Karyological analysis of an interspecific hybrid between the dioecious Silene latifolia and the hermaphroditic Silene viscosa
Jazyk angličtina Země Kanada Médium print
Typ dokumentu srovnávací studie, časopisecké články, práce podpořená grantem
PubMed
16699557
DOI
10.1139/g05-112
PII: g05-112
Knihovny.cz E-zdroje
- MeSH
- chiméra genetika MeSH
- chromozom X ultrastruktura MeSH
- chromozomy rostlin ultrastruktura MeSH
- fylogeneze MeSH
- genom rostlinný MeSH
- hybridizace in situ fluorescenční metody MeSH
- karyotypizace metody MeSH
- křížení genetické * MeSH
- meióza genetika MeSH
- poruchy sexuálního vývoje genetika MeSH
- segregace chromozomů genetika MeSH
- Silene genetika MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- srovnávací studie MeSH
The genus Silene is a good model for studying evolution of the sex chromosomes, since it includes species that are hermaphroditic and dioecious, while maintain a basic chromosome number of 2n = 24. For some combinations of Silene species it is possible to construct interspecific hybrids. Here, we present a detailed karyological analysis of a hybrid between the dioecious Silene latifolia as the maternal plant and a related species, hermaphroditic Silene viscosa, used as a pollen partner. Using genomic probes (the genomic in situ hybridization (GISH) technique), we were able to clearly discriminate parental genomes and to show that they are largely separated in distinct nuclear domains. Molecular GISH and fluorescence in situ hybridization (FISH) markers document that the hybrid genome of somatic cells was strictly additive and stable, and that it had 12 chromosomes originating from each parent, including the only X chromosome of S. latifolia. Meiotic analysis revealed that, although related, respective parental chromosomes did not pair or paired only partially, which resulted in frequent chromosome abnormalities such as bridges and irregular non-disjunctions. GISH and FISH markers clearly document that the larger genome of S. latifolia and its largest chromosome component, the X chromosome, were mostly employed in chromosome lagging and misdivision.
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