Genomic distribution of MITEs in barley determined by MITE-AFLP mapping

Genome ◽  
2006 ◽  
Vol 49 (12) ◽  
pp. 1616-1620 ◽  
Author(s):  
H. Takahashi ◽  
H. Akagi ◽  
K. Mori ◽  
K. Sato ◽  
K. Takeda
Keyword(s):  
Fragment Length Polymorphism ◽  
Linkage Groups ◽  
Entire Genome ◽  
Ssr Loci ◽  
Plant Genes ◽  
Flanking Sequences ◽  
Average Marker Density ◽  
Simple Sequence ◽  
Map Distance ◽  
Hordeum Vulgare Ssp

Miniature inverted-repeat transposable elements (MITEs) represent a large superfamily of transposons that are moderately to highly repetitive and frequently found near or within plant genes. To elucidate the organization of MITEs in the barley genome, MITEs were integrated into the genetic map of barley. In this report, we describe the use of MITEs in amplified fragment length polymorphism (AFLP) mapping, and demonstrate their superiority over conventional AFLP mapping. Barley MITEs include members of the Stowaway, Barfly, and Pangrangja families. By amplifying the flanking sequences of these MITEs, a total of 214 loci were mapped from a population of 93 doubled-haploid segregating individuals between Hordeum vulgare ssp. vulgare and H. vulgare ssp. spontaneum. The 214 MITE-AFLP and 40 anchor simple sequence repeat (SSR) loci were distributed on 7 linkage groups, covering a total map distance of 1 165 cM. The average marker density on each chromosome ranged between 3.4 and 9.6 cM per locus. Only 1 MITE-based locus was frequently found to be associated with MITE loci from the same family, resulting in clusters in chromosomal subregions. In barley, it will be possible to cover the entire genome with a limited set of MITE-based primers and to build highly dense maps of specific regions.

scholarly journals Identification of Simple-sequence Repeats in Malus (Apple)

HortScience ◽  
1995 ◽  
Vol 30 (4) ◽  
pp. 855D-855 ◽  
Author(s):  
Amy K. Szewc-McFadden ◽  
Sharon Bliek ◽  
Christopher G. Alpha ◽  
Warren F. Lamboy ◽  
James R. McFerson
Keyword(s):  
Simple Sequence Repeats ◽  
Fragment Length Polymorphism ◽  
Random Amplified Polymorphic Dna ◽  
Germplasm Characterization ◽  
The Core ◽  
Marker Data ◽  
Core Subset ◽  
Germplasm Collections ◽  
Ssr Loci ◽  
Simple Sequence

Simple-sequence repeats (SSRs) are efficient and informative DNA markers with great potential for germplasm characterization. When used to characterize large arrays of accessions, such as the core subset of the USDA/ARS Malus collection, SSRs may be more effective than other approaches, such as restriction fragment length polymorphism (RFLP) and random amplified polymorphic DNA (RAPD). For example, SSRs can be PCR-amplified and fluorescence-based detected; they also appear to be abundantly disbursed throughout plant genomes and yield abundant polymorphisms in most taxa studied. We are conducting an extensive screening of a size-fractionated library of Malus ×domestica cv. Golden Delicious to identify and characterize selected SSR loci. We are applying genetic information revealed by SSR loci in combination with passport and horticultural data to better comprehend genetic identity and relatedness in Malus germplasm collections and help develop the Malus core subset. Ultimately, application of molecular marker data will permit improved conservation and use of genetic resources.

A gene controlling sex in grapevines placed on a molecular marker-based genetic map

Genome ◽  
2000 ◽  
Vol 43 (2) ◽  
pp. 333-340 ◽  
Author(s):  
M A Dalbó ◽  
G N Ye ◽  
N F Weeden ◽  
H Steinkellner ◽  
K M Sefc ◽  
...  
Keyword(s):  
Molecular Marker ◽  
Dna Markers ◽  
Fragment Length Polymorphism ◽  
Random Amplified Polymorphic Dna ◽  
Basic Number ◽  
Genetic Maps ◽  
Hybrid Population ◽  
Linkage Groups ◽  
Starting Point ◽  
Map Distance

Genetic maps of Vitis (2n = 38) have been constructed from an interspecific hybrid population of 58 seedlings of the cross 'Horizon' ('Seyval' × 'Schuyler') × Illinois 547-1 (V. cinerea B9 × V. rupestris B38). The maps were initially constructed based on 277 RAPD (random amplified polymorphic DNA) markers using a double-pseudotestcross strategy. Subsequently, 25 microsatellites, 4 CAPS (cleaved amplified polymorphic sequence), and 12 AFLP (amplified fragment length polymorphism) markers were added to the maps. Another 120 markers, mostly those segregating 3:1, were also assigned but not positioned on the linkage groups in the two maps. The 'Horizon' map consisted of 153 markers covering 1199 cM, with an average map distance of 7.6 cM between markers. The Illinois 547-1 map had 179 markers covering 1470 cM, with an average map distance of 8.1 cM. There were 20 linkage groups in each map, one more than the basic number of chromosomes in grapes. Ten linkage groups in each map were identified as homologous using 16 microsatellite and 2 CAPS markers polymorphic in both parents. A single locus controlling sex in grapes mapped close to a microsatellite marker. These maps provide enough coverage of the genome for QTL (quantitative trait loci) analysis and as a starting point for positional gene cloning in grapes. Key words: Vitis, RAPD, microsatellite, SSR, CAPS.

Development and characterization of EST-derived simple sequence repeat (SSR) markers for pasture grass endophytes

Genome ◽  
2003 ◽  
Vol 46 (2) ◽  
pp. 277-290 ◽  
Author(s):  
Eline van Zijll de Jong ◽  
Kathryn M Guthridge ◽  
German C Spangenberg ◽  
John W Forster
Keyword(s):  
Genetic Diversity ◽  
Ssr Markers ◽  
Expressed Sequence Tags ◽  
Simple Sequence Repeat ◽  
Fragment Length Polymorphism ◽  
Sequence Repeat ◽  
Pasture Grass ◽  
Ssr Loci ◽  
Expressed Sequence ◽  
Simple Sequence

Fungal endophytes of the genus Neotyphodium are common in temperate pasture grass species and confer both beneficial and deleterious agronomic characteristics to their hosts. The aim of this study was to develop molecular markers based on simple sequence repeat (SSR) loci for the identification and assessment of genetic diversity among Neotyphodium endophytes in grasses. Expressed sequence tags (ESTs) from both Neptyphodium coenophialum and Neotyphodium lolii were examined, and unique SSR loci were identified in 9.7% of the N. coenophialum sequences and 6.3% of the N. lolii sequences. A variety of SSRs were present, although perfect trinucleotide repeat arrays were the most common. Primers were designed to 50 SSR loci from N. coenophialum and 57 SSR loci from N. lolii and were evaluated using 20 Neotyphodium and Epichloë isolates. A high proportion of the N. coenophialum and N. lolii primers produced amplification products from the majority of isolates and most of these primers detected genetic variation. SSR markers from both N. coenophialum and N. lolii detected high levels of polymorphism between Neotyphodium and Epichloë species, and low levels of polymorphism within N. coenophialum and N. lolii. SSR markers may be used in appropriate combinations to discriminate between species. Comparison with amplified fragment length polymorphism (AFLP) data demonstrated that the SSR markers were informative for the assessment of genetic variation within and between endophyte species. These markers may be used to identify endophyte taxa and to evaluate intraspecific population diversity, which may be correlated with variation for endophyte-derived agronomic traits.Key words: Neotyphodium, simple sequence repeats, expressed sequence tags, amplified fragment length polymorphism, genetic diversity.

The first genetic linkage map of Luohanguo (Siraitia grosvenorii ) based on ISSR and SRAP markers

Genome ◽  
2011 ◽  
Vol 54 (1) ◽  
pp. 19-25 ◽  
Author(s):  
Lihua Liu ◽  
Xiaojun Ma ◽  
Jianhe Wei ◽  
Jiaming Qin ◽  
Changming Mo
Keyword(s):  
Molecular Breeding ◽  
Genetic Linkage Map ◽  
Distal Region ◽  
Inter Simple Sequence Repeat ◽  
Linkage Groups ◽  
Srap Markers ◽  
Reference Information ◽  
Siraitia Grosvenorii ◽  
Simple Sequence ◽  
Map Distance

In this study, the first genetic map of Luohanguo ( Siraitia grosvenorii (Swingle) C. Jeffrey) was constructed with 150 F2 population individuals using inter-simple sequence repeat (ISSR) and sequence-related amplified polymorphism (SRAP) markers. A total of 100 ISSRs and 196 SRAP primer combinations generated 51 and 222 polymorphic markers, respectively. Among the 273 markers obtained, 199 markers (29 ISSRs and 170 SRAPs) were mapped to 25 linkage groups. The map covered 1463.3 cM with a mean map distance of 7.35 cM between adjacent markers and a maximum map distance of 52.6 cM between two markers. The markers were distributed randomly in 25 groups except for minor clusters in the distal region of linkage groups. All 25 linkage groups consisted of 2–36 loci ranging in length from 19.5 to 152.6 cM and accounted for 59.8% of the total map distance. This map provides reference information for future molecular breeding work on Luohanguo.

scholarly journals A Molecular Genetic Map and Electrophoretic Karyotype of the Plant Pathogenic Fungus Cochliobolus sativus

2002 ◽  
Vol 15 (5) ◽  
pp. 481-492 ◽  
Author(s):  
Shaobin Zhong ◽  
Brian J. Steffenson ◽  
J. Patrick Martinez ◽  
Lynda M. Ciuffetti
Keyword(s):  
Genetic Map ◽  
Length Polymorphism ◽  
Fragment Length Polymorphism ◽  
Molecular Genetic ◽  
Aflp Markers ◽  
Cochliobolus Sativus ◽  
Electrophoretic Karyotype ◽  
Linkage Groups ◽  
Molecular Genetic Map ◽  
Map Distance

A molecular genetic map was constructed and an electrophoretic karyotype was resolved for Cochliobolus sativus, the causal agent of spot blotch of barley and wheat. The genetic map consists of 27 linkage groups with 97 amplified fragment length polymorphism (AFLP) markers, 31 restriction fragment length polymorphism (RFLP) markers, two polymerase chain reaction amplified markers, the mating type locus (CsMAT), and a gene (VHv1) conditioning high virulence on barley cv. Bowman. These linkage groups covered a map distance of 849 cM. The virulence gene VHv1 cosegregated with six AFLP markers and was mapped on one of the major linkage groups. Fifteen chromosome-sized DNAs were resolved in C. sativus isolates ND93-1 and ND90Pr with contour-clamped homogeneous electric field (CHEF) electrophoresis combined with telo-mere probe analysis of comigrating chromosome-sized DNAs. The chromosome sizes ranged from 1.25 to 3.80 Mbp, and the genome size of the fungus was estimated to be approximately 33 Mbp. By hybridizing genetically mapped RFLP and AFLP markers to CHEF blots, 25 of the 27 linkage groups were assigned to specific chromosomes. The barley-specific virulence locus VHv1 was localized on a chromosome of 2.80 Mbp from isolate ND90Pr in the CHEF gel. The total map length of the fungus was estimated to be at least 1,329 cM based on the map distance covered by the linked markers and the estimated gaps. Therefore, the physical to genetic distance ratio is approximately 25 kb/cM. Construction of a high-resolution map around target loci will facilitate the cloning of the genes conferring virulence and other characters in C. sativus by a map-based cloning strategy.

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.

Enrichment of a papaya high-density genetic map with AFLP markers

Genome ◽  
2009 ◽  
Vol 52 (8) ◽  
pp. 716-725 ◽  
Author(s):  
Andrea L. Blas ◽  
Qingyi Yu ◽  
Cuixia Chen ◽  
Olivia Veatch ◽  
Paul H. Moore ◽  
...  
Keyword(s):  
Genetic Map ◽  
High Density ◽  
Aflp Markers ◽  
Comparative Genomic ◽  
Linkage Groups ◽  
Genomic Studies ◽  
Average Marker Density ◽  
Male Specific ◽  
Development And Evolution ◽  
Map Distance

A high-density genetic linkage map of papaya, previously developed using an F2 mapping population derived from the intraspecific cross AU9 × SunUp, was enriched with AFLP markers. The comprehensive genetic map presented here spans 945.2 cM and covers 9 major and 5 minor linkage groups containing 712 SSR, 277 AFLP, and 1 morphological markers. The average marker density for the 9 major linkage groups is 0.9 cM between adjacent markers, and the total number of gaps >5 cM was reduced from 48 to 27 in the current map. AFLPs generated by EcoRI/MseI primer combinations were distributed throughout the 14 linkage groups and resulted in several large locus order rearrangements within the 9 major linkage groups. Integration of AFLP markers provided tighter linkage association between loci, leading to a reduction in map distance on LGs 1, 2, and 4, which were inflated in the previous map, and correction of the marker order on LG8. Suppression of recombination in the male-specific Y region (MSY) of LG1 is further validated by the addition of 27 sex co-segregating AFLP markers. A large region of distorted segregation surrounding the MSY spans 54.4 cM and represents ∼71% of the linkage group. This comprehensive high-density genetic map provides a framework for mapping quantitative trait loci and for fine mapping as well as for comparative genomic studies of crop plant development and evolution.

scholarly journals Microsatellite Marker Development in Rose and its Application in Tetraploid Mapping

2006 ◽  
Vol 131 (3) ◽  
pp. 380-387 ◽  
Author(s):  
L.H. Zhang ◽  
D.H. Byrne ◽  
R.E. Ballard ◽  
S. Rajapakse
Keyword(s):  
Ssr Markers ◽  
Genomic Library ◽  
Cultivar Identification ◽  
Genetic Maps ◽  
Linkage Groups ◽  
Specific Primers ◽  
Pcr Products ◽  
Ssr Loci ◽  
Tetraploid Parent ◽  
Simple Sequence

Microsatellite or simple sequence repeat (SSR) markers were developed from Rosa wichurana Crépin to combine two previously constructed tetraploid rose (Rosa hybrida L.) genetic maps. To isolate SSR-containing sequences from rose a small-insert genomic library was constructed from diploid Rosa wichurana and screened with several SSR probes. Specific primers were designed for 43 unique SSR regions, of which 30 primer pairs gave rise to clear PCR products. Seventeen SSR primer pairs (57%) produced polymorphism in the tetraploid rose 90-69 mapping family. These markers were incorporated into existing maps of the parents 86-7 and 82-1134, which were constructed primarily with AFLP markers. The current map of the male parent, amphidiploid 86-7, consists of 286 markers assigned to 14 linkage groups and covering 770 cm. The map of the female tetraploid parent, 82-1134, consists of 256 markers assigned to 20 linkage groups and covering 920 cm. Nineteen rose SSR loci were mapped on the 86-7 map and 11 on the 82-1134 map. Several homeologous linkage groups within maps were identified based on SSR markers. In addition, some of the SSR markers provided anchoring points between the two parental maps. SSR markers were also useful for joining small linkage groups. Based on shared SSR markers, consensus orders for four rose linkage groups between parental maps were generated. Microsatellite markers developed in this study will provide valuable tools for many aspects of rose research including future consolidation of diploid and tetraploid rose genetic linkage maps, genetic, phylogenetic and population analyses, cultivar identification, and marker-assisted selection.

scholarly journals Parental and Consensus Linkage Maps of Eucalyptus globulus Using AFLP and Microsatellite Markers

2006 ◽  
Vol 55 (1-6) ◽  
pp. 202-217 ◽  
Author(s):  
J. S. Freeman ◽  
B. M. Potts ◽  
M. Shepherd ◽  
R. E. Vaillancourt
Keyword(s):  
Ssr Markers ◽  
Length Polymorphism ◽  
Eucalyptus Globulus ◽  
Fragment Length Polymorphism ◽  
Female Parent ◽  
Linkage Maps ◽  
Linkage Groups ◽  
Integrated Map ◽  
Gender Specific ◽  
Simple Sequence

AbstractParental and consensus maps were constructed in an F2 inter-provenance cross of Eucalyptus globulus, using amplified fragment length polymorphism (AFLP) and microsatellite (or simple sequence repeats [SSR]) markers. The female map had 12 linkage groups and 118 markers, comprising 33 SSR and 85 AFLP loci. The male map had 14 linkage groups and 130 markers comprising 36 SSR and 94 AFLP loci. The integrated map featured 10 linkage groups and 165 markers, including 33 SSR and 132 AFLP loci, a small 11th group was identified in the male parent. Moderate segregation distortion was detected, concentrated in gender specific groups. The strongest distortion was detected in the female parent for which causal mechanisms are discussed. The inclusion of SSR markers previously mapped in several different eucalypt species within the subgenus Symphyomyrtus (E. globulus, E. camaldulensis, and predominantly E. grandis and E. urophylla), allowed comparison of linkage groups across species and demonstrated that linkage orders previously reported in E. globulus, E. grandis and E. urophylla were largely conserved.

scholarly journals Genepool Variation in Genus Glycine Subgenus Soja Revealed by Polymorphic Nuclear and Chloroplast Microsatellites

Genetics ◽  
1996 ◽  
Vol 144 (2) ◽  
pp. 793-803 ◽  
Author(s):  
W Powell ◽  
M Morgante ◽  
J J Doyle ◽  
J W McNicol ◽  
S V Tingey ◽  
...  
Keyword(s):  
Fragment Length Polymorphism ◽  
Diversity Indices ◽  
Chloroplast Microsatellites ◽  
The Core ◽  
Phenetic Relationships ◽  
Allelic Variability ◽  
Soybean Genotypes ◽  
Ssr Loci ◽  
Nuclear Ssrs ◽  
Simple Sequence

Abstract A combination of nuclear and chloroplast simple sequence repeats (SSRs) have been used to investigate the levels and pattern of variability detected in Glycine max and G. soja genotypes. Based on the analysis of 700 soybean genotypes with 115 restriction fragment length polymorphism (RFLP) probes, 12 accessions were identified that represent 92% of the allelic variability detected in this genepool. These 12 core genotypes together with a sample of G. max and G. soja accessions were evaluated with 11 nuclear SSRs that detected 129 alleles. Compared with the other G. max and G. soja genotypes sampled, the core genotypes represent 40% of the allelic variability detected with SSRs. Despite the multi-allelic nature of soybean SSRs, dendrograms representing phenetic relationships between accessions clustered according to their subspecies origin. In addition to biparentally inherited nuclear SSRs, two uniparentally (maternally) transmitted chloroplast SSRs were also studied. A total of seven haplotypes were identified, and diversity indices of 0.405 ± 0.088 and 0.159 ± 0.071 were obtained for the two chloroplast SSRs. The availability of polymorphic SSR loci in the chloroplast genome provides new opportunities to investigate cytonuclear interactions in plants.

Sign in / Sign up

Export Citation Format

Share Document