Biology
12th Edition
ISBN: 9780134813448
Author: Audesirk, Teresa, Gerald, Byers, Bruce E.
Publisher: Pearson,
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Chapter 14, Problem 2AC
Summary Introduction
To determine: The reason why all the children born with SCID are boys.
Introduction: Severe combined immunodeficiency (SCID) is a rare disorder that results in affecting the development and function of immune cells due to mutation in different genes. Infants affected by SCID appear normal; initially, but later they become prone to several infections.
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An individual with 46, XX genotype is diagnosed with Duchenne-type Muscular Dystrophy, a recessive X-linked disorder. Genetic tests confirm that this individual is a heterozygote for this disorder. Briefly, but specifically, explain how it’s possible that they are showing symptoms of this disorder.
3) Queen Victoria of England, who ruled from 1837-1901, is believed to have been the carrier of
hemophilia. Hemophilia is an X-linked disease in which the blood is unable to form clots. Please
make a Punnet Square using the scenario below and answer the following questions.
Queen Victoria married a man who did not have the hemophilia trait or disease.
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What is the likelihood that they would have a son with hemophilia?
What is the likelihood that they would have a daughter with hemophilia?
Hemophilia is determined by genes on the X chromosome in humans. Assume that a phenotypically normal woman whose father had hemophilia is married to a normal man. 1) What is the probability that their first son will have hemophilia? 2) What is the probability that their first daughter will have hemophilia?
Chapter 14 Solutions
Biology
Ch. 14.1 - define biotechnology?Ch. 14.1 - Prob. 2CYLCh. 14.1 - define GMO and transgenic organism?Ch. 14.2 - describe natural processes that recombine DNA,...Ch. 14.3 - Prob. 1CSCCh. 14.3 - Prob. 1CYLCh. 14.3 - summarize how CRISPR-Cas9 works and explain why it...Ch. 14.4 - For any single person, a given STR always has...Ch. 14.4 - There are many other applications in which DNA...Ch. 14.4 - Prob. 1CYL
Ch. 14.4 - Prob. 2CYLCh. 14.5 - Restriction enzymes are isolated from bacteria....Ch. 14.5 - Many countries regulate the use of genetically...Ch. 14.5 - explain how genes are inserted into a plasmid, and...Ch. 14.5 - Prob. 2CYLCh. 14.6 - Prob. 1CTCh. 14.6 - Prob. 1HYEWCh. 14.6 - describe the advantages of genetically modified...Ch. 14.6 - list some examples of how genetically modified...Ch. 14.6 - Prob. 3CYLCh. 14.7 - Explain how fetal DNA could be used to establish...Ch. 14.7 - explain how biotechnology is used to diagnose both...Ch. 14.7 - describe how transgenic organisms are used to...Ch. 14.7 - describe the procedures and advantages of gene...Ch. 14.8 - explain why people might be opposed to the use of...Ch. 14.8 - Prob. 2CYLCh. 14.8 - Prob. 1CTCh. 14 - Prob. 1MCCh. 14 - Prob. 3MCCh. 14 - A restriction enzyme a. cuts DNA at a specific...Ch. 14 - Prob. 5MCCh. 14 - Prob. 1FIBCh. 14 - _________is the process whereby bacteria pick up...Ch. 14 - The _______ is a technique tor multiplying DNA in...Ch. 14 - Matching DNA samples in forensics uses a specific...Ch. 14 - Prob. 5FIBCh. 14 - Describe two natural forms of genetic...Ch. 14 - Prob. 2RQCh. 14 - Prob. 3RQCh. 14 - Prob. 4RQCh. 14 - Prob. 5RQCh. 14 - Prob. 6RQCh. 14 - How does gel electrophoresis separate pieces of...Ch. 14 - Prob. 8RQCh. 14 - Prob. 9RQCh. 14 - Prob. 10RQCh. 14 - As you may know, many Insects have evolved...Ch. 14 - Prob. 2AC
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- Hemophilia A is caused by a recessive X-linked allele that encodes a defective form of a clotting protein. If a affected father and a mother who is known to not be a carrier have children, what percentage of female offspring will have hemophilia?arrow_forwardAchondroplasia is a form of dwarfism in humans. It is caused by a mutant allele of the fibroblast growth factor receptor 3 gene ( FGFR3) that produces an overactive protein. Having one copy of the mutant allele results in dwarfism. Two copies of the mutant allele results in death before birth. If a man with Achondroplasia marries a woman who is Sickle Cell Anemia carrier and they have a child together, what is the probability that their child will Achondroplasia AND be a Sickle Cell Anemia carrier? ½ 2/3 ¼ 1 ½ 1/16arrow_forwardWhat type of Monogenic Immune disorders are there? Is X-linked inheritance syndrome a type of monogenic immune disorder?arrow_forward
- A form of hemophilia is caused by a sex-linked (X-linked) recessive gene. A phenotypically normal woman whose father had hemophilia marries a man who suffers with hemophilia. What is the probability that their first daughter will have hemophilia?arrow_forwardLauren reports that she had a maternal male cousin (through a maternal aunt) and a maternal great uncle (maternal grandmother’s brother) both pass away from the same x-linked lethal condition. Both affected individuals did not have genetic testing. Lauren has a normal carrier screen for x-linked lethal conditions, which you know identifies 40% of causative mutations. If Lauren is currently pregnant with a male child, what is the chance that this child will have the condition?arrow_forwardThe X chromosome has a lot of traits for things besides the traits we consider female. It carries traits forthings like the ability of your blood to clot correctly and the ability to see differences in the colors red andgreen. If you blood doesn’t clot correctly, it’s called Hemophilia. If you can’t see the difference betweenred and green, you are colorblind. Therefore, these are referred to as X-Linked or Sex-Linked Traits.Notice that those are on the X chromosome only. That means they are missing from the Y. In fact, the Y iscalled Y because it is physically missing a section at the end. This means the Y chromosome is missing genes that the X chromosome has. If you are XY, you only haveone copy of the gene, or one allele. Given what we just said above, can a XY parent pass a X-Linked Trait to his XY offspring?arrow_forward
- Mutations in the genes for clotting factor VIII and IX cause hemophilia A and B, respectively. A woman may be heterozygous for mutations in both genes, with a mutated factor VIII allele on one X chromosome, and a mutated factor IX allele on the other. All of her sons should have either hemophilia A or B. However, on rare occasions, one of these women gives birth to a son who does not have hemophilia, and his one X chromosome does not have either mutated allele. Explain.arrow_forwardHemophilia is an X-linked recessive phenotype. Suppose a man who expresses the hemophilia phenotype has children with a woman who has the normal phenotype (and does not have a family history of hemophilia). If the couple have a son, what are the chances that he will have hemophilia? A) 50% B) 25% C) 0% D) 100%arrow_forwardHemophilia is called "the royal disease" because many European royal families had members with the condition. Hemophilia is a recessive, X-linked disorder. Queen Victoria was unaffected by hemophilia, but was a carrier of the hemophilia gene (X X ). Suppose Queen Victoria's husband, Prince Albert, was affected with hemophilia (X Y). What is the percent probability that a son of Queen Victoria and Prince Albert would be unaffected by hemophilia? probability of unaffected son: What is the percent probability that a daughter or son of Queen Victoria and Prince Albert would be affected by hemophilia? probability of affected child: What is the percent probability Queen Victoria and Prince Albert would have two affected females? probability of two affected females: % % %arrow_forward
- X-linked disorders (like hemophilia) are more likely to affect people of one gender than the other. Which gender is this, and why are x-linked disorders more likely to affect people of this gender?arrow_forwardThe Xg cell-surface antigen is coded for by a gene located on the X chromosome. No equivalent gene exists on the Y chromosome. Two codominant alleles of this gene have been identified: Xg1 and Xg2. A woman of genotype Xg2/Xg2 bears children with a man of genotype Xg1/Y, and they produce a son with Klinefelter syndrome of genotype Xg1/Xg2Y. Using proper genetic terminology, briefly explain how this individual was generated. In which parent and in which meiotic division did the mistake occur?arrow_forwardIn humans, the Rh factor genetic information is inherited from our parents, but it is inherited independently of the ABO blood type alleles. In humans, Rh+ individuals have the Rh antigen on their red blood cells, while Rh- individuals do not. There are two different alleles for the Rh factor known as Rh+ and rh. Assume that a dominant gene Rh produces the Rh+ phenotype, and that the recessive rh allele produces the Rh- phenotype. In a population that is in Hardy-Weinberg equilibrium, if 160 out of 200 individuals are Rh+, calculate the frequencies of both alleles.arrow_forward
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