An inheritance is something passed from one generation to another. In some contexts, this means stuff like houses and money. In the context of biology, however, the study of genes and how they are inherited, is called genetics. Gregor Mendel is credited with being the father of modern genetics. His work is responsible for our understanding of how noticeable physical traits, or phenotypes, are passed from one generation to the next. Famously, he studied such traits in pea plants.
The pieces of information controlling those phenotypes are called genes. As there are two copies of each gene, known as alleles, we can represent these as letters. Here, we'll use the letter P. This is the first step of Mendel's famous experiment on pea flower coloration, represented here, using a tool called the Punnett square. Mendel found that when he crossed purple flowers with white ones, all of the progeny, or the first-generation plants, had purple flowers. This is because the purple color is dominant, shown using uppercase P. And carrying even one dominant allele means the phenotype will be expressed. But interestingly, when these purple flowers were crossed again, 1/4 of them were white. Where were the white flowers in the first generation? All of the first generation of purple-flowered plants were heterozygous, meaning that they had one capital purple P and one lowercase, or white, P. When they passed on their alleles in the F2 generation cross, this meant that 1/4 of the offspring received two small P alleles, and so, expressed the white phenotype. Mendel didn't have the Punnett square tool to use, he had to figure all of this out by keeping track of thousands of plants, and then noticing patterns in their numbers.
From this evidence, and a lot more, we now know that genes are also present in two copies in other organisms, too, like humans, and flies. In following up on Mendel's work, several scientists found that not all inheritance patterns followed the simple, basic model that Mendel proposed. For example, in hemophilia, a genetic clotting disorder, unaffected mothers were capable of transmitting the disease to their male children. The reason behind this lies in chromosomes, which were studied by Thomas Hunt Morgan, using his famous fruit flies, Drosophila. Because of Morgan and others, we now know that chromosomes are long strands of DNA that typically exist in pairs. Here, we can see that Drosophila has four of them. These chromosomes have genes on them for different traits, much like how a cookbook contains lots of different recipes. Nowadays, using modern microscopy, we can actually see these chromosomes and even organize them. The product of this process is called a karyotype. Here, you can see a human one. In both humans and flies, there are autosomes, and sex chromosomes. Humans, like flies, have X and Y chromosomes controlling their sex. However, most of the genes on these chromosomes control things that have nothing to do with sex. In the rare form of hemophilia that we mentioned earlier, the reason that it occurs more frequently in males, is because the phenotype is controlled by a gene found on the X chromosome, in a section which has no partner on the Y chromosome. If a female has a bad copy of the gene, and her male child inherits this copy, he will have the disorder, he has no backup copy of the X chromosome. Since one copy of the gene is sufficient for a person to clot normally, a female must inherit two bad alleles of the gene, one from each parent, in order to exhibit the disease. Which, in this case, is not possible, because the father is unaffected. As a result, this type of hemophilia affects more males than females.
In this lab, we'll look at inheritance in Drosophila. Eye color in flies is controlled by a series of genes, some controlling what kinds of pigments are made, and one particularly important gene, called the ABC transporter, which controls transports of pigments into granules in the eye. If that gene is broken, even if the fly is making pigment, that pigment will be invisible, and the fly will have white eyes. The lab exercise is to recreate one of Thomas Hunt Morgan's most famous experiments, and explore the genetic inheritance pattern of the gene encoding the pigment transporter. Is it inherited like the purple color of Mendel's pea flowers, or is it sex-linked, like hemophilia?
At the end of this lab, students should know...
Alleles are different versions of a gene encoding similar, but distinct, versions of a gene product.
An allele is considered dominant if the trait it encodes is expressed when only one copy of the allele is present. A recessive allele will only be expressed if there are two copies of that allele.
Animal cells, such as humans and flies, have autosomes and sex chromosomes. Most of the chromosomes are autosomes, while the single pair of sex chromosomes determine the sex of the individual.
A sex-linked gene is a gene that encodes a product that has nothing to do with sex determination, but is found on one of the sex chromosomes. This is most frequently the X chromosome.
Males have one X chromosome, while females have two. If a mutation is present in a gene contained on the single X chromosome a male has, then he will express the mutant trait. A female is less likely to inherit the two copies of the allele necessary to express the trait. This is not impossible, just less frequent in a population.
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