Explain what a gene pool is

explain what a gene pool is

Chapter 14 - Mendel and the Gene Idea

Mar 22,  · Eugenics is a now-discredited, pseudoscientific movement based on the belief that there are certain genes that are “best” to pass on to improve the human race, and that those with so-called. evolution, or change in gene pool frequencies, resulting from random chance. Genetic drift occurs most rapidly in small populations. In large populations, random deviations in allele frequencies in one direction are more likely to be cancelled out by random changes in the opposite direction. genetics. the study of gene structure and action and.

Concept By the law of segregation, the two alleles for a character are separated during the formation of gametes. By the law of independent assortment, each pair of alleles segregates independently into gametes. We hope your visit has been a productive one. If you're having any problems, or would like to give some feedback, we'd love to hear from you. For general help, questions, and suggestions, try our dedicated support forums. If you need to contact the Course-Notes. Org web experience team, please use our contact form.

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Printer Friendly. Chapter 14 Mendel and the Gene Idea Lecture Outline Overview: Drawing from the Deck of Genes Every day we observe heritable variations such as brown, green, or blue eyes among individuals in a population. These traits are transmitted from parents to offspring. This hypothesis proposes that genetic material contributed by each parent mixes in a manner analogous to the way blue and yellow paints blend to make green. With blending inheritance, a freely mating population will eventually give rise to a uniform population of individuals.

Everyday observations and the results of breeding experiments tell us that heritable traits do not blend to become uniform. Genes can be sorted and passed on, generation after generation, in undiluted form. Modern genetics began in an abbey garden, where a monk named Gregor Mendel documented a particulate mechanism of inheritance.

Mendel grew up on a small farm in what is today the Czech Republic. InMendel entered an Augustinian monastery. After university, Mendel taught at the Brunn Modern School and lived in the local monastery. The monks at this monastery had a long tradition of interest in the breeding us plants, including peas.

GenMendel began breeding garden peas to study inheritance. Pea plants have several advantages for genetic study.

Pea plants are available in many varieties with distinct heritable dhat, or characters, with different variant traits. Mendel could strictly control which plants mated with which. Each pea plant has male stamens and female carpal sexual organs. In nature, pea plants typically self-fertilize, fertilizing ova with the sperm nuclei from their own pollen. However, Mendel could also use pollen from another plant for cross-pollination.

For example, he worked with flowers that were either purple or white. He avoided traits, such as seed weight, that varied on a continuum. Mendel started his experiments with varieties that were true-breeding. When true-breeding plants self-pollinate, all their offspring have the same traits. In a typical breeding experiment, Mendel would cross-pollinate hybridize two wha, true-breeding pea varieties.

The true-breeding parents are the P generation, and their hybrid offspring are the F1 generation. Mendel would then allow the F1 hybrids to self-pollinate to produce an F2 generation. If the blending model was correct, the F1 hybrids from a cross between purple-flowered and white-flowered pea plants would have pale purple explain what a gene pool is. Instead, F1 what is my house worth calculator canada all have purple flowers, just as purple as their purple-flowered parents.

When Mendel allowed the F1 plants to self-fertilize, the F2 generation included both purple-flowered and white-flowered plants. The white trait, absent in the F1, reappeared in the F2. Mendel used very large sample sizes and kept accurate records of his results. Mendel recorded purple-flowered F2 plants geme white-flowered F2 plants. This cross produced a traits ratio of three purple to one white in the F2 offspring.

Mendel reasoned that the heritable how to convert exe file to video file explain what a gene pool is white flowers was present in the F1 plants, but did not affect flower color. Purple flower color is a dominant trait, and white flower color is a recessive trait. Mendel found similar 3-to-1 ratios of two traits among F2 offspring when he conducted crosses for six other characters, each represented by two different traits.

For example, when Mendel crossed two true-breeding varieties, one producing round seeds and the other producing wrinkled seeds, all the F1 offspring had round seeds. Mendel developed a hypothesis to explain these results that consisted of four related ideas. We will explain each idea with the modern understanding of genes and chromosomes. Alternative versions of genes account for variations poool inherited characters. The gene for flower color in pea plants exists in two versions, one for purple flowers and one for white flowers.

These alternate versions are called alleles. Each gene resides at a specific locus on a specific chromosome. The DNA at that locus can vary in its sequence of nucleotides.

The purple-flower and white-flower alleles are two DNA variations at the flower-color locus. For each character, an organism inherits two alleles, one from each parent. A diploid organism inherits one set of chromosomes from each parent. Each diploid organism has a explain what a gene pool is of homologous chromosomes and, therefore, two copies of each gene. These homologous loci may be identical, as in the true-breeding plants of the P generation.

Alternatively, the two alleles may differ. In the flower-color example, the F1 plants inherited a purple-flower allele from one parent and a white-flower allele from the other.

They had purple flowers because the allele for that trait is dominant. This segregation of alleles corresponds to the distribution of homologous chromosomes to different gametes in meiosis. If an organism has two identical alleles for a particular character, then that allele xeplain present as a single copy explqin all gametes. The F1 hybrids produce two classes of gametes, half with fene purple-flower allele and half with the white-flower allele. During self-pollination, the gametes of these two classes unite randomly.

This produces four equally likely combinations of sperm and ovum. A Punnett square predicts the results of a genetic cross between individuals of known genotype.

Let us describe a Punnett square ggene of the flower-color example. We will use a capital letter to symbolize the dominant allele and a lowercase letter to symbolize the recessive allele.

P is the purple-flower allele, and p is the white-flower allele. What will be the physical appearance of the F2 offspring? One in four F2 offspring will inherit two white-flower alleles and produce white flowers. Half of the F2 offspring will inherit one white-flower allele and one purple-flower allele wyat produce purple flowers. One in four F2 offspring will inherit two purple-flower alleles and produce purple flowers.

An organism with two identical alleles for a character is homozygous for that character. Organisms with two different alleles for a character is heterozygous for that how to wire smoke alarms. Its genetic makeup is called its genotype.

Two organisms can have the same phenotype but have different genotypes if one is homozygous dominant and the other is heterozygous. For flower color in peas, the only individuals with white flowers are those that are homozygous recessive pp for the flower-color gene. However, PP and Pp plants have the same phenotype purple flowers but different genotypes homozygous dominant and heterozygous.

How can we tell explaij genotype of an individual with the dominant phenotype? The organism must have one dominant allele, but could be homozygous dominant or heterozygous. The answer is to carry out a testcross. The mystery individual is bred with a homozygous recessive individual. If any of the offspring display the recessive phenotype, the mystery parent must be heterozygous.

All F1 progeny produced in these crosses were monohybrids, heterozygous for one character. A cross between two heterozygotes is a monohybrid cross. Mendel identified the second law fxplain inheritance by following two characters at the same time. In one such dihybrid cross, Mendel studied the inheritance of seed color and seed shape.

The allele for yellow seeds Y is dominant to the allele for green seeds y. The allele for round seeds R is dominant to the allele for wrinkled seeds r. Mendel crossed true-breeding plants that had yellow, round seeds YYRR with true-breeding plants that has green, wrinkled seeds yyrr.

One possibility is that the two characters are transmitted from parents to offspring as a package. The Y and R alleles and y and r alleles explain what a gene pool is together. If this were the case, the Explain what a gene pool is offspring would produce yellow, round seeds.

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Gene flow is a fundamental agent of evolution based on the dispersal of genes between populations of a species. It involves the active or passive movement of individual plants, animals, gametes, or seeds. Gene flow involves not just dispersal but also the successful establishment of the immigrant genotypes in the new population. In epistasis, a gene at one locus alters the phenotypic expression of a gene at a second locus. For example, in mice and many other mammals, coat color depends on two genes. One, the epistatic gene, determines whether pigment will be deposited in hair or not. Presence (C) . A transgene is a gene that has been transferred naturally, or by any of a number of genetic engineering techniques from one organism to another. The introduction of a transgene, in a process known as transgenesis, has the potential to change the phenotype of an organism. Transgene describes a segment of DNA containing a gene sequence that has been isolated from one organism and is .

Select the first letter of the word you are seeking from the list above to jump to the appropriate section of the glossary or scroll down to it. Purebred is the same as true breeding. Back to Top - Q - Back to Top - R - recessive allele an allele that is masked in the phenotype by the presence of a dominant allele. Recessive alleles are expressed in the phenotype when the genotype is homozygous recessive aa.

Regulator genes control the timing of production of a variety of chemicals in humans and other organisms. Shortly after conception, regulator genes work as master switches orchestrating the timely development of our body parts. They are also responsible for changes that occur in our bodies as we grow older. Regulator genes are also called homeotic genes.

Back to Top - S - sex cell a gamete, either a sperm or an ovum. Sex cells are produced by the meiosis process. See somatic cell. See sex-limited gene. See sex-controlled gene. Sickle-cell trait is the result of a pleiotropic gene. Sickle-cell trait is also known as sickle-cell anemia. Most cells in multicellular plants and animals are somatic cells. They reproduce by mitosis. See sex cell. In the case of genetically inherited diseases, the result is increasingly severe symptoms each generation.

The myotonic form of muscular dystrophy is an example. Stuttering alleles are also known as unstable alleles. Back to Top - T - Tay-Sachs Disease a genetically inherited condition caused by the inability to produce the enzyme hexosaminidase A.

This results in progressively increased fluid pressure on the brain and the subsequent degeneration of the brain and nervous system beginning about 6 months of age and inevitably resulting in death usually by age The gene responsible for Tay-Sachs Disease is recessive.

Back to Top - U - unit inheritance Gregor Mendel's idea that the characteristics of parents are passed on to descendants unchanged as units. In other words, the hereditary material of any organism is made up of discrete units now called genes. Back to Top - V - virus a category of extremely small microscopic parasites of plants, animals, and bacteria.

Since viruses cannot reproduce without a host cell, they are not strictly speaking living organisms. More precisely, this is a cell that is formed when a sperm and an ovum combine their chromosomes at conception.

A zygote contains the full complement of chromosomes in humans 46 and has the potential of developing into an entire organism. All rights reserved. Return to Last Page Return to Menu. An individual with these traits is an "albino. This is a pleiotropic trait. The alleles for a trait occupy the same locus or position on homologous chromosomes and thus govern the same trait.

However, because they are different, their action may result in different expressions of that trait. There are 20 different kinds of amino acids in living things. Proteins are composed of different combinations of amino acids assembled in chain-like molecules. Amino acids are primarily composed of carbon, oxygen, hydrogen, and nitrogen.

The inheritance of this syndrome is subject to genome imprinting. Children with Angleman syndrome typically also have small heads, experience seizures, have pronounced speech impairment, are hyperactive, and have balance disorders.

It proposed that inherited traits blend from generation to generation. Through his plant cross-breeding experiments, Gregor Mendel proved that this was wrong. Carriers often do not show any signs of the trait but can pass it on to their offspring. This is the case with hemophilia. Cataracts are common in elderly people.

They may be inherited or caused by diabetes and environmental factors. In contrast, an acute disease is one with a rapid onset and a short but usually severe course. Chromosomes are composed primarily of DNA and protein. They are visible only under magnification during certain stages of cell division. Humans have 46 chromosomes in each somatic cell and 23 in each sex cell. Neither allele is dominant or recessive, so that both appear in the phenotype or influence it.

Type AB blood is an example. Such traits are said to be codominant. Usually, the term is used in reference to the crossing of two pure breeding homozygous plants. This disease also prevents normal absorption of fats and other nutrients from food. Cystic fibrosis occurs as a result of inheriting a recessive allele for it from both parents.

About 30, people have cystic fibrosis in the U. In advanced stages, this often results in blindness from cataracts , nerve damage, gangrene in the feet and legs leading to amputation, heart disease, and kidney failure. Type 1 diabetes melitis juvenile onset diabetes is due to decreased production of insulin by the pancreas. Type 2 diabetes melitis is due to increased resistance of cells in the body to insulin. The gene or genes for diabetes are incompletely penetrant. Dominant alleles for a trait are usually expressed if an individual is homozygous dominant or heterozygous.

DNA is composed of sugars, phosphates and bases arranged in a double helix shaped molecular structure. Segments of DNA in chromosomes correspond to specific genes. The term is also frequently used to refer to the appearance of a new species. The next and subsequent generations are referred to as f2, f3, etc. Since it is an X-linked trait, males more often have it expressed in their phenotypes.

Most fragile-X males have large testes, big ears, narrow faces, and sensory integration dysfunctions that result in learning disabilities. It is likely to occur 1 in births. Approximately 1 in females are carriers of the gene for this trait. The loss or addition of individuals can easily change the gene pool frequencies of both the recipient and donor populations--that is, they can evolve.

More precisely, it is the collective genotype of a population. Physically, a gene is a sequence of DNA bases that specify the order of amino acids in an entire protein or, in some cases, a portion of a protein.

A gene may be made up of hundreds of thousands of DNA bases. Genes are responsible for the hereditary traits in plants and animals. Genetic drift occurs most rapidly in small populations. In large populations, random deviations in allele frequencies in one direction are more likely to be cancelled out by random changes in the opposite direction.

Genetic mechanisms are the underlying foundation for evolutionary change. Genetics is the branch of science that deals with the inheritance of biological characteristics. In humans, it is estimated that each individual possesses approximately 2. See Human Genome Project. Genome imprinting is also known as genetic imprinting.

Genotype can refer to an organism's entire genetic makeup or the alleles at a particular locus. See phenotype. Symptoms include painfully inflamed joints, especially of the feet and hands, that can become chronic and result in deformity. Usually, only one joint is involved, most commonly the base of a big toe. Gout is a sex-controlled trait, usually being more severe in men.

This results in prolonged bleeding from even minor cuts and injuries. Swollen joints caused by internal bleeding is a common problem for hemophiliacs. Hemophilia most often afflicts males. Individuals who are heterozygous for a trait are referred to as heterozygotes. See homozygous. The HLA system has the most genes of any other known human multiple-allele series. There are at least 30,, possible HLA genotypes.

HLA stands for " human leukocyte antigen". Such chromosomes are alike with regard to size and also position of the centromere. They also have the same genes, but not necessarily the same alleles , at the same locus or location. Homozygous also refers to a genotype consisting of two identical alleles of a gene for a particular trait.

2 thoughts on“Explain what a gene pool is

  1. Very helpful video and the explanation was really great. You are speaking like a native american, just go ahead

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