Abstract
Speciation via interspecific or intergeneric hybridization and polyploidization triggers genomic responses involving genetic and epigenetic alterations. Such modifications may be induced by small RNAs, which affect key cellular processes, including gene expression, chromatin structure, cytosine methylation and transposable element (TE) activity. To date, the role of small RNAs in the context of wide hybridization and polyploidization has received little attention. In this work, we performed high-throughput sequencing of small RNAs of parental, intergeneric hybrid, and allopolyploid plants that mimic the genomic changes occurring during bread wheat speciation. We found that the percentage of small RNAs corresponding to miRNAs increased with ploidy level, while the percentage of siRNAs corresponding to TEs decreased. The abundance of most miRNA species was similar to midparent values in the hybrid, with some deviations, as seen in overrepresentation of miR168, in the allopolyploid. In contrast, the number of siRNAs corresponding to TEs strongly decreased upon allopolyploidization, but not upon hybridization. The reduction in corresponding siRNAs, together with decreased CpG methylation, as shown here for the Veju element, represent hallmarks of TE activation. TE-siRNA downregulation in the allopolyploid may contribute to genome destabilization at the initial stages of speciation. This phenomenon is reminiscent of hybrid dysgenesis in Drosophila.
Original language | English |
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Pages (from-to) | 263-272 |
Number of pages | 10 |
Journal | Genetics |
Volume | 188 |
Issue number | 2 |
DOIs | |
Publication status | Published - 1 Jun 2011 |
Funding
Israeli Science Foundation [616/09]We thank Naomi Avivi-Ragolski and other members of the Levy laboratory for their help and discussions; Idan Efroni for help in data analysis; Yehudit Posen for editing the manuscript; and members of the bioinformatics unit, especially Jaime Prilusky for writing the quality-control script and Ester Feldmesser for help with statistical analysis. This work was funded by a grant from the Israeli Science Foundation, no. 616/09, to A.A.L.
All Science Journal Classification (ASJC) codes
- Genetics