Age-dependent genetic architecture across ontogeny of body size in sticklebacks

被引:4
作者
Fraimout, Antoine [1 ]
Li, Zitong [1 ,2 ]
Sillanpaeae, Mikko J. [3 ]
Merilae, Juha [1 ,4 ]
机构
[1] Univ Helsinki, Fac Biol & Environm Sci, Organismal & Evolutionary Biol Res Programme, Ecol Genet Res Unit, FI-00014 Helsinki, Finland
[2] CSIRO Agr & Food, GPO Box 1600, Canberra, ACT 2601, Australia
[3] Univ Oulu, Res Unit Math Sci, FI-90014 Oulu, Finland
[4] Univ Hong Kong, Sch Biol Sci, Area Ecol & Biodivers, Hong Kong, Peoples R China
基金
芬兰科学院;
关键词
QTL mapping; genetic architecture; genetic correlation; heritability; ontogeny; Pungitius; QUANTITATIVE TRAIT LOCI; PUNGITIUS-PUNGITIUS; NATURAL-SELECTION; REPEATED EVOLUTION; GROWTH; PARALLEL; PATTERNS; CONVERGENCE; DIVERGENCE; WILD;
D O I
10.1098/rspb.2022.0352
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Heritable variation in traits under natural selection is a prerequisite for evolutionary response. While it is recognized that trait heritability may vary spatially and temporally depending on which environmental conditions traits are expressed under, less is known about the possibility that genetic variance contributing to the expected selection response in a given trait may vary at different stages of ontogeny. Specifically, whether different loci underlie the expression of a trait throughout development and thus providing an additional source of variation for selection to act on in the wild, is unclear. Here we show that body size, an important life-history trait, is heritable throughout ontogeny in the nine-spined stickleback (Pungitius pungitius). Nevertheless, both analyses of quantitative trait loci and genetic correlations across ages show that different chromosomes/loci contribute to this heritability in different ontogenic time-points. This suggests that body size can respond to selection at different stages of ontogeny but that this response is determined by different loci at different points of development. Hence, our study provides important results regarding our understanding of the genetics of ontogeny and opens an interesting avenue of research for studying age-specific genetic architecture as a source of non-parallel evolution.
引用
收藏
页数:10
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