An estimate of the average number of recessive lethal mutations carried by humans - PubMed (original) (raw)

An estimate of the average number of recessive lethal mutations carried by humans

Ziyue Gao et al. Genetics. 2015 Apr.

Abstract

The effects of inbreeding on human health depend critically on the number and severity of recessive, deleterious mutations carried by individuals. In humans, existing estimates of these quantities are based on comparisons between consanguineous and nonconsanguineous couples, an approach that confounds socioeconomic and genetic effects of inbreeding. To overcome this limitation, we focused on a founder population that practices a communal lifestyle, for which there is almost complete Mendelian disease ascertainment and a known pedigree. Focusing on recessive lethal diseases and simulating allele transmissions, we estimated that each haploid set of human autosomes carries on average 0.29 (95% credible interval [0.10, 0.84]) recessive alleles that lead to complete sterility or death by reproductive age when homozygous. Comparison to existing estimates in humans suggests that a substantial fraction of the total burden imposed by recessive deleterious variants is due to single mutations that lead to sterility or death between birth and reproductive age. In turn, comparison to estimates from other eukaryotes points to a surprising constancy of the average number of recessive lethal mutations across organisms with markedly different genome sizes.

Keywords: autosomal recessive disease; consanguinity; human; inbreeding; recessive lethal mutation.

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Figures

Figure 1

The analysis pipeline for estimating the average number of recessive lethal mutations carried by humans. (A) A schematic diagram of the approach. The analysis procedures are described in black. Specific values and estimates for the Hutterites are provided in blue, including the point estimate of the mean number of mutations carried by a founder. (B) The posterior distribution of the mean number of recessive lethal mutations carried by each haploid human genome, given the probability of manifestation and the number of diseases observed.

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An estimate of the average number of recessive lethal mutations carried by humans - PubMed (original) (raw)