![Genetics: From Genes to Genomes, 5th edition](https://www.bartleby.com/isbn_cover_images/9780073525310/9780073525310_largeCoverImage.gif)
Concept explainers
a.
To explain:
The differences between the dominant allele P and the recessive allele p of the gene that is responsible for the flower colors.
Introduction:
Different varieties of the same trait are coded by different alleles of the same gene. Alleles can be present in homozygous (both are same) or in heterozygous (different alleles) condition in a gene.
b.
To determine:
Whether some different gene would have been the one that governs Mendel’s flower colors or not based on the given biochemical pathway
Introduction:
![Check Mark](/static/check-mark.png)
Want to see the full answer?
Check out a sample textbook solution![Blurred answer](/static/blurred-answer.jpg)
Chapter 2 Solutions
Genetics: From Genes to Genomes, 5th edition
- Construct a map for the genes d,e,f. Assume that: d and e = 3%; e and f = 5%. Give 2arrangements of the genes/maps.arrow_forwardA. Deletion of the SOX9 gene leads to sex reversal resulting in a person with karyotype 46XY being phenotypically Explain the genetic basis for this. B. Describe what would happen to the phenotype of a male with a mutation in the gene encoding SF1? Explain your answer.arrow_forwardHere is a family pedigree for an imprinting disorder caused by a loss of function mutation in a single imprinted gene. After generation I only related individuals are shown. You can assume that the parents not included in the pedigree did not carry the mutation. %3D II IV V Male O Female Affected Carrier a) Does the mutation involve a gene that is normally expressed from the maternal or from the paternal allele? Briefly explain your logic. b) Identify two ways in which the pattern of inheritance shown in the pedigree is different from X-linked inheritance I. Parthenogenesis has been documented in most vertebrate Classes (e.g. birds, fish) but never in mammals. Genomic imprinting provides one explanation for this observation. Why?arrow_forward
- Some sweet-pea plants have purple flowers and others have white flowers. A homozygous variety of sweet pea that has purple flowers is crossed with a homozygous variety that has white flowers. All the F1have purple flowers. When these F1 self-fertilize, the F2 appear in a ratio of 916 purple to 716 white. a.Draw a hypothetical biochemical pathway to explain the production of purple and white flowers in sweet peas.arrow_forwardIn rats, the following genotypes of two independently assorting autosomal genes determinecoat color:A–B– (gray)A–bb (yellow)aaB– (black)aabb (cream)A third gene pair on a separate autosome determines whether or not any color will be produced.The CC and Cc genotypes allow color according to the expression of the A and B alleles.However, the cc genotype results in albino rats regardless of the A and B alleles present.Determine the F1 phenotypic ratio of the following crosses: (1) AaBBCc × AaBBCc (2) AABbCc × AABbcc (3) AaBbCc × AaBbccarrow_forwardPigments in some bears are the result of epistasis between 2 genes. The black coat color is only produced when both wildtype forms of genes D and E are present. When gene D (D-ee) is wildtype alone, offspring are white. When gene E (ddE-) is wildtype alone, offspring are brown. When no wildtype alleles are present (ddee) offspring are all white. Based on this describe the relationship between the genes D and E. Group of answer choices A-D is dominant to E B- E is dominant to D C- D is epistatic to E D- E is epistatic to Darrow_forward
- In rats, the following genotypes of two independently assorting autosomal genes determine coat color: A-B- (gray) A-bb (yellow) aaB- (black) aabb (cream) A third gene pair on a separate autosome determines whether or not any color will be produced. The CC and Cc genotypes allow color according to the expression of the A and B alleles. However, the cc genotype results in albino rats regardless of the A and B alleles present. Determine the F1 phenotypic ratio of the following crosses: (a) AAbbCC * aaBBcc (b) AaBBCC * AABbcc (c) AaBbCc * AaBbcc (d) AaBBCc * AaBBCc (e) AABbCc * AABbccarrow_forwardWith regard to the T and t alleles, explain what the wordsegregation means.arrow_forwarda. How many generations are presented in this pedigree? b. What are the most probable genotype of III-3, IlI-5, and III-8? c. What is the probability that II- 1 and Il-2 will have another normal offspring? Show punnet square and explain your answer. d. Who among the individuals are affected?arrow_forward
- Leber Congenital Amaurosis (LCA) causes progressive vision loss due to defects in the gene that encodes RPE65 isomerase. Affected individuals are homozygous recessive for mutant alleles of the RPE65 gene. You are trying to determine the molecular nature of the mutations in three individuals with LCA. For ease of analysis, you may assume that each individual is homozygous for the same mutant allele (though the three individuals have different mutations than each other). You use the polymerase chain reaction to amplify DNA from each patient and you determine the sequence of the DNA and compare it to unaffected individuals. You identify the following differences. Note that the non-template strand of DNA is given and the changes are highlighted using red boldface. You can assume that the sequences are in the first reading frame (eg. the first three nucleotides of each sequence is a codon). The coding region of the gene is 1602 bp and the position of the sequences shown below is…arrow_forwardFamilial retinoblastoma, a rare autosomal dominant defect, arose in a large family that had no prior history of the disease. Consider the following pedigree (the darkly colored symbols represent affected individuals): a. Circle the individual(s) in which the mutation most likely occurred. b. Is the person who is the source of the mutation affected by retinoblastoma? Justify your answer. c. Assuming that the mutant allele is fully penetrant, what is the chance that an affected individual will have an affected child?arrow_forwardThe gene controlling ABO blood type and the gene underlying nail-patella syndrome are said to show linkage. What does that mean in terms of their relative locations in the genome? What does it mean in terms of how the two traits are inherited with respect to each other?arrow_forward
- Human Heredity: Principles and Issues (MindTap Co...BiologyISBN:9781305251052Author:Michael CummingsPublisher:Cengage Learning
![Text book image](https://www.bartleby.com/isbn_cover_images/9781305251052/9781305251052_smallCoverImage.gif)