SummaryThe p38 mitogen-activated protein kinase (p38 MAPK) family, which is comprised of four protein isoforms, p38, p38, p38 and p38, forms one of the key MAPK pathways. The p38 MAPKs are implicated in many cellular processes including inflammation, differentiation, cell growth, cell cycle and cell death. The function of p38 MAPKs in mitotic entry has been well established, but their role in mitotic progression has remained controversial. We identify p38 MAPK as a modulator of mitotic progression and mitotic cell death. In HeLa cells, loss of p38 results in multipolar spindle formation and chromosome misalignment, which induce a transient M phase arrest. The majority of p38-depleted cells die at mitotic arrest or soon after abnormal exit from M-phase. We show that p38 MAPKs are activated at the kinetochores and spindle poles throughout mitosis by kinase(s) that are stably bound to these structures. Finally, p38 is required for the normal kinetochore localization of polo-like kinase 1 (Plk1), and this contributes to the activity of the p38 MAPK pathway. Our data suggest a link between mitotic regulation and the p38 MAPK pathway, in which p38 prevents chromosomal instability and supports mitotic cell viability.
The addition of formylphenylboronic acid derivatives to urea and ethyl acetoacetate proceeds in the absence of an additional Lewis acid catalyst to give the corresponding dihydropyrimidinones (Biginelli products) in good yields. Novel boron-containing dihydropyrimidinones have been investigated for their ability to act as anticancer agents against the breast cancer cell line MCF7.Key words: anticancer, Biginelli compounds, boronic acids, breast cancer, dihydropyrimidinones.
Tomato is one of the most important crops worldwide. DNA barcoding is a molecular based method that has been successfully used for species identification, but a few studies have used this method for cultivated varieties identification. The aim of this study was to test the utility of DNA barcoding for the identification of five local salt tolerant tomato varieties and two commercial varieties. To assess the genetic diversity of tomato varieties, the non-coding plastid trnH-psbA intergenic spacer and three plastid regions (rbcL, rpoC1, rpoB) were used. Based on the sequence variation of the trnH-psbA barcode, three haplotypes were detected among the seven tomato varieties. A neighbor-joining tree was generated and separated the local tomato varieties from the commercial varieties into two distinct clusters. We found very low levels of variation in the chosen plastial markers, but additional markers could be tested in order to assess the utility of DNA barcodes in tomato varieties identification.
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