The relation between the genetic architecture of quantitative traits and long-term genetic response

2014 ◽  
Vol 55 (3) ◽  
pp. 373-381 ◽  
Author(s):  
Rostam Abdollahi-Arpanahi ◽  
Abbas Pakdel ◽  
Ardeshir Nejati-Javaremi ◽  
Mohammad Moradi Shahrbabak ◽  
Farhad Ghafouri-Kesbi
2010 ◽  
Vol 365 (1552) ◽  
pp. 2431-2438 ◽  
Author(s):  
Josephine M. Pemberton

Recent advances in the quantitative genetics of traits in wild animal populations have created new interest in whether natural selection, and genetic response to it, can be detected within long-term ecological studies. However, such studies have re-emphasized the fact that ecological heterogeneity can confound our ability to infer selection on genetic variation and detect a population's response to selection by conventional quantitative genetics approaches. Here, I highlight three manifestations of this issue: counter gradient variation, environmentally induced covariance between traits and the correlated effects of a fluctuating environment. These effects are symptomatic of the oversimplifications and strong assumptions of the breeder's equation when it is applied to natural populations. In addition, methods to assay genetic change in quantitative traits have overestimated the precision with which change can be measured. In the future, a more conservative approach to inferring quantitative genetic response to selection, or genomic approaches allowing the estimation of selection intensity and responses to selection at known quantitative trait loci, will provide a more precise view of evolution in ecological time.


2016 ◽  
Vol 283 (1835) ◽  
pp. 20160569 ◽  
Author(s):  
M. E. Goddard ◽  
K. E. Kemper ◽  
I. M. MacLeod ◽  
A. J. Chamberlain ◽  
B. J. Hayes

Complex or quantitative traits are important in medicine, agriculture and evolution, yet, until recently, few of the polymorphisms that cause variation in these traits were known. Genome-wide association studies (GWAS), based on the ability to assay thousands of single nucleotide polymorphisms (SNPs), have revolutionized our understanding of the genetics of complex traits. We advocate the analysis of GWAS data by a statistical method that fits all SNP effects simultaneously, assuming that these effects are drawn from a prior distribution. We illustrate how this method can be used to predict future phenotypes, to map and identify the causal mutations, and to study the genetic architecture of complex traits. The genetic architecture of complex traits is even more complex than previously thought: in almost every trait studied there are thousands of polymorphisms that explain genetic variation. Methods of predicting future phenotypes, collectively known as genomic selection or genomic prediction, have been widely adopted in livestock and crop breeding, leading to increased rates of genetic improvement.


Crop Science ◽  
2014 ◽  
Vol 54 (3) ◽  
pp. 939-943 ◽  
Author(s):  
Jill R. Recker ◽  
Joseph W. Burton ◽  
Andrea Cardinal ◽  
Lilian Miranda

2008 ◽  
Vol 24 (13) ◽  
pp. 1552-1553 ◽  
Author(s):  
S. Neuenschwander ◽  
F. Hospital ◽  
F. Guillaume ◽  
J. Goudet

2018 ◽  
Vol 14 (6) ◽  
pp. 20180186
Author(s):  
Jo S. Hermansen ◽  
Jostein Starrfelt ◽  
Kjetil L. Voje ◽  
Nils C. Stenseth

Intralocus sexual conflicts arise whenever the fitness optima for a trait expressed in both males and females differ between the sexes and shared genetic architecture constrains the sexes from evolving independently towards their respective optima. Such sexual conflicts are commonplace in nature, yet their long-term evolutionary consequences remain unexplored. Using a Bayesian phylogenetic comparative framework, we studied the macroevolutionary dynamics of intersexual trait integration in stalk-eyed flies (Diopsidae) spanning a time frame of more than 25 Myr. We report that increased intensity of sexual selection on male eyestalks is associated with reduced intersexual eyestalk integration, as well as sex-specific rates of eyestalk evolution. Despite this, lineages where males have been under strong sexual selection for millions of years still exhibit high levels of intersexual trait integration. This low level of decoupling between the sexes may indicate that exaggerated female eyestalks are in fact adaptive—or alternatively, that there are strong constraints on reducing trait integration between the sexes. Future work should seek to clarify the relative roles of constraints and selection in contributing to the varying levels of intersexual trait integration in stalk-eyed flies, and in this way clarify whether sexual conflicts can act as constraints on adaptive evolution even on macroevolutionary time scales.


Crop Science ◽  
2013 ◽  
Vol 53 (4) ◽  
pp. 1375-1383 ◽  
Author(s):  
Jill R. Recker ◽  
Joseph W. Burton ◽  
Andrea Cardinal ◽  
Lilian Miranda

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.


2014 ◽  
Vol 85 (5) ◽  
pp. 511-516 ◽  
Author(s):  
Motohide Nishio ◽  
Masahiro Satoh

2014 ◽  
Vol 74 (1) ◽  
pp. 93
Author(s):  
Rudrasen Singh Raikwar ◽  
A. K. Upadhyay ◽  
U. S. Gautam ◽  
V. K. Singh

1989 ◽  
Vol 49 (2) ◽  
pp. 163-169 ◽  
Author(s):  
G. Teepker ◽  
C. Smith

ABSTRACTRepeated cloning of bovine embryos by nuclear transfer, producing large clones of monozygous animals, may be possible in the future. Initially, clones could be tested and the best one selected and spread over the commercial population by embryo transfer. Further genetic improvement could be obtained by rebreeding a number of the best clones to produce a new set of clones. However, the testing and selection systems to pick the best clone (for short-term clonal response) and to pick clones with the best breeding values (for long-term genetic response) are different. The objective of this study was to derive a system which achieves both high clonal and high genetic responses. An adult MOET (multiple ovulation and embryo transfer) scheme with 40 breeding males and 40 breeding females per generation (cycle) was used to maintain adequate genetic variation for continued genetic response. For a fixed set of testing facilities and a given family structure initial clonal response is maximized by testing several members per clone. Long-term genetic response is usually greatest when testing one member per clone. Compromises to obtain both high clonal response and high genetic responses were from 95 to 100% efficient.


Sign in / Sign up

Export Citation Format

Share Document