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Krela, R.

Publications and source records attributed to Krela, R..

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Expression of AtCAN1 and AtCAN2 genes of the plant SNc nuclease family correlates with programmed cell death and endoreduplication, indicating their role in the recycling of nucleic acid components.

BackgroundControlled degradation of genomic DNA is a common feature of all known cases of programmed cell death (PCD) in animals and plants. In plants, nucleic acid degradation during PCD facilitates the redistribution of their constituent building blocks. Previous studies have shown that nucleases from the S1/P1 family are involved in this process; however, due to the complexity of the process, it has been hypothesized that nucleases from other families, including staphylococcal-like nucleases (SNc), may also participate. In Arabidopsis, this family comprises two nucleases with atypical plasma membrane localization for this enzyme class: AtCAN1 and AtCAN2. ResultsUsing the promoter-driven GUS reporter assay, we showed that genes encoding SNc nucleases are expressed in tissues grouped into three main categories. The first category includes plant structures that are clear examples of organs undergoing PCD, such as the root cap, vascular bundle elements, the tapetum, maturing seed pods, and senescent leaves. The second category comprises cells whose function involves interaction with the external environment and which are susceptible to pathogen attack. This group includes root hairs, stomatal guard cells, and hydathodes. The third group of plant structures showing SNc nuclease activity consists of elements characterized by endoreduplication, i.e., stipules, trichomes, and the basal parts of the hypocotyl. The analysis of microarray and RNA-seq transcriptomic data further confirmed the expression of both SNc genes in these three categories. Moreover, we presented the effects of a mutation that eliminates AtCAN1 expression on plant development. ConclusionsOur studies show that SNc nucleases are as broadly involved in the DNA degradation during plant PCD as the previously reported S1/P1 proteins. The frequent overlap in their expression profiles suggests cooperative action. Whereas SNc nucleases localize to the plasma membrane, S1/P1 nucleases are nuclear, indicating distinct yet complementary nucleolytic pathways. We further demonstrate that SNc nucleases are specifically expressed in organs that do not undergo PCD but are characterized by endoreduplication, implicating them in an unexplored mechanism for redistributing polyploid DNA components.

plant biology↗

The expansion and diversification of epigenetic regulatory networks underpins major transitions in the evolution of land plants

Epigenetic silencing is essential for regulating gene expression and cellular diversity in eukaryotes. While DNA and H3K9 methylation silence transposable elements (TEs), H3K27me3 marks deposited by the Polycomb repressive complex 2 (PRC2) silence varying proportions of TEs and genes across different lineages. Despite the major development role epigenetic silencing plays in multicellular eukaryotes, little is known about how epigenetic regulatory networks were shaped over evolutionary time. Here, we analyse epigenomes from diverse species across the green lineage to infer the chronological epigenetic recruitment of genes during land plant evolution. We first reveal the nature of plant heterochromatin in the unicellular chlorophyte microalga Chlorella sorokiniana and identify several genes marked with H3K27me3, highlighting the deep origin of PRC2-regulated genes in the green lineage. By incorporating genomic phylostratigraphy, we show how genes of differing evolutionary age occupy distinct epigenetic states in plants. While young genes tend to be silenced by H3K9 methylation, genes that emerged in land plants are preferentially marked with H3K27me3, some of which form part of a common network of PRC2-repressed genes across distantly-related species. Finally, we analyse the potential recruitment of PRC2 to plant H3K27me3 domains and identify conserved DNA-binding sites of ancient transcription factor (TF) families known to interact with PRC2. Our findings shed light on the conservation and potential origin of epigenetic regulatory networks in the green lineage, while also providing insight into the evolutionary dynamics and molecular triggers that underlie the adaptation and elaboration of epigenetic regulation, laying the groundwork for its future consideration in other eukaryotic lineages.

evolutionary biology↗