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Ch. 9 Patterns of Inheritance
Taylor - Campbell Biology: Concepts & Connections 10th Edition
Taylor, Simon, Dickey, Hogan10th EditionCampbell Biology: Concepts & ConnectionsISBN: 9780136538783Not the one you use?Change textbook
Chapter 9, Problem 12

Why do more men than women have colorblindness?

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1
Understand the genetic basis of colorblindness: Colorblindness is primarily caused by mutations in the genes that are responsible for the production of photopigments in the cone cells of the retina. These genes are located on the X chromosome.
Recognize the difference in genetic inheritance between males and females: Males have one X chromosome and one Y chromosome (XY), while females have two X chromosomes (XX).
Consider the impact of having only one X chromosome in males: In males, the presence of a mutation in the only X chromosome will result in colorblindness because there is no second X chromosome to potentially provide a normal copy of the gene.
Examine the inheritance in females: Females must inherit two copies of the mutated gene (one from each parent) to exhibit colorblindness. If they inherit only one mutated gene, the normal gene on the other X chromosome can compensate, typically preventing the development of colorblindness.
Conclude why colorblindness is more common in males: Since males are hemizygous for the X chromosome (having only one X chromosome), any mutation on it expresses the trait of colorblindness. Females, having two X chromosomes, are less likely to be affected as they would require mutations in both copies of the gene.

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Key Concepts

Here are the essential concepts you must grasp in order to answer the question correctly.

X-Linked Inheritance

Colorblindness is primarily caused by mutations in genes located on the X chromosome. Since men have one X and one Y chromosome, a single mutated gene on their X chromosome will result in colorblindness. In contrast, women have two X chromosomes, so a mutation must occur in both to express the condition, making it less common among females.
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X-Linked Inheritance

Genetic Mutation

Colorblindness is often the result of genetic mutations that affect the photopigments in the retina, which are responsible for color perception. These mutations can alter the way light is absorbed by the cones in the eyes, leading to difficulties in distinguishing certain colors, particularly red and green.
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Prevalence and Population Genetics

The prevalence of colorblindness varies between genders due to the genetic mechanisms involved. Statistically, about 8% of men and only about 0.5% of women are affected by colorblindness, illustrating how X-linked traits can lead to significant differences in expression between sexes in a population.
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Mendelian and Population Genetics
Related Practice
Textbook Question

A fruit fly with a gray body and red eyes (genotype BbPp) is mated with a fly having a black body and purple eyes (genotype bbpp).

What ratio of offspring would you expect if the body-color and eye-color genes are on different chromosomes (unlinked)?

When this mating is actually carried out, most of the offspring look like the parents, but 3% have a gray body and purple eyes, and 3% have a black body and red eyes.

Are these genes linked or unlinked?

What is the recombination frequency?

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Textbook Question

A series of matings shows that the recombination frequency between the black-body gene and the gene for dumpy (shortened) wings is 36%. The recombination frequency between purple eyes and dumpy wings is 41%. What is the sequence of these three genes on the chromosome?

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Textbook Question

A couple are both phenotypically normal, but their son suffers from hemophilia, a sex-linked recessive disorder.

What fraction of their children are likely to suffer from hemophilia?

What fraction are likely to be carriers?

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Textbook Question

In fruit flies, the genes for wing shape and body stripes are linked. In a fly whose genotype is WwSs, W is linked to S, and w is linked to s. Show how this fly can produce gametes containing four different combinations of alleles.

Which are parental-type gametes?

Which are recombinant gametes? How are the recombinants produced?

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Textbook Question
Skin color in humans is at least partially hereditary; dark-skinned parents tend to have dark-skinned children. But humans come in a range of skin tones. Which extension of Mendel's model accounts for the hereditary variation in human skin color?
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Textbook Question
Heather was surprised to discover she suffered from red-green colorblindness. She told her biology professor, who said, 'Your father is colorblind, too, right?' How did her professor know this? Why did her professor not say the same thing to the colorblind males in the class?
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