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Unstable Inheritance of 45S rRNA Genes in Arabidopsis thaliana
FA. Rabanal, V. Nizhynska, T. Mandáková, PY. Novikova, MA. Lysak, R. Mott, M. Nordborg,
Jazyk angličtina Země Spojené státy americké
Typ dokumentu časopisecké články, práce podpořená grantem
NLK
Directory of Open Access Journals
od 2011
Free Medical Journals
od 2011
Freely Accessible Science Journals
od 2011-06-01 do 2020
PubMed Central
od 2011
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od 2011
Open Access Digital Library
od 2011-01-01
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od 2011-01-01
Oxford Journals Open Access Collection
od 2011-06-01
ROAD: Directory of Open Access Scholarly Resources
od 2011
PubMed
28188182
DOI
10.1534/g3.117.040204
Knihovny.cz E-zdroje
- MeSH
- Arabidopsis genetika MeSH
- genetické lokusy MeSH
- genová dávka MeSH
- inbreeding MeSH
- křížení genetické MeSH
- organizátor jadérka genetika MeSH
- rekombinace genetická genetika MeSH
- repetitivní sekvence nukleových kyselin genetika MeSH
- RNA ribozomální genetika MeSH
- rostlinné geny * MeSH
- typy dědičnosti genetika MeSH
- variabilita počtu kopií segmentů DNA genetika MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
The considerable genome size variation in Arabidopsis thaliana has been shown largely to be due to copy number variation (CNV) in 45S ribosomal RNA (rRNA) genes. Surprisingly, attempts to map this variation by means of genome-wide association studies (GWAS) failed to identify either of the two likely sources, namely the nucleolus organizer regions (NORs). Instead, GWAS implicated a trans-acting locus, as if rRNA gene CNV was a phenotype rather than a genotype. To explain these results, we investigated the inheritance and stability of rRNA gene copy number using the variety of genetic resources available in A. thaliana - F2 crosses, recombinant inbred lines, the multiparent advanced-generation inter-cross population, and mutation accumulation lines. Our results clearly show that rRNA gene CNV can be mapped to the NORs themselves, with both loci contributing equally to the variation. However, NOR size is unstably inherited, and dramatic copy number changes are visible already within tens of generations, which explains why it is not possible to map the NORs using GWAS. We did not find any evidence of trans-acting loci in crosses, which is also expected since changes due to such loci would take very many generations to manifest themselves. rRNA gene copy number is thus an interesting example of "missing heritability"-a trait that is heritable in pedigrees, but not in the general population.
Central European Institute of Technology Masaryk University 625 00 Brno Czech Republic
Gregor Mendel Institute Austrian Academy of Sciences Vienna Biocenter 1030 Austria
Citace poskytuje Crossref.org
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