MadSci Network: General Biology |
Hi James, This is a great question and one many Cell Biologists have been working on for years. As you may know there are many proteins which regulate the process of cell division and the cell cycle as a whole. The two main class of proteins are the cyclins and the Cyclin-Dependent Kinases or CDK's. The regulation of these proteins are well conserved but the timing of the cell cycle vary mainly because of individual differences in each cell type. In general, there are two GAP phases where the cell determines it stage and fate. One GAP before it commits to duplicate it's chromosomes (called S phase) and another after DNA duplication but before cell division (also called mitosis, M phase). These GAP phases are called G1 and G2 respectively. The GAP phases can vary for a number of reasons. Some cells, like frog oocytes, have GAP phases that are very small to no time at all. They go to and from S phase to M phase so quickly that the two GAP phases are not seen. Factors that control cell division are mainly external. If an organism needs rapid growth the the signals to induce a longer GAP phase will not be present and these cells would divide faster. The opposite would also be true. So one answer to your question is in how each organism or cell decides to dictate the time it needs to spend in each GAP phase. Studies in many cell types, but first shown in yeast, have shown the presence of checkpoints. These are regulatory proteins that monitor if a cell is capable of entering S phase and/or M phase. If a cell gets into troube in these phases they can arrest, or stop growing, which allows the cell either time to fix the problem or commit cell suicide (apoptosis). Timing of S-phase and M-phase are also cell specific. Many scientists have formulated that the timing is equivalent to the complexity, amount of DNA and specificity of each cell in determining why one grows faster than another. As for mitosis, each separate phase within mitosis are classified primariyl on how the DNA is arranged and organized. There is prophase, which is where you will see the DNA condensing. Therefore the amount of time it takes to condense will equal how long this process is. There is no clear timeframe for each phase. Metaphase is the time is takes for the newly condensed DNA, now called chromosomes to align in the center of the cell. This timing will also vary as this is the site of the major mitotic checkpoint. During this checkpoint all of the chromosomes must be connected to the spindle pole. Studies have shown that if you inhibit this, either chemically or mechanically, the cell will just sit there and wait. Once the cell has given the signal that all is ok, the spindles will pull the chromosomes to each pole initializing the next step in mitosis, anaphase. Telophase is next were the cell begins to form an invagination of its membrane to form two cells. The DNA decondenses and cytokinesis starts. Cytokinesis is seen as the new membranes form and two new cells are seen. Since all these events take a number of regulatory proteins, why one is timed faster than another is more speculation than scientific proof. One thing that can be said is that the outside or external signals will dictate when cell division takes place. Internal signals will monitor this process and slow the cell down or arrest it if any problems arise. These internal cellular clocks are rather interesting and still a topic of research and debate. I hope this answer helps you out and I encourage you to Google your questions as there is load of information out there that may help you see it better. Good luck, Matt
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