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. 1998 Apr 14;95(8):4441-6.
doi: 10.1073/pnas.95.8.4441.

Investigation of the bottleneck leading to the domestication of maize

Affiliations

Investigation of the bottleneck leading to the domestication of maize

A Eyre-Walker et al. Proc Natl Acad Sci U S A. .

Abstract

Maize (Zea mays ssp. mays) is genetically diverse, yet it is also morphologically distinct from its wild relatives. These two observations are somewhat contradictory: the first observation is consistent with a large historical population size for maize, but the latter observation is consistent with strong, diversity-limiting selection during maize domestication. In this study, we sampled sequence diversity, coupled with simulations of the coalescent process, to study the dynamics of a population bottleneck during the domestication of maize. To do this, we determined the DNA sequence of a 1,400-bp region of the Adh1 locus from 19 individuals representing maize, its presumed progenitor (Z. mays ssp. parviglumis), and a more distant relative (Zea luxurians). The sequence data were used to guide coalescent simulations of population bottlenecks associated with domestication. Our study confirms high genetic diversity in maize-maize contains 75% of the variation found in its progenitor and is more diverse than its wild relative, Z. luxurians-but it also suggests that sequence diversity in maize can be explained by a bottleneck of short duration and very small size. For example, the breadth of genetic diversity in maize is consistent with a founding population of only 20 individuals when the domestication event is 10 generations in length.

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Figures

Figure 1
Figure 1
Schematic representation of the coalescent models used in simulation. See text for details.
Figure 2
Figure 2
The neighbor-joining reconstruction of Adh1 sequences. Bootstrap values greater than 50% are given above nodes. Abbreviations are given in Table 1.
Figure 3
Figure 3
Results of simulations based on model 1 and model 2. The right-hand y-axis of both graphs represents the population size N; N is calculated from θ assuming a mutation rate of 6.5 × 10−9 mutations per nucleotide site per year (29) over 997 nucleotide sites. For each graph, the top three lines represent estimates of θB based on different parameter values for d and θP. For ease of presentation, symbols are removed where lines overlap. The lowest plotted line represents estimates of lower 95% confidence of θB for θP = 24.3. This last line was nearly indistinguishable from lower 95% confidence intervals estimated with θP = 243 and θP = 2.43.

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