Concept explainers
a. Is
b. Does this family give evidence of genetic linkage between
c. Using N and n to represent alleles at the
d. Explain why
e. Explain why
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Genetic Analysis: An Integrated Approach (3rd Edition)
- 3) Achondroplasia is a common form of hereditary dwarfism that causes very short limbs, stubby hands, and an enlarged forehead. Below are three pedigrees depicting families with this specific type of dwarfism. A. What is the most likely mode of inheritance?arrow_forwardThe pedigree below shows a family affected by a disease. Assume that the individuals marked with an asterisk (*) do not carry any allele associated with the affected phenotype, no other mutation spontaneously occurred, and complete penetrance. Answer the following questions below. Use the notation XR for the allele associated with the dominant phenotype and Xr for the allele associated with the recessive phenotype. Q1) Give the genotypes for as many individuals in the pedigree as possible.arrow_forwardEctrodactyly is a rare condition in which the fingers are absent, and the hand is split. It is usually inherited as an autosomal dominant trait. What do the double horizontal lines mean between III-1 and III-4? Is the pedigree below consistent with autosomal dominant inheritance?arrow_forward
- 15. The following pedigree shows inheritance of Huntington's disease, a fatal genetic disorder that causes neurodegeneration. Since signs and symptoms usually do not appear until adulthood, many who are carriers may not realize their risk of passing on the disease-causing allele. The following pedigree represents a family in which some people are affected by Huntington's disease. Reeessive Trit er btmnt be Mec yplicalty Hinheteearrow_forwardPlease consider the following pedigree. Assume that people who marry in to the family do not carry the allele. Assume complete penetrance. I II III 3 IV 1 2 a. Is it possible for the inheritance pattern for the trait illustrated in this pedigree to be as a result of each of the following? Answer yes or no. (i) an autosomal recessive allele (AR) (ii) an autosomal dominant allele (AD) (iii) a X-linked recessive allele (XR) (iv) a X-linked dominant allele (XD) b. Based strictly on the characteristic patterns of inheritance that define the four different options in (a), give a definitive motivation for the most likely mode of inhertance.arrow_forwardthe pedigree below shows the inheritance of a newly identified eye color gene. Assume 100% penetrance and expressivity. Use the pedigree to find: 1. Identify the mode of inheritance (either autosomal dominant, or autosomal recessive) 2. Argue why your mode of inheritance must be correct. Your argument should cite specific individuals from the pedigree. (For example, the top left individual is person I-1).arrow_forward
- The inheritance pattern of a rare form of Xeroderma pigmentosum is exhibited in the pedigree shown below. The pattern of inheritance of the Xeroderma pigmentosum phenotype suggests what type of inheritance. Explain your conclusion.arrow_forwardRefer to the pedigree below which shows inheritance for achondroplasia (dwarfism), a dominantly inherited trait (denoted as D), which are the darkened circles and squares. Dwarfism (darkened shapes) are dominantly inherited, while normal height is recessively inherited (hh). Based on the pedigree, what is the correct genotype for individual #II-6? Dominant Autosomal Pedigree 2 II 2 3 II 1 2 3 6 9 10 Dd DD DD or Dd ddarrow_forwardBelow is a pedigree of a family with a rare genetic disorder. I. IV. a. What is the mode of inheritance for this rare disorder and what is the genotype of I.1 and 1.2? b. Write the genotypes for the following individuals (if the genotype is unknown write all possible genotypes): i.) III.2 - ii) III.3 -arrow_forward
- Take the example of B-thalassemia, an autosomal recessive genetic disease that particularly affects people from around the Mediterranean. This disease is associated with an anomaly of hemoglobin, a protein essential for the transport of oxygen, which is composed of four chains: two alpha (a) and two beta (B). In case of B-thalassemia, the ẞ chains are produced in insufficient or no quantity in an individual homozygous recessive resulting in insufficient production of overall hemoglobin leading to anemia and other physiological challenges. The gene that controls the synthesis of the ẞ chains is located on chromosome 11. Here is part of the coding portion of this gene (which controls a total of 146 amino acids and of which you only see the portion 36 to 41) and one of the targeted mutations: 1. Give the sequence of amino acids from the template and mutated strands. 2. What type of point mutation is it? 3. Using the principles of the theory of evolution, explain briefly and generally why…arrow_forwardUse the following information to answer the next question. The shape of the fruit of summer squash plants is determined by the interaction of two genes. The genotypes and corresponding phenotypes for the shapes of summer squash are given below. a. DDee b. ddee In order to determine the genotype of a squash with disc-shaped fruit a plant breeder would cross the disc- shaped plant with which of the following? Select one: c. ddEE Genotype D_E_ D_ee, ddE_ ddee d. DDEE Phenotype disc-shaped fruit sphere-shaped fruit long-shaped fruitarrow_forwardEctrodactyly is a rare condition in which the fingers are absent and the hand is split. This condition is usually inherited as an autosomal dominant trait. Ademar Freire-Maia reported the appearance of ectrodactyly in a family in São Paulo, Brazil, whose pedigree is shown here. Is this pedigree consistent with autosomal dominant inheritance? If not, what mode of inheritance is most likely? Explain your reasoning.arrow_forward
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