French Canadians are genetically special (not that that’s a good thing)

By Razib Khan | September 30, 2013 2:40 am

Jack Kerouac, credit: Tom Palumbo

The Pith: Higher Mendelian disease rates among French Canadians may be due to their demographic history.

As I have noted before, demographic bottlenecks with extremely strong effects on the character of population genetic variation need to be very radical in their nature to be of any significance. The population pinhole has to be on the order of hundreds, rather than thousands, of individuals. But that does not preclude more modest bottlenecks generating subtle shifts in the genetic site frequency spectrum. Strong bottlenecks may be needed to drive wholesale extinction of once common alleles (or the fixation of those at moderate frequencies), but mild bottlenecks may nevertheless perturb the allele frequency distribution. In particular, the number of alleles which are present at very low frequencies can be strongly impacted by demographic variation and natural selection. This is the logical rationale which serves as the basis for nucleotide sequence based tests for detecting natural selection, such as Tajima’s D. An excess of low frequency variants suggest a bottleneck and subsequent population expansion, or positive and/or purifying selection. In contrast, balanced polymorphism frequencies point to a shrinking population or balancing selection.

Citation: Casals F, Hodgkinson A, Hussin J, Idaghdour Y, Bruat V, et al. (2013) Whole-Exome Sequencing Reveals a Rapid Change in the Frequency of Rare Functional Variants in a Founding Population of Humans. PLoS Genet 9(9): e1003815. doi:10.1371/journal.pgen.1003815

These basic ideas have been around for decades, but it is with powerful genomic technologies that they are truly giving us actionable insights. A new paper in PLOS Genetics lays it out simply enough, Whole-Exome Sequencing Reveals a Rapid Change in the Frequency of Rare Functional Variants in a Founding Population of Humans. To the left you see a site frequency distribution for French and French Canadian populations. What is clear is that for the derived allele (i.e., mutations from the ancestral state) distribution in exonic regions of the genome French Canadians are much more skewed toward the low frequency portion of the spectrum than French proper. This skew is more noticeable for deleterious mutations, such as nonsense and missense mutations (nonsense mutations usually produce nonfunctional protein, while missense mutations may alter the nature of the protein in some specific detail through amino acid substitution).

The focus here is on exons, ~1% of the genome, because these are the regions that are translated into the final protein product, and the authors seem particularly interested in the functional consequences of the site frequency spectrum of the French Canadians. This makes sense, because the French Canadian population has long been known to have a somewhat high burden of recessive diseases. Why? As noted in the paper the French Canadian ancestry derives overwhelmingly from a founding population of less than 10,000. Not only that, but this expanding population exhibits geographic substructure, with demographic expansion being particularly powerful along the edge of the pale of Quebecois settlement. This results in increased genetic drift on the edge, as a smaller portion of the population contributes to descendants pushing over the frontier. The key is to note how striking it is that a few hundred years of demographic separation can result in the emergence of ‘private alleles.’ To a great extent this is intuitively obvious, as private alleles emerge de novo in families, and many French Canadian families have had many of generations separated from the ancestral homeland to accumulate distinctive markers specific to their lineage.

Over the long term many “x” whole-genome coverage (so on average the same base can be found in 10 or 20 or 30 reads to reduce possible false positives) is going to be ubiquitous, and we’ll get a sense of the distribution of genetic load within and across families. One major demographic-historical dynamic highlighted in this paper is that serial bottleneck events in human history (e.g., the “Out of Africa” migration) may endow different populations with different site frequency spectra, and so imply diverse genetic disease loads. Seeing as how genomic work tends to be focused on populations of European descent we haven’t truly explored these sorts of inter-population possibilities in great depth, but they’re in the offing. I suspect for example that Indian subcastes will tend to have many private alleles due to bottlenecks and recent expansions. And, in the short-term this may also redound to the benefit of those who argue for the benefits of genetic diversity through random mating across populations.

Citation: Casals F, Hodgkinson A, Hussin J, Idaghdour Y, Bruat V, et al. (2013) Whole-Exome Sequencing Reveals a Rapid Change in the Frequency of Rare Functional Variants in a Founding Population of Humans. PLoS Genet 9(9): e1003815. doi:10.1371/journal.pgen.1003815

CATEGORIZED UNDER: Population Genetics
  • James

    In English please? Lol.. What does the gene do? I’m French Canadian and would like to know if this has any consequences or evolutionary rewards?

    • razibkhan

      more disease.

  • Dmitry Pruss

    The same level of excess of rare variation in comparison with the ancestral Europeans is seen in many other descendants of American Frontier settlers who came to the new World in time for the population expansion boom of roughly 1850-1950. From Texas to Minnesota, we repeatedly find evidence of rare deleterious mutations which emerged in immigrant farmers in those years.

    Bottlenecks are largely irrelevant for the recently emerged deleterious mutations not just in dominant traits which we study the most, but also in recessive traits which Razib seems to have in mind, simply because even combined per-locus prevalences of those recent mutations are relatively small. Bottlenecks make genetic diseases widespread precisely because they work on the opposite end of the frequency spectrum, elevating frequencies of some of the old alleles.

    BTW could you please qualify the statement equating “missense” with “deleterious”? Surely most missense variants aren’t deleterious, and some silent ones are. We should be talking not about equality but about elevated likelihood of deleteriousness, right?

  • Joe Q.

    So the interesting thing is that many Francophone Quebecois have Irish ancestry that dates from the mid-19th century (especially those from outside of Montreal). I wonder how that skews (or does not skew) the results.

    • Karl Zimmerman

      I’ve noticed that on 23andme I am a distant relative to a ton of French Canadians. They seem to all be related to me from my Father’s side. My father had no Quebecois ancestry. He was half German, with the remainder a mixture of Irish, English, and Sephardic. I presume that one of his Irish ancestors had a sibling who migrated to Quebec.

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This blog is about evolution, genetics, genomics and their interstices. Please beware that comments are aggressively moderated. Uncivil or churlish comments will likely get you banned immediately, so make any contribution count!

About Razib Khan

I have degrees in biology and biochemistry, a passion for genetics, history, and philosophy, and shrimp is my favorite food. In relation to nationality I'm a American Northwesterner, in politics I'm a reactionary, and as for religion I have none (I'm an atheist). If you want to know more, see the links at http://www.razib.com

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