RFLP linkage map and genome analysis of Saccharum spontaneum

Genome ◽  
1993 ◽  
Vol 36 (4) ◽  
pp. 782-791 ◽  
Author(s):  
Jorge A. G. da Silva ◽  
Mark E. Sorrells ◽  
William L Burnquist ◽  
Steven D. Tanksley
Keyword(s):  
Linkage Map ◽  
Genome Size ◽  
Genome Analysis ◽  
Dna Probes ◽  
Rflp Markers ◽  
Saccharum Spontaneum ◽  
Linkage Groups ◽  
Rflp Map ◽  
Dna Libraries ◽  
Rice Cdna

An RFLP linkage map of the wild sugarcane species Saccharum spontaneum L. (2n = 8x = 40–128) was constructed, comprising 216 loci, detected by 116 DNA probes, and distributed over 44 linkage groups. At a density of at least one marker every 25-cM interval, the coverage of the genome was estimated as 86%. For the generation of RFLP markers, probes were surveyed from seven DNA libraries: three sugarcane cDNA, one oat cDNA, one rice cDNA, and one barley cDNA, as well as one sugarcane genomic. Sixty-two maize genomic clones that were previously mapped on maize were used to initiate a comparative map between the sugarcane, sorghum, and maize genomes. Based on the RFLP segregation data, we conclude that this species is an autopolyploid, with an estimated genome size of 2107 cM.Key words: sugarcane, polyploid, RFLP, map, genome.

Combined AFLP and RFLP mapping in two hexaploid oat recombinant inbred populations

Genome ◽  
2000 ◽  
Vol 43 (1) ◽  
pp. 94-101 ◽  
Author(s):  
Hua Jin ◽  
Leslie L Domier ◽  
Xuejen Shen ◽  
Frederic L Kolb
Keyword(s):  
Linkage Map ◽  
Recombinant Inbred ◽  
Barley Yellow Dwarf Virus ◽  
Aflp Markers ◽  
Rflp Markers ◽  
Linkage Groups ◽  
Data Set ◽  
Rflp Map ◽  
Barley Yellow Dwarf ◽  
Yellow Dwarf Virus

A combined RFLP and AFLP map was constructed for hexaploid oat (Avena spp.). The segregation of AFLP markers was scored in two hexaploid oat recombinant inbred line (RIL) populations, the 'Kanota' × 'Ogle' RFLP population, and a population derived from 'Clintland64' and 'IL86-5698', barley yellow dwarf virus (BYDV)-sensitive and BYDV-tolerant lines, respectively. More than 300 AFLP markers were scored in each population, of which 97 could be scored in both populations. AFLP markers were linked to RFLP markers in 32 of 36 'Kanota' × 'Ogle' RFLP linkage groups. The addition of the AFLP markers to the 'Kanota' × 'Ogle' RFLP data set combined markers from four pairs of linkage groups and increased the size of the map from 1402 cM to 2351 cM. Thirty linkage groups were observed in the 'Clintland64' × 'IL86-5698' population, two of which could be consolidated by comparing the maps from both populations. The AFLP and RFLP markers showed very similar distributions in the 'Kanota' × 'Ogle' population with a tendency of each type of marker to cluster with markers of the same type. The placement of a set of AFLP markers on the 'Kanota' × 'Ogle' linkage map will enrich the RFLP map and allow others to relate AFLP markers for agronomically important genes to the reference 'Kanota' × 'Ogle' linkage map. Key words: amplified fragment length polymorphism, Avena, comparative mapping.

Construction of a sorghum RFLP linkage map using sorghum and maize DNA probes

Genome ◽  
1994 ◽  
Vol 37 (4) ◽  
pp. 590-594 ◽  
Author(s):  
R. A. Ragab ◽  
S. Dronavalli ◽  
M. A. Saghai Maroof ◽  
Y. G. Yu
Keyword(s):  
Linkage Map ◽  
Fragment Length Polymorphism ◽  
Genomic Library ◽  
Restriction Enzymes ◽  
Rflp Markers ◽  
Linkage Groups ◽  
Rflp Map ◽  
Hybridization Probes ◽  
Low Copy Number ◽  
Marker Distance

Previous reports on sorghum restriction fragment length polymorphism (RFLP) mapping have been limited to the use of heterologous maize clones. In this study, both sorghum and maize probes were used to construct an RFLP map based on an F2 population from a cross between sorghum lines BSC 35 and BTX 631. A set of single-or low-copy number clones from a sorghum genomic library was preselected to use as hybridization probes. Forty-nine of the 101 clones (49%) tested were polymorphic between the two parental lines. In comparison, 53 of the 135 maize probes (39%) detected polymorphism with the same restriction enzymes. In total, 71 RFLP markers (38 sorghum and 33 maize) were placed into 15 linkage groups spanning 633 cM with an average marker distance of 8.9 cM. Comparison of our linkage map with other published sorghum maps, based on maize probes, showed resemblance for several linkage groups, indicating that these maps can be integrated. Homologous sorghum probes are useful in improving the coverage and resolution of RFLP linkage map in sorghum.Key words: RFLP, Sorghum bicolor, chromosomes, Zea mays.

Two genetic linkage maps of mungbean using RFLP and RAPD markers

2000 ◽  
Vol 51 (4) ◽  
pp. 415 ◽  
Author(s):  
C. J. Lambrides ◽  
R. J. Lawn ◽  
I. D. Godwin ◽  
J. Manners ◽  
B. C. Imrie
Keyword(s):  
Linkage Map ◽  
Segregation Distortion ◽  
Recombinant Inbred ◽  
Genetic Linkage ◽  
Rapd Markers ◽  
Rflp Markers ◽  
Linkage Maps ◽  
Linkage Groups ◽  
Genetic Linkage Maps ◽  
Map Distance

Two genetic linkage maps of mungbean derived from the cross Berken ACC 41 are reported. The F2 map constructed from 67 individuals consisted of 110 markers (52 RFLP and 56 RAPD) that grouped into 12 linkage groups. The linked markers spanned a total map distance of 758.3 cM. A recombinant inbred (RI) population derived from the 67 F2 individuals was used for the generation of an additional linkage map. The RI map, composed entirely of RAPD markers, consisted of 115 markers in 12 linkage groups. The linked markers spanned a total map distance of 691.7 cM. Using a framework set of RFLP markers, the F2 map was compared with another F2 mungbean map constructed in Minnesota. In general, the order of these markers was consistent between maps. Segregation distortion was observed for some markers. 14.5% (16/110) of mapped F2 markers and 24% (28/115) of mapped RI markers segregated with distorted ratios. Segregation distortion occurred in each successive generation after the F2 . The regions of distortion identified in the Australian maps did not coincide with regions of the Minnesota map.

scholarly journals Generation of a Highly Saturated Linkage Map in Peach [Prunus persica (L.) Batsch] Using AFLP and RFLP Markers

HortScience ◽  
1996 ◽  
Vol 31 (4) ◽  
pp. 592b-592
Author(s):  
Bryon Sosinski ◽  
W.V. Baird ◽  
S. Rajapakse ◽  
R.E. Ballard ◽  
A.G. Abbott
Keyword(s):  
Linkage Map ◽  
Genetic Linkage Map ◽  
Prunus Persica ◽  
Quality Characteristics ◽  
Soluble Solids ◽  
Rflp Markers ◽  
Linkage Groups ◽  
Flesh Color ◽  
Peach Genome ◽  
The Cross

We have developed a highly saturated genetic linkage map in peach (diploid, 2n = 16) using two separate crosses. The first population consists of 48 randomly selected F2 individuals which were generated by selfing an F1 from the cross of `New Jersey Pillar' x KV 77119. This progeny set exhibits segregation for gross morphological traits including: canopy shape, fruit flesh color, and flower petal color, size, and number. The second population contains 48 F2 progeny derived from the cross of `Suncrest' x `Bailey'. These progeny segregate for quality traits such as fruit diameter, weight, flesh color, cling vs. free stone, soluble solids, pH of juice extract, and fruit developmental period. Nine linkage groups were identified in the first cross, which cover 590 cM of the genome. In the second cross, eight linkage groups were found that contain several significant chromosomal intervals contributing to fruit quality characteristics by QTL analysis. Anchor loci present in both maps were used to join the linkage groups to create a single combined map of the peach genome. Physical mapping is currently underway to assign the each linkage group to the appropriate chromosome.

Generation of a restriction fragment length polymorphism linkage map for Toxoplasma gondii.

Genetics ◽  
1992 ◽  
Vol 132 (4) ◽  
pp. 1003-1015 ◽  
Author(s):  
L D Sibley ◽  
A J LeBlanc ◽  
E R Pfefferkorn ◽  
J C Boothroyd
Keyword(s):  
Toxoplasma Gondii ◽  
Linkage Map ◽  
Restriction Fragment ◽  
Fragment Length ◽  
Genetic Linkage ◽  
Genetic Linkage Map ◽  
Close Correlation ◽  
Rflp Markers ◽  
Linkage Groups ◽  
Restriction Fragment Length

Abstract We have constructed a genetic linkage map for the parasitic protozoan, Toxoplasma gondii, using randomly selected low copy number DNA markers that define restriction fragment length polymorphisms (RFLPs). The inheritance patterns of 64 RFLP markers and two phenotypic markers were analyzed among 19 recombinant haploid progeny selected from two parallel genetic crosses between PLK and CEP strains. In these first successful interstrain crosses, these RFLP markers segregated into 11 distinct genetic linkage groups that showed close correlation with physical linkage groups previously defined by molecular karyotype. Separate linkage maps, constructed for each of the 11 chromosomes, indicated recombination frequencies range from approximately 100 to 300 kb per centimorgan. Preliminary linkage assignments were made for the loci regulating sinefungin resistance (snf-1) on chromosome IX and adenine arabinoside (ara-1) on chromosome V by linkage to RFLP markers. Despite random segregation of separate chromosomes, the majority of chromosomes failed to demonstrate internal recombination events and in 3/19 recombinant progeny no intramolecular recombination events were detected. The relatively low rate of intrachromosomal recombination predicts that tight linkage for unknown genes can be established with a relatively small set of markers. This genetic linkage map should prove useful in mapping genes that regulate drug resistance and other biological phenotypes in this important opportunistic pathogen.

Integration of a molecular linkage group containing the broomrape resistance gene Or5 into an RFLP map in sunflower

Genome ◽  
1999 ◽  
Vol 42 (3) ◽  
pp. 453-456 ◽  
Author(s):  
Yun Hai Lu ◽  
Geneviève Gagne ◽  
Bruno Grezes-Besset ◽  
Philippe Blanchard
Keyword(s):  
Linkage Group ◽  
Linkage Map ◽  
Resistance Gene ◽  
Scar Marker ◽  
Rapd Marker ◽  
Rflp Marker ◽  
Rflp Markers ◽  
Scar Markers ◽  
Molecular Linkage Group ◽  
Rflp Map

A linkage group containing the Or5 gene conferring resistance to Orobanche cumana race E, as well as 5 SCAR markers and 1 RAPD marker has been recently identified in sunflower. A SCAR marker RTS05, mapped 5.6 cM proximal to the Or5 locus, was analysed in an F2 population for which the segregation data of 80 RFLP markers (GIE cartisol - Phase II, France) were available. An association was found between the SCAR marker RTS05 and an RFLP marker S009 (32.1 cM, LOD = 4.7) that had been mapped to the linkage group 17 of the GIE Cartisol RFLP map. Another RFLP marker S010, tightly linked to S009 (0.0 cM) in the same linkage group, was screened in the F2 population that had been previously used for the Or5 linkage map identification. S010 was found to be significantly linked to all 5 SCAR markers as well as to the single RAPD marker with a LOD > 3.0 in each case. This RFLP marker was mapped between two SCAR markers and was situated at 35.1 cM from the resistance gene with a LOD = 2.7. These results showed that the Or5 linkage group could be integrated with the linkage group 17 of the GIE Cartisol RFLP map.Key words: Helianthus, Orobanche, RFLP, SCAR, linkage map.

A linkage map of hexaploid oat based on grass anchor DNA clones and its relationship to other oat maps

Genome ◽  
2001 ◽  
Vol 44 (2) ◽  
pp. 249-265 ◽  
Author(s):  
V A Portyanko ◽  
D L Hoffman ◽  
M Lee ◽  
J B Holland
Keyword(s):  
Linkage Map ◽  
Fragment Length ◽  
Rflp Markers ◽  
Linkage Groups ◽  
Sequence Tagged Sites ◽  
Length Polymorphisms ◽  
Amplified Fragment Length Polymorphisms ◽  
Incomplete Coverage ◽  
Marker Loci ◽  
Isozyme Loci

A cultivated oat linkage map was developed using a recombinant inbred population of 136 F6:7 lines from the cross 'Ogle' × 'TAM O-301'. A total of 441 marker loci, including 355 restriction fragment length polymorphism (RFLP) markers, 40 amplified fragment length polymorphisms (AFLPs), 22 random amplified polymorphic DNAs (RAPDs), 7 sequence-tagged sites (STSs), 1 simple sequence repeat (SSR), 12 isozyme loci, and 4 discrete morphological traits, was mapped. Fifteen loci remained unlinked, and 426 loci produced 34 linkage groups (with 2–43 loci each) spanning 2049 cM of the oat genome (from 4.2 to 174.0 cM per group). Comparisons with other Avena maps revealed 35 genome regions syntenic between hexaploid maps and 16–34 regions conserved between diploid and hexaploid maps. Those portions of hexaploid oat maps that could be compared were completely conserved. Considerable conservation of diploid genome regions on the hexaploid map also was observed (89–95%); however, at the whole-chromosome level, colinearity was much lower. Comparisons among linkage groups, both within and among Avena mapping populations, revealed several putative homoeologous linkage group sets as well as some linkage groups composed of segments from different homoeologous groups. The relationships between many Avena linkage groups remain uncertain, however, due to incomplete coverage by comparative markers and to complications introduced by genomic duplications and rearrangements.Key words: Avena, linkage map, comparative mapping, homoeology.

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 A Genetic Map of Gibberella fujikuroi Mating Population A (Fusarium moniliforme)

Genetics ◽  
1996 ◽  
Vol 143 (1) ◽  
pp. 175-189 ◽  
Author(s):  
Jin-rong Xu ◽  
John F Leslie
Keyword(s):  
Fusarium Moniliforme ◽  
Fragment Length Polymorphism ◽  
Fumonisin B1 ◽  
Gibberella Fujikuroi ◽  
Female Sterility ◽  
Rflp Markers ◽  
Linkage Groups ◽  
Mating Population ◽  
Spore Killer ◽  
Chiasma Interference

Abstract We constructed a recombination-based map of the fungal plant pathogen Gibberella fujikuroi mating population A (asexual stage Fusarium moniliforme). The map is based on the segregation of 142 restriction fragment length polymorphism (RFLP) markers, two auxotrophic genes (arg1, nic1), mating type (matA+ / matA−), female sterility (ste1), spore-killer (Sk), and a gene governing the production of the mycotoxin fumonisin B1 (fum1) among 121 random ascospore progeny from a single cross. We identified 12 linkage groups corresponding to the 12 chromosome-sized DNAs previously observed in contour-clamped homogeneous electric field (CHEF) gels. Linkage groups and chromosomes were correlated via Southern blots between appropriate RFLP markers and the CHEF gels. Eleven of the 12 chromosomes are meiotically stable, but the 12th (and smallest) is subject to deletions in 3% (4/121) of the progeny. Positive chiasma interference occurred on five of the 12 chromosomes, and nine of the 12 chromosomes averaged more than one crossover per chromosome. The average kb/cM ratio in this cross is ~32.

scholarly journals An enhanced molecular marker based genetic map of perennial ryegrass (Lolium perenne) reveals comparative relationships with other Poaceae genomes

Genome ◽  
2002 ◽  
Vol 45 (2) ◽  
pp. 282-295 ◽  
Author(s):  
Elizabeth S Jones ◽  
Natalia L Mahoney ◽  
Michael D Hayward ◽  
Ian P Armstead ◽  
J Gilbert Jones ◽  
...  
Keyword(s):  
Molecular Marker ◽  
Linkage Map ◽  
Genetic Map ◽  
Lolium Perenne ◽  
Perennial Ryegrass ◽  
Genetic Linkage Map ◽  
Population Based ◽  
Genetic Maps ◽  
Linkage Groups ◽  
Integrated Genetic Map

A molecular-marker linkage map has been constructed for perennial ryegrass (Lolium perenne L.) using a one-way pseudo-testcross population based on the mating of a multiple heterozygous individual with a doubled haploid genotype. RFLP, AFLP, isoenzyme, and EST data from four collaborating laboratories within the International Lolium Genome Initiative were combined to produce an integrated genetic map containing 240 loci covering 811 cM on seven linkage groups. The map contained 124 codominant markers, of which 109 were heterologous anchor RFLP probes from wheat, barley, oat, and rice, allowing comparative relationships between perennial ryegrass and other Poaceae species to be inferred. The genetic maps of perennial ryegrass and the Triticeae cereals are highly conserved in terms of synteny and colinearity. This observation was supported by the general agreement of the syntenic relationships between perennial ryegrass, oat, and rice and those between the Triticeae and these species. A lower level of synteny and colinearity was observed between perennial ryegrass and oat compared with the Triticeae, despite the closer taxonomic affinity between these species. It is proposed that the linkage groups of perennial ryegrass be numbered in accordance with these syntenic relationships, to correspond to the homoeologous groups of the Triticeae cereals.Key words: Lolium perenne, genetic linkage map, RFLP, AFLP, conserved synteny.

Sign in / Sign up

Export Citation Format

Share Document