additive genetic variation
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BMC Genomics ◽  
2021 ◽  
Vol 22 (1) ◽  
Author(s):  
Noah DeWitt ◽  
Mohammed Guedira ◽  
Edwin Lauer ◽  
J. Paul Murphy ◽  
David Marshall ◽  
...  

Abstract Background Genetic variation in growth over the course of the season is a major source of grain yield variation in wheat, and for this reason variants controlling heading date and plant height are among the best-characterized in wheat genetics. While the major variants for these traits have been cloned, the importance of these variants in contributing to genetic variation for plant growth over time is not fully understood. Here we develop a biparental population segregating for major variants for both plant height and flowering time to characterize the genetic architecture of the traits and identify additional novel QTL. Results We find that additive genetic variation for both traits is almost entirely associated with major and moderate-effect QTL, including four novel heading date QTL and four novel plant height QTL. FT2 and Vrn-A3 are proposed as candidate genes underlying QTL on chromosomes 3A and 7A, while Rht8 is mapped to chromosome 2D. These mapped QTL also underlie genetic variation in a longitudinal analysis of plant growth over time. The oligogenic architecture of these traits is further demonstrated by the superior trait prediction accuracy of QTL-based prediction models compared to polygenic genomic selection models. Conclusions In a population constructed from two modern wheat cultivars adapted to the southeast U.S., almost all additive genetic variation in plant growth traits is associated with known major variants or novel moderate-effect QTL. Major transgressive segregation was observed in this population despite the similar plant height and heading date characters of the parental lines. This segregation is being driven primarily by a small number of mapped QTL, instead of by many small-effect, undetected QTL. As most breeding populations in the southeast U.S. segregate for known QTL for these traits, genetic variation in plant height and heading date in these populations likely emerges from similar combinations of major and moderate effect QTL. We can make more accurate and cost-effective prediction models by targeted genotyping of key SNPs.


2020 ◽  
Author(s):  
Franziska S. Brunner ◽  
Alan Reynolds ◽  
Ian W. Wilson ◽  
Stephen Price ◽  
Steve Paterson ◽  
...  

ABSTRACTGenotype-by-environment interactions (G x E) underpin the evolution of plastic responses in natural populations. Theory assumes that G x E interactions exist but empirical evidence from natural populations is equivocal and difficult to interpret because G x E interactions are normally univariate plastic responses to a single environmental gradient. We compared multivariate plastic responses of 43 Daphnia magna clones from the same population in a factorial experiment that crossed temperature and food environments. Multivariate plastic responses explained more than 30% of the total phenotypic variation in each environment. G x E interactions were detected in most environment combinations irrespective of the methodology used. However, the nature of G x E interactions was context-dependent and led to environment-specific differences in additive genetic variation (G-matrices). Clones that deviated from the population average plastic response were not the same in each environmental context and there was no difference in whether clones varied in the nature (phenotypic integration) or magnitude of their plastic response in different environments. Plastic responses to food were aligned with additive genetic variation (gmax) at both temperatures, whereas plastic responses to temperature were not aligned with additive genetic variation (gmax) in either food environment. These results suggest that fundamental differences may exist in the potential for our population to evolve novel responses to food versus temperature changes, and challenges past interpretations of thermal adaptation based on univariate studies.


Forests ◽  
2020 ◽  
Vol 11 (12) ◽  
pp. 1356
Author(s):  
Judith S. Nantongo ◽  
Brad M. Potts ◽  
Hugh Fitzgerald ◽  
Jessica Newman ◽  
Stephen Elms ◽  
...  

Bark stripping by mammals is a major problem for conifer forestry worldwide. In Australia, bark stripping in the exotic plantations of Pinus radiata is mainly caused by native marsupials. As a sustainable management option, we explored the extent to which natural variation in the susceptibility of P. radiata is under genetic control and is thus amenable to genetic improvement. Bark stripping was assessed at ages four and five years in two sister trials comprising 101 and 138 open-pollinated half-sib families. A third younger trial comprising 74 full-sib control-pollinated families was assessed at two and three years after planting. Significant additive genetic variation in bark stripping was demonstrated in all trials, with narrow-sense heritability estimates between 0.06 and 0.14. Within sites, the amount of additive genetic variation detected increased with the level of bark stripping. When strongly expressed across the two sister trials, the genetic signal was stable (i.e., there was little genotype × environment interaction). No significant non-additive effect (specific combining ability effect) on bark stripping was detected in the full-sib family trial, where it was estimated that up to 22.1% reduction in bark stripping might be achieved by selecting 20% of the less susceptible families. Physical traits that were genetically correlated, and likely influenced the amount of bark removed from the trees by the marsupials, appeared to depend upon tree age. In the older trials, these traits included bark features (presence of rough bark, rough bark height, and bark thickness), whereas in the younger trial where rough bark was not developed, it was the presence of obstructive branches or needles on the stem. In the younger trial, a positive genetic correlation between prior height and bark stripping was detected, suggesting that initially faster growing trees exhibit more bark stripping than slower growing trees but later develop rough bark faster and became less susceptible. While the presence of unexplained genetic variation after accounting for these physical factors suggests that other explanatory plant traits may be involved, such as chemical traits, overall the results indicate that selection for reduced susceptibility is possible, with potential genetic gains for deployment and breeding.


Author(s):  
Addison Doudu ◽  
Serekye Yaw Annor ◽  
James Kwame Kagya-Agyemang ◽  
Godson Aryee Zagbede ◽  
Clement Gyeabour Kyere

This study on indigenous Guinea fowls in Ghana was undertaken to estimate genetic variation and heritability of traits in these birds. The study was conducted at the Poultry Section of the Animal farm of the Department of Animal Science Education, University of Education, Winneba, Mampong-Ashanti campus, Ghana, from 2015 to 2018. The data used in the present experiment were collected from six hundred keets (300 males and 300 females) produced from randomly selecting and mating 110 dams and 22 sires and consisted of 780 records collected over a period of 3 years. The genetic parameters were estimated using sire-son, sire-daughter and dam-daughter regression analysis.  Body weight and 8-month weight gain showed the greatest additive genetic variation, with survival, docility, dressing percentage, age at first egg, egg weight, egg number, fertility, hatchability traits, feed intake and FCR showing relatively low additive genetic variation.  Moderate to high heritability estimates were obtained for body weight, weight gain at ages 1day to 2 months, 2-4 months in females, 4-6 months in males, docility, feed intake in females and feed conversion ratio in both males and females. Similarly, moderate to high heritability estimates were also obtained for age at first egg, egg weight and egg numbers. However, all other parameters considered in this study had low heritability estimates. This study concludes that, the results could be used to initiate Guinea fowl selection breeding programmes.


2020 ◽  
Vol 10 (7) ◽  
pp. 2435-2443 ◽  
Author(s):  
Nicholas G. Karavolias ◽  
Anthony J. Greenberg ◽  
Luz S. Barrero ◽  
Lyza G. Maron ◽  
Yuxin Shi ◽  
...  

Quantitative traits are important targets of both natural and artificial selection. The genetic architecture of these traits and its change during the adaptive process is thus of fundamental interest. The fate of the additive effects of variants underlying a trait receives particular attention because they constitute the genetic variation component that is transferred from parents to offspring and thus governs the response to selection. While estimation of this component of phenotypic variation is challenging, the increasing availability of dense molecular markers puts it within reach. Inbred plant species offer an additional advantage because phenotypes of genetically identical individuals can be measured in replicate. This makes it possible to estimate marker effects separately from the contribution of the genetic background not captured by genotyped loci. We focused on root growth in domesticated rice, Oryza sativa, under normal and aluminum (Al) stress conditions, a trait under recent selection because it correlates with survival under drought. A dense single nucleotide polymorphism (SNP) map is available for all accessions studied. Taking advantage of this map and a set of Bayesian models, we assessed additive marker effects. While total genetic variation accounted for a large proportion of phenotypic variance, marker effects contributed little information, particularly in the Al-tolerant tropical japonica population of rice. We were unable to identify any loci associated with root growth in this population. Models estimating the aggregate effects of all measured genotypes likewise produced low estimates of marker heritability and were unable to predict total genetic values accurately. Our results support the long-standing conjecture that additive genetic variation is depleted in traits under selection. We further provide evidence that this depletion is due to the prevalence of low-frequency alleles that underlie the trait.


Genetics ◽  
2020 ◽  
Vol 215 (2) ◽  
pp. 343-357 ◽  
Author(s):  
David Steinsaltz ◽  
Andy Dahl ◽  
Kenneth W. Wachter

We consider the problem of interpreting negative maximum likelihood estimates of heritability that sometimes arise from popular statistical models of additive genetic variation. These may result from random noise acting on estimates of genuinely positive heritability, but we argue that they may also arise from misspecification of the standard additive mechanism that is supposed to justify the statistical procedure. Researchers should be open to the possibility that negative heritability estimates could reflect a real physical feature of the biological process from which the data were sampled.


2019 ◽  
Author(s):  
Natasha Tigreros ◽  
Anurag A. Agrawal ◽  
Jennifer S. Thaler

ABSTRACTDespite the ubiquity of parental effects and their potential impact on evolutionary dynamics, their contribution to the evolution of ecologically relevant adaptations remains poorly understood. Using quantitative genetics, here we demonstrate that parental effects contribute substantially to the evolutionary potential of larval antipredator responses in a leaf beetle (Leptinotarsa decemlineata). Previous research showed that larger L. decemlineata larvae elicit stronger antipredator responses, and mothers perceiving predators improved offspring responses by increasing intraclutch cannibalism –an extreme form of offspring provisioning. We now report substantial additive genetic variation underlying maternal ability to induce intraclutch cannibalism, indicating the potential of this adaptive maternal effect to evolve by natural selection. We also show that paternal size, a heritable trait, impacted larval responses to predation risk, but that larval responses themselves had little additive genetic variation. Together, these results demonstrate how larval responses to predation risk can evolve via two types of parental effects, both of which provide indirect sources of genetic variation for offspring traits.


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