Cytological heterozygosity and the hybrid origin of sweet orange [Citrus sinensis (L.) Osbeck]
Identifieur interne : 000990 ( PascalFrancis/Corpus ); précédent : 000989; suivant : 000991Cytological heterozygosity and the hybrid origin of sweet orange [Citrus sinensis (L.) Osbeck]
Auteurs : A. Pedrosa ; D. Schweizer ; M. GuerraSource :
- Theoretical and Applied Genetics [ 0040-5752 ] ; 2000.
Descripteurs français
- Pascal (Inist)
English descriptors
- KwdEn :
Abstract
Citrus sinensis chromosomes, although small in size, present a remarkable differentiation of bands with the fluorochromes CMA and DAPI. These bands suggest that some heteromorphisms are fixed in this species. To investigate the extension of these heteromorphisms, ten cultivars of C. sinenesis were analysed with CMA/DAP1 staining and, in some of them, the 18S-5.8S-25S rRNA and 5S rRNA genes were located by in situ hybridization. CMA/DAPI staining showed exactly the same CMA+/DAPI- banding pattern for all cultivars. In situ hybridization revealed three 18S-5.8S-25S rRNA gene sites, two proximally located on two similar chromosomes and one terminally located on a third non-related chromosome. Two 5S rRNA gene sites were observed in this species, with one located proximal to the telomeric 18S-5.8S-25S rDNA site. Both cytological approaches revealed an invariable, heterozygotic karyotype among sweet orange cultivars. Based on these data, the putative hybrid origin of the species is discussed.
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Format Inist (serveur)
NO : | PASCAL 00-0166955 INIST |
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ET : | Cytological heterozygosity and the hybrid origin of sweet orange [Citrus sinensis (L.) Osbeck] |
AU : | PEDROSA (A.); SCHWEIZER (D.); GUERRA (M.) |
AF : | Department of Cytology and Genetics, Institute of Botany, University of Vienna, Rennweg 14/1030, Vienna/Autriche (1 aut., 2 aut., 3 aut.) |
DT : | Publication en série; Niveau analytique |
SO : | Theoretical and Applied Genetics; ISSN 0040-5752; Coden THAGA6; Allemagne; Da. 2000; Vol. 100; No. 3-4; Pp. 361-367; Bibl. 1 p.1/4 |
LA : | Anglais |
EA : | Citrus sinensis chromosomes, although small in size, present a remarkable differentiation of bands with the fluorochromes CMA and DAPI. These bands suggest that some heteromorphisms are fixed in this species. To investigate the extension of these heteromorphisms, ten cultivars of C. sinenesis were analysed with CMA/DAP1 staining and, in some of them, the 18S-5.8S-25S rRNA and 5S rRNA genes were located by in situ hybridization. CMA/DAPI staining showed exactly the same CMA+/DAPI- banding pattern for all cultivars. In situ hybridization revealed three 18S-5.8S-25S rRNA gene sites, two proximally located on two similar chromosomes and one terminally located on a third non-related chromosome. Two 5S rRNA gene sites were observed in this species, with one located proximal to the telomeric 18S-5.8S-25S rDNA site. Both cytological approaches revealed an invariable, heterozygotic karyotype among sweet orange cultivars. Based on these data, the putative hybrid origin of the species is discussed. |
CC : | 002A07D02B |
FD : | Cultivar; Hybridation interspécifique; Cytogénétique; Bande chromosomique; RNA ribosomique; Gène; Citrus sinensis; Agrume; Bande chromosomique CMA |
FG : | Rutaceae; Dicotyledones; Angiospermae; Spermatophyta |
ED : | Cultivar; Interspecific hybridization; Cytogenetics; Chromosome banding; Ribosomal RNA; Gene; Citrus sinensis; Citrus fruit |
EG : | Rutaceae; Dicotyledones; Angiospermae; Spermatophyta |
SD : | Cultivar; Hibridación interespecífica; Citogenética; Banda cromosómica; RNA ribosómico; Gen; Citrus sinensis; Agrios |
LO : | INIST-395.354000086661830040 |
ID : | 00-0166955 |
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Pascal:00-0166955Le document en format XML
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<front><div type="abstract" xml:lang="en">Citrus sinensis chromosomes, although small in size, present a remarkable differentiation of bands with the fluorochromes CMA and DAPI. These bands suggest that some heteromorphisms are fixed in this species. To investigate the extension of these heteromorphisms, ten cultivars of C. sinenesis were analysed with CMA/DAP1 staining and, in some of them, the 18S-5.8S-25S rRNA and 5S rRNA genes were located by in situ hybridization. CMA/DAPI staining showed exactly the same CMA<sup>+</sup>
/DAPI<sup>-</sup>
banding pattern for all cultivars. In situ hybridization revealed three 18S-5.8S-25S rRNA gene sites, two proximally located on two similar chromosomes and one terminally located on a third non-related chromosome. Two 5S rRNA gene sites were observed in this species, with one located proximal to the telomeric 18S-5.8S-25S rDNA site. Both cytological approaches revealed an invariable, heterozygotic karyotype among sweet orange cultivars. Based on these data, the putative hybrid origin of the species is discussed.</div>
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<ET>Cytological heterozygosity and the hybrid origin of sweet orange [Citrus sinensis (L.) Osbeck]</ET>
<AU>PEDROSA (A.); SCHWEIZER (D.); GUERRA (M.)</AU>
<AF>Department of Cytology and Genetics, Institute of Botany, University of Vienna, Rennweg 14/1030, Vienna/Autriche (1 aut., 2 aut., 3 aut.)</AF>
<DT>Publication en série; Niveau analytique</DT>
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<EA>Citrus sinensis chromosomes, although small in size, present a remarkable differentiation of bands with the fluorochromes CMA and DAPI. These bands suggest that some heteromorphisms are fixed in this species. To investigate the extension of these heteromorphisms, ten cultivars of C. sinenesis were analysed with CMA/DAP1 staining and, in some of them, the 18S-5.8S-25S rRNA and 5S rRNA genes were located by in situ hybridization. CMA/DAPI staining showed exactly the same CMA<sup>+</sup>
/DAPI<sup>-</sup>
banding pattern for all cultivars. In situ hybridization revealed three 18S-5.8S-25S rRNA gene sites, two proximally located on two similar chromosomes and one terminally located on a third non-related chromosome. Two 5S rRNA gene sites were observed in this species, with one located proximal to the telomeric 18S-5.8S-25S rDNA site. Both cytological approaches revealed an invariable, heterozygotic karyotype among sweet orange cultivars. Based on these data, the putative hybrid origin of the species is discussed.</EA>
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