bacterial artificial chromosome library for soybean and identification of clones near a major cyst nematode resistance gene

We constructed a bacterial artificial chromosome (BAC) library for soybean (Glycine max) consisting of approximately 30000 clones with an average insert size of 120 kilobase pairs. The library was successfully screened with restriction fragment length polymorphism (RFLP) and microsatellite markers t...

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Veröffentlicht in:Theoretical and applied genetics 1998-02, Vol.96 (2), p.196-202
Hauptverfasser: Danesh, D, Penuela, S, Mudge, J, Denny, R.L, Nordstrom, H, Martinez, J.P, Young, N.D
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container_end_page 202
container_issue 2
container_start_page 196
container_title Theoretical and applied genetics
container_volume 96
creator Danesh, D
Penuela, S
Mudge, J
Denny, R.L
Nordstrom, H
Martinez, J.P
Young, N.D
description We constructed a bacterial artificial chromosome (BAC) library for soybean (Glycine max) consisting of approximately 30000 clones with an average insert size of 120 kilobase pairs. The library was successfully screened with restriction fragment length polymorphism (RFLP) and microsatellite markers tightly linked to a major resistance gene for the cyst nematode, Heterodera glycines. Since many soybean RFLPs hybridize to duplicate loci, BACs homologous to duplicate RFLP loci were distinguished by digestion with the restriction enzyme originally used to map the RFLP, followed by a comparison of the hybridizing fragments. Linkage mapping of BAC clones identified with markers linked to the cyst nematode resistance gene demonstrated that these clones were located at the expected chromosomal positions and that there were no indications of chimeras within the genomic inserts.
doi_str_mv 10.1007/s001220050727
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The library was successfully screened with restriction fragment length polymorphism (RFLP) and microsatellite markers tightly linked to a major resistance gene for the cyst nematode, Heterodera glycines. Since many soybean RFLPs hybridize to duplicate loci, BACs homologous to duplicate RFLP loci were distinguished by digestion with the restriction enzyme originally used to map the RFLP, followed by a comparison of the hybridizing fragments. Linkage mapping of BAC clones identified with markers linked to the cyst nematode resistance gene demonstrated that these clones were located at the expected chromosomal positions and that there were no indications of chimeras within the genomic inserts.</abstract><cop>Heidelberg</cop><cop>Berlin</cop><pub>Springer</pub><doi>10.1007/s001220050727</doi><tpages>7</tpages></addata></record>
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ispartof Theoretical and applied genetics, 1998-02, Vol.96 (2), p.196-202
issn 0040-5752
1432-2242
language eng
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source SpringerNature Journals
subjects Biological and medical sciences
chromosome mapping
Classical genetics, quantitative genetics, hybrids
clones
cloning
Cysts
DNA libraries
Fundamental and applied biological sciences. Psychology
Genetic aspects
genetic markers
Genetics
Genetics of eukaryotes. Biological and molecular evolution
Genomic libraries
Glycine max
Heterodera glycines
Libraries
linkage (genetics)
major genes
microsatellite repeats
Nematoda
pest resistance
Plant genetics
Plant immunology
Pteridophyta, spermatophyta
repetitive sequences
restriction fragment length polymorphism
Soybean
Soybeans
Vegetals
title bacterial artificial chromosome library for soybean and identification of clones near a major cyst nematode resistance gene
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