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Meiosis quizlet
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Meiosis is specialized cellular division of sex cells. This type of cellular division occurs in single and multi-cellular organisms that undergo sexual reproduction. This process is split into two cycles: Meiosis I and Meiosis II. Prior to the start of meiosis, interphase occurs. Although interphase is not a stage of meiosis it is a vital preparatory step. It allows cellular growth, DNA replication and prepares for cellular division. Each cycle of meiosis is broken down into four stages for a total of eight stages. Meiosis I is composed of prophase I, metaphase I, anaphase I, and telophase I. Meiosis II is a repeat of each phase of meiosis I. Once meiosis is complete, the result will be four haploid daughter cells meaning that each daughter …show more content…
cell will only have half the amount of chromosomes as the diploid parent cell. These haploid cells will mature and turn into gametes. Each phase occurs in succession but is a clearly defined process. During prophase I, chromosomes coil or condense.
One chromosome has been donated from each parent cell in order to create a homologous chromosome pair. These chromosomes have identical lengths and gene placement but can contain different alleles. When homologous chromosomes attach at the centromere they create a tetrad, which is defined as a pair of sister chromatids. Once the sister chromatids are attached, the non-sister chromatids participate in crossing over. Crossing over is the transfer of genetic information in order to create greater genetic variability. In metaphase I, the centromere of each tetrad attaches to spindle fibers. These spindle fibers slowly shift the tetrads position to the center of the cell until they are side by side. Immediately after they line up, homologous chromosomes are separated by microtubules called kinetochore fibers that are used to pull sister chromatids to opposite poles of the cell. Once the sister chromatids are on opposite poles of the cell, anaphase I is complete and the cytoplasm of the cell begins to separate. This is known as cytokinesis and occurs during telophase. Once meiosis I is complete, meiosis II begins and repeats each step, however, instead of two haploid cells there will be a total of …show more content…
four. Mendel’s Laws of inheritance are concepts that explain how variability occurs within gametes. Mendel’s First law, the principal of segregation, states that diploid organisms separate during the formation of sex cells in order to create genetic variability. For example a person that is heterozygous for a trait has two alleles that are responsible for eye color. The alleles will separate into two different cells during meiosis in order to increase the chances of genetic variability. Independent assortment, Mendel’s second law, states that gametes can end up with any combination of parental chromosomes. Simply put, traits act independently of one another, meaning that the gene that determines height has no influence the gene for eye color. During cellular division homologues chromosomes may lack a piece of information from a gene.
This can result in single gene disorders that may or may not be life threatening depending on the mutation. For example, the Maple Syrup Urine Disorder, or MSUD, is a potentially fatal disease that disables the body from breaking down valine, leucine and isoleucine. These three amino acids are used to build proteins and are eventually broken down by branched –chain alpha ketoacid dehydrogenase (BCKD). Individuals who are affected by MSUD have a mutation that lack one of the six proteins that assist in the breakdown of the three amino acids. As a result, increased levels of valine, leucine and isoleucine end up in the blood stream and cause degradation of brain cells. In order for the disease to be inherited the child must obtain an altered gene from each parent, which makes MSUD an autosomal recessive
disorder
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.
Genetic disorders can be caused by many of the 46 chromosomes in human cells. This specific disorder is linked to a mutation in the long arm of the X, or 23rd chromosome. The mutation is recessive, meaning a normal X chromosome can hide it. Females have two X chromosomes allowing them to hide the mutated recessive one, making them a carrier of the gene, while males only have one X chromosome, meaning that they are unable to hide the mutation and they become effected by the disease. Therefore if a male carries the gene, he is affected because he has no way of dominating the recessive gene, but if a female carries it, she is only a carrier and has a 50/50 chance of passing it on to her baby. This may seem like a high probability however, only one in every fifty thousand male births will have this immunodeficiency disease.
A genetic disorder is a sickness caused by one or many abnormalities or absentees in the genes or chromosomes. One interesting genetic disorder such as cancer, are found genetic but, can also be caused and affected by many by environmental factors such as being exposed to asbestos which may increase the risk of lung cancer and many other cancers. While on the other hand most disorders like Williams Syndrome are genetic and are primarily rare and only affect a limited amount of people about one in every several thousand. Because it is a genetic disorder that is estimated between 1 in 10,000 people worldwide, primarily caused by a micro-deletion on the seventh chromosome is what indicates the disorder being Williams Syndrome.
In telophase, these separate chromatids uncoil to become chromosomes. This division produces two identical cells.
It is important to note that genes themselves do not cause disease genetic disorders are caused by mutations that make a gene function improperly. For example, when people say that someone has the cystic fibrosis gene, they are usually referring to a mutated version of the Cystic Fibrosis Transmembrane Conductance Regulator gene, which causes the disease. All people, including those without cystic fibrosis, have a version of the Cystic Fibrosis Transmembrane Conductance Regulator gene.
This means that all the sperm in males and eggs in females are produced from meiosis. Sperm and egg cells are haploid cells-they contain only one of each type of chromosome. Meiosis actually starts with a diploid cell that undergoes two divisions; the end products are four gametes, all genetically different. Meiosis is known as a reduction division because the daughter cells always contain half the amount of chromosomes as the diploid beginner cell. Chromosomes come in pairs and these pairs are called homologous pairs. Homologous chromosomes mean that both of the chromosomes in the pair have the same gene sequence. Human somatic cells(diploid) contain 46 chromosomes consisting of 23 homologous pairs; therefore, human gametes, which are haploid, have 23 total chromosomes-one from each homologous pair. Just like in mitosis, meiosis undergoes all of the same phases. However, because meiosis involves two divisions, the cell goes through all the phases twice. When referring to the first time the cell undergoes a phase, we say 1, and when referring to the second time, we say 2. For example, when a cell starts prophase the first time in meiosis, we say it is going through prophase 1(P1). Also, there are some differences in the process itself. During P1, homologous chromosomes exchange a section of themselves in what is known as crossing over. This provides a source of genetic variation since part of each chromosome switched places with each other, thus making both chromosomes distinct from the original. Another important difference to know is that in anaphase 1, the doubled chromosomes are not separated into sister chromatids. This doesn’t happen until A2 to ensure that each of the four gametes receives one of each kind of chromosome. There are many key points to understand about meiosis. The first being that cells in meiosis do not go through interphase twice. Interphase is a “one-time” thing; DNA
Adrenoleukodystrophy Adrenoleukodystrophy is a genetically transferred disease which causes the human body to not be able to breakdown “very-long-chain-fatty-acids” (VLCFA). This inability to break down these acids eventually leads to myelin deterioration as well as the deterioration of the nervous system. Although there is no cure for this terrible disease, there are a variety of effective treatments. Adrenoleukodystrophy is a sex-linked trait carried on the X-chromosome and is carried by the mother. It is only passed on to male children, and every male child that a carrier mother gives birth to has a fifty-fifty chance of acquiring adrenoleukodystrophy.
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.
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 two phases of meiosis are that in meiosis I, while the cell undergoes the phases, prophase I, metaphase I, anaphase I, and telophase I, it causes the cell to divide into two with each of the cells having a double stranded chromosome. But in meiosis II, it is just the division of the the cells from meiosis I. The ending result being that four haploid daughter
Meiosis is when each daughter cell ends up with exactly half the number of chromosomes as the parent cell, one of each. type, which is known as the haploid state. Meiosis is associated with sexual reproduction and generally takes place in the formation of gametes or in some cases spores. Asexual reproduction is the process of one individual organism. producing one or more new individuals.
The cell cycle is an ordered set of events, culminating in cell growth and division into two daughter cells. There are different stages to the cell cycle such as mitosis and meiosis. During, the course of this paper I will explain, what causes a cell to divide, whether cells rapidly grow constantly, how easy it is to grow cell in culture, and what cells holds the liver together.
The Ashram’s develop self-fulfillment, spiritual culture and completion to one-self in the Hindu religion. In ancient Hinduism, the human life is divided into four stages; the Brahmacarya, Grihastha, Vanaprastha, and Sanyasa. Each stage is known as an ashrama and is a part of the Ashram system. Ashram, meaning “a place of spiritual shelter”# can be viewed as a religious journey in which each Hindu must go through to gain spirituality. Typically, the males were the ones who went through the four stages of ashram. In order to fully experience a stage of ashram, one must achieve self-realization. “The individual must go through severe training and disciplines to develop a spirit of self-detachment in the four stages of life- or the four Ashramas. # The Ashram system was instilled in Vedic society in order to guide the life of man to reach fulfillment. It was the Dharma, meaning the righteous duty, of one to reach this fulfillment in life.
This brings us to metaphase II. In this stage the chromosomes line up at the metaphase plate in the cell's center waiting to be pulled to the other side. Anaphase II consists of the sister chromatids and chromosomes separate. The spindles will pull the sister chromatids to the opposite pole. Lastly comes telophase II where the nuclei from at both poles and the spindles start to break down and the nuclear membrane start to form. Lastly is cytokinesis that separates these two cells to four haploid cells that contain half the genetic material. The end product is four cell that have each twenty-three chromosomes and chromatids. This only happens in the gametes or sex cells that are eukaryotic because it must a have membrane-bound nucleus. Meiosis is important because this keeps our species going, and makes us not to be extinct. Without this we wouldn't be able reproduce because when a sperm comes to fertilize an egg they combine to have a full forty-six chromosome cell that will go through the process of maturing to be a zygote and then an embryo. Meiosis occurs when a germ or gamete goes through interphase and then the process of meiosis I and
Once the sperm fuses with the ovum both chromosomes will pair up and begin the first stages of cell division.