Interpopulation hybridization generates meiotically stable rDNA epigenetic variants in allotetraploid Tragopogon mirus

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Publikace nespadá pod Fakultu sportovních studií, ale pod Přírodovědeckou fakultu. Oficiální stránka publikace je na webu muni.cz.
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MATYÁŠEK Roman KUTÍLKOVÁ Eva HÚSKA Dalibor JEŽKOVÁ Ivana SOLTIS Pamela SOLTIS Douglas KOVAŘÍK Aleš

Rok publikování 2016
Druh Článek v odborném periodiku
Časopis / Zdroj The Plant Journal
Fakulta / Pracoviště MU

Přírodovědecká fakulta

Citace
www http://www.ncbi.nlm.nih.gov/pubmed/26711705
Doi http://dx.doi.org/10.1111/tpj.13110
Obor Biofyzika
Klíčová slova allopolyploid; chromatin modification; epigenetic variants
Popis Uniparental silencing of 35S rRNA genes (rDNA), known as nucleolar dominance (ND), is common in inter- speci?c hybrids. Allotetraploid Tragopogon mirus composed of Tragopogon dubius (d) and Tragopogon por- rifolius (p) genomes shows highly variable ND. To examine the molecular basis of such variation, we studied the genetic and epigenetic features of rDNA homeologs in several lines derived from recently and independently formed natural populations. Inbred lines derived from T. mirus with a dominant d-rDNA homeolog transmitted this expression pattern over generations, which may explain why it is prevalent among natural populations. In contrast, lines derived from the p-rDNA dominant progenitor were meioti- cally unstable, frequently switching to co-dominance. Interpopulation crosses between progenitors display- ing reciprocal ND resulted in d-rDNA dominance, indicating immediate suppression of p-homeologs in F 1 hybrids. Original p-rDNA dominance was not restored in later generations, even in those segregants that inherited the corresponding parental rDNA genotype, thus indicating the generation of additional p-rDNA and d-rDNA epigenetic variants. Despite preserved intergenic spacer (IGS) structure, they showed altered cytosine methylation and chromatin condensation patterns, and a correlation between expression, hypomethylation of RNA Pol I promoters and chromatin decondensation was apparent. Reversion of such epigenetic variants occurred rarely, resulting in co-dominance maintained in individuals with distinct geno- types. Generally, interpopulation crosses may generate epialleles that are not present in natural popula- tions, underlying epigenetic dynamics in young allopolyploids. We hypothesize that highly expressed variants with distinct IGS features may induce heritable epigenetic reprogramming of the partner rDNA arrays, harmonizing the expression of thousands of genes in allopolyploids.
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