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Almost all eukaryotic proteins are subject to post-translational modifications during mitosis and cell cycle, and in particular, reversible phosphorylation being a key event. The recent use of high-throughput experimental analyses has revealed that more than 70% of all eukaryotic proteins are regulated by phosphorylation; however, the mechanism of dephosphorylation, counteracting phosphorylation, is relatively unknown. Recent discoveries have shown that many of the protein phosphatases are involved in the temporal and spatial control of mitotic events, such as mitotic entry, mitotic spindle assembly, chromosome architecture changes and cohesion, and mitotic exit. This implies that certain phosphatases are tightly regulated for timely dephosphorylation of key mitotic phosphoproteins and are essential for the control of various mitotic processes. This review describes the physiological and pathological roles of mitotic phosphatases, as well as the versatile role of various protein phosphatases in several mitotic events.
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Nutrition autotrophs ingestive heterotrophs absorptive heterotrophs mixotrophs movement flagella cilia pseudopods non-motile.
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A) results in haploid cells
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The difference in pCO 2 is related to the amount of carbon that is converted from CO 2 gas to other nongaseous carbon species in the sea water, like bicarbonate and carbonate ions. This so-called "buffer capacity" is what allows the oceans to hold so much carbon.
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