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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 thatKerrys were true breeding. Dexters, on the other hand, were not true breeding and never produced as many offspring as Kerrys. Provide a genetic explanation for these observations.

Short Answer

Expert verified
Based on the given information, the inheritance pattern of traits in cattle can be analyzed as follows: 1. The polled trait (hornless) is dominant over the horned trait. 2. The short legs (Dexter) trait is recessive, while the long legs (Kerry) trait is dominant. 3. When polled Kerrys (PP KK) are mated with horned Dexters (pp DD), the F1 generation consists of 50% polled Dexters (PP DK) and 50% polled Kerrys (PP KD). 4. In the F2 generation, we observe a ratio of 3/8 polled Dexters (PP DD), 3/8 polled Kerrys (PP KK), 1/8 horned Dexters (Pp DD), and 1/8 horned Kerrys (Pp KK). This inheritance pattern explains why Kerrys are true breeding but polled Dexters are not. The presence of the heterozygous genotype (Pp DD) in the F2 generation results in 12.5% of offspring being horned Dexters, causing the breed to not produce as many polled offspring as Kerrys.

Step by step solution

01

Identifying traits and inheritance pattern

From the data, we can identify the following traits: 1. Polled (hornless) or Horned 2. Short legs (Dexter) or Long legs (Kerry) When polled Kerrys and horned Dexters are mated, we get half polled Dexters and half polled Kerrys. This demonstrates that the polled trait is dominant over the horned trait.
02

Analyze the \(\mathrm{F}_{2}\) generation data

In the \(\mathrm{F}_{2}\) generation, we observe that: 1. \(3 / 8\) (37.5%) are polled Dexters 2. \(3 / 8\) (37.5%) are polled Kerrys 3. \(1 / 8\) (12.5%) are horned Dexters 4. \(1 / 8\) (12.5%) are horned Kerrys These observed ratios indicate that at least two independently assorting genes are involved in controlling the inheritance of these traits, with the polled trait showing a dominant gene action over horned, and the Dexter trait showing a recessive gene action over Kerry.
03

Propose gene symbols

Let's use the following gene symbols: 1. "P" for polled (dominant) and "p" for horned (recessive) 2. "D" for short legs (Dexter, recessive) and "K" for long legs (Kerry, dominant) According to the data, polled Kerrys and horned Dexters were true breeding, so their genotypes should be PP KK and pp DD, respectively.
04

Analyze the \(\mathrm{F}_{1}\) generation data

The cross between polled Kerry (PP KK) and horned Dexter (pp DD) cattle results in the \(\mathrm{F}_{1}\) generation with the same polled phenotype and different breed phenotypes (50% polled Kerrys, 50% polled Dexters). This means that their genotypes are as follows: 1. Polled Kerrys: PP KD (50%) 2. Polled Dexters: PP DK (50%)
05

Analyze the \(\mathrm{F}_{2}\) generation data

When the \(\mathrm{F}_{1}\) generation cattle (PP KD and PP DK) are mated, we will get offspring in the following proportions: 1. \(3 / 8\) polled Dexters: PP DD 2. \(3 / 8\) polled Kerrys: PP KK 3. \(1 / 8\) horned Dexters: Pp DD 4. \(1 / 8\) horned Kerrys: Pp KK The observed data in the \(\mathrm{F}_{2}\) generation are consistent with this explanation.
06

Explain breeding observations

From the genotype analysis, we can explain the breeding observations mentioned in the problem: 1. Kerrys are true breeding because they have the dominant "K" allele for leg length, and the "PP" genotype for polled trait allows them to remain hornless. 2. Dexters are not true breeding because they have the recessive "D" allele for leg length. Although 50% of polled Dexters' offspring will be polled Dexters (PP DD), the presence of the heterozygous genotype (Pp DD) in the \(\mathrm{F}_{2}\) generation results in 12.5% of offspring being horned Dexters, causing the breed to not produce as many polled offspring as Kerrys.

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Key Concepts

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

Dominant and Recessive Traits
In the world of genetics, traits are often categorized as either dominant or recessive. This classification describes how traits are inherited from one generation to the next. Dominant traits, like the polled (hornless) characteristic in cattle, overshadow recessive traits when the individual carries both versions, or alleles, of a gene. So, if an animal has one polled allele (P) and one horned allele (p), it will be polled because the dominant trait (P) expresses itself.

Recessive traits, on the other hand, like the horned trait in cattle, only express themselves when the individual has two copies of the recessive allele (pp). This means that for a horned animal to appear, both of its parents must carry the recessive allele and pass it on to their offspring.

In Dexter and Kerry cattle, the polled trait is dominant, while having short legs is a recessive characteristic. Therefore, even if a Dexter only has one copy of the dominant allele, they will appear polled. This results in more visible polled traits in successive generations, as long as one parent has the dominant allele. Understanding the hierarchy of dominant vs. recessive traits is essential for predicting how traits will be inherited.
Mendelian Genetics
Gregor Mendel, known as the father of genetics, laid the groundwork for understanding how traits are inherited through his experiments with pea plants. Mendel's principles apply universally, including to cattle, as shown in the example of Dexter and Kerry cattle. His laws highlight the predictable patterns of trait inheritance.

Mendel's Law of Segregation tells us that each parent contributes one allele for a trait to their offspring, resulting in a blend of genetic material. When we analyze the \(\mathrm{F}_1\) generation of crosses between Kerry and Dexter cattle, Mendelian genetics helps explain the resulting distribution of traits. Each parent passes on an allele for both traits: polled vs. horned and short legs vs. long legs.

Furthermore, Mendel's Law of Independent Assortment shows that traits are passed independently from one another. This principle is evident when offspring inherit traits from a blended parental mix, producing new combinations like those seen in \(\mathrm{F}_2\) generation cattle, where different mixes of polled and horned alongside short and long legs appear. Thanks to Mendel's groundwork, we can predict outcomes based on these fundamental laws of genetics.
True Breeding and Hybridization
True breeding refers to organisms that consistently produce offspring with the same phenotype when self-crossed. In the case of Kerry cattle, they are true breeding for the polled trait, represented by the genotypes "PP KK." This means when two Kerry animals reproduce, all their offspring will also be hornless and have long legs, following a predictable pattern. This ensured trait consistency aligns with their dominance in polled and leg-length characteristics.

Hybridization, in contrast, occurs when different breeds or varieties are crossed, producing a hybrid. For Dexter cattle, which are not true breeding, crossing with Kerrys results in offspring like the \(\mathrm{F}_1\) generation, which exhibit a mix of characteristics from both original breeds. The hybrids display a range of genotypic combinations like the polled short-legged or long-legged phenotypes, shown in the cattle study.

The concept of hybrid vigor often comes into play, where hybrids might show greater traits than their parents due to the combination of genetic material from diverse gene pools. Understanding the difference between true breeding and hybridization is crucial for those engaged in breeding programs, as it allows for controlled manipulation of genetic outcomes and more predictable characteristics in the next generation of animals or plants.

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Most popular questions from this chapter

When summer squash plants (Cucurbita pepo) with discshaped fruits are crossed to ones with long fruits, the \(\mathrm{F}_{1}\) generation all have disc-shaped fruits. When the \(F_{1}\) plants are crossed to each other, the \(\mathrm{F}_{2}\) produce spherical fruits as well as exhibit the two parental strains. The phenotypic ratio is 9: 6: 1 (disc-shaped:spherical:long). (a) Which type of gene interaction is this an example of? (b) Explain the phenotypes observed in terms of the number of gene pairs involved and by designating genotypes for all the fruit shapes in the cross. (Use dashes where required.)

While vermilion is X-linked in Drosophila and causes the eye color to be bright red, brown is an autosomal recessive mutation that causes the eye to be brown. Flies carrying both mutations lose all pigmentation and are white-eyed. Predict the \(\mathrm{F}_{1}\) and \(\mathrm{F}_{2}\) results of the following crosses: (a) vermilion females \(\times\) brown males (b) brown females \(\times\) vermilion males (c) white females \(\times\) wild-type males

In a unique species of plants, flowers may be yellow, blue, red, or mauve. All colors may be true breeding, If plants with blue flowers are crossed to red- flowered plants, all \(\mathrm{F}_{1}\) plants have yellow flowers. When these produced an \(\mathrm{F}_{2}\) generation, the following ratio was observed: \(9 / 16\) yellow: \(3 / 16\) blue: \(3 / 16\) red: \(1 / 16\) mauve In still another cross using true-breeding parents, yellow-flowered plants are crossed with mauve-flowered plants. Again, all \(\mathrm{F}_{1}\) plants had yellow flowers and the \(\mathrm{F}_{2}\) showed a 9: 3: 3: 1 ratio, as just shown. (a) Describe the inheritance of flower color by defining gene symbols and designating which genotypes give rise to cach of the four phenotypes. (b) Determine the \(F_{1}\) and \(F_{2}\) results of a cross between truebreeding red and true-breeding mauve-flowered plants.

In goats, the development of the beard is due to a recessive gene. The following cross involving true-breeding goats was made and carried to the \(\mathrm{F}_{2}\) generation: Offer an explanation for the inheritance and expression of this trait, diagramming the cross. Propose one or more crosses to test your hypothesis.

In Drosophila , the \(\mathrm{X}\) -linked recessive mutation vermilion \((v)\) causes bright red eyes, in contrast to the brick-red eyes of wild type. A separate autosomal recessive mutation, suppressor of vermilion \((s u-v),\) causes flies homozygous or hemizygous for \(v\) to have wild-type eyes. In the absence of vermilion alleles, \(s u-v\) has no effect on eye color. Determine the \(\mathrm{F}_{1}\) and \(\mathrm{F}_{2}\) phenotypic ratios from a cross between a female with wild-type alleles at the vermilion locus, but who is homozygous for \(s u-v,\) with a vermilion male who has wild-type alleles at the \(s u-v\) locus.

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