"These four mutations gave us the exact mutation rate - one in 30 million nucleotides each generation - that we had expected," says the study's coordinator, Chris Tyler-Smith, also from The Wellcome Trust Sanger Institute. "This was reassuring because the methods we used - harnessing next-generation sequencing technology - had not previously been tested for this kind of research. New mutations are responsible for an array of genetic diseases. The ability to reliably measure rates of DNA mutation means we can begin to ask how mutation rates vary between different regions of the genome and perhaps also between different individuals."

This work was supported by the Joint Project from the NSFC and The Royal Society, and the Wellcome Trust.


Story Source:

The above story is based on materials provided by Wellcome Trust Sanger Institute. Note: Materials may be edited for content and length.


Journal Reference:

  1. Xue Y et al. Human Y chromosome base substitution mutation rate measured by direct sequencing in a deep-rooting pedigree. Current Biology, (in press)

Cite This Page:

Wellcome Trust Sanger Institute. "We Are All Mutants: Measurement Of Mutation Rate In Humans By Direct Sequencing." ScienceDaily. ScienceDaily, 1 September 2009. <www.sciencedaily.com/releases/2009/08/090827123210.htm>.
Wellcome Trust Sanger Institute. (2009, September 1). We Are All Mutants: Measurement Of Mutation Rate In Humans By Direct Sequencing. ScienceDaily. Retrieved November 28, 2014 from www.sciencedaily.com/releases/2009/08/090827123210.htm
Wellcome Trust Sanger Institute. "We Are All Mutants: Measurement Of Mutation Rate In Humans By Direct Sequencing." ScienceDaily. www.sciencedaily.com/releases/2009/08/090827123210.htm (accessed November 28, 2014).

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