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The process of meiosis 1 essay
The process of meiosis 1 essay
The process of meiosis 1 essay
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Sometimes when you look at two children from one family, and they look so different, you think one of them must be adopted. However, this is not necessarily the case. It is possible for parents to have children that look completely different from their parents. Each parent has 46 chromosomes divided into pairs of two. The pairs are one from the maternal side and one from the paternal side. Each parent passes on 23 chromosomes, one from each pair. This is randomly selected which chromosome gets passed on. Alleles are a variant of the gene within the chromosomes. With various combinations of alleles, there are over 8 million different human possibilities to occur from one couple. This is why two parents can have children that are all different. …show more content…
Meiosis is a process of cell division, chromosomes are copied, sometimes incorrectly, paired up and divided. In meiosis there is crossing over in which there is an exchange of the genetic material. In the crossing over, it becomes a woven network of the proteins until they have switched places. This is the same for certain processes, which can also affect the DNA. There are two stages of meiosis, also known as meiosis I and meiosis II. The chromosomes are diploid, meaning into two segments and then divide again into four haploid daughter cells. Mendel came up with the Law of Independence, which is that the alleles separate different from each other during gamete formation or meiosis. The different traits are inherited separate from each other. Within meiosis I the first stage is prophase I is where the chromosomes condense and the crossing starts to happen after the nuclear envelope breaks down. Next comes metaphase I. In Metaphase I, the paired homologous chromosomes move to the center of the cell. Anaphase I is next, the chromosomes now move to the opposite poles of the cell. Telophase I, the chromosomes gather at the poles or end of the cells and there is a division of the cytoplasm. Now we begin with meiosis II, which occurs in four stages. In prophase II, a spindle forms around the chromosome. Next comes metaphase II, which the chromosomes line up at the middle of the cell or the equator. In …show more content…
These mistakes like our own have a range of causes and effects, however these mistakes cause mutations in our body. Changes or mutations are not always bad and, sometimes changes that matter to evolution are naturally occurring and can happen slowly over time. When a cell divides, it makes a copy of its DNA, and sometimes copying incorrectly causing errors due to either incomplete or imperfect replication. This imperfection can even be a complete deletion of a genetic code. That small difference from the original DNA is a mutation. Mutations can affect a group of genes or whole chromosome and usually happens during meiosis. It can happen during the crossing over, random fertilization, or different arrangement of chromosomes. Mutations can cause either a large problems such as cystic fibrosis, small problems such an extra toe or even webbed
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.
Introduction In our genes, multiple different alleles determine whether one person will have a certain trait or not. Alleles are what make up our genotypes and in this lab, we wanted to determine the genotypes of our class in the two loci: TAS2R38 and PV92. The TAS2R38 locus codes for a protein that involves the bitter taste of PTC; the gene determines whether or not a person will taste the PTC paper as very bitter or no taste at all. People with the “T” allele are tasters, while those that are homozygous recessive (tt) are non-tasters. The taster locus can be found in chromosome 7.3.
On a normal person, you have 23 pairs of chromosomes. In each pair, 1 gene comes from the mother, and 1 gene comes from the father. This is how things get passed down from parents to children (like eye color, height, skin tone etc...).
Each cell contains the same genetic code as the parent cell, it is able to do this because it has copied it’s own chromosomes prior to cell death. division. The. Meiosis consists of two divisions whilst mitosis is followed. in one division; both these processes involve the stages of interphase, prophase, metaphase, anaphase, and telophase.
Sexual reproduction is that the union of male and feminine gametes to create a fertilised egg or zygote. The ensuing offspring inherit one-half their traits from every parent. Consequently, they 're not genetically similar to either parent or siblings, except within the case of identical twins. As theorised by Mendel, adults are diploid, meaning as 2N, having 2 alleles offered to code for one attribute. The gametes should be haploid, signified by N, containing just one allele in order that once 2 haploid gametes mix, they manufacture a traditional diploid individual. The method where haploid sex cells are created from diploid parents is known as meiosis, and it happens solely within the reproductive organs.
These mutations also are referred to as gremlin mutations as a result of they 're the gift within the parent 's egg or spermatozoa cells that also are referred to as microorganism cells [3]. First of all, the associate degree union of an egg and sperm takes place. The ensuing creature cell receives deoxyribonucleic acid from each folk. In condition that this acid features a mutation, every cell and feature of the kid developing from those genes will face the mutation and sudden changes in the sequencing of the genes. The other type of mutations known as bodily changes occur at your time throughout a life of an individual and are gift solely inbound cells, instead of having in each cell within the body [2]. Non heritable mutations incorporeal cells (cells apart from spermatozoa) are unable to become one generation to the later generations. In a number of cases, mutation may take place during the egg or sperm development but this may not result to major differences in terms of cell structure [4]. In different cases, some changes take place within the creature in a minute once after the union of eggs and sperms [5].Because the creature divides, every ensuing cell within the growing embryo can have the alteration. De Novo mutations could make a case for genetic disorders within which associate degree affected kid features a mutation in
A chromosome is made up of two identical structures called chromatids. The process of nuclear division is called interphase; each DNA molecule in a nucleus makes an identical copy of itself. Each copy is contained in the chromatid and a characteristic narrow region called the centromere holds the two chromatids together. The centromere can be found anywhere along a chromosome but the position is the characteristic for a particular chromosome. Each Chromatid contains one DNA molecule. DNA is the molecule of inheritance and is made up of a series of genes. The fact that the two DNA molecules in the sister chromatids, and hence their genes, are identical is the key to precise nuclear division.
...generations. If it is a beneficial mutation, then it will likely not only pass on through reproduction, but those offspring will have better odds of reproducing in order to “spread” that trait onto future offspring. This is the process of natural selection. If there are enough changes or the change is drastic enough, a new species can evolve. So, evolution comes about as a result of changes to DNA and some of those changes to DNA can come from external factors such as environment, climate, and culture.
Mutation happens when the DNA gene gets changed, moves, or is damaged. When this happens it causes the genetic message to be carried by that gene to be different. This process can occur in somatic cells. The somatic cells are all the cells that are a living organism except the reproductive cells, meaning the body. For example, the skin cells on your legs are and will not be passed on to ones offsprings. In addition those leg cells will not effect the evolution. Another occurrence is called gametic mutations, which is in a woman's eggs and or in a man's sperm. These are cells that are and can be passed on to ones offsprings, and they are the essentials for the evolution. There are three effects mutation causes to a species. Species can only takes on one of the three. The three effects are bad, neutral, and good. Having a bad mutation can cause one to have a harder time being able to survive. Having a neutral mutation will not change or help one to survive. Having a good mutation will help one to survive and have a better chance of survival. However, mutation is random in the evolution, and provides raw material for natural selection, genetic drift, and gene flow...
In Meiosis 1, chromosomes in a diploid cell resegregate, producing four haploid daughter cells. It is this step in Meiosis that generates genetic diversity.Meiosis 2 is similar to mitosis. However, there is no "S" phase. The chromatids of each chromosome are no longer identical because of recombination. Meiosis II separates the chromatids producing two daughter cells each with 23 chromosomes (haploid), and each chromosome has only one chromatid.
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.
A genetic mutation is a permanent change in the sequence of the DNA that makes up a gene. A mutation of these sorts can be caused by either inheritance from the parent or caused sometime during the life of someone. The mutation that has been inherited is called a germline mutation. Germline mutations affect virtually the entire body, and they seem to be present in every cell. A somatic mutation, or one that is caused in the DNA of a single cell sometime during the life, can be caused by an environmental factor or a wrong bonding in the DNA molecule. These cannot be passed down to the next generation of children because they occur in a specific cell as opposed to in a reproductive cell. Some mutations occur in the embryo as it is growing. These may occur during cell division, and some of the cells may or may not inherit this mutation. Some mutations are extremely rare, and others are incredibly common. Those that occur in more than one percent across a population are considered polymorphisms. Polymorphisms are considered normal variations in DNA, and they are known to cause simple changes such as variations in blood types and hair color. Although these are not typically fatal, they can influence the creation of some disorders (Lister Hill National Center for Biomedical Communications, U.S. National Library of Medicine, National Institutes of Health, Department of Health and Human Services, USA.gov, 2013).
Human beings are born, formed and changed from one generation to the other through genetics. When a child enters the world, there is always a lot of excitement and uncertainty as which parent will the baby look like? Genes of the both parents determines the physical makeup of a child and therefore, genetics plays a very big role in human development. Genetics chromosomes are distributed equally by the parents to the child and they play a big role in the development of the child. Genes determines the development of a fetus inside its mother’s womb and outside of the mother’s womb.
There are certain things that must happen first before the cell can actually split. There is a six step process required during Mitosis. The first five steps of mitosis are called prophase, prometaphase, metaphase, anaphase, and telophase. This is where all the training and preparation is done for cell division. The sixth step is Cytokinesis, and that is when the cell literally splits into two. Like I said, there are certain things in order to happen before it can enter the M phase. first, it must meet the requirements of the certain size and environment. Since in the S phase the cell duplicated it’s amount of chromosomes it be represented as 2N, where N equals the number of chromosomes in the cell. Cells about to enter M phase, which have passed through S phase and replicated their DNA, have 4N chromosomes. Because of this they are now allowed to enter within the M phase to prophase. Here is where the cell thickens up its chromosomes and begin to sprout microtubules from clone centrosomes. Microtubules tub-like are protein filaments and where the chromosomes migrate but are still within the nuclear envelope in the nucleus. There are centromeres, that are inside the chromosomes and during the later process of this phase, specialized microtubules called kinetochores, assemble on the centromere then later attach to these sites. They act like magnets and go
Another mechanism is a hereditable type of evolution is mutations. Mutations are alterations to a gene. Mutation can be harmful, beneficial or neutral. Mutations are the origin of the source of genetic diversity (9).Mutation that are harmful, hinders the chances of the organism chances of survival and are likely to die along with the mutations. Beneficial mutations increase the chances of the individual to survive in its environment, and they will be more likely to reproduce and pass on the gene to future generations (9).