Genetic Analysis: An Integrated Approach (2nd Edition)
2nd Edition
ISBN: 9780321948908
Author: Mark F. Sanders, John L. Bowman
Publisher: PEARSON
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Chapter 19, Problem 10P
Most large protein complexes in mitochondria and chloroplasts are composed both of proteins encoded in the organelle genome and proteins encoded in the nuclear genome. What complexities does this introduce for gene regulation (i.e., for ensuring that the appropriate relative numbers of the proteins in a complex are produced)?
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A mutation creates a dominant negative allele of a particular gene. The gene encodes a protein that forms a trimer within the cell. If one or more of the subunits has the mutant structure, the entire trimeric protein is inactive. In a heterozygous cell, if the proteins of both alleles are present at the same levels, what percent of the trimers present in the cell will be active?
A) 100%
B) 5%
C) 50%
D) 33%
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In humans, the average length of a gene on chromosome 7 is 69,000 base pairs, but
the average MRNA length on chromosome 7 is only 2,500 base pairs. Chromosome
7 has 863 protein-coding genes, but many more than 863 proteins are made from
the genes on chromosome 7.
The observation that the length of the average gene on chromosome 7 is longer
than the average mRNA length is explained by the process of
while the observation that more proteins are produced from the genes on
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O heterogeneity; complementation
splicing of introns; alternative splicing
O chromatin remodeling; micro RNA binding
acetylation; methylation
alternative splicing; splicing of introns
The Saccharomyces cerevisiae nuclear gene ARG8encodes an enzyme that catalyzes a key step in biosynthesis of the amino acid arginine. This protein isnormally synthesized on cytoplasmic ribosomes, butthen is transported into mitochondria, where the enzyme conducts its functions. In 1996, T. D. Fox andhis colleagues constructed a strain of yeast in which agene encoding the Arg8 protein was itself moved intomitochondria, where functional protein could besynthesized on mitochondrial ribosomes.a. How could these investigators move the ARG8gene from the nucleus into the mitochondria, whilepermitting the synthesis of active enzyme? In whatways would the investigators need to alter theARG8 gene to allow it to function in the mitochondria instead of in the nucleus?b. Why might these researchers have wished to movethe ARG8 gene into mitochondria in the firstplace?
Chapter 19 Solutions
Genetic Analysis: An Integrated Approach (2nd Edition)
Ch. 19 - 17.1 Reciprocal crosses of experimental animals or...Ch. 19 - 17.2 How are some of the characteristics of the...Ch. 19 - 17.3 The human mitochondrial genome encodes...Ch. 19 - What is the evidence that transfer of DNA from the...Ch. 19 - Draw a graph depicting the relative amounts of...Ch. 19 - Prob. 6PCh. 19 - 17.7 What is the evidence that the ancient...Ch. 19 - 17.8 Outline the steps required for a gene...Ch. 19 - 17.9 Consider the phylogenetic tree presented in...Ch. 19 - Most large protein complexes in mitochondria and...
Ch. 19 - What insights have analyses of human mitochondrial...Ch. 19 - You are a genetic counselor, and several members...Ch. 19 - A mutation in Arabidopsis immutans results in the...Ch. 19 - What type or types of inheritance are consistent...Ch. 19 - You have isolated (1) a streptomycin-resistant...Ch. 19 - You have isolated two petite mutants, pet1 and...Ch. 19 - 17.15 Consider this human pedigree for a vision...Ch. 19 - A 50- year - old man has been diagnosed with MELAS...Ch. 19 - 17.17 The first person in a family to exhibit...Ch. 19 - Prob. 20PCh. 19 - Prob. 21PCh. 19 - 17.19 What is the most likely mode of inheritance...Ch. 19 - 17.20 In , the Russian Tsar Nicholaswas deposed,...Ch. 19 - 17.21 The dodo bird (Raphus cucullatus) lived on...Ch. 19 - Cytoplasmic male sterility (CMS) in plants has...Ch. 19 - 17.23 Wolves and coyotes can interbreed in...Ch. 19 - Prob. 27PCh. 19 - Prob. 28P
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- Metabolic syndrome is a genetic disorder with symptoms of hypertension, elevated blood cholesterol concentrations, and lower-than-normal blood magnesium concentrations. This syndrome is caused by a mutation in mitochondrial DNA (mtDNA) in which a thymine nucleotide is replaced by a cytosine nucleotide. Which of the following identifies the mutated mtDNA and the corresponding mRNA and tRNA produced in a person with metabolic syndrome if the normal mtDNA triplet is TCG? Select one: a. Mutated mtDNA: CCG mRNA: GGC tRNA: GGC b. Mutated mtDNA: TCG mRNA: UGC tRNA: ACG c. Mutated mtDNA: CCG mRNA: GGC tRNA: CCG d. Mutated mtDNA: TTG mRNA: AAC tRNA: UUCarrow_forwardAn old genetic observation is that a normally active gene will be silenced if it is moved by transposition or crossing over from an uncondensed (euchromatic) region to a heavily condensed (heterochromatic) region of a chromosome. Assume the euchromatic chromatin containing the active gene is surrounded by heterochromatic chromatin immediately after insertion. Please explain in terms of the control of histone modification why the normally active gene is silenced when it becomes surrounded by condensed regions. (Do not explain how histone modification causes chromatin condensation.)arrow_forwardWhen high levels of unfolded proteins are detected in the endoplasmic reticulum (ER), a eukaryotic cell responds by increasing the gene expression of chaperone proteins, which help proteins to fold correctly. BiP is a chaperone protein. You detect amounts of BiP mRNA and protein in the absence and presence of unfolded protein in the ER of a eukaryotic cell as shown in the figure below. a. Describe two specific biological processes that the cell could regulate in order to increase the amount of BiP protein. Briefly explain your answer using the information from figures A & B. A BİP MRNA expression В BiP protein expression No unfolded Unfolded No unfolded Unfolded proteins in ER proteins in ER proteins in ER proteins in ERarrow_forward
- When high levels of unfolded proteins are detected in the endoplasmic reticulum (ER), a eukaryotic cell responds by increasing the gene expression of chaperone proteins, which help proteins to fold correctly. BiP is a chaperone protein. You detect amounts of BiP mRNA and protein in the absence and presence of unfolded protein in the ER of a eukaryotic cell as shown in the figure below. a. Describe two specific biological processes that the cell could regulate in order to increase the amount of BiP protein. Briefly explain your answer using the information from figures A & B. A BİP MRNA expression BiP protein expression No unfolded Unfolded No unfolded Unfolded proteins in ER proteins in ER proteins in ER proteins in ERarrow_forwardMany aspects of gene function can be nicely explained with the one-gene-one-enzyme hypothesis, which states that a gene controls the production of an enzyme. Which of the following findings about gene expression, though, requires an expansion of this simple concept? Choose an answer below: Non-enzyme proteins are made from genes too. Some genes code for RNA molecules only. Enzymes composed of different polypeptides are coded for by more than one gene. a and c, but not b a, b, and carrow_forwardScientists are working to develop gene therapy to treat Batten disease, also known as Late Infantile Neuronal Ceroid Lipofuscinosis (LINCL). This fatal, autosomal recessive neurodegenerative disorder results from a mutation in the gene that codes for the enzyme TPP1 (Tripeptidyl peptidase 1). In the absence of this enzyme, a substance called ceroid lipofuscin accumulates in lysosomes in the brain, resulting in seizures, blindness, decline in cognitive function and motor skills, dementia, and death by the late teens or early 20’s. The TPP1 gene is 6695 bp in length. Think about the characteristics of Batten disease, and then suggest an approach to gene therapy that might be effective for this specific genetic disorder. You may assume that your research team is working in the U.S. and your research is funded by a grant from the National Institutes of Health (NIH). 1. Briefly outline a procedure that you could use to carry out the gene therapy for Batten disease.arrow_forward
- A cultured mouse cell line has a mutation in a gene encoding a ribosomal protein. The mutant protein impairs the fidelity of translation such that incorrect amino acids are incorporated at higher rates than normal during protein synthesis. It also slows the rate of mRNA translation and increases the duration of the cell cycle, i.e., the mutant cells grow and divide more slowly. Researchers noted that these cells express higher levels of chaperone proteins than normal cells. Which of the following is the most likely explanation for the elevated chaperone levels.arrow_forwardYou have created three different mutations in the histoneH1 protein (HISmut1, HISmut2, HISmut3), and each of these mutations eliminate a stretch of 5 amino acids from the primary sequence. Based on the description of where you find the mutant histoneH1 proteins when you look inside a cell in each of the cases below, describe 1) what the function is of the amino acids that were removed, and 2) what is not happening with the mutant histoneH1 protein that does happen with wild type H1: 1. HISmut2 protein is found in the cytoplasm, and never in the nucleus. 2. HISmut1 protein is found in only briefly in the cytoplasm because it is very quickly sent to the proteasome. 3. HISmut3 protein is found floating freely throughout the nucleoplasm.arrow_forwardYou are working in a lab studying Progeria. You design an expression vector containing a mutated form of the lamin gene that codes for a lamin protein that can no longer be phosphorylated. What do you predict would happen if you express this mutant form of lamin in a cell line? Lamin proteins would not be transported into the nucleus and would remain in the cytosol. Nuclear lamins will be unable to produce dimers, as the coiled-coil formation will be disrupted. Disassembly of the nuclear lamins will occur prematurely. Nuclear lamins will no longer disassemble properly during prometaphase. O Nuclear lamins will no longer assemble properly during telophase.arrow_forward
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Mitochondrial mutations; Author: Useful Genetics;https://www.youtube.com/watch?v=GvgXe-3RJeU;License: CC-BY