Concepts of Genetics (11th Edition)
11th Edition
ISBN: 9780321948915
Author: William S. Klug, Michael R. Cummings, Charlotte A. Spencer, Michael A. Palladino
Publisher: PEARSON
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Chapter 4, Problem 34PDQ
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How can you envision using this new information? Discuss how things that we do to our bodies (smoking, recreational drugs, employment environments, stress levels, eating/drinking habits, etc.) can influence genetic expression in our future child(ren).
In humans, dosage compensation is accomplished by:
inactivating one X chromosome in female somatic cells
inactivating one homolog from each homologous pair of chromosomes in female somatic cells
inactivating the Y chromosome in male somatic cells
increasing gene expression from the X chromosome in male somatic cell
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Questions:
1. How does the genetic code determine the expression of heritable traits in an organism?
2. What are the mechanisms of gene regulation that control the expression of heritable traits?
3. What are the functions of DNA segments that do not code for proteins?
Chapter 4 Solutions
Concepts of Genetics (11th Edition)
Ch. 4 - In the guinea pig, one locus involved in the...Ch. 4 - In some plants a red flower pigment, cyanidin, is...Ch. 4 - Below are three pedigrees. For each trait,...Ch. 4 - Prob. 1CSCh. 4 - Prob. 2CSCh. 4 - Prob. 3CSCh. 4 - HOW DO WE KNOW? In this chapter, we focused on...Ch. 4 - CONCEPT QUESTION Review the Chapter Concepts list...Ch. 4 - In shorthorn cattle, coat color may be red, white,...Ch. 4 - In foxes, two alleles of a single gene, P and p,...
Ch. 4 - In mice, a short-tailed mutant was discovered....Ch. 4 - List all possible genotypes for the A, B, AB, and...Ch. 4 - With regard to the ABO blood types in humans,...Ch. 4 - In a disputed parentage case, the child is blood...Ch. 4 - The A and B antigens in humans may be found in...Ch. 4 - In chickens, a condition referred to as creeper...Ch. 4 - In rabbits, a series of multiple alleles controls...Ch. 4 - Three gene pairs located on separate autosomes...Ch. 4 - As in Problem 12, flower color may be red, white,...Ch. 4 - Horses can be cremello (a light cream color),...Ch. 4 - With reference to the eye color phenotypes...Ch. 4 - Pigment in mouse fur is only produced when the C...Ch. 4 - In rats, the following genotypes of two...Ch. 4 - Given the inheritance pattern of coat color in...Ch. 4 - In a species of the cat family, eye color can be...Ch. 4 - In a plant, a tall variety was crossed with a...Ch. 4 - In a unique species of plants, flowers may be...Ch. 4 - Five human matings (15), identified by both...Ch. 4 - A husband and wife have normal vision, although...Ch. 4 - In humans, the ABO blood type is under the control...Ch. 4 - In Drosophila, an X-linked recessive mutation,...Ch. 4 - Another recessive mutation in Drosophila, ebony...Ch. 4 - In Drosophila, the X-linked recessive mutation...Ch. 4 - While vermilion is X-linked in Drosophila and...Ch. 4 - In a cross in Drosophila involving the X-linked...Ch. 4 - Consider the three pedigrees below, all involving...Ch. 4 - In goats, the development of the beard is due to a...Ch. 4 - Predict the F1 and F2 results of crossing a male...Ch. 4 - Two mothers give birth to sons at the same time at...Ch. 4 - Discuss the topic of phenotypic expression and the...Ch. 4 - Prob. 35PDQCh. 4 - Labrador retrievers may be black, brown...Ch. 4 - A true-breeding purple-leafed plant isolated from...Ch. 4 - In Dexter and Kerry cattle, animals may be polled...Ch. 4 - A geneticist from an alien planet that prohibits...Ch. 4 - The following pedigree is characteristic of an...Ch. 4 - Students taking a genetics exam were expected to...Ch. 4 - In four oclock plants, many flower colors are...Ch. 4 - Proto-oncogenes stimulate cells to progress...Ch. 4 - Below is a partial pedigree of hemophilia in the...
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- There are two genes that determine the coat colour expression in some dogs: eumelanin and merle. These genes are located on two separate chromosomes. For the eumelanin gene, black coat colour (E) is dominant over red coat colour (e). The merle gene controls the degree to which these coat colours are expressed through incomplete dominance. The following table describes the merle gene expression. Genotype Phenotype MM White Mm Half colour (Grey or light red) mm Full colour (Black or Red) Two dogs heterozygous for both traits were crossed. What phenotypic ratio is expected in the F1 generation? Answer: Phenotype: White Grey Black Light Red Redarrow_forwardThere are two genes that determine the coat colour expression in some dogs: eumelanin and merle. These genes are located on two separate chromosomes. For the eumelanin gene, black coat colour (E) is dominant over red coat colour (e). The merle gene controls the degree to which these coat colours are expressed through incomplete dominance. The following table describes the merle gene expression. Genotype Phenotype MM White Mm Half colour (Grey or light red) mm Full colour (Black or Red) A grey dog that is heterozygous for the eumelanin gene mates with a light red dog. 1. What is the probability they would have a grey puppy? 2. What is the probability they would have a grey or light red puppy?arrow_forwardContrast penetrance and expressivity as the terms relate to phenotypic expression.arrow_forward
- When the expression of alleles are affected by the presence of other genes,such as sickle cell trait carriers that experience symptoms, this is calledarrow_forwardDefine the Random Monoallelic Expression: Inactivation of the X Chromosome ?arrow_forwardFaulty Tooth Enamel Formation Amelogenesis imperfecta (AI) is a disorder of faulty tooth enamel formation. It is inherited in an autosomal dominant and X-linked dominant pattern. The expression of AI disorder is determined by mutations in the autosomal alleles. One copy of the mutated allele (A) will cause the disorder. The severity of the disorder is determined by mutations in a gene carried on the X chromosome. Normal (or non-severe) abnormality (XN) is dominant over the abnormality (or severe) (Xn) allele. In the absence of the autosomal dominant allele, the abnormality gene on the X chromosome is notexpressed. Question:A woman with normal teeth had four children with a man with non-severe form of AI: A boy was born without amelogenesis imperfecta A girl was born without amelogenesis imperfecta A boy was born with severe amelogenesis imperfecta A boy was born with non severe amelogenesis imperfecta Identify the parental genotypes. Complete the Punnett square for the parental…arrow_forward
- Duchenne Muscular Dystrophy (DMD) is a disorder that primarily affects the function of skeletal muscles used for movement and cardiac muscles used for heart beating. Dystrophin is a protein encoded by a single gene, DMD, that is expressed in skeletal and cardiac muscle. Some forms of muscular dystrophy may be caused by different mutations in the DNA sequence of the DMD gene. Because the DMD locus is on the X chromosome, males are affected at higher rates. Two brothers, one of whom has DMD and one of whom does not, worked with their genetic counselor (Links to an external site.) to have their DMD gene sequenced to identify genetic variation that may explain why one brother was affected and the other not. Because DMD is a very long gene, a fictionalized, simplified model of the results is presented here (Figure 1). The actual DMD mRNA is about 16,000 base-pairs!------Consider single nucleotide polymorphism (SNP) #1 (Figure 1). Is this mutation likely to cause Duchenne muscular…arrow_forwardWhy does a loss or an excess in genetic material lead to the expression of an abnormal phenotype?arrow_forwardEpistasis refers to the interaction of genes wherein the expression of one gene is dependent on another gene. For example, suppose there are two genes that code for flower color in a plant, where red, WW or Ww, is typically dominant over expression of white, ww, and yellow, YY or Yy, is typically dominant over green, yy. One type of epistasis expresses a pattern where a dominant allele in either gene produces a red phenotype. Classify the F1 flower color ratio that would be produced from the dihybrid cross for each type of epistasis.arrow_forward
- You are discussing the genetic pedigree of a client with a history of autosomal dominant disease in his family. You explain that while a recessive mutation requires both copies of the gene to be mutated in order to cause clinical disease, an autosomal dominant mutation can cause disease when only one copy of the gene is affected. Describe the different mechanisms by which dominance occurs, giving examples of each.arrow_forwardDefine about random monoallelic expression ?arrow_forwardAmelogenesis imperfecta (AI) is a disorder of faulty tooth enamel formation. It is inherited in an autosomal dominant and X-linked dominant pattern. The expression of AI disorder is determined by mutations in the autosomal alleles. One copy of the mutated allele (A) will cause the disorder. The severity of the disorder is determined by mutations in a gene carried on the X chromosome. Normal (or non-severe) abnormality (XN) is dominant over the abnormality (or severe) (Xn) allele. In the absence of the autosomal dominant allele, the abnormality gene on the X chromosome is not expressed. Question:A woman with normal teeth had four children with a man with non-severe form of AI: A boy was born without amelogenesis imperfecta A girl was born without amelogenesis imperfecta A boy was born with severe amelogenesis imperfecta A boy was born with non severe amelogenesis imperfecta Identify the parental genotypes. Complete the Punnett square for the parental cross, and identify the…arrow_forward
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