scholarly journals Combining Trait Physiology, Crop Modelling and Molecular Genetics to Improve Wheat Adaptation to Terminal Water-Stress Targeting Stay-Green and Root Traits

Proceedings ◽  
2020 ◽  
Vol 36 (1) ◽  
pp. 196
Author(s):  
Jack Christopher ◽  
Cecile Richard ◽  
Karine Chenu ◽  
Mandy Christopher ◽  
Valeria Paccapello ◽  
...  
Keyword(s):  
Root Length Density ◽  
Association Studies ◽  
Recombinant Inbred Lines ◽  
Physiological Adaptation ◽  
Future Climate Change ◽  
Genome Wide Association Studies ◽  
Genetic Progress ◽  
Deep Soil ◽  
Stay Green ◽  
Terminal Drought

Terminal drought stress is currently a major constraint in many wheat production regions. This is predicted to worsen with future climate change. The stay-green phenotype allows crops to remain green and photosynthesize for longer after anthesis, potentially improving yields in terminal drought environments. Root systems with greater root length density at depth can contribute by increasing access to deep soil moisture late in the season. To study the genetics of root and stay-green traits in wheat, a multi reference parent nested association mapping (NAM) population was developed. Using the “speed breeding” system of rapid generation advance, over 1500 recombinant inbred lines (RIL) were generated in approximately 18 months. Genome-wide association studies (GWAS) using a novel whole-genome NAM method (WG-NAM) identified genetic regions associated with the target traits. High-throughput techniques were developed and used for the NAM lines to (i) phenotype seedling roots in controlled conditions, and (ii) objectively characterize novel stay-green traits for hundreds of genotypes in standard yield plots in the field. NAM lines were phenotyped for yield and stay-green traits at multiple water-stressed and non-stressed environments during 4 seasons. Particular traits were associated with superior adaptation to certain environments. Many lines with adaptive root and stay-green traits exhibited superior yield to the reference parent in relevant target environments and 54 such lines have been provided to commercial Australian wheat breeders for cultivar development. This combination of technologies is increasing understanding of physiological adaptation to water-limited environments in wheat and helping accelerate genetic progress.

scholarly journals Genomic Analysis, Progress and Future Perspectives in Dairy Cattle Selection: A Review

Animals ◽  
2021 ◽  
Vol 11 (3) ◽  
pp. 599
Author(s):  
Miguel A. Gutierrez-Reinoso ◽  
Pedro M. Aponte ◽  
Manuel Garcia-Herreros
Keyword(s):  
Dairy Cattle ◽  
Production Efficiency ◽  
Association Studies ◽  
Phenotypic Traits ◽  
Progeny Testing ◽  
Genome Wide Association Studies ◽  
Genetic Progress ◽  
Breeding Programs ◽  
Increased Risk ◽  
Selection Of

Genomics comprises a set of current and valuable technologies implemented as selection tools in dairy cattle commercial breeding programs. The intensive progeny testing for production and reproductive traits based on genomic breeding values (GEBVs) has been crucial to increasing dairy cattle productivity. The knowledge of key genes and haplotypes, including their regulation mechanisms, as markers for productivity traits, may improve the strategies on the present and future for dairy cattle selection. Genome-wide association studies (GWAS) such as quantitative trait loci (QTL), single nucleotide polymorphisms (SNPs), or single-step genomic best linear unbiased prediction (ssGBLUP) methods have already been included in global dairy programs for the estimation of marker-assisted selection-derived effects. The increase in genetic progress based on genomic predicting accuracy has also contributed to the understanding of genetic effects in dairy cattle offspring. However, the crossing within inbred-lines critically increased homozygosis with accumulated negative effects of inbreeding like a decline in reproductive performance. Thus, inaccurate-biased estimations based on empirical-conventional models of dairy production systems face an increased risk of providing suboptimal results derived from errors in the selection of candidates of high genetic merit-based just on low-heritability phenotypic traits. This extends the generation intervals and increases costs due to the significant reduction of genetic gains. The remarkable progress of genomic prediction increases the accurate selection of superior candidates. The scope of the present review is to summarize and discuss the advances and challenges of genomic tools for dairy cattle selection for optimizing breeding programs and controlling negative inbreeding depression effects on productivity and consequently, achieving economic-effective advances in food production efficiency. Particular attention is given to the potential genomic selection-derived results to facilitate precision management on modern dairy farms, including an overview of novel genome editing methodologies as perspectives toward the future.

scholarly journals Adaptive Traits to Improve Durum Wheat Yield in Drought and Crown Rot Environments

2020 ◽  
Vol 21 (15) ◽  
pp. 5260 ◽  
Author(s):  
Samir Alahmad ◽  
Yichen Kang ◽  
Eric Dinglasan ◽  
Elisabetta Mazzucotelli ◽  
Kai P. Voss-Fels ◽  
...  
Keyword(s):  
Durum Wheat ◽  
Field Experiments ◽  
Triticum Turgidum ◽  
Association Studies ◽  
Wheat Yield ◽  
Crown Rot ◽  
Physiological Traits ◽  
Yield Potential ◽  
Genome Wide Association Studies ◽  
Stay Green

Durum wheat (Triticum turgidum L. ssp. durum) production can experience significant yield losses due to crown rot (CR) disease. Losses are usually exacerbated when disease infection coincides with terminal drought. Durum wheat is very susceptible to CR, and resistant germplasm is not currently available in elite breeding pools. We hypothesize that deploying physiological traits for drought adaptation, such as optimal root system architecture to reduce water stress, might minimize losses due to CR infection. This study evaluated a subset of lines from a nested association mapping population for stay-green traits, CR incidence and yield in field experiments as well as root traits under controlled conditions. Weekly measurements of normalized difference vegetative index (NDVI) in the field were used to model canopy senescence and to determine stay-green traits for each genotype. Genome-wide association studies using DArTseq molecular markers identified quantitative trait loci (QTLs) on chromosome 6B (qCR-6B) associated with CR tolerance and stay-green. We explored the value of qCR-6B and a major QTL for root angle QTL qSRA-6A using yield datasets from six rainfed environments, including two environments with high CR disease pressure. In the absence of CR, the favorable allele for qSRA-6A provided an average yield advantage of 0.57 t·ha−1, whereas in the presence of CR, the combination of favorable alleles for both qSRA-6A and qCR-6B resulted in a yield advantage of 0.90 t·ha−1. Results of this study highlight the value of combining above- and belowground physiological traits to enhance yield potential. We anticipate that these insights will assist breeders to design improved durum varieties that mitigate production losses due to water deficit and CR.

scholarly journals QTL Mapping for Seedling and Adult Plant Resistance to Leaf and Stem Rusts in Pamyati Azieva × Paragon Mapping Population of Bread Wheat

Agronomy ◽  
2020 ◽  
Vol 10 (9) ◽  
pp. 1285 ◽  
Author(s):  
Yuliya Genievskaya ◽  
Saule Abugalieva ◽  
Aralbek Rsaliyev ◽  
Gulbahar Yskakova ◽  
Yerlan Turuspekov
Keyword(s):  
Association Studies ◽  
Recombinant Inbred Lines ◽  
Adult Plant ◽  
Growth Stages ◽  
Genome Wide Association Studies ◽  
Rust Diseases ◽  
Plant Growth Stages ◽  
Local Breeding ◽  
Disease Resistances ◽  
Grain Yield And Quality

Leaf rust (LR) and stem rust (SR) pose serious challenges to wheat production in Kazakhstan. In recent years, the susceptibility of local wheat cultivars has substantially decreased grain yield and quality. Therefore, local breeding projects must be adjusted toward the improvement of LR and SR disease resistances, including genetic approaches. In this study, a spring wheat segregating population of Pamyati Azieva (PA) × Paragon (Par), consisting of 98 recombinant inbred lines (RILs), was analyzed for the resistance to LR and SR at the seedling and adult plant-growth stages. In total, 24 quantitative trait loci (QTLs) for resistance to rust diseases at the seedling and adult plant stages were identified, including 11 QTLs for LR and 13 QTLs for SR resistances. Fourteen QTLs were in similar locations to QTLs and major genes detected in previous linkage mapping and genome-wide association studies. The remaining 10 QTLs are potentially new genetic factors for LR and SR resistance in wheat. Overall, the QTLs revealed in this study may play an important role in the improvement of wheat resistance to LR and SR per the marker-assisted selection approach.

scholarly journals Precision Mapping of a Maize MAGIC Population Identified a Candidate Gene for the Senescence-Associated Physiological Traits

2021 ◽  
Vol 12 ◽  
Author(s):  
Marlon Caicedo ◽  
Eduardo D. Munaiz ◽  
Rosa A. Malvar ◽  
José C. Jiménez ◽  
Bernardo Ordas
Keyword(s):  
Candidate Gene ◽  
Defense Mechanism ◽  
Agronomic Traits ◽  
Association Studies ◽  
Recombinant Inbred Lines ◽  
Sugar Transport ◽  
Genome Wide Association ◽  
Genome Wide Association Studies ◽  
Genome Wide ◽  
Important Trait

Senescence is an important trait in maize (Zea mais L.), a key crop that provides nutrition values and a renewable source of bioenergy worldwide. Genome-wide association studies (GWAS) can be used to identify causative genetic variants that influence the major physiological measures of senescence, which is used by plants as a defense mechanism against abiotic and biotic stresses affecting its performance. We measured four physiological and two agronomic traits that affect senescence. Six hundred seventy-two recombinant inbred lines (RILs) were evaluated in two consecutive years. Thirty-six candidate genes were identified by genome-wide association study (GWAS), and 11 of them were supported by additional evidence for involvement in senescence-related processes including proteolysis, sugar transport, and sink activity. We identified a candidate gene, Zm00001d043586, significantly associated with chlorophyll, and independently studied its transcription expression in an independent panel. Our results showed that Zm00001d043586 affects chlorophyl rate degradation, a key determinant of senescence, at late plant development stages. These results contribute to better understand the genetic relationship of the important trait senescence with physiology related parameters in maize and provide new putative molecular markers that can be used in marker assisted selection for line development.

scholarly journals Unstable inheritance of 45S rRNA genes in Arabidopsis thaliana

2016 ◽  
Author(s):  
Fernando A. Rabanal ◽  
Viktoria Nizhynska ◽  
Terezie Mandáková ◽  
Polina Yu. Novikova ◽  
Martin A. Lysak ◽  
...  
Keyword(s):  
Arabidopsis Thaliana ◽  
Copy Number ◽  
Association Studies ◽  
Recombinant Inbred Lines ◽  
Gene Copy Number ◽  
Rrna Genes ◽  
Gene Copy ◽  
Nucleolar Organizer Regions ◽  
Rrna Gene ◽  
Genome Wide Association Studies

AbstractThe considerable genome size variation in Arabidopsis thaliana has been shown largely to be due to copy number variation (CNV) in 45S ribosomal RNA (rRNA) genes. Surprisingly, attempts to map this variation by means of genome-wide association studies (GWAS) failed to identify either of the two likely sources, namely the nucleolar organizer regions (NORs). Instead, GWAS implicated a trans-acting locus, as if rRNA CNV was a phenotype rather than a genotype. To explain these results, we investigated the inheritance and stability of rRNA gene copy number using the variety of genetic resources available in A. thaliana — F2 crosses, recombinant inbred lines, the multiparent advanced generation inter-cross population, and mutation accumulation lines. Our results clearly show that rRNA gene CNV can be mapped to the NORs themselves, with both loci contributing equally to the variation. However, NOR size is unstably inherited, and dramatic copy number changes are visible already within tens of generations, which explains why it is not possible to map the NORs using GWAS. We did not find any evidence of trans-acting loci in crosses, which is also expected since changes due to such loci would take very many generations to manifest themselves. rRNA gene copy number is thus an interesting example of “missing heritability” — a trait that is heritable in pedigrees, but not in the general population.

scholarly journals Accurate, ultra-low coverage genome reconstruction and association studies in Hybrid Swarm mapping populations

2021 ◽  
Vol 11 (4) ◽  
Author(s):  
Cory A Weller ◽  
Susanne Tilk ◽  
Subhash Rajpurohit ◽  
Alan O Bergland
Keyword(s):  
Genetic Variation ◽  
Sequence Data ◽  
Association Studies ◽  
Recombinant Inbred Lines ◽  
Natural Populations ◽  
Inbred Lines ◽  
Genome Wide Association Studies ◽  
Hybrid Swarm ◽  
Genome Wide ◽  
Low Coverage

Abstract Genetic association studies seek to uncover the link between genotype and phenotype, and often utilize inbred reference panels as a replicable source of genetic variation. However, inbred reference panels can differ substantially from wild populations in their genotypic distribution, patterns of linkage-disequilibrium, and nucleotide diversity. As a result, associations discovered using inbred reference panels may not reflect the genetic basis of phenotypic variation in natural populations. To address this problem, we evaluated a mapping population design where dozens to hundreds of inbred lines are outbred for few generations, which we call the Hybrid Swarm. The Hybrid Swarm approach has likely remained underutilized relative to pre-sequenced inbred lines due to the costs of genome-wide genotyping. To reduce sequencing costs and make the Hybrid Swarm approach feasible, we developed a computational pipeline that reconstructs accurate whole genomes from ultra-low-coverage (0.05X) sequence data in Hybrid Swarm populations derived from ancestors with phased haplotypes. We evaluate reconstructions using genetic variation from the Drosophila Genetic Reference Panel as well as variation from neutral simulations. We compared the power and precision of Genome-Wide Association Studies using the Hybrid Swarm, inbred lines, recombinant inbred lines (RILs), and highly outbred populations across a range of allele frequencies, effect sizes, and genetic architectures. Our simulations show that these different mapping panels vary in their power and precision, largely depending on the architecture of the trait. The Hybrid Swam and RILs outperform inbred lines for quantitative traits, but not for monogenic ones. Taken together, our results demonstrate the feasibility of the Hybrid Swarm as a cost-effective method of fine-scale genetic mapping.

scholarly journals Genetic Dissection of Seedling Root System Architectural Traits in a Diverse Panel of Hexaploid Wheat through Multi-Locus Genome-Wide Association Mapping for Improving Drought Tolerance

2021 ◽  
Vol 22 (13) ◽  
pp. 7188
Author(s):  
T. Danakumara ◽  
Jyoti Kumari ◽  
Amit Kumar Singh ◽  
Subodh Kumar Sinha ◽  
Anjan Kumar Pradhan ◽  
...  
Keyword(s):  
Drought Tolerance ◽  
Root Length Density ◽  
Association Studies ◽  
Average Diameter ◽  
Genome Wide Association ◽  
Phenotypic Variance ◽  
Genome Wide Association Studies ◽  
Association Panel ◽  
Genome Wide ◽  
Genomic Regions

Cultivars with efficient root systems play a major role in enhancing resource use efficiency, particularly water absorption, and thus in drought tolerance. In this study, a diverse wheat association panel of 136 wheat accessions including mini core subset was genotyped using Axiom 35k Breeders’ Array to identify genomic regions associated with seedling stage root architecture and shoot traits using multi-locus genome-wide association studies (ML-GWAS). The association panel revealed a wide variation of 1.5- to 50- fold and were grouped into six clusters based on 15 traits. Six different ML-GWAS models revealed 456 significant quantitative trait nucleotides (QTNs) for various traits with phenotypic variance in the range of 0.12–38.60%. Of these, 87 QTNs were repeatedly detected by two or more models and were considered reliable genomic regions for the respective traits. Among these QTNs, eleven were associated with average diameter and nine each for second order lateral root number (SOLRN), root volume (RV) and root length density (RLD). A total of eleven genomic regions were pleiotropic and each controlled two or three traits. Some important candidate genes such as Formin homology 1, Ubiquitin-like domain superfamily and ATP-dependent 6-phosphofructokinase were identified from the associated genomic regions. The genomic regions/genes identified in this study could potentially be targeted for improving root traits and drought tolerance in wheat.

scholarly journals Quantitative and population genomics suggest a broad role of staygreen loci in the drought adaptation of sorghum

2021 ◽  
Author(s):  
Jacques M Faye ◽  
Eyanawa A Akata ◽  
Bassirou Sine ◽  
Cyril Diatta ◽  
Daniel Fonceka ◽  
...  
Keyword(s):  
Drought Tolerance ◽  
Yield Components ◽  
Population Genomics ◽  
Association Studies ◽  
Tolerance Index ◽  
Genome Wide Association Studies ◽  
Drought Adaptation ◽  
Stay Green ◽  
Broad Role

Drought is a major constraint on plant productivity globally. Sorghum (Sorghum bicolor) landraces have evolved in drought-prone regions, but the genetics of their adaptation is not yet understood. Loci underlying stay-green post-flowering drought tolerance (Stg), have been identified in a temperate breeding line, but their role in drought adaptation of tropical sorghum is to be elucidated. We phenotyped 590 diverse sorghum accessions from West Africa under field-based managed drought stress, pre-flowering (WS1) and post-flowering (WS2) over several years and conducted genome-wide association studies (GWAS). Broad-sense heritability for grain and biomass yield components was high (33-92%) across environments. There was a significant correlation between stress tolerance index (STI) for grain weight across WS1 and WS2. GWAS revealed that SbZfl1 and SbCN12, orthologs of maize flowering genes, likely underlie flowering time variation under these conditions. GWAS further identified associations (n = 134) for STI and drought effects on yield components, including 16 putative pleiotropic associations. Thirty of the associations colocalized with Stg1-4 loci and had large effects. Seven lead associations, including some within Stg1, overlapped with positive selection outliers. Our findings reveal natural genetic variation for drought tolerance-related traits, and suggest a broad role of Stg loci in drought adaptation of sorghum.

TLR1 and PRKAA1 Gene Polymorphisms in the Development of Atrophic Gastritis and Gastric Cancer

2018 ◽  
Vol 27 (4) ◽  
pp. 363-369 ◽  
Author(s):  
Gintare Dargiene ◽  
Greta Streleckiene ◽  
Jurgita Skieceviciene ◽  
Marcis Leja ◽  
Alexander Link ◽  
...  
Keyword(s):  
Gastric Cancer ◽  
Atrophic Gastritis ◽  
Genetic Polymorphisms ◽  
Association Studies ◽  
Control Group ◽  
Similar Distribution ◽  
Genome Wide Association Studies ◽  
Increased Risk ◽  
Infection Susceptibility ◽  
H Pylori

Background & Aims: Previous genome-wide association studies showed that genetic polymorphisms in toll-like receptor 1 (TLR1) and protein kinase AMP-activated alpha 1 catalytic subunit (PRKAA1) genes were associated with gastric cancer (GC) or increased Helicobacter pylori (H. pylori) infection susceptibility. The aim of this study was to evaluate the association between TLR1 and PRKAA1 genes polymorphisms and H.pylori infection, atrophic gastritis (AG) or GC in the European population.Methods: Single-nucleotide polymorphisms (SNPs) were analysed in 511 controls, 340 AG patients and 327 GC patients. TLR1 C>T (rs4833095) and PRKAA1 C>T (rs13361707) were genotyped by the real-time polymerase chain reaction. H. pylori status was determined by testing for anti-H. pylori IgG antibodies in the serum.Results: The study included 697 (59.2%) H. pylori positive and 481 (40.8%) H. pylori negative cases. We observed similar distribution of TLR1 and PRKAA1 alleles and genotypes in H. pylori positive and negative cases. TLR1 and PRKAA1 SNPs were not linked with the risk of AG. TC genotype of TLR1 gene was more prevalent in GC patients compared to the control group (29.7% and 22.3% respectively, p=0.002). Carriers of TC genotype had a higher risk of GC (aOR=1.89, 95% CI: 1.26–2.83, p=0.002). A similar association was observed in a dominant inheritance model for TLR1 gene SNP, where comparison of CC+TC vs. TT genotypes showed an increased risk of GC (aOR=1.86, 95% CI: 1.26–2.75, p=0.002). No association between genetic polymorphism in PRKAA1 gene and GC was observed.Conclusions: TLR1 rs4833095 SNP was associated with an increased risk of GC in a European population, while PRKAA1 rs13361707 genetic variant was not linked with GC. Both genetic polymorphisms were not associated with H. pylori infection susceptibility or the risk of AG.

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