FISH landmarks for barley chromosomes (Hordeum vulgare L.)
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Brown, SE
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Colorado State Univ, Coll Agr Sci, Dept Bioagr Sci & Pest Management, Ft Collins, CO 80523 USAColorado State Univ, Coll Agr Sci, Dept Bioagr Sci & Pest Management, Ft Collins, CO 80523 USA
Brown, SE
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Stephens, JL
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机构:Colorado State Univ, Coll Agr Sci, Dept Bioagr Sci & Pest Management, Ft Collins, CO 80523 USA
Stephens, JL
Lapitan, NLV
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机构:Colorado State Univ, Coll Agr Sci, Dept Bioagr Sci & Pest Management, Ft Collins, CO 80523 USA
Lapitan, NLV
Knudson, DL
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机构:Colorado State Univ, Coll Agr Sci, Dept Bioagr Sci & Pest Management, Ft Collins, CO 80523 USA
Knudson, DL
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[1] Colorado State Univ, Coll Agr Sci, Dept Bioagr Sci & Pest Management, Ft Collins, CO 80523 USA
[2] Colorado State Univ, Dept Soil & Crop Sci, Ft Collins, CO 80523 USA
Barley metaphase chromosomes (2n = 14) can be identified by fluorescence in situ hybridization (FISH) and digital imaging microscopy using heterologous 18S rDNA and 5S rDNA probe sequences. When these sequences are used together, FISH landmark signals were seen so that all 7 chromosomes were uniquely identified and unambiguously oriented. The chromosomal location of the landmark signals was determined by FISH to a barley trisomic series using the 18S and 5S probes labeled with different fluorophores. The utility of these FISH landmarks for barley physical mapping was also demonstrated when an Amy-2 cDNA clone and a BAC clone were hybridized with the FISH landmark probes.