Cellular information passes from one generation to the next in the form of Dna through a process called meiosis. Cellular information is stored in Dna, which is wound tightly around proteins in a double helix to form chromatin strands, which in turn are wound tightly to form chromatids. A normal human has 92 chromatids. After dna replication occurs in the S phase of meiosis, these chromatids duplicate themselves to form sister chromatids that are held together by a centromere. This becomes a chromosome, which then travels through the process of meiosis. Meiosis is how cellular information passes from one generation to the next because in this cycle, the egg and sperm containing genetic information from the paternal and maternal figure are created. When the egg and sperm go through fertilization, the cellular information from the parents are within the new, …show more content…
ALD is a mutation that is carried on the X chromosome, which of course is passed down from parents to child like all other chromosome. In females, this gene does not affect them greatly or at all because females have two X chromosomes. If one sex chromosome has a mutation, females have a “backup” X chromosome to compensate. This is why females are usually only carriers of ALD, like how Mrs.Odone was. In males however, they have no backup X chromosome, they have only one X chromosome. Their father will give them their Y chromosome, and their mother will give them their X one. If the mother was a carrier of ALD, then the mutation gets passed down to the son, who unfortunately will be affected to the full extent of symptoms. This happened to Lorenzo. His mother was a carrier of the ALD gene, so when she went through meiosis, she had a 50-50 chance of passing down the mutation. Unfortunately the odds were not in her favor, and the X chromosome she passed down to her son was the one containing the ALD mutation. Therefore, Lorenzo inherited ALD from his mother,
“Because it is unlikely that females will have two altered copies of this gene, it is very rare for females to have hemophilia. A characteristic of X-linked inheritance is that fathers cannot pass X-linked traits to their sons. ” says the US National Library of
In males (who have only one X chromosome), one altered copy of the COL4A5 gene in each cell is sufficient to cause kidney failure and other severe symptoms of the disorder. In females (who have two X chromosomes), a mutation in one copy of the COL4A5 gene usually only results in hematuria, but some women experience more severe symptoms. A characteristic of X-linked inheritance is that fathers cannot pass X-linked traits to their sons. In approximately 15 percent of cases, Alport syndrome results from mutations in both copies of the COL4A3 or COL4A4 gene and is inherited in an autosomal recessive pattern. The parents of an individual with the autosomal recessive form of this condition each have one copy of the mutated gene and are
There is only one cell which is able to survive in total of four cell which then develops into a female gametophyte. The pollination occurs in female gametophyte. Fertilization occurs after successful pollination in which one sperm cell will meet with the egg and will make a diploid embryo which will be surrounded by seed coat of tissue from the parent
Later it was discovered that it was the result of an extra copy of chromosome 21. The nondisjunction that results in an extra copy of chromosome 21 occurs during anaphase I in meiosis I. The genetic mutation is trisomy 21 (3 copies of chromosome 21). The characteristic phenotypic occurrences that are distinct to the disorder: poor muscle tone, stout neck, flat face, small head, mouth, and ears, eyes slanting upwardly, Brushfield spots, and stout fingers and
If a male offspring is diagnosed with this defective gene the results are usually fatal.
Therefore, males experience a more severe case than females as the X chromosome in males is only one, whereas in females there are two X chromosomes. Therefore, in females, there is another one to mask the effects of the one that has the mutation, in males; the one X chromosome is enough to cause disease. Question
Males have one X chromosome and one Y chromosome whilst females have two X chromosomes. Therefore if females have one of their X chromosomes containing the faulty gene F8, there is a chance they may have that gene working in their other X chromosome. On the other hand, if the one X chromosome that males have contains the faulty gene, they will have Haemophilia A. Therefore most people with Haemophilia A are males, . After treatment for Haemophilia A, inhibitors can develop in the body and attach to the protein factor VIII that has been inserted causing it to restrain its function of blood clotting.
Mitosis leads to production of cells that are genetically identical to their parent and as the basis for producing new cells, whereas meiosis leads to production of cells with half the genetic content of the parent and as the basis for producing new sexually reproducing organisms. With these two types of cell division
Turner Syndrome Assignment 1. The name of the most common abnormal chromosome disorder in female is Turner Syndrome. 2. This disease only occurs in females. It affects 1 in 2000- 2500 females, in the world.
If you get the gene from your parents, you can pass it on to your children,
The building blocks of life revolve around Meiosis and Mitosis, two processes of reproduction. Without them there would be no living organisms on the planet, or anywhere for that matter. Although they possess some similarities, Meiosis and Mitosis also have key differences. Meiosis and Mitosis, on a basic scale, are fairly similar throughout processes of reproduction. For starters, Meiosis and Mitosis both use the basic four steps of reproduction such as prophase, metaphase, anaphase, and telophase.
The idea of cell division, mitosis and binary fission, are ideas that make me stop and think. Mitosis is a type of cell division that happens in cells with a nucleus, and ends in two identical daughter cells. Mitosis interests me because of how complex the process is. It is amazing how it goes through various stages without hardly ever a mistake, and ends with two identical daughter cells. Binary Fission is a type of cell division that happens in cells without a nucleus, and also ends with two identical cells.
Meiosis and mitosis are forms of nucleus division in eukaryotic cells that occur after the Interphase or DNA replication of cell division occurs (OpenStax, 2013). Mitosis and meiosis are similar in their function to split the cell nucleus and form new cells however, the process for meiosis is much more involved. The process of meiosis is broken into two phase Meiosis I and Meiosis II with each having similar sub-phases where mitosis is one phase broken down into sub-phases similar to Meiosis II. The reason for meiosis to have two phases is that there are actually two separate cell divisions that will occur over meiosis. In Meiosis I the sub-phases consist of the following six phase.
This is due to the fact the majority of the cytoplasm (containing mtDNA) is inherited from the maternal ova rather then the paternal sperm, meaning the mother’s mitochondrial disorder is passed onto the offspring (NSW Government, 2015). In the case of LHON disorder, symptoms normally begin to show around adulthood. This means that for Felicity, it will be hard to distinguish whether the mutation has been passed onto her offspring. Furthermore, LHON symptoms are seen much more frequently in men then women. In fact, males are four to five times more likely to be affected than females (Yu-Wai-Man et al. 2000).
Turner Syndrome Turner Syndrome also known as Ullrich- Turner Syndrome or Gonadal dysgenesis, is a chromosomal disease that affects only females wherein one of the two X-chromosomes is defective or completely absent. . The name “Turner Syndrome” comes from an endocrinologist, Dr. Henry Turner, who first described the collection of findings in 1938 (Chen et al., 2006). The first published report of a female with a 45,X karyotype was in 1959 by Dr. Charles Ford and colleagues in Harwell, Oxfordshire (Chen et al., 2006). It was found in a 14-year-old girl with signs of Turner syndrome. Having one X-chromosome was identified soon after this.