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虹鳟鱼的杂合性-适合度相关性:等位酶位点的影响还是关联超显性?

Heterozygosity-fitness correlations in rainbow trout: effects of allozyme loci or associative overdominance?

作者信息

Thelen G C, Allendorf F W

机构信息

Division of Biological Sciences, University of Montana, Missoula 59812, USA.

出版信息

Evolution. 2001 Jun;55(6):1180-7. doi: 10.1111/j.0014-3820.2001.tb00637.x.

Abstract

Previous studies with rainbow trout (Oncorhynchus mykiss) have shown that increased heterozygosity at allozyme loci is correlated with several phenotypic traits associated with fitness. We expected to find a similar effect of heterozygosity at other nuclear loci if these associations are due to loci in linkage disequilibrium with the allozyme loci (i.e., associative overdominance), rather than the allozymes themselves. We examined the association between multiple locus heterozygosity and condition factor at 10 allozyme and 10 microsatellite loci. Individuals that were more heterozygous at allozyme loci had significantly greater condition factor in two hatchery cohorts of rainbow trout (1996 P = 0.006; 1997 P < 0.001). In contrast, there was no evidence at microsatellite loci that increased heterozygosity was associated with greater condition factor. Our results suggest that the observed relationship between heterozygosity at allozyme loci and condition factor in rainbow trout appears to be due to the allozyme loci themselves, rather than associative overdominance. We cannot, however, rule out that differences in the mutation process between allozymes and microsatellites may be responsible for these observations. Regardless of the underlying mechanism, these results support the view that allozymes and microsatellites are differentially affected by natural selection.

摘要

先前对虹鳟(Oncorhynchus mykiss)的研究表明,等位酶位点杂合性的增加与几个与适应性相关的表型性状相关。如果这些关联是由于与等位酶位点处于连锁不平衡的位点(即关联超显性),而不是等位酶本身,我们预计在其他核位点也会发现类似的杂合性效应。我们研究了10个等位酶位点和10个微卫星位点的多位点杂合性与条件因子之间的关联。在虹鳟的两个孵化群体中,等位酶位点杂合性更高的个体具有显著更高的条件因子(1996年P = 0.006;1997年P < 0.001)。相比之下,在微卫星位点没有证据表明杂合性增加与更高的条件因子相关。我们的结果表明,虹鳟中等位酶位点杂合性与条件因子之间观察到的关系似乎是由于等位酶位点本身,而不是关联超显性。然而,我们不能排除等位酶和微卫星之间突变过程的差异可能是这些观察结果的原因。无论潜在机制如何,这些结果支持了等位酶和微卫星受到自然选择不同影响的观点。

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