scholarly journals Generation Mean Analysis using Six Parameters Genetic Model for Quantitative Traits in Cowpea [(Vigna unguiculata (L.) Walp.]

Author(s):  
Pal lavi ◽  
Alankar Singh ◽  
Sumit Chaudhary
Author(s):  
Anand Singh ◽  
Y. V. Singh ◽  
Asheesh Sharma ◽  
Amit Visen ◽  
Mithilesh Kumar Singh ◽  
...  

Generation Mean Analysis was carried out using six basic generations in 3 different crosses of cowpea to determine suitable breeding methods. For most of the studied traits, additive, dominance, additive x additive, additive x dominance and dominance x dominance effects were significant. Additive effect significantly contributed for days to 1st flowering and seed yield per plant. Dominance effect was significant for the incidence of cowpea mosaic virus in family 1, while for pod maturity in family 2. Additive x dominance type of interaction contributed significantly for days to 1st flowering, days to pod maturity and seed yield per hectare. Duplicate type of epistasis was observed for days to 1st flowering and incidence of cowpea mosaic virus in family 1, number of pods per plant and pod length in family 2 and 3. The findings suggested that pureline, pedigree and recurrent selection could be followed in cowpea improvement.


2019 ◽  
Vol 97 (Supplement_3) ◽  
pp. 259-260
Author(s):  
Ashley Ling ◽  
Romdhane Rekaya

Abstract Gene editing (GE) is a form of genetic engineering in which DNA is removed, inserted or replaced. For simple monogenic traits, the technology has been successfully implemented to create heritable modifications in animals and plants. The benefits of these niche applications are undeniable. For quantitative traits the benefits of GE are hard to quantify mainly because these traits are not genetic enough (low to moderate heritability) and their genetic architecture is often complex. Because its impact on the gene pool through the introduction of heritable modifications, the potential gain from GE must be evaluated within reasonable production parameters and in comparison, with available tools used in animal selection. A simulation was performed to compare GE with genomic selection (GS) and QTN-assisted selection (QAS) under four experimental factors: 1) heritability (0.1 or 0.4), 2) number of QTN affecting the trait (1000 or 10000) and their effect distribution (Gamma or uniform); 3) Percentage of selected females (100% or 33%); and 4) fixed or variable number of edited QTNs. Three models GS (M1), GS and GE (M2), and GS and QAS (M3) were implemented and compared. When the QTN effects were sampled from a Gamma distribution, all females were selected, and non-segregating QTNs were replaced, M2 clearly outperformed M1 and M3, with superiority ranging from 19 to 61%. Under the same scenario, M3 was 7 to 23% superior to M1. As the complexity of the genetic model increased (10000 QTN; uniform distribution), only one third of the females were selected, and the number of edited QTNs was fixed, the superiority of M2 was significantly reduced. In fact, M2 was only slightly better than M3 (2 to 6%). In all cases, M2 and M3 were better than M1. These results indicate that under realistic scenarios, GE for complex traits might have only limited advantages.


Genetics ◽  
1995 ◽  
Vol 141 (4) ◽  
pp. 1633-1639 ◽  
Author(s):  
J Zhu

Abstract A genetic model with additive-dominance effects and genotype x environment interactions is presented for quantitative traits with time-dependent measures. The genetic model for phenotypic means at time t conditional on phenotypic means measured at previous time (t-1) is defined. Statistical methods are proposed for analyzing conditional genetic effects and conditional genetic variance components. Conditional variances can be estimated by minimum norm quadratic unbiased estimation (MINQUE) method. An adjusted unbiased prediction (AUP) procedure is suggested for predicting conditional genetic effects. A worked example from cotton fruiting data is given for comparison of unconditional and conditional genetic variances and additive effects.


2013 ◽  
Vol 280 (1769) ◽  
pp. 20131552 ◽  
Author(s):  
Etienne Rajon ◽  
Joshua B. Plotkin

In the classic view introduced by R. A. Fisher, a quantitative trait is encoded by many loci with small, additive effects. Recent advances in quantitative trait loci mapping have begun to elucidate the genetic architectures underlying vast numbers of phenotypes across diverse taxa, producing observations that sometimes contrast with Fisher's blueprint. Despite these considerable empirical efforts to map the genetic determinants of traits, it remains poorly understood how the genetic architecture of a trait should evolve, or how it depends on the selection pressures on the trait. Here, we develop a simple, population-genetic model for the evolution of genetic architectures. Our model predicts that traits under moderate selection should be encoded by many loci with highly variable effects, whereas traits under either weak or strong selection should be encoded by relatively few loci. We compare these theoretical predictions with qualitative trends in the genetics of human traits, and with systematic data on the genetics of gene expression levels in yeast. Our analysis provides an evolutionary explanation for broad empirical patterns in the genetic basis for traits, and it introduces a single framework that unifies the diversity of observed genetic architectures, ranging from Mendelian to Fisherian.


1999 ◽  
Vol 74 (3) ◽  
pp. 271-277 ◽  
Author(s):  
DAHLIA M. NIELSEN ◽  
B. S. WEIR

We examine the relationships between a genetic marker and a locus affecting a quantitative trait by decomposing the genetic effects of the marker locus into additive and dominance effects under a classical genetic model. We discuss the structure of the associations between the marker and the trait locus, paying attention to non-random union of gametes, multiple alleles at the marker and trait loci, and non-additivity of allelic effects at the trait locus. We consider that this greater-than-usual level of generality leads to additional insights, in a way reminiscent of Cockerham's decomposition of genetic variance into five terms: three terms in addition to the usual additive and dominance terms. Using our framework, we examine several common tests of association between a marker and a trait.


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