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A breeder of black Labrador puppies notices that in his line a gene predisposing his dogs for white spots has arisen. He believes the white spot allele is autosomal recessive, and he wants to prevent it from continuing in his dogs. He sees that one of his female dogs, Speckle, has white spots, and he therefore assumes she is homozygous for the gene. But he must determine which males in his pack are heterozygous to avoid breeding them in the future. What is a reasonable plan? (A) Stop breeding Speckle. (B) Pair Speckle with a male with white spots. (C) Perform a testcross of Speckle with a black Labrador male. If any pups are born with white spots, stop breeding that male because he is heterozygous. (D) Breed Speckle with a chocolate Labrador.

Short Answer

Expert verified
The best plan is to perform a testcross of Speckle with a black Labrador male. If any pups are born with white spots, stop breeding that male because he is heterozygous. (C)

Step by step solution

01

Understanding the given options

It's important to first understand the given options and their implications: (A) Stop breeding Speckle: This option suggests that by not breeding Speckle, the issue of spreading the white spot allele can be prevented. However, this would not help in identifying heterozygous males. (B) Pair Speckle with a male with white spots: This option will mate Speckle with another dog showing the white spot trait. This may perpetuate the white spot allele but does not address the concern of identifying heterozygous males. (C) Perform a testcross of Speckle with a black Labrador male: If any pups are born with white spots, stop breeding that male because he is heterozygous. This option suggests using a testcross to identify heterozygous males. (D) Breed Speckle with a chocolate Labrador: This option suggests breeding with a different color Labrador. However, it doesn't specifically help in identifying heterozygous males or preventing the spread of the white spot allele.
02

Choosing the best option

Option C is the best choice because it proposes a focused and logical way to identify heterozygous males, which was the main concern of the breeder. A testcross is performed with a black Labrador male, as they cannot have white spots (meaning they have at least one dominant allele). If they produce offspring with white spots, it means that the male carries the recessive white spot allele (heterozygous), and the breeder should avoid breeding that male. Therefore, the best plan is: (C) Perform a testcross of Speckle with a black Labrador male. If any pups are born with white spots, stop breeding that male because he is heterozygous.

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Most popular questions from this chapter

In pea plants, tall ( \(T\) ) is dominant over short ( \(t\) ) and green \((G)\) is dominant over yellow \((g)\). If a pea plant that is heterozygous for both traits is crossed with a plant that is recessive for both traits, approximately what percentage of the progeny plants will be tall and yellow? (A) \(0 \%\) (B) \(25 \%\) (C) \(66 \%\) (D) \(75 \%\)

The gene for coat color in some breeds of cats is found on the X chromosome. Calico cats are mottled with orange and black colorings. What is a possible explanation for the fact that true calico cats are only female? (A) The allele for coat color is randomly chosen by Xinactivation. (B) The coat color is linked with genes that are lethal to male cats, so male calico cats never live past birth. (C) Coat orange and black color is expressed only in female cats; males have only one color. (D) Male cats have Y chromosomes.

Which of the following is a reason why certain traits do not follow Mendel's Law of Independent Assortment? (A) The genes are linked on the same chromosome. (B) It applies only to eukaryotes. (C) Certain traits are not completely dominant. (D) Heterozygotes have both alleles.

Neuronal ceroid lipofuscinosis (NCL) is a group of autosomal recessive diseases characterized by blindness, loss of cognitive and motor function, and early death. One of the genes that is mutated in this disease is CLN3. When functional CLN3 protein is absent, neurons die because of increased storage material in the cells, presumably because the lysosomes aren't working properly. What is a valid explanation as to why parents of children with this devastating disease can be completely normal? (A) Parents of the autosomal recessive disease must both be carriers of the mutation on the CLN3 gene. (B) Carriers of the CLN3 mutation genotype do not show the phenotype because one normal CLN3 allele is present to provide a functioning CLN3 protein. (C) Redundant proteins take over the function of the mutant CLN3 protein in the parents. (D) X inactivation prevents expression of the CLN3 mutated protein in the parents.

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