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Poreba, E.

Publications and source records attributed to Poreba, E..

2 recordsLinked to original sources

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↗

Single nucleus RNA sequencing reveals glial cell type-specific responses to ischemic stroke

Reactive neuroglia critically shape the brains response to ischemic stroke. However, their phenotypic heterogeneity impedes a holistic understanding of the cellular composition and microenvironment of the early ischemic lesion. Here we generated a single cell resolution transcriptomics dataset of the injured brain during the acute recovery from permanent middle cerebral artery occlusion. This approach unveiled infarction and subtype specific molecular signatures in oligodendrocyte lineage cells and astrocytes, which ranged among the most transcriptionally perturbed cell types in our dataset. Specifically, we characterized and compared infarction restricted proliferating oligodendrocyte precursor cells (OPCs), mature oligodendrocytes and heterogeneous reactive astrocyte populations. Our analyses unveiled unexpected commonalities in the transcriptional response of oligodendrocyte lineage cells and astrocytes to ischemic injury. Moreover, OPCs and reactive astrocytes were involved in a shared immuno-glial cross talk with stroke specific myeloid cells. In situ, osteopontin positive myeloid cells accumulated in close proximity to proliferating OPCs and reactive astrocytes, which expressed the osteopontin receptor CD44, within the perilesional zone specifically. In vitro, osteopontin increased the migratory capacity of OPCs. Collectively, our study highlights molecular cross talk events which might govern the cellular composition and microenvironment of infarcted brain tissue in the early stages of recovery.

neuroscience↗