Genetics: Analysis and Principles
6th Edition
ISBN: 9781259616020
Author: Robert J. Brooker Professor Dr.
Publisher: McGraw-Hill Education
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Chapter 5, Problem 3EQ
Summary Introduction
To review:
One of the techniques to show that nurse cells can transfer the maternal effect genes (gene B) to the oocyte.
Introduction:
Maternal effect genes are those genes from the mother's genome whose RNA (ribonucleic acid) and protein are accumulated in the zygote even before the expression of zygotic genes. The expression of this gene is not at all affected by the zygote. Northern and western blotting techniques are used to detect the specific RNA and protein fragments that are separated via the gel electrophoresis.
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Chapter 21 describes two blotting methods (i.e., Northern blotting
and Western blotting) used to detect gene products. Northern blotting
detects RNA and Western blotting detects proteins. Suppose
that a female fruit fly is heterozygous for a maternal effect gene,
which we will call gene B. The female is Bb. The normal allele, B,
encodes a functional mRNA that is 550 nucleotides long. A recessive
allele, b, encodes a shorter mRNA that is 375 nucleotides
long. (Allele b is due to a deletion within this gene.) How could
you use one or more of these techniques to show that nurse cells
transfer gene products from gene B to developing oocytes? You
may assume that you can dissect the ovaries of fruit flies and isolate
oocytes separately from nurse cells. In your answer, describe
your expected results.
Imagine a scenario in which prenatal testing of a human female fetus indicates that the baby will have a normal XX karyotype but is heterozygous for a mutation that inactivates the Xist promoter. Allele “Xr” represents the mutated version of the Xist promoter, and “XR” represents the normal version of the Xist promoter.
How will this mutation affect the process of X inactivation?A. "X inactivation will still be random with both mutant and normal X chromosomes being randomly inactivated"
B. "The chromosome with the mutant Xist promoter will always be active"
C. "The chromosome with the mutant Xist promoter will always be inactivated"
D. "The normal X chromosome (no mutation in Xist) will always be active"
E. "The normal X chromosome (no mutation in Xist) will always be inactivated"
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
Chapter 5 Solutions
Genetics: Analysis and Principles
Ch. 5.1 - A female snail that coils to the left has...Ch. 5.1 - 2. What is the molecular explanation for maternal...Ch. 5.2 - 1. In fruit flies, dosage compensation is achieved...Ch. 5.2 - 2. According to the Lyon hypothesis,
a. one of...Ch. 5.2 - Prob. 3COMQCh. 5.3 - 1. In mice, the copy of the Igf2 gene that is...Ch. 5.3 - 2. A female mouse that is is crossed to a male...Ch. 5.3 - Prob. 3COMQCh. 5.3 - Prob. 4COMQCh. 5.4 - 1. Extranuclear inheritance occurs due to
a....
Ch. 5.4 - 2. A cross is made between a green four-o’clock...Ch. 5.4 - 3. Some human diseases are caused by mutations in...Ch. 5.4 - 4. Chloroplasts and mitochondria evolved from an...Ch. 5 - Define the term epigenetic inheritance, and...Ch. 5 - 2. Describe the inheritance pattern of maternal...Ch. 5 - A maternal effect gene exists in a dominant N...Ch. 5 - 4. A Drosophila embryo dies during early...Ch. 5 - 5. For Mendelian inheritance, the nuclear genotype...Ch. 5 - Suppose a maternal effect gene exists as a...Ch. 5 - Suppose that a gene affects the anterior...Ch. 5 - Explain why maternal effect genes exert their...Ch. 5 - As described in Chapter 22, researchers have been...Ch. 5 - 10. With regard to the numbers of sex chromosomes,...Ch. 5 - 11. What is a Barr body? How is its structure...Ch. 5 - Among different species, describe three distinct...Ch. 5 - 13. Describe when X-chromosome inactivation occurs...Ch. 5 - 14. Describe the molecular process of X-chromosome...Ch. 5 - Prob. 15CONQCh. 5 - 16. How many Barr bodies would you expect to find...Ch. 5 - 17. Certain forms of human color blindness are...Ch. 5 - A black female cat (XBXB) and an orange male cat...Ch. 5 - Prob. 19CONQCh. 5 - When does the erasure and reestablishment phase of...Ch. 5 - In what types of cells would you expect de novo...Ch. 5 - 22. On rare occasions, people are born with a...Ch. 5 - Genes that cause Prader-Willi syndrome and...Ch. 5 - Prob. 24CONQCh. 5 - What is extranuclear inheritance? Describe three...Ch. 5 - Prob. 26CONQCh. 5 - Among different species, does extranuclear...Ch. 5 - Extranuclear inheritance often correlates with...Ch. 5 - Prob. 29CONQCh. 5 - Prob. 30CONQCh. 5 - Which of the following traits or diseases is (are)...Ch. 5 - Prob. 32CONQCh. 5 - 33. Describe how a biparental pattern of...Ch. 5 - Figure 5.1 describes an example of a maternal...Ch. 5 - 2. Discuss the types of experimental observations...Ch. 5 - Prob. 3EQCh. 5 - As a hypothetical example, a trait in mice results...Ch. 5 - You have a female snail that coils to the right,...Ch. 5 - Prob. 6EQCh. 5 - 7. Figure 5.6 describes the results of...Ch. 5 - Prob. 8EQCh. 5 - In the experiment of Figure 5.6, why does a clone...Ch. 5 - Prob. 10EQCh. 5 - 11. A variegated trait in plants is analyzed using...Ch. 5 - 1. Recessive maternal effect genes are identified...Ch. 5 - Prob. 2QSDC
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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
- In the Fast Forward Box Visualizing X Chromosome Inactivation in Transgenic Mice, suppose the investigators had looked at the expression of green and red fluorescent protein in early mouse embryos, when the embryos have fewer than 500 cells. What patterns would they likely have observed?arrow_forwardDraw a basket mutant embryo. What does basket encode? Why do the mutant embryos have this phenotype?arrow_forwardTwo methods for functionally inactivating a gene without altering the gene sequence involve dominant negative alleles and RNA interference (RNAi). Describe how each method can inhibit expression of a gene.arrow_forward
- Figure 19.25 shows that the Sxl protein binds to the mRNA of the msl-2 gene, inhibiting translation of the mRNA’s proper reading frame. The MSL-2 protein is a transcription factor that binds to the X chromosome in XY males to double the level of X-linked gene transcription, thus equalizing X-linked gene expression in XY males and XX females. a. In which sex, XY males or XX females, would the Sxl protein bind to the msl-2 mRNA? b. As discussed in Problem 35, some Sxl alleles are lethal to females and others are lethal to males. Is the function of Sxl in regulating the synthesis of Msl-2 protein sufficient to explain the sex-specific lethality caused by both kinds of alleles? c. Predict the effect of loss-of-function mutations in msl-2 on male and female fertility and viability.arrow_forwardA normal appearing female infant was identified with a positive newborn screen, linked to chromosome 12. Few years ago, her older sibling had developed profound hypoglycemia, liver failure leading to coma, and subsequent irreparable brain damage, following a viral illness. The sibling was subsequently shown by clinical testing to have the same disorder that this female infant is screened positive for. a. What is the most likely diagnosis? b. What biomarkers would confirm this on the newborn screening process? Describe the mechanism that causes this metabolic defect.arrow_forwardWhen the organization of adjacent genes with highly similar sequences is in an inverted orientation, this can reduce the expression of other genes that have similar sequence and are located on other chromosomes. Explain the mechanism of how this generally occurs.arrow_forward
- Drosophila females homozygous for loss-of-functionmutations in the gene aubergine are sterile. RNA-Seqexperiments show that in the ovaries of these females,the levels of RNAs for many kinds of transposable elements are more than 10× higher than in wild-type ovaries. The aubergine gene encodes a Piwi-family protein.a. Why do you think these females are sterile?b. Piwi proteins interact with piRNAs that are transcribed from piRNA gene clusters. Given that thelevels of many kinds of TEs are elevated in mutantovaries, what kinds of DNA sequences do youthink are located in these clusters?c. Many investigators think of piRNAs as a kind ofdefensive mechanism that protects organisms fromthe effects of new transposable elements that mightbe introduced into genomes, for example fromother species. Explainarrow_forwardGiven a mutation in the promoter, coding region, and/or non-coding region of a gene, explain how these three scenarios create new alleles of the same gene.arrow_forwardWhat effect does the transposon have on the function of gene X in this figure?arrow_forward
- Briefly discuss why mutant allele 1 fails to produce functional protein. Note that this mutation has no impact on the length of the mRNA transcribed from the gene.arrow_forwardExplain how a loss-of-function allele in a gene encoding a cohesin protein could be dominant to itswild-type counterpart.arrow_forwardKnockout mice are mice in which a functional gene or a group of functional genes are rendered nonfunctional by a special technique involving homologous recombination. Predict what happen to knockout mice which have their RAG-1 and RAG-2 genes “removed".arrow_forward
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