scholarly journals A Consensus Genetic Map and Linkage Panel for Fresh-market Tomato

2022 ◽  
Vol 147 (1) ◽  
pp. 53-61
Author(s):  
Prashant Bhandari ◽  
Reza Shekasteband ◽  
Tong Geon Lee
Keyword(s):  
Genetic Map ◽  
Genetic Recombination ◽  
The United States ◽  
Snp Markers ◽  
Chromosome 2 ◽  
Consensus Map ◽  
Fresh Market ◽  
Recombination Rates ◽  
Breeding Programs ◽  
Genomic Association

The first consensus genetic map in fresh-market tomato (Solanum lycopersicum) was constructed, combining genetic recombination data from two biparental F2 segregating populations derived from four different fresh-market tomatoes. Each F2 population was nominated by different academic tomato breeding programs located in major fresh-market tomato-producing areas of the United States, and chromosome-wide variation in recombination rates was observed between tomato populations based on the origin of their breeding programs. A consensus map constructed using 335 common single nucleotide polymorphism (SNP) sites found in both populations spanned 737.3 cM across 12 tomato chromosomes, with chromosome 2 containing more than 40% of the total SNPs and chromosomes 4, 5, 7, and 10 together representing less than 10% of the SNPs. There was a high degree of collinearity between the genetic and physical positions of those 335 SNP markers. The integration of 6553 SNP sites that were detected in either of the two populations with 335 common sites resulted in an extended consensus genetic map. The total length of the extended map was estimated to be 1997.9 cM, which was compatible with a previous estimate for large-fruited fresh-market tomato. A linkage panel for fresh-market tomato was also established using the combined dataset of the consensus map of 335 SNP loci and 73 SNP-genotyped core fresh-market tomatoes. An empirical genetic mapping study of the tomato brachytic trait using the linkage panel demonstrated the value of the consensus map and linkage panel for tomato research. The allelic information in the linkage panel will serve as a basis for SNP marker implementation, such as genotyping platforms and genomic association map, in tomato.

scholarly journals Meta-Analysis of Quantitative Traits Loci (QTL) Identified in Drought Response in Rice (Oryza sativa L.)

Plants ◽  
2021 ◽  
Vol 10 (4) ◽  
pp. 716
Author(s):  
Nurhanis Selamat ◽  
Kalaivani K. Nadarajah
Keyword(s):  
Drought Stress ◽  
Drought Tolerance ◽  
Qtl Analysis ◽  
Oryza Sativa L ◽  
Genetic Maps ◽  
Chromosome 1 ◽  
Chromosome 2 ◽  
Consensus Map ◽  
Breeding Programs ◽  
Stable Qtls

Rice is an important grain that is the staple food for most of the world’s population. Drought is one of the major stresses that negatively affects rice yield. The nature of drought tolerance in rice is complex as it is determined by various components and has low heritability. Therefore, to ensure success in breeding programs for drought tolerant rice, QTLs (quantitative trait loci) of interest must be stable in a variety of plant genotypes and environments. This study identified stable QTLs in rice chromosomes in a variety of backgrounds and environments and conducted a meta-QTL analysis of stable QTLs that have been reported by previous research for use in breeding programs. A total of 653 QTLs for drought tolerance in rice from 27 genetic maps were recorded for analysis. The QTLs recorded were related to 13 traits in rice that respond to drought. Through the use of BioMercartor V4.2, a consensus map containing QTLs and molecular markers were generated using 27 genetic maps that were extracted from the previous 20 studies and meta-QTL analysis was conducted on the consensus map. A total of 70 MQTLs were identified and a total of 453 QTLs were mapped into the meta-QTL areas. Five meta-QTLs from chromosome 1 (MQTL 1.5 and MQTL 1.6), chromosome 2 (MQTL2.1 and MQTL 2.2) and chromosome 3 (MQTL 3.1) were selected for functional annotation as these regions have high number of QTLs and include many traits in rice that respond to drought. A number of genes in MQTL1.5 (268 genes), MQTL1.6 (640 genes), MQTL 2.1 (319 genes), MQTL 2.2 (19 genes) and MQTL 3.1 (787 genes) were annotated through Blast2GO. Few major proteins that respond to drought stress were identified in the meta-QTL areas which are Abscisic Acid-Insensitive Protein 5 (ABI5), the G-box binding factor 4 (GBF4), protein kinase PINOID (PID), histidine kinase 2 (AHK2), protein related to autophagy 18A (ATG18A), mitochondrial transcription termination factor (MTERF), aquaporin PIP 1-2, protein detoxification 48 (DTX48) and inositol-tetrakisphosphate 1-kinase 2 (ITPK2). These proteins are regulatory proteins involved in the regulation of signal transduction and gene expression that respond to drought stress. The meta-QTLs derived from this study and the genes that have been identified can be used effectively in molecular breeding and in genetic engineering for drought resistance/tolerance in rice.

scholarly journals Multi-Locus Genome-Wide Association Studies Reveal Fruit Quality Hotspots in Peach Genome

2021 ◽  
Vol 12 ◽  
Author(s):  
Cassia da Silva Linge ◽  
Lichun Cai ◽  
Wanfang Fu ◽  
John Clark ◽  
Margaret Worthington ◽  
...  
Keyword(s):  
Fruit Quality ◽  
The United States ◽  
Genome Wide Association ◽  
Genome Wide Association Studies ◽  
Quality Traits ◽  
Fresh Market ◽  
Breeding Programs ◽  
Genome Wide ◽  
Fruit Quality Traits ◽  
Peach Breeding

Peach is one of the most important fruit crops in the world, with the global annual production about 24.6 million tons. The United States is the fourth-largest producer after China, Spain, and Italy. Peach consumption has decreased over the last decade, most likely due to inconsistent quality of the fruit on the market. Thus, marker-assisted selection for fruit quality traits is highly desired in fresh market peach breeding programs and one of the major goals of the RosBREED project. The ability to use DNA information to select for desirable traits would enable peach breeders to efficiently plan crosses and select seedlings with desired quality traits early in the selection process before fruiting. Therefore, we assembled a multi-locus genome wide association study (GWAS) of 620 individuals from three public fresh market peach breeding programs (Arkansas, Texas, and South Carolina). The material was genotyped using 9K SNP array and the traits were phenotyped for three phenological (bloom date, ripening date, and days after bloom) and 11 fruit quality-related traits (blush, fruit diameter, fruit weight, adherence, fruit firmness, redness around pit, fruit texture, pit weight, soluble solid concentration, titratable acidity, and pH) over three seasons (2010, 2011, and 2012). Multi-locus association analyses, carried out using mrMLM 4.0 and FarmCPU R packages, revealed a total of 967 and 180 quantitative trait nucleotides (QTNs), respectively. Among the 88 consistently reliable QTNs detected using multiple multi-locus GWAS methods and/or at least two seasons, 44 were detected for the first time. Fruit quality hotspots were identified on chromosomes 1, 3, 4, 5, 6, and 8. Out of 566 candidate genes detected in the genomic regions harboring the QTN clusters, 435 were functionally annotated. Gene enrichment analyses revealed 68 different gene ontology (GO) terms associated with fruit quality traits. Data reported here advance our understanding of genetic mechanisms underlying important fruit quality traits and further support the development of DNA tools for breeding.

scholarly journals A Genetic Map and Linkage Panel for the Large-fruited Fresh-market Tomato

2021 ◽  
pp. 1-7
Author(s):  
Prashant Bhandari ◽  
Tong Geon Lee
Keyword(s):  
Genetic Map ◽  
Recombination Frequency ◽  
Average Distance ◽  
Genetic Research ◽  
Snp Markers ◽  
Genetic Maps ◽  
Nucleotide Polymorphism ◽  
Fresh Market ◽  
Crop Breeding ◽  
Single Nucleotide

Genetic maps saturated with genetic markers are useful for genetic research and crop breeding; however, the genetic map for the large-fruited fresh-market tomato (Solanum lycopersicum) has never been constructed, and the recombination frequency between DNA fragments is only partly understood for fresh-market tomato. We constructed a novel fresh-market tomato genetic map by using 3614 single nucleotide polymorphism (SNP) markers and a 93 F2 segregating progeny derived from a cross between two United States large-fruited fresh-market tomato lines. The average distance between markers was less than 1 cM, and substantial recombination densities between markers were observed across the approximate centromere locations. A linkage panel for large-fruited fresh-market tomato was also established using the combined dataset of the genetic map and 58 SNP-genotyped core tomato lines. The allelic information in the linkage panel will be a significant resource for both tomato genetics and future breeding approaches.

scholarly journals VARIATION FOR GENETIC RECOMBINATION AMONG TOMATO PLANTS REGENERATED FROM THREE TISSUE CULTURE SYSTEMS

HortScience ◽  
1990 ◽  
Vol 25 (9) ◽  
pp. 1164e-1164 ◽  
Author(s):  
Michael E. Compton ◽  
Richard E. Veilleux
Keyword(s):  
Tissue Culture ◽  
Genetic Recombination ◽  
Shoot Tips ◽  
Chromosome 3 ◽  
Chromosome 2 ◽  
Recombination Rates ◽  
Culture Systems ◽  
Thin Cell Layers ◽  
Cell Layers ◽  
Map Distance

Genetic recombination rates of hybrid plants regenerated from three tissue culture. systems were compared by backcrossing regenerated plants with mutant parents and comparing the observed crossover frequencies with those expected based on control plants raised from seed. Increased recombination rates and map distances were observed among plants from micropropagated shoot tips (4.5%-5.9%), cotyledon calli (3.7%-8.5%), and thin cell layers (2.8%-6.5%) between the sunny (sy) and baby leaf syndrome (bls) markers which flank the centromere on chromosome 3. Conversely, a decrease in map distance was observed between bls and the solanifolia (sf) locus which is more distal to the centromere on the same arm of chromosome 3 as bls. Increased map distance among plants regenerated from micropropagated shoot tips, cotyledon calli, and thin cell layers was also observed between white virescence (wv) and anthocyanin reduced (are) loci on chromosome 2.

scholarly journals Genetic Diversity and Population Structure Analysis of the USDA Olive Germplasm Using Genotyping-By-Sequencing (GBS)

Genes ◽  
2021 ◽  
Vol 12 (12) ◽  
pp. 2007
Author(s):  
A. S. M. Faridul Islam ◽  
Dean Sanders ◽  
Amit Kumar Mishra ◽  
Vijay Joshi
Keyword(s):  
Genetic Diversity ◽  
Population Structure ◽  
Structure Analysis ◽  
Genotyping By Sequencing ◽  
The United States ◽  
Snp Markers ◽  
Breeding Programs ◽  
The Us ◽  
The Mediterranean ◽  
Olive Breeding

Olives are one of the most important fruit and woody oil trees cultivated in many parts of the world. Olive oil is a critical component of the Mediterranean diet due to its importance in heart health. Olives are believed to have been brought to the United States from the Mediterranean countries in the 18th century. Despite the increase in demand and production areas, only a few selected olive varieties are grown in most traditional or new growing regions in the US. By understanding the genetic background, new sources of genetic diversity can be incorporated into the olive breeding programs to develop regionally adapted varieties for the US market. This study aimed to explore the genetic diversity and population structure of 90 olive accessions from the USDA repository along with six popular varieties using genotyping-by-sequencing (GBS)-generated SNP markers. After quality filtering, 54,075 SNP markers were retained for the genetic diversity analysis. The average gene diversity (GD) and polymorphic information content (PIC) values of the SNPs were 0.244 and 0.206, respectively, indicating a moderate genetic diversity for the US olive germplasm evaluated in this study. The structure analysis showed that the USDA collection was distributed across seven subpopulations; 63% of the accessions were grouped into an identifiable subpopulation. The phylogenetic and principal coordinate analysis (PCoA) showed that the subpopulations did not align with the geographical origins or climatic zones. An analysis of the molecular variance revealed that the major genetic variation sources were within populations. These findings provide critical information for future olive breeding programs to select genetically distant parents and facilitate future gene identification using genome-wide association studies (GWAS) or a marker-assisted selection (MAS) to develop varieties suited to production in the US.

Variation for genetic recombination among tomato plants regenerated from three tissue culture systems

Genome ◽  
1991 ◽  
Vol 34 (5) ◽  
pp. 810-817 ◽  
Author(s):  
Michael E. Compton ◽  
Richard E. Veilleux
Keyword(s):  
Tissue Culture ◽  
Genetic Recombination ◽  
Shoot Tips ◽  
Chromosome 3 ◽  
Chromosome 2 ◽  
Recombination Rates ◽  
Culture Systems ◽  
Hybrid Plants ◽  
Map Distance ◽  
Pedicel Explants

Shoot morphogenesis was compared among two tomato inbred lines, two mutant lines, and their eight reciprocal F1 hybrids in three tissue culture systems. The number of shoots per explant was greatest on tomato pedicel explants, intermediate on cotyledon calli, and poor on micropropagated shoot tips. Genetic recombination rates of F1 hybrid plants regenerated from three tissue culture systems were analyzed by backcrossing the regenerated plants with mutant parents and comparing the observed crossover frequencies with those expected based on control plants raised from seed. Increased recombination rates and map distance were observed among plants from micropropagated shoot tips (18.8%), cotyledon calli (17.3%), and pedicel explants (13.5%) between the markers sunny (sy) and baby leaf syndrome (bls), which flank the centromere on chromosome 3. Conversely, decreased recombination rates and map distance were observed between bls and the locus solanifolia (sf), which is more distal to the centromere on the same arm of chromosome 3 as bls. Increased recombination rates and map distance among plants from micropropagated shoot tips, cotyledon calli, and pedicel explants were also observed between the loci white virescence (wv) and anthocyanin reduced (are) on chromosome 2.Key words: genetic recombination, tomato, Lycopersicon esculentum, pedicel explants, micropropagation, callus culture, plant regeneration.

Sex-Specific Recombination Rates in Zebrafish (Danio rerio)

Genetics ◽  
2002 ◽  
Vol 160 (2) ◽  
pp. 649-657 ◽  
Author(s):  
Amy Singer ◽  
Hodel Perlman ◽  
YiLin Yan ◽  
Charlene Walker ◽  
Graham Corley-Smith ◽  
...  
Keyword(s):  
Genetic Map ◽  
Positional Cloning ◽  
Genetic Recombination ◽  
Physical Distance ◽  
Male Meiosis ◽  
Female Meiosis ◽  
Recombination Rates ◽  
Practical Applications ◽  
Mapping Panel ◽  
Haploid Embryos

Abstract In many organisms, the rate of genetic recombination is not uniform along the length of chromosomes or between sexes. To compare the relative recombination rates during meiosis in male and female zebrafish, we constructed a genetic map based on male meiosis. We developed a meiotic mapping panel of 94 androgenetic haploid embryos that were scored for genetic polymorphisms. The resulting male map was compared to female and sex-average maps. We found that the recombination rate in male meiosis is dramatically suppressed relative to that of female meiosis, especially near the centromere. These findings have practical applications for experimental design. The use of exclusively female meiosis in a positional cloning project maximizes the ratio of genetic map distance to physical distance. Alternatively, the use of exclusively male meiosis to localize a mutation initially to a linkage group or to maintain relationships of linked alleles minimizes recombination, thereby facilitating some types of analysis.

scholarly journals Heterogeneity in Rates of Recombination Across the Mouse Genome

Genetics ◽  
1996 ◽  
Vol 142 (2) ◽  
pp. 537-548 ◽  
Author(s):  
Michael W Nachman ◽  
Gary A Churchill
Keyword(s):  
Linkage Map ◽  
Genetic Map ◽  
Large Scale ◽  
Physical Map ◽  
Genetic Maps ◽  
Recombination Rates ◽  
Physical Maps ◽  
Genomic Patterns ◽  
Mary Lyon ◽  
Microsatellite Linkage

Abstract If loci are randomly distributed on a physical map, the density of markers on a genetic map will be inversely proportional to recombination rate. First proposed by MARY LYON, we have used this idea to estimate recombination rates from the Drosophila melanogaster linkage map. These results were compared with results of two other studies that estimated regional recombination rates in D. melanogaster using both physical and genetic maps. The three methods were largely concordant in identifying large-scale genomic patterns of recombination. The marker density method was then applied to the Mus musculus microsatellite linkage map. The distribution of microsatellites provided evidence for heterogeneity in recombination rates. Centromeric regions for several mouse chromosomes had significantly greater numbers of markers than expected, suggesting that recombination rates were lower in these regions. In contrast, most telomeric regions contained significantly fewer markers than expected. This indicates that recombination rates are elevated at the telomeres of many mouse chromosomes and is consistent with a comparison of the genetic and cytogenetic maps in these regions. The density of markers on a genetic map may provide a generally useful way to estimate regional recombination rates in species for which genetic, but not physical, maps are available.

scholarly journals Genetic diversity and population structure of ridge gourd (Luffa acutangula) accessions in a Thailand collection using SNP markers

2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Grimar Abdiel Perez ◽  
Pumipat Tongyoo ◽  
Julapark Chunwongse ◽  
Hans de Jong ◽  
Anucha Wongpraneekul ◽  
...  
Keyword(s):  
Genetic Diversity ◽  
Population Structure ◽  
Germplasm Collection ◽  
Snp Markers ◽  
Fixation Index ◽  
Breeding Programs ◽  
Total Fixation ◽  
Unrooted Phylogenetic Tree ◽  
Luffa Acutangula ◽  
Selection Of

AbstractThis study explored a germplasm collection consisting of 112 Luffa acutangula (ridge gourd) accessions, mainly from Thailand. A total of 2834 SNPs were used to establish population structure and underlying genetic diversity while exploring the fruit characteristics together with genetic information which would help in the selection of parental lines for a breeding program. The study found that the average polymorphism information content value of 0.288 which indicates a moderate genetic diversity for this L. acutangula germplasm. STRUCTURE analysis (ΔK at K = 6) allowed us to group the accessions into six subpopulations that corresponded well with the unrooted phylogenetic tree and principal coordinate analyses. When plotted, the STRUCTURE bars to the area of collection, we observed an admixed genotype from surrounding accessions and a geneflow confirmed by the value of FST = 0.137. AMOVA based on STRUCTURE clustering showed a low 12.83% variation between subpopulations that correspond well with the negative inbreeding coefficient value (FIS =  − 0.092) and low total fixation index (FIT = 0.057). There were distinguishing fruit shapes and length characteristics in specific accessions for each subpopulation. The genetic diversity and different fruit shapes in the L. acutangula germplasm could benefit the ridge gourd breeding programs to meet the demands and needs of consumers, farmers, and vegetable exporters such as increasing the yield of fruit by the fruit width but not by the fruit length to solve the problem of fruit breakage during exportation.

High Frequency Recombination During the Sexual Cycle of Dictyostelium discoideum

Genetics ◽  
1998 ◽  
Vol 148 (4) ◽  
pp. 1829-1832 ◽  
Author(s):  
David Francis
Keyword(s):  
Dictyostelium Discoideum ◽  
Genetic Map ◽  
High Frequency ◽  
Cell Biology ◽  
Physical Map ◽  
Genetic System ◽  
Sexual Cycle ◽  
Chromosome 2 ◽  
New Combinations ◽  
Restriction Sites

Abstract Analysis of Dictyostelium development and cell biology has suffered from the lack of an ordinary genetic system whereby genes can be arranged in new combinations. Genetic exchange between two long ignored strains, A2Cycr and WS205 is here reexamined. Alleles which differ in size or restriction sites between these two strains were found for seven genes. Six of these are in two clusters on chromosome 2. Frequencies of recombinant progeny indicate that the genetic map of the two mating strains is colinear with the physical map recently worked out for the standard nonsexual strain, NC4. The rate of recombination is high, about 0.1% per kilobase in three different regions of chromosome 2. This value is comparable to rates found in yeast, and will permit fine dissection of the genome.

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