EBK GENETICS: FROM GENES TO GENOMES
5th Edition
ISBN: 8220100255250
Author: HARTWELL
Publisher: YUZU
expand_more
expand_more
format_list_bulleted
Concept explainers
Textbook Question
Chapter 21, Problem 8P
Human geneticists have found the Finnish population to be very useful for studies of a variety of conditions. The population is small; Finns have extensive church records documenting lineages; and few people have migrated into Finland. The frequency of some recessive disorders is higher in the Finnish population than elsewhere in the world, and diseases such as PKU and cystic fibrosis that are common elsewhere do not occur in the Finnish population.
a. | How would a population geneticist explain these variations in disease occurrence? |
b. | The Finnish population is also a source of information for the study of quantitative traits. The genetic basis of schizophrenia is one question that can be explored in this population. What advantage(s) and disadvantage(s) can you imagine for studying complex traits based on the Finnish population structure? |
Expert Solution & Answer
Trending nowThis is a popular solution!
Students have asked these similar questions
Discuss the role of mutation in the origin of genetic polymorphisms. Suppose that a genetic polymorphism involves two alleles at frequencies of 0.45 and 0.55. Describe three different scenarios to explain these observed allele frequencies. You can propose that the mutations that produced the polymorphism are neutral, beneficial, or deleterious.
Please help with the following:
How does penetrance differ from expressivity in genetics?
A. Penetrance is the percentage of individuals with a specific genotype that exhibit the expected phenotype while expressivity is the degree to which a phenotypic character is expressed.
B. Penetrance is the degree of lethality of a specific genotype while expressivity is how frequently that genotype is seen in the population.
C. Penetrance is the presence of more than two alleles at a locus within a group of individuals while expressivity is the influence of sex on which alleles express themselves.
D. None of the above.
E. Penetrance refers to the paternal effects of a gene while expressivity refers to the maternal effects of a gene.
.. Nowadays, newborn babies are required to be tested for
phynylketonuria (PKU), an autosomal recessive genetic disorder. If
untreated, individual homozygous for PKU suffer mental retardation. In a
recent year, 4 PKU babies were detected out of 126,000 tested. Assuming
Hardy-Weinberg conditions, what is the frequency of the PKU gene in this
population (Give your answer in decimal number with 3 decimal places)?
Chapter 21 Solutions
EBK GENETICS: FROM GENES TO GENOMES
Ch. 21 - Choose the best matching phrase in the right...Ch. 21 - Prob. 2PCh. 21 - How can each of the following be used in...Ch. 21 - Which of the following statements would be true of...Ch. 21 - Prob. 5PCh. 21 - Prob. 6PCh. 21 - Prob. 7PCh. 21 - Human geneticists have found the Finnish...Ch. 21 - Prob. 9PCh. 21 - Prob. 10P
Ch. 21 - In a certain plant, leaf size is determined by...Ch. 21 - Compare and contrast the use of SNP genotyping: i...Ch. 21 - Prob. 13PCh. 21 - Prob. 14PCh. 21 - Canavan disease, caused by homozygosity for a...Ch. 21 - Prob. 16PCh. 21 - Prob. 17PCh. 21 - Consider the triangle diagram shown in Fig. 21.15....Ch. 21 - Prob. 19PCh. 21 - Prob. 20PCh. 21 - Suppose a GWAS investigation found a particular LD...Ch. 21 - In domesticated dogs, size has a high...Ch. 21 - Prob. 23P
Knowledge Booster
Learn more about
Need a deep-dive on the concept behind this application? Look no further. Learn more about this topic, biology and related others by exploring similar questions and additional content below.Similar questions
- population is black in colour but about 1/4 of them are white. gene (B) that produces an enzyme that converts a pigment molecule to produce the Black colour. There are 2 alleles of this gene - the dominant B and the recessive b. DNA analysis shows that black individuals have either a BB or Bb genotype and that white individuals have a bb phenotype. However, you have discovered that a small percentage of White individuals have either a BB or Bb genotype. Explain two reasons that could explain this apparent anomaly. They have a BB or Bb genotype but a white phenotype.arrow_forwardThe eugenic movement was created in the early 20th century by Sir Francis Galton. Its aim was to improve the genetic pool of the human population by selective breeding. One idea was to discourage individuals with Mendelian autosomal recessive diseases to have children. However, the fallacy of this idea is shown by the fact that recessive lethal alleles (that are never found in homozygosity) can persist in populations for hundreds to thousands of generations. Which one of the following statements best explains the persistence of those alleles in populations? There is heterozygote advantage in those populations. Recessive alleles keep being produced by mutation. Recessive alleles cannot be selected against when present in heterozygotes. Genetic drift keeps recessive alleles at a relative high frequency in populations. Consider the action of mutation and of genetic drift in a population. What do you expect genetic variation will be in a…arrow_forwardYou are studying an autosome trait. There are two alleles, one showing complete dominance over the other. In a population, 84% of the individuals show the dominant phenotype. Assuming that this population is under Hardy-Weinberg equilibrium, which of the following statement is TRUE? 36% of individuals have the homozygous dominant genotype. 40% of the alleles in the population is recessive. 16% of the alleles in the population is recessive. 60% of individuals have the dominant alleles.arrow_forward
- You are studying the genetics of a newly discovered small animal. You note that most of the population is black in colour but about 1/4 of them are white. You have determined that there is a gene (B) that produces an enzyme that converts a pigment molecule to produce the Black colour. There are 2 alleles of this gene - the dominant B and the recessive b. DNA analysis shows that black individuals have either a BB or Bb genotype and that white individuals have a bb phenotype. However, after extensive DNA analysis, you have discovered that a small percentage of White individuals have either a BB or Bb genotype. Describe two reasons (at a molecular level) that could explain this apparent anomaly. There wasn't a mistake in analysis! These individuals did have a BB or Bb genotype but a white phenotype.arrow_forwardSickle cell anemia is caused by a recessive allele at a single gene. As we discussed in class, being a homozygote for the sickle cell allele is almost always lethal, but heterozygotes tend to be resistant against malaria although they have a mild form of anemia. Because of this heterozygote advantage, the allele for sickle cell anemia has a frequency of more than 10% in some human populations. How would present allele frequencies of the sickle cell allele change, if there was no heterozygote advantage or disadvantage (that is, that heterozygotes would be identical to ‘normal’ homozygotes – no malaria resistance, no anemia)? How would the change in sickle cell allele frequencies compare to scenario a (extirpation of malaria)arrow_forwardThe population risk of NIDDM is highly dependent on the population under consideration; in most populations, this risk is 1%-5%, although it is 6% to 7% in the United States. If a patient has one affected sibling, the risk increases to 10%; an affected sibling and another first-degree relative, the risk is 20%; an affected monozygotic twin, the risk is 50%-100%. 1) Is this a single gene inheritance or multifactorial disease? 2) Is there a strong genetic or environmental cause to the development of this disease? If both genetic and environmental causes are implicated, you have to indicate each of them separately.arrow_forward
- Consider the case of a hypothetical genetic disease called WhySciEleven (WSE), an inherited disease that results to the inability to complete production of an amino acid “moduleactivity” that results in brain damage if untreated. WSE is due to a recessive allele. Given one WSE occurrence per 10,000 births. 1. What is the frequency of the dominant allele? 2. What is the frequency of the recessive allele for WSE in population? 3. What is the frequency of the heterozygous people?arrow_forwardYou are investigating a newly emerging bacteriophage infecting your bacteria. There is a population of bacteria that are resistant to the disease. The allele frequency of the resistant allele is q=0.43. The mutation rate (Aàa) of the locus is 3.2 x 10-2. Assuming no back mutations, how do you expect the allele frequency of the recessive allele to change in the next generation? a. It will decrease a little b. It will not change c. It will decrease a lot d. It will increase a little e. It will increase a lotarrow_forwardPeople who like certain purebred dog breeds, such as German shepherd dogs, are often saddened to learn that some individuals of these purebred breeds have specific genetic defects that might be due to single mutations that are present in the breed. For example, German shepherd dogs often suffer from hip dysplasia. Not all German shepherd individuals seem to have this mutant allele for hip dysplasia. 1. How would linkage help select a German shepherd population that has all the phenotypic traits you want with this breed while no longer having a genetic predisposition to hip dysplasia?arrow_forward
- To understand this research, you must be familiar with some basic genetic terminology. Drag the terms on the left to the appropriate blanks on the right to complete the sentences. Not all terms will be used. dominant allele phenotype The possession of two different alleles of a particular gene is referred to as Reset Help A variation in a DNA sequence at one particular position is called a heterozygosity genotype recessive allele homozygosity single nucleotide polymorphism The appearance of the organism, its observable traits, are referred to as the A variant of a gene for which an individual must be homozygous in order for it to influence the appearance of the organism is a The set of alleles an organism has for a particular trait is the organism's Submit Request Answerarrow_forward.A) To determine if a human trait is heritable, we would best study Group of answer choices. I think it's A. Please explain your answer I'm trying to understand the material a. monozygotic twins that were raised separately, in different environments. b. monozygotic twins that have been raised under similar conditions. c.only distantly related individuals. d. all males or all females. B). To say that a trait exhibits “high heritability” is to say that a. a given set of genes has no influence on a trait. b. there is no difference in genotype between members of the population at the loci in question. c. in a given environment and population, genetic differences have a high degree of influence on the trait compared to environmental influences. d. there is no difference in character between two individuals with the same genotype in question. C). If two populations with identical genetic makeup are raised in different environments, the narrow-sense heritability of a trait of…arrow_forwardIf the frequency of those homozygous for a rare clinically relevant allele that causes an autosomal monogenic recessive condition in a given population of 15 million individuals is 1/8500, how many individuals are likely to be carriers of the causative mutation? Please give your answer as a whole number.arrow_forward
arrow_back_ios
SEE MORE QUESTIONS
arrow_forward_ios
Recommended textbooks for you
- Human Anatomy & Physiology (11th Edition)BiologyISBN:9780134580999Author:Elaine N. Marieb, Katja N. HoehnPublisher:PEARSONBiology 2eBiologyISBN:9781947172517Author:Matthew Douglas, Jung Choi, Mary Ann ClarkPublisher:OpenStaxAnatomy & PhysiologyBiologyISBN:9781259398629Author:McKinley, Michael P., O'loughlin, Valerie Dean, Bidle, Theresa StouterPublisher:Mcgraw Hill Education,
- Molecular Biology of the Cell (Sixth Edition)BiologyISBN:9780815344322Author:Bruce Alberts, Alexander D. Johnson, Julian Lewis, David Morgan, Martin Raff, Keith Roberts, Peter WalterPublisher:W. W. Norton & CompanyLaboratory Manual For Human Anatomy & PhysiologyBiologyISBN:9781260159363Author:Martin, Terry R., Prentice-craver, CynthiaPublisher:McGraw-Hill Publishing Co.Inquiry Into Life (16th Edition)BiologyISBN:9781260231700Author:Sylvia S. Mader, Michael WindelspechtPublisher:McGraw Hill Education
Human Anatomy & Physiology (11th Edition)
Biology
ISBN:9780134580999
Author:Elaine N. Marieb, Katja N. Hoehn
Publisher:PEARSON
Biology 2e
Biology
ISBN:9781947172517
Author:Matthew Douglas, Jung Choi, Mary Ann Clark
Publisher:OpenStax
Anatomy & Physiology
Biology
ISBN:9781259398629
Author:McKinley, Michael P., O'loughlin, Valerie Dean, Bidle, Theresa Stouter
Publisher:Mcgraw Hill Education,
Molecular Biology of the Cell (Sixth Edition)
Biology
ISBN:9780815344322
Author:Bruce Alberts, Alexander D. Johnson, Julian Lewis, David Morgan, Martin Raff, Keith Roberts, Peter Walter
Publisher:W. W. Norton & Company
Laboratory Manual For Human Anatomy & Physiology
Biology
ISBN:9781260159363
Author:Martin, Terry R., Prentice-craver, Cynthia
Publisher:McGraw-Hill Publishing Co.
Inquiry Into Life (16th Edition)
Biology
ISBN:9781260231700
Author:Sylvia S. Mader, Michael Windelspecht
Publisher:McGraw Hill Education
Mitochondrial mutations; Author: Useful Genetics;https://www.youtube.com/watch?v=GvgXe-3RJeU;License: CC-BY