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Cell Cycle Progression through the cell cycle requires the coordination of variety of macromolecular syntheses, assemblies and movements. The chromosomes must be replicated, condensed, segregated, and decondensed. The spindle poles must duplicate, separated, and migrate to opposite ends of the nucleus. Coordination of these complex processes is thought to be achieved by series of changes in the cyclin-dependent kinases (CDKs). The active forms of the CDKs are a complex of at lest two proteins, kinase and cyclin. These complexes undergo changes in the kinase and cyclin components that are believed to drive the cell from one stage of the cell cycle to another. According to this paradigm, cell cycle stage is determined by the constellation of proteins activated or inactivated by phosphorylation as result of the activity of the CDKs during that stage. Progression through the cell cycle is tightly controlled by cell-cycle checkpoints in phases G1 and G2. Interphase: The period when the cell is not in mitosis is referred to as "interphase". Chromosomes are replicated beginning at the origins of replication and proceed bidirectionally from the origins across the chromosome. Euchromatin makes up most of interphase chromosomes. Interphase contains the following phases:
Mitosis (M phase): Chromosomes become highly condensed and then are separated and distributed to the two daughter nuclei. The condensation of interphase chromosomes into mitotic chromosomes requires a class of proteins called condensins which are large protein complexes that contain SMC proteins; these are long, dimeric protein molecules that use the energy of ATP hydrolysis to make large right handed loops in DNA. When the 46 human chromosomes at mitosis are stained with dyes, one can see a reproducible banding patter. The centromere attaches to the duplicated chromosomes to the mitotic spindle so that one copy is distributed to each daughter cell. |
Copyright © 2002-2005 YPatent
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