Non-apoptotic programmed cell death with paraptotic-like features in bleomycin-treated plant cells is suppressed by inhibition of ATM/ATR pathways or NtE2F overexpression
Jazyk angličtina Země Velká Británie, Anglie Médium print-electronic
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
22268149
DOI
10.1093/jxb/err439
PII: err439
Knihovny.cz E-zdroje
- MeSH
- bleomycin farmakologie MeSH
- buněčná smrt účinky léků MeSH
- down regulace účinky léků MeSH
- exprese genu účinky léků MeSH
- fragmentace DNA účinky léků MeSH
- kontrolní body buněčného cyklu účinky léků MeSH
- protein-serin-threoninkinasy genetika metabolismus MeSH
- rostlinné proteiny genetika metabolismus MeSH
- tabák cytologie účinky léků genetika metabolismus MeSH
- transkripční faktory E2F genetika metabolismus MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- bleomycin MeSH
- protein-serin-threoninkinasy MeSH
- rostlinné proteiny MeSH
- transkripční faktory E2F MeSH
In plants, different forms of programmed cell death (PCD) have been identified, but they only partially correspond to those described for animals, which is most probably due to structural differences between animal and plant cells. Here, the results show that in tobacco BY-2 cells, bleomycin (BLM), an inducer of double-strand breaks (DSBs), triggers a novel type of non-apoptotic PCD with paraptotic-like features. Analysis of numerous PCD markers revealed an extensive vacuolization, vacuolar rupture, and chromatin condensation, but no apoptotic DNA fragmentation, fragmentation of the nuclei, or sensitivity to caspase inhibitors. BLM-induced PCD was cell cycle regulated, occurring predominantly upon G(2)/M cell cycle checkpoint activation. In addition, this paraptotic-like PCD was at least partially inhibited by caffeine, a known inhibitor of DNA damage sensor kinases ATM and ATR. Interestingly, overexpression of one NtE2F transcriptional factor, whose homologues play a dual role in animal apoptosis and DNA repair, reduced PCD induction and modulated G(2)/M checkpoint activation in BY-2 cells. These observations provide a solid ground for further investigations into the paraptotic-like PCD in plants, which might represent an ancestral non-apoptotic form of PCD conserved among animals, protists, and plants.
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