BIOLOGY:THE ESSENTIALS (LL) W/CONNECT
3rd Edition
ISBN: 9781260670929
Author: Hoefnagels
Publisher: MCG CUSTOM
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Textbook Question
Chapter 10, Problem 2WIO
List three genes (mentioned in this chapter or not) that do not affect physical appearance. Do these genes contribute to an organism’s
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In man, muscular dystrophy is a condition in which the muscles waste away during early life and may result in a shorter life expectancy. It is due to a sex-linked, recessive gene. A certain couple has five children – three boys (ages 1yr, 3yrs, and 10yrs old) and two girls (ages 5yrs and 7yrs old). The oldest boy shows the symptoms of this disease. You are their family physician and they come to you for advice. What would you tell them about the chances of their other children developing the disease?
Albinism is characterized by the lack of a dark pigment called melanin in the hair, skin and eyes. Albinism is caused by the absence of an functioning enzyme called thyrosinase, which is necessary for the synthesis of melanin. Given this bit of information, what can you assume about the heredity pattern of this trait?
A) It is caused by a recessive allele of the gene coding for thyrosinase.
B) It is caused by a dominant allele of the gene coding for melanin.
C) It is caused by a dominant allele of the gene coding for thyrosinase.
D) It is caused by a recessive allele of the gene coding for melanin.
E) There is not enough information here to tell
1. What is an allele?
2. What is a point mutation?
3. How are point mutations related to alleles?
Use these sites to find the answer please:
https://www.britannica.com/story/whats-the-difference-between-a-gene-and-an-allele
http://rosalind.info/glossary/point-mutation/
Chapter 10 Solutions
BIOLOGY:THE ESSENTIALS (LL) W/CONNECT
Ch. 10.1 - How are chromosomes, DNA, genes, and alleles...Ch. 10.1 - Prob. 2MCCh. 10.2 - Why did Gregor Mendel choose pea plants as his...Ch. 10.2 - Distinguish between dominant and recessive;...Ch. 10.3 - Prob. 1MCCh. 10.3 - How are Punnett squares helpful in following the...Ch. 10.3 - Prob. 3MCCh. 10.3 - Prob. 4MCCh. 10.4 - What is a dihybrid cross, and what is the...Ch. 10.4 - Prob. 2MC
Ch. 10.4 - Prob. 3MCCh. 10.5 - How do the patterns of inheritance differ for...Ch. 10.5 - What is the difference between recombinant and...Ch. 10.5 - Prob. 3MCCh. 10.6 - Prob. 1MCCh. 10.6 - What is pleiotropy?Ch. 10.6 - Prob. 3MCCh. 10.6 - Prob. 4MCCh. 10.7 - Prob. 1MCCh. 10.7 - Prob. 2MCCh. 10.7 - Prob. 3MCCh. 10.8 - How are pedigrees helpful in determining a...Ch. 10.8 - Prob. 2MCCh. 10.9 - Prob. 1MCCh. 10.9 - Prob. 2MCCh. 10 - In the list of four terms below, which term is the...Ch. 10 - Prob. 2MCQCh. 10 - Prob. 3MCQCh. 10 - Prob. 4MCQCh. 10 - Prob. 5MCQCh. 10 - Prob. 6MCQCh. 10 - Prob. 1WIOCh. 10 - List three genes mentioned in this chapter or not...Ch. 10 - Prob. 3WIOCh. 10 - Prob. 4WIOCh. 10 - Prob. 5WIOCh. 10 - Explain how each of the following appears to...Ch. 10 - Prob. 8WIOCh. 10 - Calico cats have large patches of orange and...Ch. 10 - Prob. 10WIOCh. 10 - Review Burning Question 10.10, which describes the...Ch. 10 - Prob. 1PITCh. 10 - Analyze the concept map and then explain the...Ch. 10 - Add meiosis, gametes, mutations, incomplete...Ch. 10 - In rose bushes, red flowers FF or Ff are dominant...Ch. 10 - In Mexican hairless dogs, a dominant allele...Ch. 10 - Prob. 3GPCh. 10 - Two lizards have green skin and large dewlaps...Ch. 10 - A fern with a genotype AA Bb Cc dd Ee mates with...Ch. 10 - In Fraggles, males are genotype XY and females are...
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- Tay Sachs is a rare autosomal recessive disorder that causes mental and physical disabilities leading to death in infants. Affected individuals are lacking the enzyme hexosaminidase, causing lipids to build up in the brain.The HEXA gene on chromosome 15 codes for hexosaminidase, and a four base pair insertion in the gene results in an altered reading frame and non-functional enzyme being produced. Individuals who are carriers (heterozygotes) of the Tay-Sachs allele are not affected by the disease but appear to have increased protection against tuberculosis.The incidence of Tay-Sachs disease is much higher among Ashkenazi Jews originating from Eastern Europe than the general population of the United States. About 1 in 3 500 babies of Ashkenazi Jewish heritage are born with Tay-Sachs disease and about 1 in 30 Ashkenazi Jews are carriers compared to about 1 in 320 000 babies born with the disease and about 1 in 300 carriers in the general United States population. Ashkenazi Jews living in…arrow_forwardPlace each description of a mutation in the appropriate column based on whether it is most likely to show a dominant or recessive pattern of inheritance. (Each box is used only once.) Mutation that results in death before the age of reproduction Mutation that results in an inactive enzyme Mutation that results in a misfolded protein that aggregates with normal cellular proteins Mutation that results in no protein being produced Mutation that results in increased synthesis of a protein Mutation that results in a protein with increased enzymatic activity Dominant Recessivearrow_forwardIndividuals, such as Ryan Clark and Geno Atkins, heterozygous for the sickle cell allele show effects of the allele under some circumstances (refer to the linked article and Mendelian patterns of inheritance in your text). Explain in terms of gene expression. http://www.nfl.com/news/story/0ap3000000714754/article/coleman-unsure-on-denver-game-due-to-sickle-cell-traitarrow_forward
- Lesch-Nyhan syndrome is due to a mutation in a gene that encodesa protein called hypoxanthine-guanine phosphoribosyltransferase(HPRT). HPRT is an enzyme that functions in purine metabolism.People afflicted with this syndrome have severe neurodegenerationand loss of motor control. The pedigree below contains severalindividuals with Lesch-Nyhan syndrome, shown with blacksymbols. Based on this pedigree, does this syndrome appearto be inherited by an autosomal recessive, autosomal dominant,X-linked recessive, or X-linked dominant pattern? Explainyour reasoning.arrow_forwardIn genetics, what does a genotype of Hh signify? Choose 1 answer: Choose 1 answer: (Choice A) A Homozygous; two dominant alleles (Choice B) B Homozygous; two recessive alleles (Choice C) C Heterozygous; one dominant allele and one recessive allele (Choice D) D Homozygous; one dominant allele and one recessive allelearrow_forwardChoose one human multifactorial condition and describe it in detail. Include a description of the condition, possible genetic and environmental components that cause the condition as well as an explanation of why it is difficult to study multifactorial conditions. Include references. PDF https://www.genetics.edu.au/PDF/Environmental_and_genetic_interactions_fact_sheet-CGE.pdfarrow_forward
- Phenylketonuria (PKU) is a disorder caused by a defect in the gene that codes for the phenylalanine hydroxylase (PAH), an enzyme required to break down the amino acid phenylalanine. The results of a newborn screening test indicated that Jack and Jill’s baby has phenylketonuria (PKU). Neither Jack nor Jill has PKU. A DNA test indicated that there was no switching of babies - Jack and Jill are the baby's real parents. What is the probability that their next child will have PKU?arrow_forwardPhenylketonuria (PKU) is a disorder caused by a defect in the gene that codes for the phenylalanine hydroxylase (PAH), an enzyme required to break down the amino acid phenylalanine. The results of a newborn screening test indicated that Jack and Jill’s baby has phenylketonuria (PKU). Neither Jack nor Jill has PKU. A DNA test indicated that there was no switching of babies - Jack and Jill are the baby's real parents. What is the probability that their next child will have PKU? Answer in fraction:arrow_forwardThere are some genes where the phenotype of an individual is dependent on the mother's genotype. These are called maternal genes. Find some examples. Why is the mother's genotype more important?arrow_forward
- A couple is planning a family, but since each has a brother having the sickle-cell disorder, they are worried that their kids might develop the disorder too. Neither of them nor their respective parents have the disorder. Which of the following will be your smartest advice as a genetic counsellor? One of four of their children can be expected to have sickle cell. It is possible that none of their kids will have the disorder, but tests should be carried out on both of them to confirm. All of their children will have sickle-cell disorder. There is no chance of any of their kids having sickle cell.arrow_forwardAlbinism is caused by an autosomal recessive allele that interferes with skin pigmentation in mammals. Two normally pigmented human parents already have an albino boy. They plan to continue to have children until they get a girl. Some or all of this information is important for each of the questions below. a) What is the probability that their next child (currently unborn) will be a girl with albinism? Explain your reasoning. b) What is the probability their first female child will be albino? Explain your reasoning. c) The answer to part (b) is different (and, yes, the answer is different) from the answer to part (a). Explain why. (Hint: it has something to do with the underlined words.)arrow_forwardWhat is recessive mutation ?arrow_forward
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