Mitosis how does it happen




















During mitosis one cell divides once to form two identical cells. The major purpose of mitosis is for growth and to replace worn out cells. If not corrected in time, mistakes made during mitosis can result in changes in the DNA that can potentially lead to genetic disorders.

Mitosis is divided into five phases: 1. Interphase: The DNA in the cell is copied in preparation for cell division, this results in two identical full sets of chromosomes. Outside of the nucleus are two centrosomes, each containing a pair of centrioles, these structures are critical for the process of cell division.

During interphase, microtubules extend from these centrosomes. Prophase: The chromosomes condense into X-shaped structures that can be easily seen under a microscope. Each chromosome is composed of two sister chromatids, containing identical genetic information.

The chromosomes pair up so that both copies of chromosome 1 are together, both copies of chromosome 2 are together, and so on.

At the end of prophase the membrane around the nucleus in the cell dissolves away releasing the chromosomes. The mitotic spindle, consisting of the microtubules and other proteins, extends across the cell between the centrioles as they move to opposite poles of the cell.

Metaphase: The chromosomes line up neatly end-to-end along the centre equator of the cell. The centrioles are now at opposite poles of the cell with the mitotic spindle fibres extending from them.

The mitotic spindle fibres attach to each of the sister chromatids. Anaphase: The sister chromatids are then pulled apart by the mitotic spindle which pulls one chromatid to one pole and the other chromatid to the opposite pole. Telophase: At each pole of the cell a full set of chromosomes gather together. A membrane forms around each set of chromosomes to create two new nuclei.

During prophase, the parent cell chromosomes — which were duplicated during S phase — condense and become thousands of times more compact than they were during interphase. Because each duplicated chromosome consists of two identical sister chromatids joined at a point called the centromere , these structures now appear as X-shaped bodies when viewed under a microscope. Several DNA binding proteins catalyze the condensation process, including cohesin and condensin.

Cohesin forms rings that hold the sister chromatids together, whereas condensin forms rings that coil the chromosomes into highly compact forms. The mitotic spindle also begins to develop during prophase. As the cell's two centrosomes move toward opposite poles, microtubules gradually assemble between them, forming the network that will later pull the duplicated chromosomes apart.

When prophase is complete, the cell enters prometaphase — the second stage of mitosis. During prometaphase, phosphorylation of nuclear lamins by M-CDK causes the nuclear membrane to break down into numerous small vesicles. As a result, the spindle microtubules now have direct access to the genetic material of the cell. As prometaphase ends and metaphase begins, the chromosomes align along the cell equator. Every chromosome has at least two microtubules extending from its kinetochore — with at least one microtubule connected to each pole.

At this point, the tension within the cell becomes balanced, and the chromosomes no longer move back and forth. In addition, the spindle is now complete, and three groups of spindle microtubules are apparent. Kinetochore microtubules attach the chromosomes to the spindle pole; interpolar microtubules extend from the spindle pole across the equator, almost to the opposite spindle pole; and astral microtubules extend from the spindle pole to the cell membrane.

Metaphase leads to anaphase , during which each chromosome's sister chromatids separate and move to opposite poles of the cell. Enzymatic breakdown of cohesin — which linked the sister chromatids together during prophase — causes this separation to occur. Upon separation, every chromatid becomes an independent chromosome.

Meanwhile, changes in microtubule length provide the mechanism for chromosome movement. More specifically, in the first part of anaphase — sometimes called anaphase A — the kinetochore microtubules shorten and draw the chromosomes toward the spindle poles. Then, in the second part of anaphase — sometimes called anaphase B — the astral microtubules that are anchored to the cell membrane pull the poles further apart and the interpolar microtubules slide past each other, exerting additional pull on the chromosomes Figure 2.

Figure 2: Types of microtubules involved in mitosis During mitosis, several types of microtubules are active. The motor proteins associated with the interpolar microtubules drive the assembly of the spindle. Note the other types of microtubules involved in anchoring the spindle pole and pulling apart the sister chromatids.

Figure Detail. Cytokinesis is the physical process that finally splits the parent cell into two identical daughter cells. During cytokinesis, the cell membrane pinches in at the cell equator, forming a cleft called the cleavage furrow. The position of the furrow depends on the position of the astral and interpolar microtubules during anaphase. The cleavage furrow forms because of the action of a contractile ring of overlapping actin and myosin filaments. As the actin and myosin filaments move past each other, the contractile ring becomes smaller, akin to pulling a drawstring at the top of a purse.

When the ring reaches its smallest point, the cleavage furrow completely bisects the cell at its center, resulting in two separate daughter cells of equal size Figure 3. Figure 3: Mitosis: Overview of major phases The major stages of mitosis are prophase top row , metaphase and anaphase middle row , and telophase bottom row. This page appears in the following eBook.

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