Centromere Repeat DNA Originated from Brassica rapa is Detected in the Centromere Region of Raphanus sativus Chromosomes

Fluorescence in situ hybridization (FISH) is a powerful tool for the detection of DNA sequences in the specific region of the chromosomes. As well as for the integrated physical mapping, FISH karyotype analysis has to be preceded. Karyotype of Raphanus sativus 'Wonkyo 10039' was analyzed b...

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Published inWeon'ye gwahag gi'sulji Vol. 30; no. 6; pp. 751 - 756
Main Authors Hwang, Y.J., Kyungpook National University, Daegu, Republic of Korea, Yu, H.J., The Catholic University of Korea, Bucheon, Republic of Korea, Mun, J.H., National Academy of Agricultural Science, RDA, Suwon, Republic of Korea, Ryu, K.B., Kyungpook National University, Daegu, Republic of Korea, Park, B.S., National Academy of Agricultural Science, RDA, Suwon, Republic of Korea, Lim, K.B., Kyungpook National University, Daegu, Republic of Korea
Format Journal Article
LanguageEnglish
Published 한국원예학회HST 01.12.2012
한국원예학회
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ISSN1226-8763
2465-8588
DOI10.7235/hort.2012.12168

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Abstract Fluorescence in situ hybridization (FISH) is a powerful tool for the detection of DNA sequences in the specific region of the chromosomes. As well as for the integrated physical mapping, FISH karyotype analysis has to be preceded. Karyotype of Raphanus sativus 'Wonkyo 10039' was analyzed by a dual-color FISH technique; using various repetitive DNA probes, including 5S rDNA, 45S rDNA, and centromere retrotransposon. The length of the somatic metaphase chromosome ranged from 1.35 to 2.06 ㎛ with a total length of 15.29 ㎛. The chromosome complements comprised of eight pairs of metacentrics and one pair of submetacentric. Bleached DAPI Band analysis revealed a heterochromatin region, covering 28.6% to 50.4% each chromosomes. 5S and 45S rDNA sequences were located on two and three pairs of chromosomes, respectively. The centromere retrotransposon of Brassica (CRB) is a major component in Brassica related species that has been maintained as a common centromere component. CRB signals were detected on the centromere and pericentromeric region of R. sativus 'Wonkyo 10039' and three basic Brassica species (B. rapa, B. nigra, and B. oleracea). These results will provide a valuable background for physical mapping and elucidation of the evolutionary relationship among the Brassica related species.
AbstractList Fluorescence in situ hybridization (FISH) is a powerful tool for the detection of DNA sequences in the specific region of the chromosomes. As well as for the integrated physical mapping, FISH karyotype analysis has to be preceded. Karyotype of Raphanus sativus ‘Wonkyo 10039’ was analyzed by a dual-color FISH technique; using various repetitive DNA probes, including 5S rDNA, 45S rDNA, and centromere retrotransposon. The length of the somatic metaphase chromosome ranged from 1.35 to 2.06 µm with a total length of 15.29 µm. The chromosome complements comprised of eight pairs of metacentrics and one pair of submetacentric. Bleached DAPI Band analysis revealed a heterochromatin region, covering 28.6% to 50.4%each chromosomes. 5S and 45S rDNA sequences were located on two and three pairs of chromosomes,respectively. The centromere retrotransposon of Brassica (CRB) is a major component in Brassica related species that has been maintained as a common centromere component. CRB signals were detected on the centromere and pericentromeric region of R. sativus ‘Wonkyo 10039’ and three basic Brassica species (B. rapa, B. nigra, and B. oleracea). These results will provide a valuable background for physical mapping and elucidation of the evolutionary relationship among the Brassica related species. KCI Citation Count: 8
Fluorescence in situ hybridization (FISH) is a powerful tool for the detection of DNA sequences in the specific region of the chromosomes. As well as for the integrated physical mapping, FISH karyotype analysis has to be preceded. Karyotype of Raphanus sativus 'Wonkyo 10039' was analyzed by a dual-color FISH technique; using various repetitive DNA probes, including 5S rDNA, 45S rDNA, and centromere retrotransposon. The length of the somatic metaphase chromosome ranged from 1.35 to 2.06 ㎛ with a total length of 15.29 ㎛. The chromosome complements comprised of eight pairs of metacentrics and one pair of submetacentric. Bleached DAPI Band analysis revealed a heterochromatin region, covering 28.6% to 50.4% each chromosomes. 5S and 45S rDNA sequences were located on two and three pairs of chromosomes, respectively. The centromere retrotransposon of Brassica (CRB) is a major component in Brassica related species that has been maintained as a common centromere component. CRB signals were detected on the centromere and pericentromeric region of R. sativus 'Wonkyo 10039' and three basic Brassica species (B. rapa, B. nigra, and B. oleracea). These results will provide a valuable background for physical mapping and elucidation of the evolutionary relationship among the Brassica related species.
Author Lim, K.B., Kyungpook National University, Daegu, Republic of Korea
Yu, H.J., The Catholic University of Korea, Bucheon, Republic of Korea
Mun, J.H., National Academy of Agricultural Science, RDA, Suwon, Republic of Korea
Ryu, K.B., Kyungpook National University, Daegu, Republic of Korea
Hwang, Y.J., Kyungpook National University, Daegu, Republic of Korea
Park, B.S., National Academy of Agricultural Science, RDA, Suwon, Republic of Korea
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10.1139/g97-076
10.1002/cyto.a.10013
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10.1186/gb-2010-11-9-r94
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Snippet Fluorescence in situ hybridization (FISH) is a powerful tool for the detection of DNA sequences in the specific region of the chromosomes. As well as for the...
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SubjectTerms bleached DAPI band
BRASSICACEAE
GENOMAS
GENOME
GENOMES
heterochromatin
radish
농학
Title Centromere Repeat DNA Originated from Brassica rapa is Detected in the Centromere Region of Raphanus sativus Chromosomes
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