An updated doubled haploid oat linkage map and QTL mapping of agronomic and grain quality traits from Canadian field trials

Genome ◽  
2012 ◽  
Vol 55 (4) ◽  
pp. 289-301 ◽  
Author(s):  
Pirjo Tanhuanpää ◽  
Outi Manninen ◽  
Aaron Beattie ◽  
Peter Eckstein ◽  
Graham Scoles ◽  
...  
Keyword(s):  
Linkage Map ◽  
Doubled Haploid ◽  
Avena Sativa ◽  
Dna Markers ◽  
Grain Quality ◽  
Field Trials ◽  
Diversity Array Technology ◽  
Linkage Groups ◽  
Array Technology ◽  
Reference Map

The first doubled haploid oat linkage map constructed at MTT Agrifood Research Finland was supplemented with additional microsatellites and Diversity Array Technology (DArT) markers to produce a map containing 1058 DNA markers and 34 linkage groups. The map was used to locate quantitative trait loci (QTLs) for 11 important breeding traits analyzed from Finnish and Canadian field trials. The new markers enabled most of the linkage groups to be anchored to the ‘Kanota’ × ‘Ogle’ oat ( Avena sativa L.) reference map and allowed comparison of the QTLs located in this study with those found previously. Two to 12 QTLs for each trait were discovered, of which several were expressed consistently across several environments.

QTLs for important breeding characteristics in the doubled haploid oat progeny

Genome ◽  
2010 ◽  
Vol 53 (6) ◽  
pp. 482-493 ◽  
Author(s):  
Pirjo Tanhuanpää ◽  
Outi Manninen ◽  
Elina Kiviharju
Keyword(s):  
Quantitative Trait Loci ◽  
Linkage Map ◽  
Doubled Haploid ◽  
Avena Sativa ◽  
Quantitative Trait ◽  
Oil Content ◽  
Mapping Population ◽  
Field Trials ◽  
Quality Traits ◽  
Leaf Blotch

A homozygous mapping population, consisting of doubled haploid (DH) oat ( Avena sativa L.) plants generated through anther culture of F1 plants from the cross between the Finnish cultivar ‘Aslak’ and the Swedish cultivar ‘Matilda’, was used to construct an oat linkage map. Ten agronomic and quality traits were analyzed in the DH plants from field trials in 2005 and 2006. Leaf blotch (caused by Pyrenophora avenae ) resistance was also evaluated in a greenhouse test with 2 different isolates. One to 8 quantitative trait loci (QTLs) were found to be associated with each trait studied. Some chromosomal regions affected more than 1 trait; for example, 4 regions affected both protein and oil content. This study gives valuable information to oat breeders concerning the inheritance of important traits, and it provides potential tools to assist breeding.

Mapping of quantitative trait loci underlying resistance to cassava anthracnose disease

2015 ◽  
Vol 154 (7) ◽  
pp. 1209-1217 ◽  
Author(s):  
A. BOONCHANAWIWAT ◽  
S. SRAPHET ◽  
S. WHANKAEW ◽  
O. BOONSENG ◽  
D. R. SMITH ◽  
...  
Keyword(s):  
Quantitative Trait Loci ◽  
Linkage Map ◽  
Dna Markers ◽  
Quantitative Trait ◽  
Genetic Linkage ◽  
Genetic Linkage Map ◽  
Gene Annotation ◽  
Linkage Groups ◽  
Anthracnose Disease ◽  
Trait Loci

SUMMARYCassava (Manihot esculenta Crantz) is an economically important root crop in Thailand, which is ranked the world's top cassava exporting country. Production of cassava can be hampered by several pathogens and pests. Cassava anthracnose disease (CAD) is an important disease caused by the fungus Colletotrichum gloeosporioides f. sp. manihotis. The pathogen causes severe stem damage resulting in yield reductions and lack of stem cuttings available for planting. Molecular studies of cassava response to CAD will provide useful information for cassava breeders to develop new varieties with resistance to the disease. The current study aimed to identify quantitative trait loci (QTL) and DNA markers associated with resistance to CAD. A total of 200 lines of two F1 mapping populations were generated by reciprocal crosses between the varieties Huabong60 and Hanatee. The F1 samples were genotyped based on simple sequence repeat (SSR) and expressed sequence tag-SSR markers and a genetic linkage map was constructed using the JoinMap®/version3·0 program. The results showed that the map consisted of 512 marker loci distributed on 24 linkage groups with a map length of 1771·9 centimorgan (cM) and a mean interval between markers of 5·7 cM. The genetic linkage map was integrated with phenotypic data for the response to CAD infection generated by a detached leaf assay test. A total of three QTL underlying the trait were identified on three linkage groups using the MapQTL®/version4·0 program. Those DNA markers linked to the QTL that showed high statistically significant values with the CAD resistance trait were identified for gene annotation analysis and 23 candidate resistance genes to CAD infection were identified.

scholarly journals Molecular Marker Development and High Throughput with Microarrays using Diversity Array Technology (DArT)

HortScience ◽  
2005 ◽  
Vol 40 (4) ◽  
pp. 1113D-1114
Author(s):  
Mikel R. Stevens ◽  
Shawn A. Chrisensen ◽  
Ammon B. Marshall ◽  
JoLynn J. Stevens ◽  
Peter Wenzl ◽  
...  
Keyword(s):  
Polymorphic Band ◽  
Marker Development ◽  
Polymorphic Markers ◽  
Microarray Technology ◽  
Diversity Array Technology ◽  
Linkage Groups ◽  
Large Numbers ◽  
Array Technology ◽  
Molecular Marker Development ◽  
Laboratory Time

Recently, a technology known as DArT (diversity array technology) has been developed to increase throughput in marker assisted selection (MAS). DArT utilizes microarray technology as a method to potentially compare thousands of molecular markers in one test to a single DNA sample. We used DArT on two sets of interspecific tomato [Solanum lycopersicum (Fla 7613) × S. pennellii (LA 716 or LA 2963)] segregating populations (BC, F2, and F1). We compared over 300 segregating plants to 3840 random tomato genomic fragments. After the 3840 markers were prepared, it took about 2 weeks of laboratory time to perform the experiments. With experience, this time can be reduced. We identified a total of 654 polymorphic markers usable for developing a DArT tomato genetic map. Depending on the particular cross, 13 to 17 linkage groups were identified (LOD 3) per population. Most recently, the amplified polymorphic DNA (AFLP) technique has been used for rapid genetic mapping of large numbers of anonymous genomic fragments. Besides the additional effort and reagents using AFLPs compared to DArT, a desired AFLP polymorphic band is often difficult to clone and process into a PCR based marker, whereas in DArT all markers are already cloned and immediately available for such experiments. A drawback to DArT is that it requires specialized software and equipment and is technically demanding. However, once the equipment and software are secured, techniques are optimized, and segregating populations developed, marker throughput is increased by orders of magnitude. Although challenging, the application of DArT can dramatically increase MAS throughput, thus facilitating quantitative trait and saturated mapping research.

Construction of an intraspecific integrated linkage map of pepper using molecular markers and doubled-haploid progenies

Genome ◽  
1995 ◽  
Vol 38 (1) ◽  
pp. 112-121 ◽  
Author(s):  
Véronique Lefebvre ◽  
Alain Palloix ◽  
Carole Caranta ◽  
Edmond Pochard
Keyword(s):  
Linkage Map ◽  
Capsicum Annuum ◽  
Doubled Haploid ◽  
Linkage Groups ◽  
Hypersensitive Resistance ◽  
Integrated Linkage Map ◽  
New Genes ◽  
Rflp Rapd ◽  
Pepper Genome ◽  
Genomic Regions

An integrated molecular linkage map of pepper (Capsicum annuum L.), including mainly RFLP and RAPD markers, has been constructed by alignment of three intraspecific linkage maps generated by segregating doubled-haploid progenies. A total of 85 markers covered approximately 820 cM in 14 linkage groups. Four linkage groups were assigned to 4 chromosomes. Two new genes of agronomic interest were located: L controlling hypersensitive resistance to TMV and up controlling the erect habit of the fruits. The C gene controlling the fruit pungency was more precisely located. This map is estimated to represent from 36 to 59% of the total pepper genome. An examination of segregation data has revealed several genomic regions with aberrant segregation ratios often favouring the agronomic big-fruited parents, particularly in crosses involving the exotic parent CM334, suggesting that these genome regions are subjected to selection during the process of doubled-haploid production. The suitability of doubled-haploid progenies for mapping projects and the differences observed between this intraspecific integrated map with earlier published interspecific pepper maps are discussed.Key words: Capsicum annuum, RFLP, RAPD, integrated linkage map, doubled-haploid progenies.

Genetic map of triticale compiling DArT, SSR, and AFLP markers

Genome ◽  
2011 ◽  
Vol 54 (5) ◽  
pp. 391-401 ◽  
Author(s):  
M. Tyrka ◽  
P.T. Bednarek ◽  
A. Kilian ◽  
M. Wędzony ◽  
T. Hura ◽  
...  
Keyword(s):  
Linkage Map ◽  
Genetic Map ◽  
Genetic Linkage Map ◽  
Fragment Length Polymorphism ◽  
Aflp Markers ◽  
Structural Rearrangements ◽  
Linkage Groups ◽  
Array Technology ◽  
Dh Lines ◽  
Simple Sequence

A set of 90 doubled haploid (DH) lines derived from F1plants that originated from a cross between × Triticosecale Wittm. ‘Saka3006’ and ×Triticosecale Wittm. ‘Modus’, via wide crossing with maize, were used to create a genetic linkage map of triticale. The map has 21 linkage groups assigned to the A, B, and R genomes including 155 simple sequence repeat (SSR), 1385 diversity array technology (DArT), and 28 amplified fragment length polymorphism (AFLP) markers covering 2397 cM with a mean distance between two markers of 4.1 cM. Comparative analysis with wheat consensus maps revealed that triticale chromosomes of the A and B genomes were represented by 15 chromosomes, including combinations of 2AS.2AL#, 2AL#2BL, 6AS.6AL#, and 2BS.6AL# instead of 2A, 2B, and 6A. In respect to published maps of rye, substantial rearrangements were found also for chromosomes 1R, 2R, and 3R of the rye genome. Chromosomes 1R and 2R were truncated and the latter was linked with 3R. A nonhomogeneous distribution of markers across the triticale genome was observed with evident bias (48%) towards the rye genome. This genetic map may serve as a reference linkage map of triticale for efficient studies of structural rearrangements, gene mapping, and marker-assisted selection.

Construction of a linkage map of the Rennell Island Tall coconut type (Cocos nucifera L.) and QTL analysis for yield characters

Genome ◽  
2001 ◽  
Vol 44 (6) ◽  
pp. 962-970 ◽  
Author(s):  
P Lebrun ◽  
L Baudouin ◽  
R Bourdeix ◽  
J Louis Konan ◽  
J HA Barker ◽  
...  
Keyword(s):  
Linkage Map ◽  
Qtl Analysis ◽  
Dna Markers ◽  
Marker Assisted Selection ◽  
Ssr Marker ◽  
Cocos Nucifera ◽  
Genome Length ◽  
Linkage Groups ◽  
Consecutive Sampling ◽  
Cocos Nucifera L

AFLP and SSR DNA markers were used to construct a linkage map in the coconut (Cocos nucifera L.; 2n = 32) type Rennell Island Tall (RIT). A total of 227 markers were arranged into 16 linkage groups. The total genome length corresponded to 1971 cM for the RIT map, with 5–23 markers per linkage group. QTL analysis for yield characters in two consecutive sampling periods identified nine loci. Three and two QTLs were detected for number of bunches and one and three QTLs for number of nuts. The correlation of trait values between characters and evaluation periods is partially reflected in identical QTLs. The QTLs represent characters that are important in coconut breeding. The cosegregation of markers with these QTLs provides an opportunity for marker-assisted selection in coconut breeding programmes.Key words: coconut, QTL, AFLP, SSR, marker-assisted selection (MAS).

Development of an AFLP-based linkage map and localization of QTLs for seed fatty acid content in condiment mustard (Brassica juncea)

Genome ◽  
2002 ◽  
Vol 45 (6) ◽  
pp. 1203-1215 ◽  
Author(s):  
E Lionneton ◽  
S Ravera ◽  
L Sanchez ◽  
G Aubert ◽  
R Delourme ◽  
...  
Keyword(s):  
Fatty Acids ◽  
Linkage Map ◽  
Brassica Juncea ◽  
Doubled Haploid ◽  
Genetic Linkage ◽  
Genetic Linkage Map ◽  
Major Gene ◽  
Fatty Acid Content ◽  
Eicosenoic Acid ◽  
Linkage Groups

A genetic linkage map of Brassica juncea based on AFLP and RAPD markers was constructed using 131 F1-derived doubled-haploid (DH) plants from a cross between two mustard lines. The map included 273 markers (264 AFLP, 9 RAPD) arranged on 18 linkage groups, and covered a total genetic distance of 1641 cM; 18.3% of the AFLP markers showed a segregation distortion (P < 0.01). The markers with biased segregation were clustered on seven linkage groups. QTLs for oil contents, palmitic acid (16:0), stearic acid (18:0), oleic acid (18:1), linoleic acid (18:2), linolenic acid (18:3), eicosenoic acid (20:1), and erucic acid (22:1), were mapped on the AFLP linkage map. Correlation studies among fatty acids in the DH population and the localization of QTLs involved in their control indicated that a major gene located on linkage group (LG) 2 controlled the elongation step of erucic acid.Key words: Brassica juncea, doubled haploid, AFLP genetic linkage map, fatty acids, QTL.

scholarly journals Diversity Array Technology Markers: Genetic Diversity Analyses and Linkage Map Construction in Rapeseed (Brassica napus L.)

DNA Research ◽  
2011 ◽  
Vol 19 (1) ◽  
pp. 51-65 ◽  
Author(s):  
H. Raman ◽  
R. Raman ◽  
M. N. Nelson ◽  
M. N. Aslam ◽  
R. Rajasekaran ◽  
...  
Keyword(s):  
Genetic Diversity ◽  
Brassica Napus ◽  
Linkage Map ◽  
Diversity Array Technology ◽  
Brassica Napus L ◽  
Map Construction ◽  
Array Technology

scholarly journals Secondary Trisomics and Telotrisomics of Rice: Origin, Characterization, and Use in Determining the Orientation of Chromosome Map

Genetics ◽  
1996 ◽  
Vol 143 (1) ◽  
pp. 517-529
Author(s):  
Kuldeep Singh ◽  
D S Multani ◽  
Gurdev S Khush
Keyword(s):  
Linkage Map ◽  
Large Population ◽  
Marker Genes ◽  
Linkage Groups ◽  
Breeding Behavior ◽  
Specific Chromosome ◽  
Chromosome Map ◽  
Primary Trisomics ◽  
Correct Orientation ◽  
Genetic Segregation

Abstract Secondary trisomics and telotrisomics representing the 12 chromosomes of rice were isolated from the progenies of primary trisomics. A large population of each primary trisomic was grown. Plants showing variation in gross morphology compared to the primary trisomics and disomic sibs were selected and analyzed cytologically at diakinesis and pachytene. Secondary trisomics for both arms of chromosomes 1, 2, 6, 7 and 11 and for one arm of chromosomes 4, 5, 8, 9 and 12 were identified. Telotrisomics for short arm of chromosomes 1, 8, 9 and 10 and for long arms of chromosomes 2, 3 and 5 were isolated. These secondary and telotrisomics were characterized morphologically and for breeding behavior. Secondary trisomics 2n + 1S · 1S, 2n + 1L · 1L, 2n + 2S · 2S, 2n + 2L · 2L, 2n + 6S · 6S, 2n + 6L · 6L and 2n + 7L · 7L are highly sterile, and 2n + 1L · 1L, 2n + 2L · 2L and 2n + 7L · 7L do not set any seed even upon backcrossing. Telotrisomics are fertile and vigorous. Genetic segregation of 43 marker genes was studied in the F2 or backcross progenies. On the basis of segregation data, these genes were delimited to specific chromosome arms. Correct orientation of 10 linkage groups was determined and centromere positions on nine linkage groups were approximated. A revised linkage map of rice is presented.

scholarly journals QTL analysis of seed germination traits in tobacco (Nicotiana tabacum L.)

2021 ◽  
Author(s):  
Monika Agacka-Mołdoch ◽  
Mian Abdur Rehman Arif ◽  
Ulrike Lohwasser ◽  
Teresa Doroszewska ◽  
Ramsey S. Lewis ◽  
...  
Keyword(s):  
Nicotiana Tabacum ◽  
Seed Germination ◽  
Doubled Haploid ◽  
Mapping Population ◽  
Area Under The Curve ◽  
Linkage Groups ◽  
Polygenic Control ◽  
Nicotiana Tabacum L ◽  
Controlled Deterioration ◽  
Germination Traits

AbstractGenetic mapping of seed germination traits has been performed with many plant species. In tobacco, however, investigations are rare. In the present study, a bi-parental mapping population consisting of 118 doubled haploid lines and derived from a cross between ‘Beinhart-1000’ and ‘Hicks’ was investigated. Four germination-related traits, total germination (TG), normal germination (NG), time to reach 50% of total germination (T50), and the area under the curve after 200 h of germination (AUC) were considered by examining seeds either untreated or after a moderate controlled deterioration (CD). Quantitative trait loci were found for all traits distributed on 11 out of the 24 linkage groups. It was demonstrated that, as in many other species, germination-related traits are very complex and under polygenic control.

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