Cell division in the unicellular microalga Dunaliella viridis depends on phosphorylation of extracellular signal-regulated kinases (ERKs)

In mammalian cells, MAPKs are involved in both stress response (JNK and p38 pathways) and cell proliferation and differentiation [extracellular signal-regulated kinase (ERK)] through protein kinase cascades. Exposure of Dunaliella viridis cell cultures to PD98059, a very specific inhibitor of the ER...

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Veröffentlicht in:Journal of experimental botany. - 1985. - 58(2007), 5 vom: 15., Seite 1001-11
1. Verfasser: Jiménez, Carlos (VerfasserIn)
Weitere Verfasser: Cossío, Belén R, Rivard, Christopher J, Berl, Tomás, Capasso, Juan M
Format: Aufsatz
Sprache:English
Veröffentlicht: 2007
Zugriff auf das übergeordnete Werk:Journal of experimental botany
Schlagworte:Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't Flavonoids Plant Proteins RNA, Messenger Extracellular Signal-Regulated MAP Kinases EC 2.7.11.24 2-(2-amino-3-methoxyphenyl)-4H-1-benzopyran-4-one SJE1IO5E3I
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100 1 |a Jiménez, Carlos  |e verfasserin  |4 aut 
245 1 0 |a Cell division in the unicellular microalga Dunaliella viridis depends on phosphorylation of extracellular signal-regulated kinases (ERKs) 
264 1 |c 2007 
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500 |a Date Revised 15.08.2018 
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520 |a In mammalian cells, MAPKs are involved in both stress response (JNK and p38 pathways) and cell proliferation and differentiation [extracellular signal-regulated kinase (ERK)] through protein kinase cascades. Exposure of Dunaliella viridis cell cultures to PD98059, a very specific inhibitor of the ERK signalling pathway, resulted in a total arrest of cell proliferation and a complete dephosphorylation of ERK. As shown by flow cytometry analysis of propidium iodide-stained cells, PD98059 stopped mitosis at the G(2) phase after the S phase has been completed. Multiple physiological parameters such as cell motility and reducing power generation (NADPH) clearly indicate that the treated cells are wholly viable. Exposure of D. viridis to environmental stresses that impair cell division, such as hyperosmotic shock, nitrogen starvation, or sublethal UV irradiation, caused a marked decrease in the phospho-ERK levels as detected by western blot. Two 400 bp polynucleotides from D. viridis with high homologies to published sequences of ERK1 and ERK2 were cloned, sequenced, and submitted to GenBank. Northern blot analysis revealed two mRNA bands of approximately 1.9 kb, consistent with the expected size of ERK proteins ( approximately 40 kDa). Sequence analysis showed that they contained several mitogen-activated protein kinase (MAPK) conserved domains, including II, III, VIb, VII, and the double phosphorylation motif. Interestingly, in D. viridis, this motif was T*DY* instead of the canonic T*EY*. Based on this finding, ERK plant sequences can be divided into two groups, one termed the T*DY* branch and the other termed the T*EY* branch. The molecular and functional data presented here suggest that ERK is a very ancient signalling pathway and that it was already present in the last common ancestor of all eukaryotic cells 
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650 4 |a Research Support, N.I.H., Extramural 
650 4 |a Research Support, Non-U.S. Gov't 
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650 7 |a Plant Proteins  |2 NLM 
650 7 |a RNA, Messenger  |2 NLM 
650 7 |a Extracellular Signal-Regulated MAP Kinases  |2 NLM 
650 7 |a EC 2.7.11.24  |2 NLM 
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700 1 |a Cossío, Belén R  |e verfasserin  |4 aut 
700 1 |a Rivard, Christopher J  |e verfasserin  |4 aut 
700 1 |a Berl, Tomás  |e verfasserin  |4 aut 
700 1 |a Capasso, Juan M  |e verfasserin  |4 aut 
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