Mitosis, Meiosis, Linked Genes, and Chromosomal Abnormalities
Similarities between Mitosis and Meiosis
Both Mitosis and Meiosis are involved in the reproduction of eukaryotic cells in multicellular organisms. Both start from a diploid parent cell, where the process of cell nuclear division starts with one cell. The DNA of the primary cell is replicated once prior to nuclear partitioning. Meiosis and Mitosis are multistage processes, including an Interphase, a Prophase, a metaphase, an anaphase, and a telophase, or multiples thereof. Both go through a period of growth with the interphase, and genetic synthesis, before their cycles begin. DNA is replicated within the S, or synthesis, phase of Interphase. Mitosis is only similar to the Meiosis
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Homologous chromosomes have the same genes, in the same order, at the same locations. Furthermore, they may not be identical as the alleles may differ. For example, although gene 1 is for eye colour, one codes for blue, the other for brown. In Meiosis, during Prophase I, once these chromosomes are subjected to synapsis, or pairing, during early meiosis, reciprocity arises, and the exchange of genetic material occurs resulting in a gene swap. It is the recombination nodules, located are various points along the synaptonemal protein structure, that define the spots (chiasmata) where the crossover will take place. Consequently, recombination rearranges, or reorganizes, chromosomes in such a way as to create new allele combinations, unless they are located too close together. This is crossing over is where we get our genetic diversity. However, linked genes throw the rules out the window and contravene Mendel's Law of Independent assortment, whereby, he states that dissimilar traits are inherited independently of the other. During the recombination, or crossing over, gene assignment does not change (OpenStax College, …show more content…
One can see at a glance if there is something awry with the arrangement. The chromosome number is decreased, increased by duplication, or the amount of whole groupings of chromosomes is incorrect.
1. Nondisjunction – failure to divide of paired homologous chromosomes during Meiosis I or II
2. Aneuploidy – decrease (monosomy) or increase (trisomy) of chromosomes
45 or 47 rather than the normal 46
Decrease in the number of chromosomes
Increase in the number of chromosomes
The most common aneuploidic disorder is Trisomy 21, or Down Syndrome. This disorder is characterized by three chromosome 21s. See figure 4 for Trisomy 21 karyogram.
Common signs: Seen across all ethnic communities, a person with Down syndrome has short stature, distinct facies, short fingers & toes, broad hands, slanted eyes, thick tongue, and developmental delays.
3. Polyploidy – increased chromosome sets
Extremely rare, seen mostly among lizards, fish, amphibians
4. Sex chromosome nondisjunctions – X-inactivation
Example: Klinefelter Syndrome, one type XXY
Example: Turner Syndrome, usually characterized as X0
5. Duplications and Deletions – loss or duplication of a portion of the chromosome
Example: Cri-du-chat, deletion of
Women have two X-chromosomes so that is why they will not have the disease. They have one defected gene and one normal. Their normal
Genes, or sometimes called alleles, are the small subunits that make up DNA and create the unique traits for each species. The type of genes that are replicated and passed down during DNA replication are called alleles and these combine when forming a new offspring to yield a new combination of traits. In most cases, alleles for a single trait are seen in pairs. The singular alleles within a pair can be classified as dominant or recessive, and whichever classification it falls under decides how the gene will be expressed. Dominant alleles are typically represented with a capital letter and they are traits that will always be expressed, regardless of the other allele it is paired with.
This is because the different chromosomes that the genres are on are independently assorted into daughter cells during meiosis (Updegraff,
fertility and type of offspring depends on which cell line gave rise to the ovaries or testes; varying degrees of intersex differences may result if one set of cells is genetically female and another genetically male. Tetragametic chimerism Tetragametic chimerism is a form of congenital chimerism. This condition occurs through the fertilisation of two separate ova by two sperm, followed by aggregation of the two at the blastocyst or zygote stages. This results in the development of an organism with intermingled cell lines.
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
The same region is also amplified on both chromosomes, however they are different sizes, which are then put into gel
During random fertilization, no gamete has a greater chance than the other with fusing together in sperm and zygote fusion. These processes contribute to the production of genetic variety because of the many opportunities of unique combinations, unlike the process of mitosis, in which identical daughter cells are always the
Trisomy 21 occurs when a person has 47 chromosomes rather than the normal 46. The physician can usually diagnose the condition of Down syndrome when the baby is born, and confirms the diagnosis with an extra blood
Klinefelter syndrome, also known as ‘47,XXY’ and ‘XXY’ is found in males, this is due to the fact that the host male gets another X chromosome. The image on the right you can see the extra chromosome with the pair of sex chromosomes. Usually there are only two chromosomes that determine the sex, one from opposite sexes but when it comes to Klinefelters Syndrome there is an extra X chromosome. Because this due to the additional chromosome it can described as a chromosome disorder.
Chapter 1 INTRODUCTION A. BACKGROUND OF THE STUDY Chromosomal abnormalities which frequently cause physical and cognitive abnormalities for a child throughout life are usually evident at birth. Nondisjunction, deletion translocation, mosaicism, and isochrosome abnormalities are some of the various forms of chromosomal abnormalities (Hatfield, 2008). Nondisjunction is the most common type of chromosomal abnormalities which occur through uneven chromosomal division. During cell division of the cells reproduction, the 46 chromosomes should be divided into half having 23 chromosomes in each new cell. With the new cell having an extra or lacking chromosome, nondisjunction abnormalities occur.
The sister chromatids are pulled towards oppsite poles of the cell. (http://andrewhulse.weebly.com/archive-blog---life-in-room-213206209/archives/01-2014) Telophase:the chormatids are now called chormosomes. The nuclear envelope reforms arounds the two sets of chromosomes to form two new nuclei and in each nucleus the nucleolus reforms. The spindle fibres disappear and the chromosomes become uncoiled, elongated and are no longer visible.
When a heterozygous individual has his genetic loci separated and located on two different homologous chromosomes and the meiosis process kicks in, it all begins with the interphase process. Meiosis begins with a one diploid parent cell with 46 chromosomes, and ends in four haploid cells with 23 chromosomes each. In the interphase l process, it has three stages and then proceeds into prophase I. The stages include the G1 phase, in which the cell grows, the S phase, in which the chromosomes we started with and the centrioles replicates and the G2 phase, where the cell prepares for Meiosis. Prophase l is the beginning phase of Meiosis, in which the homologous chromosomes condense as well as become visible.
In most cases of Down syndrome, a child gets an extra chromosome 21 for a total of 47 chromosomes instead of 46. (Susan Skallerup) Research said it is this extra genetic material that causes the physical appearance and developmental delays associated with DS. Today no one knows for sure why DS happens and there's no way to prevent the chromosomal error that causes it. Scientists do know that women age 35 and older have a extremely higher risk of having a child with the condition.
Introduction The human genome consists of 23 pairs of chromosomes. 22 of those pairs are homologous and autosomal. The 23rd pair is the sex determining pair of chromosomes. In females, the chromosomes are homologous, namely the karyotype XX.
If this egg or sperm is fertilize, then the baby will have three copies of the #21 chromosome, which is called trisomy 21, or Down syndrome. The features of Down syndrome are caused by that extra copy of chromosome #21 being in every cell in the body. When this cell with three 21 chromosomes continues to multiply, and the pregnancy is carried to term, a baby with Down syndrome will be born. That what happen to your baby as well when the baby is developing in your womb. When you baby boy developing there was a random error in cell division that results that result having an extra copy of chromosome 21.