Genetics: Analysis and Principles
6th Edition
ISBN: 9781259616020
Author: Robert J. Brooker Professor Dr.
Publisher: McGraw-Hill Education
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Chapter 1, Problem 6CONQ
Summary Introduction
To review:
The term
Introduction:
DNA or deoxyribonucleic acid is the genetic material for all organisms, except vriuses. The genes are expressed in the form of proteins. These genes determine the different traits carried by an individual. For example, genes coding for the color pigment of wings determine whether it will be a dark or light colored wing.
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Students have asked these similar questions
"Coat color in rats varies from white to black and includes many shades of gray in between. If the number of different coat colors possible is 9, how many genes are involved? "
What are the causes of genetic variation?
Give specific examples.
(7) In a family-based alcohol use disorder genetic study, a total of 50 families, each with a pair of
siblings, were recruited. The result showed that 12 families have the 1" siblings with marijuana
dependence and the 2nd siblings without the disorder, while another 11 families are opposite (i.e. the 1st
siblings without the disorder but the 2nd siblings with the disorder). In contrast, 20 families have both
siblings exhibiting the disorder and another 17 families have both siblings without the disorder. What
kind of heritability can you calculate using this family study and what is the heritability value for
alcohol use disorder?
A) Narrow-sense heritability, approximately 88%
B) Narrow-sense heritability, approximately 44%
C) Broad-sense heritability, approximately 88%
D) Broad-sense heritability, approximately 44%
Chapter 1 Solutions
Genetics: Analysis and Principles
Ch. 1.1 - 1. Which of the following is not a constituent of...Ch. 1.1 - 2. A gene is a segment of DNA that has the...Ch. 1.1 - The function of the genetic code is to a. promote...Ch. 1.1 - The process of transcription directly results in...Ch. 1.2 - Gene expression can be viewed at which of the...Ch. 1.2 - 2. Variation in the traits of organisms may be...Ch. 1.2 - 3. A human skin cell has 46 chromosomes. A human...Ch. 1.2 - 4. Evolutionary change caused by natural selection...Ch. 1.3 - Which of the following is not a model organism? a....Ch. 1.3 - A person studying the rate of transcription of a...
Ch. 1.4 - The scientific method involves which of the...Ch. 1 - Pick any example of a genetic technology and...Ch. 1 - Prob. 2CONQCh. 1 - Most genes encode proteins. Explain how the...Ch. 1 - Prob. 4CONQCh. 1 - Prob. 5CONQCh. 1 - Prob. 6CONQCh. 1 - Prob. 7CONQCh. 1 - Your textbook describes how the detrimental...Ch. 1 - Prob. 9CONQCh. 1 - Prob. 10CONQCh. 1 - Prob. 11CONQCh. 1 - Prob. 12CONQCh. 1 - 13. With regard to biological evolution, which of...Ch. 1 - 14. What are the primary interests of researchers...Ch. 1 - What is a genetic cross?Ch. 1 - Prob. 2EQCh. 1 - Prob. 3EQCh. 1 - 4. Many organisms are studied by geneticists. Do...Ch. 1 - Prob. 5EQ
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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
- Albinism in humans can be caused by mutations in any one of several different genes. This situation, in which the same phenotype may result from variation in several different genes, is referred to as genetic heterogeneity. Is genetic heterogeneity common? Are most genetic traits in humans the result of variation in a single gene, or are there many genetic traits that result from variation in several genes, as albinism does?arrow_forwardWhat is polymorphism? Outside of genes (non-gene regions of genome) what are the 4 types of polymorphisms that you can have. What are their distinguishing features?arrow_forward***18. Complete this flowchart to show how different alleles can result in different characteristics. In the DNA, different alleles of a gene have a different sequence of > different sequence of transcription > different sequence of in a protein translation > different structure and function of the protein (e.g. normal enzyme vs. defective enzyme) > different characteristics (e.g. normal color vs. albino) inarrow_forward
- Part 1 - With use of Punnett diagrams discuss how the results of experiments carried out by Austrian monk Gregor Mendel on pea plants brought about the Law of Dominance, the Law of Segregation, and the Law of Independent assortment. Part 2 - In humans, the gene that produces the disease Sickle Cell Anaemia is recessive to the gene for healthy haemoglobin production. a) How can two phenotypically healthy parents have a child who suffers from Sickle cell Anaemia? In your answer use suitable letters to show the genotypes of the parents and construct a Punnett diagram to show all the possibilities of the children's genotypes. b) Based on the outcome of your Punnett diagram, state and explain the probability of a child being a sufferer of Sickle Cell Anaemia and the probability of a child not suffering from the disease. c) If an individual who suffers from Sickle cell disease has a child with someone who is healthy (and not carrying the sickle cell gene), what is the probability that…arrow_forwardInterested in exploring the genetic pathways that lead to neurological issues, you want to see if recessive mutations which generate too many neurons (tm) in flies - which many causes autistic like symptoms are in the same gene as mutations that generate too few neurons (tf) - intellectual diabilities. You cross a true-breeding homozygous tm/tm fly to a homozygous too few neuron fly tf/tf. What phenotype in the progeny would tell these mutations are in different genes?arrow_forward1. 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/arrow_forward
- 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.arrow_forwardIn a study of a muscle disorder, several affected families exhibited vision problems, muscle weakness, and deafness (M. Zeviani et al. 1990. American Journal of Human Genetics 47:904–914). Analysis of the mtDNA from affected members of these families revealed that large numbers of their mtDNA molecules possessed deletions of varying lengths. Different members of the same family and even different mitochondria from the same person possessed deletions of different sizes, so the underlying defect appeared to be a tendency for the mtDNA of affected persons to have deletions. A pedigree of one of the families studied is shown below. The researchers concluded that this disorder is inherited as an autosomal dominant trait, and they mapped the diseasecausing gene to a position on chromosome 10 in the nucleus. Q. Explain how a mutation in a nuclear gene might lead to deletions in mtDNA.arrow_forwardIn a study of a muscle disorder, several affected families exhibited vision problems, muscle weakness, and deafness (M. Zeviani et al. 1990. American Journal of Human Genetics 47:904–914). Analysis of the mtDNA from affected members of these families revealed that large numbers of their mtDNA molecules possessed deletions of varying lengths. Different members of the same family and even different mitochondria from the same person possessed deletions of different sizes, so the underlying defect appeared to be a tendency for the mtDNA of affected persons to have deletions. A pedigree of one of the families studied is shown below. The researchers concluded that this disorder is inherited as an autosomal dominant trait, and they mapped the diseasecausing gene to a position on chromosome 10 in the nucleus. Q. What characteristics of the pedigree rule out inheritance of a trait encoded by a gene in the mtDNA as the cause of this disorder?arrow_forward
- In the 1800s, a man with dwarfism who lived in Utah produced a large number of descendants: 22 children, 49 grandchildren, and 250 greatgrandchildren (see the illustration of a family pedigree to the right), many of whom also exhibited dwarfism (F. F. Stephens. 1943. Journal of Heredity 34:229–235). The type of dwarfism found in this family is called Schmid-type metaphyseal chondrodysplasia, although it was originally thought to be achondroplastic dwarfism. Among the families of this kindred, dwarfism appeared only in members who had one parent with dwarfism. When one parent exhibited dwarfism, the following numbers of children were produced. Q. Use chi-square tests to determine if the numbers of children with each phenotype in family C (1 with normal stature, 6 with dwarfism) and in family D (6 with normal stature, 2 with dwarfism) are significantlydifferent from the numbers expected on the basis of your proposed mode of inheritance. How would you explain these deviations from the…arrow_forwardHow can you use this piece of information to help you explain to your friends what is the significance of mutations in the emergence of new genetic properties (alleles) that may result (or not) in new phenotypic characteristics? (Recall that not all SNPs affect phenotype.)arrow_forwardA scientist investigating the genome of two related individuals observes a difference of a few nucleotides in one individual compared to the other. The nucleotide differences are in a region of noncoding DNA on chromosome 1. Would these differences be considered a mutation? Why or why not? Yes, the difference in nucleotide sequences between the individuals is a mutation because it will affect the phenotype of the two individuals. Yes, any heritable variation in the nucleotide sequence is considered a mutation, even if that variation is in a noncoding region of DNA. Not enough information was provided to determine if this nucleotide difference is a mutation because the effect on phenotype is unknown. No, the change in nucleotide sequence doesn't appear in a coding region of the DNA and so can't be a mutation.arrow_forward
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Genetic Variation and Mutation | 9-1 GCSE Science Biology | OCR, AQA, Edexcel; Author: SnapRevise;https://www.youtube.com/watch?v=bLP8udGGfHU;License: Standard YouTube License, CC-BY