Biology
12th Edition
ISBN: 9781260494570
Author: Raven, Peter
Publisher: MCGRAW-HILL HIGHER EDUCATION
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Textbook Question
Chapter 13, Problem 6U
How does maternal inheritance of mitochondrial genes differ from sex linkage?
a. Mitochondrial genes do not contribute to the
b. Because mitochondria are inherited from the mother, only females are affected.
c. Since mitochondria are inherited from the mother, females and males are equally affected.
d. Mitochondrial genes must be dominant. Sex-linked traits are typically recessive.
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Students have asked these similar questions
In organisms with X and Y chromosomes, many more genes can be found on the X chromosome than on the Y chromosome. In mammals, how might this deviate from traits being expressed, according to Mendel?
A.
Females might exhibit a mix of traits rather than all dominant or all recessive traits.
B.
Only females will have the traits resulting from the X-linked genes.
C.
Females will overproduce some proteins in relation to males’ production levels.
D.
This will not result in individuals deviating from Mendel’s principles.
In humans, failure to synthesize melanin leads to a condition called albinism. This is a recessive condition. If parents heterozygous (Nn) for normal skin pigmentation give rise to 4 offspring, what is the probability that:
a. they will have an albino child?
b. the second child is albino?
c. they will have all boys with normal pigmentation?
d. they will have ONE albino child, no matter the order.
In genetic maternal effect, the phenotype of the individual is determined by which of these statements?
A. The sex of the parent who transmits the gene
B. The nuclear genotype of the maternal parent
C. The sex of the individual with only one sex able to express the phenotype
D. Cytoplasmic genes usually located in the mitochondria
E. A combination of environmental factors and the genotype of the individual
Chapter 13 Solutions
Biology
Ch. 13.1 - Describe sex-linked inheritance in fruit flies.Ch. 13.1 - Prob. 2LOCh. 13.2 - Prob. 1LOCh. 13.2 - Explain the genetic consequences of dosage...Ch. 13.3 - Prob. 1LOCh. 13.4 - Prob. 1LOCh. 13.4 - Explain the relationship between frequency of...Ch. 13.4 - Prob. 3LOCh. 13.5 - Prob. 1LOCh. 13.5 - Prob. 2LO
Ch. 13.5 - Prob. 3LOCh. 13 - Inquiry question Mendel did not examine plant...Ch. 13 - What would Mendel have observed in a dihybrid...Ch. 13 - Prob. 2DACh. 13 - Why is the white-eye phenotype always observed in...Ch. 13 - In an organisms genome, autosomes are a. the...Ch. 13 - What cellular process is responsible for genetic...Ch. 13 - The map distance between two genes is determined...Ch. 13 - How many map units separate two alleles if the...Ch. 13 - How does maternal inheritance of mitochondrial...Ch. 13 - Which of the following genotypes due to...Ch. 13 - Prob. 1ACh. 13 - As real genetic distance increases, the distance...Ch. 13 - Down syndrome is the result of trisomy for...Ch. 13 - Genes that are on the same chromosome can show...Ch. 13 - The A and B genes are 10 cM apart on a chromosome....Ch. 13 - Prob. 6ACh. 13 - Color blindness is caused by a sex-linked,...Ch. 13 - Assume that the genes for seed color and seed...Ch. 13 - A low frequency of calico cats are male (about...
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- a. Explain the difference between maternal inheritanceof organelle DNAs and maternal effect inheritance.b. How do the inheritance patterns of phenotypescaused by mitochondrial genes differ from thosecaused by maternal effect genes?arrow_forwarda. Each person inherits one copy of the Huntington's Disease gene from each parent. Explain why the negative control sample (from an unaffected individual) only produced one band. b. Explain why the positive control sample (from an individual affected by Huntington’s disease) produced twobands.arrow_forwardPhenylketonuria (PKU) is a disease that results from a recessive gene. Suppose that two unaffected parents produce a child with PKU. a. What is the probability that a sperm from the father will contain the PKU allele? b. What is the probability that an egg from the mother will contain the PKU allele? c. What is the probability that their next child will have PKU? d. What is the probability that their next child will be heterozygous for the PKU gene?arrow_forward
- Phenylketonuria (PKU) is a disease that results from a recessive gene.Suppose that two unaffected parents produce a child with PKU. a. What is the probability that a sperm from the father will contain the PKU allele?b. What is the probability that an egg from the mother will contain the PKU allele?c. What is the probability that their next child will have PKU?d. What is the probability that their next child will be heterozygous for the PKU gene?arrow_forwardPlease explain mitochondrial DNA inheritance . How is it inherited ? Why is it predisposed to mutations ? How can one identical twin be normal but the other identical twin have a mitochondrial disease ?arrow_forwardWhen the phenotype of the offspring is determined by endoparasites in the father it is… a. epistasis b. due to genes located in the mitochondria. c. a maternal effect d. non-nuclear inheritance e. a non-additive genetic effectarrow_forward
- Color blindness in men is controlled by a recessive gene located on the X chromosome. Can a brother and sister with color blindness have another normal brother? A. Yes, if the mother is a carrier. B.Yes, if the mother is homozygous. C.Yes, if the father is heterogametic. D.Yes, if the father is a carrier.arrow_forwardIn mammals, males have X and Y sex chromosomes, while females have two Xs. While the Y sex chromosome has very few genes associated with it, the X sex chromosome has many that are important to maintain life. How do mammals account for this in terms of equaling out gene expression levels? A. Mammals do not need to account for this, but birds do. B. Females produce more proteins from X-linked genes than males do. C. The single X of the males works twice as hard to keep up with the female’s two Xs. D. The females have one X inactivated to permit the males to keep pace with them.arrow_forwardIn the snail Limnaea peregra, coiling of the shell is determined by the genes D for right-handed coiled shells, and d for left-handed coiled shells. The gene for the right-handed shell is dominant. However, the direction of coiling in any single individual is determined by the genotype of the maternal parent producing the egg, regardless of the progeny's genotype. Which describes this type of inheritance? A. infectious heredity B. maternal effect C. dominant X-linked D. organelle heredityarrow_forward
- Fruit fly segmentation begins during oogenesis and is affected by which maternal genes? (Note answers can be multiple or if not given from the option, provided the proper answer) a. Gap genes b. Oskar genes c. Pair-rule genes d. Gurken genesarrow_forwardWhich statement about the pattern of inheritance for a recessive X-linked allele is true? A. Unaffected parents can produce daughters who are affected. B. Unaffected parents can have sons who are affected and daughters who are carriers. C. Unaffected fathers can be carriers. D. Affected parents do not produce affected children. E. Every affected person has an affected parent.arrow_forwardin a summary use your understanding of molecular biology to explain that recessive alleles are expressed through transcription and translation, and that they may have functional gene products. Describe how the interaction of the products produced by each allele results in what we see as dominant or recessive traits.arrow_forward
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