Stages Of Cell Cycle Biotechnology Notes
Stages Of Cell Cycle -We all know that the ‘Cell is the structural, functional and the biological unit of life’. Any living organism is either unicellular or multicellular. Whatever the case, the cell follows its own life cycle. The life cycle of a eukaryotic cell can be divided into three stages: resting phase, interphase and mitotic phase (M-phase).
– The M phase is the actual division phase wherein the mother cell divides into two daughter cells. It occurs in two stages: Mitosis (nuclear division) and Cytokinesis (cytoplasmic division).
Let’s have a more detailed look at each of the phases
I. Resting Phase or G0 Phase
Cells in the G0 phase are ones that have entered a non-dividing state either reversibly or irreversibly. The cells which are reversibly or temporarily non- dividing or the quiescent cells, can enter back into cell cycle on receiving an appropriate signal and enter the G1 phase. The irreversibly non-dividing cells either become senescent or differentiated. Cells become senescent when there are DNA damage or any other problem. Cells like neurons usually get differentiated and perform their functions.
Interphase is the phase in which the cell grows till it can divide it’s genetic material and the cytoplasm into two halves i.e. capable of producing two daughter cells. This phase is also known as the Preparatory phase. Interphase is, in turn, divided into three different subphases: G1, S, and G2.
a. G1 Phase (First Gap Phase)
During this phase, the cell grows in its size. It synthesizes a group of proteins and nucleotides which are required for the synthesis (replication) of the DNA along with other normal processes.
b. S Phase (Synthesis Phase)
DNA replication takes place during the S phase. The entire genome is duplicated in this phase and the two copies of DNA are held together at the centromere region.
c. G2 Phase (Second Gap)
The main processes that take place during the G2 phase are the duplication of cell organelles and the rearrangement of the cytoskeleton. This phase is also characterized by the synthesis of other proteins required for the upcoming M phase (mitosis and the cytokinesis).
III. M phase (The Mitotic Phase)
M phase begins after the G2 phase of the interphase. During the M phase, the replicated DNA condenses to form the X shaped chromosomes, wherein each sister chromatid is the entire replicated and condensed daughter DNA.
Fig 3: A chromosome. The two sister chromatids are joined at the centromere, which is also the site for kinetochore arrangement. In the mitosis, the chromosomes are aligned and the two sister chromatids are separated, each becoming the genetic material of the daughter cells.
The M phase is divided into
A. Mitosis characterized by karyokinesis or nuclear division and
B. Cytokinesis characterized by cytoplasmic division.
Mitosis brings about the division of the nuclear material or Karyokinesis in 4 phases called prophase, metaphase, anaphase, and telophase.
During prophase, the chromosomes begin to condense, the nucleolus disappears, and the nuclear envelope disintegrates. The cytoplasmic organelles are pushed to the periphery of the cell. The centrosomes which help in the arrangement of microtubules to form spindle fibers, move to the opposite poles of the cell.
The condensed chromosomes are attached to the spindle fibers with the help of protein complex, kinetochore. Each sister chromatid has a kinetochore of its own which helps in separation and dragging of each of them to the opposite poles.
A human cell at this point has 46 chromosomes (and 92 chromatids). The two daughter cells receive one chromatid or daughter chromosomes each from the 46 chromosomes (see the previous post on chromosomes).
During metaphase, the chromosomes are most condensed. The sister chromatids are still connected at the centromere and aligned in the center of the spindle apparatus forming the metaphase plate.
During anaphase, the two sister chromatids are pulled apart to form two daughter chromosomes. As mentioned before the spindle microtubules pull the chromosomes toward opposite poles (toward the centrosome) with help of the kinetochore. The cell becomes elongated as the two chromatids move to the opposite poles and are no longer joined at the centromere.
During telophase, the separated daughter chromosomes reach the opposite poles. Once the daughter chromosomes reach the opposite poles they begin to decondense. Along with the decondensation, the transcription and the translation of important proteins begin. The nuclear envelope is formed again and nucleosomes begin to appear within the nuclear area. The spindle apparatus is dismantled and tubulin monomers begin to organize the cytoskeletal structure of the daughter cells.
The nuclear division is accompanied by the cytoplasmic division, which is known as cytokinesis. Cytokinesis leads to a separation of the cytoplasmic components into two daughter cells proportionately. There are some differences in the process of cytokinesis in a plant cell and an animal cell.
Animal cells lack cell walls. In these cells, a contractile ring composed of actin filaments forms just inside the plasma membrane along the circumference of the cell at the site of the metaphase plate. The ring contracts drawing the plasma membrane at equator closer forming the cleavage furrow (similar to the way a drawstring tightens). The cleavage furrow finally contracts completely resulting in two separate daughter cells.
Plant cells have cell walls. For the complete division, a new cell wall has to be synthesized between the two daughter cells. In-plant cells, the Golgi apparatus stores all the material for cell wall synthesis during interphase and disperses throughout the cell in the form of small vesicles. During telophase, these Golgi vesicles move at the metaphase plate, fuse with each other and the existing cell wall along with the metaphase plate. As more and more vesicles fuse and mature, the entire cell wall at the metaphase plate is formed dividing the two cell.
• Cell cycle Regulation:
The cell undergoes through different stages of the cell cycle to give two daughter cells. Each of the phases of the cell cycle is under the very strict control of cell cycle checkpoints. These checkpoints ensure that the previous stage has been completed in a successful error-free manner before initiating the next phase.
The main mechanism that regulates the cell cycle progression involves the cyclin-dependent kinases (CDKs). CDKs are a group of serine/threonine protein kinases that phosphorylate various substrates which co-ordinate and regulate the progression of the cell cycle. CDKs are constitutively present in the cell but are inactive and only activated when they bind their cyclin subunits. These cyclin subunits are synthesized at the particular phase and degraded thereafter. When cyclins are synthesized, they bind and activate specific CDKs, resulting in the progression to the next phase. The CDK activity is controlled by the various other promoters and inhibitors as well.
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