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In four o'clock plants, many flower colors are observed. In a cross involving two true-breeding strains, one crimson and the other white, all of the \(P_{1}\) generation were rose color. In the \(F_{2}\), four new phenotypes appeared along with the \(P_{1}\) and \(F_{1}\) parental colors. The following ratio was obtaincd: \(1 / 16\) erimson \(2 / 16\) orange \(1 / 16\) yellow \(2 / 16\) magenta \(4 / 16\) rose \(2 / 16\) pale yellow \(4 / 16\) white Propose an explanation for the inheritance of these flower colors.

Short Answer

Expert verified
Answer: The inheritance pattern responsible for the flower colors in this cross is a dihybrid inheritance pattern with incomplete dominance. Two separate genes with incomplete dominance, one for crimson pigment (C) and one for yellow pigment (Y), control the inheritance of the flower colors.

Step by step solution

01

Understanding the initial cross

The two parental strains with crimson and white flowers were true-breeding, meaning they were homozygous for their respective flower color genes. When crossed, the \(P_{1}\) generation showed an intermediate rose color, suggesting incomplete dominance.
02

Identifying the pattern in the \(F_{2}\) generation

Examine the ratio of flower colors in the \(F_{2}\) generation: \(1 / 16\) crimson \(2 / 16\) orange \(1 / 16\) yellow \(2 / 16\) magenta \(4 / 16\) rose \(2 / 16\) pale yellow \(4 / 16\) white The pattern follows a \(1:2:1:2:4:2:4\) ratio, which is derived from the product of two \(1:2:1\) ratios, suggesting that two separate gene interactions are responsible for the flower color inheritance.
03

Assigning alleles for flower colors

Assign two pairs of alleles, \(C\) and \(Y\), which control the crimson and yellow pigments in the flowers, respectively. The homozygous recessive genotype for both pairs of alleles will be white (e.g., \(ccyy\)).
04

Combining the genotypes with phenotypes

Now, combine the genotypes of alleles \(C\) and \(Y\) with the observed phenotypes: \(1 / 16\) crimson: \(CCYY\) \(2 / 16\) orange: \(CCYy\) \(1 / 16\) yellow: \(CCyy\) \(2 / 16\) magenta: \(CcYY\) \(4 / 16\) rose: \(CcYy\) \(2 / 16\) pale yellow: \(Ccyy\) \(4 / 16\) white: \(ccyy\)
05

Proposing an explanation for the inheritance of flower colors

The inheritance of flower colors in this case appears to be controlled by two separate genes with incomplete dominance, one responsible for crimson pigment (\(C\)) and the other for yellow pigment (\(Y\)). The \(C\) allele determines the degree of crimson pigmentation, with \(CC\) being fully crimson, \(Cc\) being partially crimson, and \(cc\) having no crimson pigment. The \(Y\) allele determines the degree of yellow pigmentation, with \(YY\) being fully yellow, \(Yy\) being partially yellow, and \(yy\) having no yellow pigment. The ratio of flower colors in the \(F_{2}\) generation can be explained by the interactions between these two genes and their alleles, revealing the \(1:2:1:2:4:2:4\) ratio. This suggests a dihybrid inheritance pattern with incomplete dominance at play.

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Key Concepts

These are the key concepts you need to understand to accurately answer the question.

Incomplete Dominance
Incomplete dominance is a fascinating situation in genetics where the phenotype of the offspring is a mix, or intermediate, between the phenotypes of the parents. In the context of four o'clock plants, this is clearly seen in the rose-colored flowers of the \(P_1\) generation. Unlike complete dominance, where one trait completely masks the other, incomplete dominance allows the traits to blend together.

Imagine the crimson and white parent plants as colors being mixed like paint. Crimson represents one pure color (let's call it "A" for full expression) and white represents another pure color ("a" for absence of expression). When combined, the result is neither fully crimson nor fully white, but instead, a beautiful rose color.

This rose color in the \(F_1\) generation represents incomplete dominance where neither the crimson nor the white completely prevail in the offspring. In the genetic symbols used, if \(C\) represents crimson and \(c\) represents lack of crimson, then the \(Cc\) genotype showcases the intermediate rose color.
Flower Color Genetics
The genetics of flower color can be quite intricate, involving not just one but sometimes multiple genes. In the case of our four o'clock plant scenario, two genes contribute to the variety of observed colors.

These two genes, represented here as \(C\) for crimson pigment and \(Y\) for yellow pigment, combine in different ways to produce the spectrum of flower colors seen in the \(F_2\) generation. Each plant can inherit combinations of these genes that lead to a wide range of colors:
  • \(CCYY\): Full pigmentation, resulting in deep crimson.
  • \(CCYy\): Slightly less pigmentation, appearing as orange.
  • \(CCyy\): Only the yellow pigment is visible, giving a yellow flower.
  • \(CcYY\): Partial pigmentation shows as magenta, a mix between crimson and rose.
  • \(CcYy\): The intermediate rose color, with both pigments present but diluted.
  • \(Ccyy\): Shows as pale yellow, less pigmented compared to "deep" shades.
  • \(ccyy\): Lack of pigmentation, resulting in white flowers.
Through these combinations, flower color genetics illustrate how variations in genetic makeup can lead to varied phenotypic outcomes.
Gene Interactions
Gene interactions occur when different genes influence a single trait, producing a variety of phenotypes. This is what occurs with the flower colors in our four o'clock plants example. Here, gene interactions between two separate gene pairs create a complex inheritance pattern.

Essentially, each flower color is the result of multiple genes working together. The two gene pairs \(C\) (crimson) and \(Y\) (yellow) contribute to the observed phenotype based on their allelic combinations.

These interactions produce a dihybrid ratio, a classic signpost of such complex genetic behavior. For instance, the resulting \(1:2:1:2:4:2:4\) ratio in the \(F_2\) generation displays the unique interactions of these genes:
  • Both dominant genes (\(CCYY\)) produce the most intense crimson shade.
  • Presence of both recessive alleles (\(ccyy\)) results in white flowers.
  • Intermediate forms (combinations of \(CcYy\), \(CCYy\)) lead to various intermediate colors like rose and magenta.
In this way, gene interactions illustrate the intricate dance genes perform to craft the visible phenotypes that we encounter in nature.

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Most popular questions from this chapter

In Dexter and Kerry cattle, animals may be polled (hornless) or horned. The Dexter animals have short legs, whereas the Kerry animals have long legs. When many offspring were obtained from matings between polled Kerrys and horned Dexters, half were found to be polled Dexters and half polled Kerrys. When these two types of \(\mathrm{F}_{1}\) cattle were mated to one another, the following \(\mathrm{F}_{2}\) data were obtained: \(3 / 8\) polled Dexters 3/8 polled Kerrys \(1 / 8\) horned Dexters \(1 / 8\) horned Kerrys A geneticist was puzzled by these data and interviewed farmers who had bred these cattle for decades. She learned that Kerrys were true-breeding. Dexters, on the other hand, were not truebreeding and never produced as many offspring as Kerrys. Provide a genetic explanation for these observations.

Horses can be cremello (a light cream color), chestnut (a reddish brown color), or palomino (a golden color with white in the horse's tail and mane).Of these phenotypes, only palominos never breed true. The following results have been observed: (a) From these results, determine the mode of inheritance by assigning gene symbols and indicating which genotypes yield which phenotypes. (b) Predict the \(\mathrm{F}_{1}\) and \(\mathrm{F}_{2}\) results of many initial matings between cremello and chestnut horses.

A husband and wife have normal vision, although both of their fathers are red- green color-blind, inherited as an X-linked recessive condition. What is the probability that their first child will be (a) a normal son, (b) a normal daughter, (c) a color-blind son, (d) a color-blind daughter?

Three gene pairs located on separate autosomes determine flower color and shape as well as plant height. The first pair exhibits incomplete dominance, where color can be red, pink (the heterozygote), or white. The second pair leads to the dominant personate or recessive peloric flower shape, while the third gene pair produces either the dominant tall trait or the recessive dwarf trait. Homozygous plants that are red, personate, and tall are crossed with those that are white, peloric, and dwarf. Determine the \(F_{1}\) genotype(s) and phenotype(s). If the \(F_{1}\) plants are inter. bred, what proportion of the offspring will exhibit the same phenotype as the \(\mathrm{P}_{1}\) plants?

In this chapter, we focused on many extensions and modifications of Mendellan principles and ratios. In the process, we encountered many opportunities to consider how this information was acquired. Answer the following fundamental questions: (a) How were early geneticists able to ascertain inheritance patterns that did not fit typical Mendelian ratios? (b) How did geneticists determine that inheritance of some phenotypic characteristics involves the interactions of two or more gene pairs? How were they able to determine how many gene pairs were involved? (c) How do we know that specific genes are located on the sexdetermining chromosomes rather than on autosomes? (d) For genes whose expression seems to be tied to the gender of individuals, how do we know whether a gene is X-linked in contrast to exhibiting sex- limited or sex-influenced inheritance? (e) How was extranuclear inheritance discovered?

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