Concepts of Genetics Plus Mastering Genetics with Pearson eText -- Access Card Package (12th Edition) (What's New in Genetics)
12th Edition
ISBN: 9780134811390
Author: William S. Klug, Michael R. Cummings, Charlotte A. Spencer, Michael A. Palladino, Darrell Killian
Publisher: PEARSON
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Chapter 18, Problem 1PDQ
HOW DO WE KNOW? In this chapter, we focused on how eukaryotic gene expression is regulated posttranscriptionally. At the same time, we found many opportunities to consider the methods and reasoning by which much of this information was acquired. From the explanations given in the chapter:
- (a) How do we know that alternative splicing enables one gene to encode different isoforms with different functions?
- (b) How do we know that misregulation of mRNA stability and decay is a contributing factor in some cancers?
- (c) How do we know that double-stranded RNA molecules can control gene expression?
- (d) How do we know that microRNAs negatively regulate target mRNAs?
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Regarding eukaryotic genes, it is correct to state that: *
A) Distal enhancer-like elements decrease the intensity of gene transcription activation B)Mutations in intronic regions of a gene can alter the levels of its corresponding protein
C)They are regulated only by promoter regions, being activated or repressed by the presence of transcription factors
D)The junctions of exons and introns are recognized by splicing factors, which ensure the production of the same mRNA regardless of cell type.
E) Activator and repressor proteins bind to the coding region of genes, regulating the intensity of their transcription
Regarding eukaryotic genes, it is correct to state that:
a) Distal enhancer-like elements decrease the intensity of gene transcription activation
b) Mutations in intronic regions of a gene can alter the levels of its corresponding protein
c) They are regulated only by promoter regions, being activated or repressed by the presence of transcription factors
d) The junctions of exons and introns are recognized by splicing factors, which guarantee the production of the same mRNA regardless of cell type.
e) Activator and repressor proteins bind to the coding region of genes, regulating the intensity of their transcription
A full-length eukaryotic gene is inserted into a bacterial chromosome. The gene contains a complete promoter sequence and a functional polyadenylation sequence, and it has wild-type nucleotides throughout the transcribed region. However, the gene fails to produce a functional protein.
a)List at least 3 possible reasons why this eukaryotic gene is not expressed in bacteria.
b)What changes would you recommend to permit expression of this eukaryotic gene in a bacterial cell?
Chapter 18 Solutions
Concepts of Genetics Plus Mastering Genetics with Pearson eText -- Access Card Package (12th Edition) (What's New in Genetics)
Ch. 18 - Some mutations in the tra gene of Drosophila cause...Ch. 18 - Some scientists use the analogy that the...Ch. 18 - Consider the example that actin mRNA localization...Ch. 18 - What is alternative splicing, where does it occur,...Ch. 18 - What role might the expanded tri- and...Ch. 18 - DM1 is characterized by a phenomenon known as...Ch. 18 - HOW DO WE KNOW? In this chapter, we focused on how...Ch. 18 - CONCEPT QUESTION Review the Chapter Concepts list...Ch. 18 - List three types of alternative splicing patterns...Ch. 18 - Consider the CT/CGRP example of alternative...
Ch. 18 - Explain how the use of alternative promoters and...Ch. 18 - Explain how a tissue-specific RNA-binding protein...Ch. 18 - The regulation of mRNA decay relies heavily upon...Ch. 18 - Nonsense-mediated decay is an mRNA surveillance...Ch. 18 - AU-rich elements (AREs) are cis-elements in mRNAs...Ch. 18 - What are processing bodies (P bodies), and what...Ch. 18 - In 1998, future Nobel laureates Andrew Fire and...Ch. 18 - Present an overview of RNA interference (RNAi)....Ch. 18 - RNAi may be directed by small interfering RNAs...Ch. 18 - Prob. 14PDQCh. 18 - In principle, RNAi may be used to fight viral...Ch. 18 - Prob. 16PDQCh. 18 - Prob. 17PDQCh. 18 - Prob. 18PDQCh. 18 - Prob. 19PDQCh. 18 - How is it possible that a given mRNA in a cell is...Ch. 18 - Prob. 21PDQCh. 18 - Prob. 22PDQCh. 18 - Prob. 23PDQCh. 18 - Prob. 24ESPCh. 18 - Prob. 25ESPCh. 18 - Mutations in the low-density lipoprotein receptor...Ch. 18 - RNA helicases are a class of proteins that bind...Ch. 18 - While miRNA response elements (MREs) may be...Ch. 18 - RNAi is currently being tested as a therapeutic...Ch. 18 - The localization and translational control of...Ch. 18 - Explain how the expression of a single gene can be...
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- We know that eukaryote gene regulation can occur at any point in the process of gene expression. (a) What is the final step where gene expression control may occur in the process of protein expression ? (b) Is this a cellular energy efficient or inefficient mechanism of gene regulation? Explain.arrow_forwardWhich of the following are possible reasons that a cell would regulate its expression of a gene? (Select all that apply.) (a) an increased need for a particular enzyme (b) a decreased need for a particular enzyme (c) increasing temperature in the external environment (d) changing needs as an organism ages (e) deatharrow_forwardThree similar proteins are expressed in human tissues: HHT1 is expressed in the liver, HHT2 is expressed in the pancreas, and HHT3 is expressed in the heart. You are given the task of investigating how these 3 similar proteins are produced. After investigation, you conclude that: all answers are correct it is possible that HHT1 and 3 are produced via alternative splicing, and HHT2 is encoded by a different gene it is possible that all 3 proteins are encoded by the same gene and produced via alternative splicing it is possible that each of these proteins are encoded by different genes (3 different genes)arrow_forward
- a. How do bacteria increase the efficiency of gene expression? Is this possible in eukaryotes? b. A mutation in the promoter of Gene K disrupts an enzyme binding site and results in the loss of Gene K expression. Is this change in gene expression likely happening at the transcriptional or the translational level? Explain. c. Propose three different mutations to prevent initiation, elongation, and termination of bacterial transcription, respectively. Explain how/why each mutation would prevent its respective step. (Hint: mutations can be in genes that encode proteins or regulatory DNA sequences)arrow_forward(a) Did deletion of any of the possible control elements cause areduction in reporter gene expression? If so, which one(s), and howcan you tell? (b) If loss of a control element causes a reduction ingene expression, what must be the normal role of that controlelement? Provide a biological explanation for how the loss of sucha control element could lead to a reduction in gene expression.arrow_forwardThe expression of genes in bacterial cells can be regulated on different levels in the production of the resulting protein.(a) Name the different levels of gene regulation in prokaryotes. (b) Discuss the different mechanisms used in each of these levels.arrow_forward
- You are teaching a class on the regulation of eukaryotic gene expression. In order to demonstrate this complex process, you decide to draw for the class a typical eukaryotic gene/transcription unit with its major regions, such as the promoter regions, where the RNA polymerase II and transcription factors would bind From the list given - choose all components that you think are part of a typical eukaryotic gene From the list given - choose all the regulatory sequences that you think would control the expression of this eukaryotic gene From the list given - choose all of the regulatory proteins that would bind the eukaryotic gene to control its expressionarrow_forwardHelp me pleasearrow_forwardYou are studying a rare form of brain cancer where the newly-discovered genes BR and AIN are known to play a role in the development of this cancer. You perform a RNA-seq analysis on a patient with this form of cancer and compare the resulting expression histogram to a healthy patient. You conclude that AIN is heavily upregulated in the cancer patient and that the cancer patient's mRNA for BR retains one of that gene's introns in the RNA-seq results. Based on this information, BR is likely a(n) _________ and AIN is likely a(n) _________ . a. oncogene; tumor-suppressor gene b. tumor-suppressor gene; tumor-suppressor gene c. oncogene; oncogene d. tumor-suppressor gene; viral gene e. tumor-suppressor gene; oncogenearrow_forward
- Answer these questions concerning promoters. a) What role do promoters play in transcription? b) What is the common structure of bacterial promoter with respect to consensus sequences? c) Eukaryotic promoters are more variable than bacterial promoters. Why? d) What is the meaning of the term alternative promoter? How does the use of alternative promoters affect transcription?arrow_forwardThe lac genotypes are as shown below: P+OcZ-Y+A+// P¯O+Z+Y+A+ (i) The lac operon consists of three structural genes, lacZ, lacY and lacA. Which structural genes are involved in lactose metabolism? Explain. (ii) Draw and explain how lactose repress the gene expression in lac IS/I- heterozygote. (iii) What is the function of the promoter in the bacterial operon?arrow_forwardExplain how the following mutations would affect transcription of the yeast GAL1 gene in the presence of galactose. (a) A deletion within the GAL4 gene that removes the region encoding amino acids 1 to 100. (b) A deletion of the entire GAL3 gene. (c) A mutation within the GAL80 gene that blocks the ability of Gal80 protein to interact with Gal3p. (d) A deletion of one of the four UASG elements upstream from the GAL1 gene. (e) A point mutation in the GAL1 core promoter that alters the sequence of the TATA box.arrow_forward
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