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The process of meiosis 1 essay
Dialectic method
The process of meiosis 1 essay
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Meiosis is the process sex cells undergo for division. Unlike mitosis where cells reproduce from a diploid number of chromosomes to a diploid number of chromosomes, meiosis produces diploid cells from haploid cells. Diploid and haploid are names for the number of chromosomes a cell has, soma cells or body cells that reproduce through mitosis are diploid, meaning they have 46 chromosomes (in humans), haploid cell have half as many chromosomes as diploid cells; 23 in humans. Sex cells or gametes are haploid, to undergo sexual reproduction. Meiosis is a process similar to mitosis in some ways, however the phases of meiosis cycle twice. The first cycle of meiosis consists of; prophase I, metaphase I, anaphase I, and telophase I. In prophase I, the Cri-du-chat syndrome was named because of the distinct cry effected babies have. Cri-du-chat syndrome was discovered by the same scientist that discovered Down syndrome, Jerome Lejeune in 1963. Of genetic disorders caused by chromosomal deletion, cri-du-chat syndrome is the most common. This disorder is cause by a region of chromosome five being broke, or deleted, which causes all of the genes located on that region of the chromosome to be deleted. The actual error of this disorder probably occurs in the synthesis period of interphase because this is when DNA replicates itself, where the error for the deletion would occur. The deletion can occur at any step in meiosis, once chromosomes are visible in prophase. The phenotypic characteristics of individuals effected by this disorder are numerous. Most individuals affected will have smaller than average heads, and unusual facial features like, widely set eyes, small chins, and round faces. Individuals can also have incorrectly developed “voice boxes”, which causes the cat cry the disorder is named after, they can also have any number of muscle, heart, and or skeletal
The fungus Sordaria fimicola is commonly used to study the different processes of cell cycles such as the assortment of genes and the crossing over during meiosis. Considering the importance of genetics in the world today, this experiment is crucially valuable in helping the students gain knowledge in the different processes of cell cycle and learning how to attempt similar experiments on their own in the future. Sordaria fimicola requires “both mitotic and meiotic nuclear divisions to manufacture eight haploid ascospores” (Helm, 1998). This fungus “spend most of its life in haploid condition” (Glase, 1995). When the haploid nuclei fuse together in the cells, they beco...
Meiosis, also called reduction division, is a distinct type of cell division that is essential for sexual reproduction to occur. It is one in which two successive divisions of diploid cell occur thereby producing four genetically different haploid daughter cells, also called gametes, each with half the number of chromosomes and thus, half the total amount of genetic material as compared to the amount before meiosis began. Interphase precedes meiosis and thus, paves the way for meiosis to eventuate as the cell’s DNA replicates in the S phase yielding corresponding, identical chromosomes. Interphase sparks the marvelous process of meiosis that allows variation to transpire within the organisms it occurs, hence, giving rise to millions of organisms with unique aspects unlike any other on Earth. Because meiosis is a form of sexual reproduction itself, it is the means through which gametes are produced, each with a reduced number of chromosomes, so that when two gametes fuse during fertilization, not only do they form a diploid zygote with 46 chromosomes, but also have manifested differing features due to the rearrangement (crossing-over) of chromosomes.
chromosome is called a haploid cell. Meioses produces haploid daughter. cells that are genetically different from each other and from the parent cell. However, mitosis is a form of cell division that produces. daughter cells identical to the parent during repair or growth.
. Other mistakes that can occur during meiosis include translocation, within which a part of one chromosome becomes connected to another, and deletion, in which part of one chromosome is lost entirely. The severity of the results of those disorders depends entirely on the dimensions of the chromosome fragment concerned and, therefore, the genetic data contained in it. Modern technology will find these genetic abnormalities early within the development of the foetus, however at the moment, very little will be done to correct or perhaps treat the diseases ensuing from
Rett syndrome is a neurological disorder that mainly affects females. According to “The Molecular Pathology of Rett syndrome: Synopsis and Update”, it states that the disorder starts to be recognizable when the child is between six to eighteen months of age. The affected child will loose their ability to speak and hand movements. Through research, MECP2 is in the X chromosome gene (2006). An estimate of females that suffer from Rett syndrome is 1 in 1,000 and in the United States, it is approximately 16,000 young and adult females that are affected (Rett Syndrome, 2008). In my paper, I will give a brief history of how Rett syndrome was first noticed, discuss the dysfunction in the brain, the development and behavior, and possible treatments.
Cri-du-chat is a rare genetic disorder discovered by Jerome Lejeune in 1963. It is caused by the deletion of genetic material on chromosome five, an autosomal chromosome. The deletion occur on the "p" arm of the chromosome. Scientists do not know the reason why this chromosome deletion occurs.
Most cases of Down syndrome are not inherited. When the condition is caused by trisomy 21, the chromosomal abnormality occurs as a random event during the formation of reproductive cells in a parent. The abnormality usually occurs in egg cells, but it occasionally occurs in sperm cells. An error in cell division called nondisjunction results in a reproductive cell with an abnormal number of chromosomes. For example, an egg or sperm cell may gain an extra copy of chromosome 21. If one of these atypical reproductive cells contributes to the genetic makeup of a child, the child will have an extra chromosome 21 in each of the body's cells.
Children with Down Syndrome have distinct physical characteristics. They are short in stature and have a small, round face with a high flattened ...
A male makes one thousand new sperm per second, that is two trillion over a lifetime and they all are one of a kind, very unique. A woman has all her eggs from birth. The process starts out as meiosis, this is where 30,000 genes are then there are forty six chromosomes. Twenty three comes from your mother and twenty three come from your father, they only come together in meiosis in pairs, but they are not the same. Chromosomes make an exact copy of themselves then they condense making an X shape, chromosomes get a partner then embrace. The chromosomes cling close together in big chunks, the cell then divides pulling the pair apart with twenty three chromosomes. The cell alone is incomplete, but holds many promises. Every cell holds di...
Cells that contain two sets on chromosomes are called diploid. This is represented as 2n, n=number of chromosomes in one set of chromosomes. Cells that contain one set of chromosomes is called haploid. This is represented as n.
Meiosis is a special type of cell division that occurs during formation of sperm and egg cells and gives them the correct number of chromosomes. Since a sperm and egg unite during fertilization, each must have only half the number of chromosomes other body cells have. Otherwise, the fertilized cell would have too many.
The differences between the phases of mitosis and meiosis are that in mitosis, it has 1 cell division, duplicates the DNA, occurs in somatic cells, and no crossing over happens. In meiosis, it has 2 cell divisions, reduces the DNA, occurs in gametes or sperm and egg cells, while crossing over happens. They are both similar in which they both create daughter cells, headed by at least one round of DNA replication, and have similar stages for cell division.
...omosomes or genetic/chromosomal disorders. The most common type of genetic or chromosomal disorder is Down Syndrome or trisomy 21 (Cherry, n.d.). The condition occurs when a child has three chromosomes at the site of the twenty-first chromosome rather than the normal two. Some of the most common signs of Down Syndrome include round face, thick tongue, slanted eyes, hearing problems, heart defects, and intellectual impairment.
Once the sperm fuses with the ovum both chromosomes will pair up and begin the first stages of cell division.
Spermatogenesis is the formation of the male sex cell, sperm. This process begins with the differentiation of germ cells to form stem cells. A first mitotic division creates spermatogonia (diploid) and a second creates spermatocytes (diploid). Each spermatocyte then goes through meiosis to firm four haploid spermatids. In the seminiferous tubules the cells move towards the centre of the tubules as they undergo shape changes. The cells go through a spermatocyte and a spermatid stage and move into the lumen then the epididymis where they finally become mobile (textbook).