The randomness in the alignment of recombined chromosomes at the metaphase plate, coupled with the crossing over events between nonsister chromatids, are responsible for much of the genetic variation in the offspring. To clarify this further, remember that the homologous chromosomes of a sexually reproducing organism are originally inherited as two separate sets, one from each parent. Using humans as an example, one set of 23 chromosomes is present in the egg donated by the mother. The father provides the other set of 23 chromosomes in the sperm that fertilizes the egg. Every cell of the multicellular offspring has copies of the original two sets of homologous chromosomes. In prophase I of meiosis, the homologous chromosomes form the tetrads. In metaphase I, these pairs line up at the midway point between the two poles of the cell to form the metaphase plate. Because there is an equal chance that a microtubule fiber will encounter a maternally or paternally inherited chromosome, the arrangement of the tetrads at the metaphase plate is random. Thus, any maternally inherited chromosome may face either pole. Likewise, any paternally inherited chromosome may also face either pole. The orientation of each tetrad is independent of the orientation of the other 22 tetrads.
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Answer:
Helper T cells stimulate B-cells to produce antibodies and killer T cells to destroy the non-self cells. Cytotoxic T cells on the other hand are direct attack cells. They can kill the micro organisms by creating pores on the invader's cell.
Explanation:
T lymphocyte mediated immunity of cell mediated immunity do not secrete antibodies but they help stimulate the B cells to produce them. Immature T cells are produced in bone marrow from where they migrate to thymus via blood. In the thymus maturation of T cells occur and then they migrate to lymphoid tissue and get differentiated into three types:
a. Helper T cells: As the name suggests, they help in activating other immune cells, in other terms they are the regulator of virtually all functions of immune system. Protein mediator called lymphokines are produced by these helper T cells in order to regulate the immune functions. Some examples of these lymphokines are: Interleukin-2 interleukin-3, interferon gamma. T helper cells stimulate the B-cells to produce antibodies.
b. Cytotoxic cells or killer T cells: The lymphokine interleukin-2 is responsible for the growth and proliferation of both cytotoxic T cells and suppressor T cells. With the help of receptor proteins on the surface of killer T cells, they bind to the specific antigen. After binding, they secrete a pore forming protein called perforins which create pores on the invaders cell membrane for water to enter into it thereby cell swells and finally lyse.
c. Suppressor T cells: They suppress the function of above two T cells.
The difference is that thymine is replaced by Uralic in mRNA.
Answer:
It is spherical in shape and directs and command all the function of the cell, Found only in eukaryotes
Explanation:
vacuole are fluid filled membrane bound space .there are many small vacuoles in plant cell and one large vacuole in animal cell
Tumor suppressor genes encode for proteins that inhibit or slow the progression of the cell cycle through a specific stage.they also encode for check point control proteins that arrests the cell cycle if the DNA is damaged or the chromosomes are abnormal. Mutation in the tumor suppressor genes that cause a loss or decreased function would lead to uncontrolled cell cycle leading to abnormal proliferation and the cell may become cancerous.