Genetic Analysis: An Integrated Approach (3rd Edition)
3rd Edition
ISBN: 9780134605173
Author: Mark F. Sanders, John L. Bowman
Publisher: PEARSON
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Textbook Question
Chapter 15, Problem 7P
Using animal models of human diseases can lead to insights into the cellular and genetic bases of the diseases. Duchenne muscular dystrophy (DMD) is the consequence of an X-linked recessive allele.
How would you make a mouse model of DMD?
How would you make a Drosophila model of DMD?
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Suppose a researcher has three different Drosophila strains that have mutations in the bicoid gene called bicoid-A, bicoid-B, and bicoid-C; the wild type is designated bicoid +. To study these mutations,
phenotypically normal female flies that are homozygous for the given bicoid mutation were obtained, and their oocytes were analyzed using a Northern blot to determine the size and/or amount of the bicoid
mRNA and in situ hybridization to determine the bicoid mRNA location within the oocyte. A wild-type strain was also analyzed as a control. In both cases, the probe was complementary to the bicoid mRNA and
the results are shown below. (Anterior is on the left; posterior is on the right.)
Northern blot
1
2
-
3 4
In situ hybridization
Wild type
Lane 1. Wild type (bicoid*)
Lane 2. bicoid-A
Lane 3. bicoid-B
Lane 4. bicoid-C
bicoid-B
bicoid-A
bicoid-C
Which mutation is likely to cause the embryo to develop two "anterior" ends?
bicoid-B
Obicoid-A
bicoid-C
For the first experiment ever on Drosophila mutations. Answer the following questions.
a. What is the title of the first published paper explained the experiment and what is the name of the Author?
b. What is the first mutation discovered in Drosophila?
c. Explain the changes in the Drosophila yellow mutant (Y)compared to wild type.
provide one example from the Drosophila AP toolkit for "Toolkit genes can be classified according to the phenotypes caused by their mutation. Similar mutant phenotypes often reflect genes that function in a single developmental pathway. Distinct pathways exist for the generation of body axes, for example, and for the formation and identity of fields."
Chapter 15 Solutions
Genetic Analysis: An Integrated Approach (3rd Edition)
Ch. 15 - 15.1 What purpose do the bla and lacZ genes serve...Ch. 15 - The human genome is 3109 bp in length. How many...Ch. 15 - 15.3 Ligase catalyzes a reaction between the...Ch. 15 - You have constructed four different libraries: a...Ch. 15 - Using the genomic libraries in Problem 4, you wish...Ch. 15 - The human genome is 3109bp. You wish to design a...Ch. 15 - 15.7 Using animal models of human diseases can...Ch. 15 - 15.8 Compare methods for constructing homologous...Ch. 15 - 15.9 Chimeric genefusion products can be used for...Ch. 15 - 15.10 Why are diseases of the blood simpler...
Ch. 15 - Injection of double-stranded RNA can lead to gene...Ch. 15 - Compare and contrast methods for making transgenic...Ch. 15 - 15.13 It is often desirable to insert cDNAs into a...Ch. 15 - 15.14 A major advance in the s was the development...Ch. 15 - 15.15 The bacteriophage lambda genome can exist in...Ch. 15 - 15.16 The restriction enzymes Xho and Sal cut...Ch. 15 - 15.17 The bacteriophage has a single-stranded DNA...Ch. 15 - 15.18 To further analyze the CRABS CLAW gene (see...Ch. 15 - You have isolated a genomic clone with an EcoR I...Ch. 15 - 15.20 You have identified a cDNA clone that...Ch. 15 - 15.21 You have isolated another cDNA clone of the...Ch. 15 - 15.22 You have identified five genes in S....Ch. 15 - You have generated three transgenic lines of maize...Ch. 15 - 15.24 Bacterial Pseudomonas species often possess...Ch. 15 - 15.25 Two complaints about some transgenic plants...Ch. 15 - 15.26 In Drosophila, lossoffunction Ultrabithorax...Ch. 15 - Prob. 27PCh. 15 - The highlighted sequence shown below is the one...Ch. 15 - Vitamin E is the name for a set of chemically...Ch. 15 - The RAS gene encodes a signaling protein that...Ch. 15 - 15.31 You have cloned a gene for an enzyme that...Ch. 15 - 15.32 About of occurrences of nonautoimmune type...Ch. 15 - Describe how having the Cas 9 gene at a genomic...Ch. 15 - 15.34 Would a gene drive system spread rapidly...
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- In Drosophila subobscura, the presence of a recessive gene called grandchildless (gs) causes the offspring of homozygous females, but not those of homozygous males, to be sterile. Can you offer an explanation as to why females and not males are affected by the mutant gene?arrow_forwardAPOE gene has been found to be a major contributor to sporadic Alzheimer's disease (AD), by acting as an age-of-onset modifier for the common relatively late-onset forms of the disease. Among four alleles causing early onset of AD, the epsilon4 allele (APOE4) disrupts this function. If you generate transgenic monkeys in which the normal allele of APOE gene is knocked out, what phenotype will you expect for those knockout monkeys? A. The APE mRNA expression will be completely suppressed. B. They slow down the development of AD. C. They develop AD early. D. They don't show any AD symptom.arrow_forwardConsider the following variations in Drosophila melanogaster, relative to the wild-type: White eyes are a recessive trait—the gene of which is found in Chromosome I (X). Vestigial wings are a recessive trait—the gene of which is found in Chromosome II. Aristapedia is a dominant trait—the gene of which is found in Chromosome III. Being homozygous for this condition is lethal. Cross the following mutant females with a wild-type (homozygous) male. Show the Punnett square and obtain the genotypic and phenotypic ratios of the first filial generation (F1). Female with white eyes Q4: Show the Punnett squares and obtain the genotypic and phenotypic ratios of the first filial generation (F1) and second filial generation (F2) of the following crosses. Note: The F2 generation can be obtained by crossing one male and one female from the F1 generation. Female with white eyes and vestigial wings and wild-type malearrow_forward
- Certain genes determine sex, fertility, and viability in Drosophila, and mutations in these genes affect the two sexes differently. Classify the descriptions below based on their occurrence in XY or XX flies. Some descriptions may be used in both categories. The expressed form of Dsx activates maleness genes and represses femaleness genes. XY XX Null mutations in the dsx gene result in an intersex phenotype. Loss-of-function mutations in the tra gene have no effect on phenotype. Sxl is expressed in early embryogenesis from the establishment promoter. Flies that produce Fru-M in brain cells from a transgene perform a mating dance and specifically court females. Loss-of-function mutations in the fru gene result in flies who court both males and females. Sxl regulates splicing of its own RNA to produce a functional protein. The expressed form of Dsx activates femaleness genes and represses maleness genes. Loss-of-function mutations in the Sxl gene have no effect on phenotype. Resetarrow_forwardDuchenne Muscular Dystrophy (DMD) is a disease that manifests in muscle weakness. It exhibits X-linked recessive inheritance pattern. The dystrophin gene is large and can have many different mutations along the DNA. From the following mutations between the gene sequence (DNA template strand) of a healthy male and an affected brother determine if they would affect the production of mRNA or the sequence of the protein. Base your analysis on the position of the mutation in the transcription unit, and the impact of the change on the codons. Mutation 1: Position -6 Healthy individual A Affected brother C Group of answer choices A. Normal mRNA, normal protein B. No mRNA produced (promoter affected) C. Abnormal mRNA, affected protein D. Normal mRNA, affected protein Base your analysis on the position of the mutation in the transcription unit, and the impact of the change on the codons.arrow_forwardHuman females who are heterozygous for an X-linked recessive allele sometimes exhibit mild expression of the trait. However, such mild expression of X-linked traits in females who are heterozygous for Xlinked alleles is not seen in Drosophila. What might cause this difference in the expression of X-linked genes between human females and female Drosophila? (Hint: In Drosophila, dosage compensation is accomplished by doubling the activity of genes on the X chromosome of males.)arrow_forward
- Here are schematic diagrams of mutant Drosophila larvae. The left side of each pair shows a wild-type larva, with gray boxes showing the sections that are missing in the mutant larva. Which type of gene is defective in each larva: a gap gene, a pair-rule gene, or a segment-polarity gene?arrow_forwardCompare and contrast the experimental advantages and disadvantages of Drosophila, C. elegans, mammals, and Arabidopsis.arrow_forwardResearchers have exploited Minute mutations in orderto study the phenotypes associated with recessive lethal mutations (l−) that decrease the rate of cell divisionand thus make only very tiny homozygous mutant clones that are difficult to analyze. Many differentstrains of Drosophila carry dominant loss-of-functionMinute (M) mutations in a variety of genes encodingribosomal protein subunits. The M genes are haploinsufficient; flies with only one wild-type M+ gene copyhave a slower pace of cell division, and thus prolongeddevelopment and subtle morphological abnormalities.To circumvent the tiny clone problem, researchersgenerate GFP-marked homozygous l−/ l− clones thatare also M+/ M+, in flies that are l−/ l+ and M−/ M+.The loss of the Minute mutation only in cells withinthe clone gives the l−/ l− cells a growth advantageover their neighbors, enabling the mutant clone togrow large enough to study. Diagram chromosomesthat could be used to generate such clonesarrow_forward
- Read the following passage carefully about some aspects of genetics involving a certain species of Drosophila and then answer the following questions in parts The gene for the production of eye colour in this species of fruit fly can be expressed as either normal red-eyes or as brown-eyes. The allele for the normal red eyes is dominant to that of brown, and is transmitted in normal Mendelian fashion. A gene involved with body colour in this species of fruit fly is located on the non-homologous portion of the X chromosome, and has two alleles, grey and yellow, where the grey allele is dominant to yellow. The two genes are NOT linked. a) Produce a key to clearly show the nature of the alleles associated with the eye colour in this species of Drosophila, and in each case justify your choice of letters and / or style of presentation to best depict the genetics involved. b) State the type of genetics involved in terms of body colour, justifying your answer with the evidence from…arrow_forwardIn Drosophila sex determination (Check all that apply.) A) XY individuals transcribe the Sxl gene early but not late. B XX individuals carry the Sxl gene, XY individuals do not. XX individuals transcribe the Sxl gene, XY individuals do not. XX individuals express the Sxl protein, XY individuals do not. E) The Sxl transcript (Pre-MRNA) is spliced differently in XX compared to XY individuals.arrow_forwardPax6 is a gene that is involved in mammalian eye development. Mutations in this gene result in a lack of iris in humans, and mice that are homozygous for the mutation lack eyes completely. Mutations in the eyeless gene in the fruitfly Drosophila result in reduced eyes. Expressing Pax6 from mammals in other tissues of Drosophila during its embryonic development can result in an ectopic eye (e.g. an eye expressed in a different tissue type). An example of an ectopic eye on the antenna of Drosophila is shown below. Part A: The eye of humans, mouse, and fly are an example of the following (check all that apply) A. Structural analog B. Structural homolog C. Developmental homolog D. Genetic homolog Part B: Darwin's hypothesis of natural selection has two components: Species are not static but change through time Species are related, and not independent. In what ways does the human, mouse, and fly eye support or contradict one or both of the two components of…arrow_forward
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