FINAL EXAM ? Flashcards
The building blocks of DNA are
A. amino acids
B. nucleotides
C. carbohydrates
D. lipids
E. enzymes
B. nucleotides
A variation of a gene is called a(n)
A) allele
B) morph
C) genome
D) proteome
E) species
A) allele
A characteristic that an organism displays is called __________.
A) trait
B) gene
C) chromosome
D) gene expression
E) DNA
A) trait
During sexual reproduction, each parent contributes one set of chromosomes. Similar chromosomes from each parent are called __________.
A) sex chromosomes
B) sister chromatids
C) homologs
D) karyotypes
C) homologs
In animals, somatic cells are ________ and gametes are __________.
A) haploid; haploid
B) diploid; haploid
C) haploid; diploid
D) diploid; diploid
B) diploid; haploid
The end result of meiosis in animals is ______.
a. four diploid cells
b. four haploid cells
c. two haploid cells
d. two diploid cells
b. four haploid cells
A diploid cell within an organism’s body that is not a reproductive cell is _______.
A) rare
B) an allele
C) a somatic cell
D) a gamete
E) a sperm cell
C) a somatic cell
Which of the following would contain genetic material that is 100% identical?
A) homologous chromosomes
B) sister chromatids
C) X and Y chromosomes
D) All of these choices are identical.
B) sister chromatids
An individual who has two different alleles for a trait is called ____________.
A) isozygous
B) true-breeding
C) homozygous
D) haploid
E) heterozygous
E) heterozygous
A true-breeding line of green pod pea plants is crossed with a true-breeding line of yellow pod plants. All of their offspring have green pods. From this information, it can be stated that the green color is _____ to the yellow color.
A) dominant
B) recessive
C) blended
D) subservient
E) None of these choices are correct.
A) dominant
The differences in inherited traits among individuals in a population are called _______.
A. genetic variation
B. homozygous
C. heterozygous
D. natural selection
A. genetic variation
When Mendel crossed two plants that were heterozygous for a single trait, what was the phenotypic ratio of their offspring?
A) 3:1
B) Varied depending on the trait
C) 1:2:1
D) 7:4
E) 9:3:3:1
A) 3:1
When Mendel crossed two plants that were heterozygous for a single trait, what was the genotypic ratio of their offspring?
A) 1:2:1
B) 3:1
C) 9:3:3:1
D) Varied depending on the trait
E) 1:1
A) 1:2:1
In a two-factor cross using Mendelian inheritance, if both parents are heterozygous for both traits, what will be the phenotypic ratio of their offspring?
A. 1:2:1
B. 9:3:3:1
C. 1:1
D. 3:1
E. Varied depending on the trait
B. 9:3:3:1
Mendel’s work with two-factor crosses led directly to which of the following?
A) chromosomal theory of inheritance
B) theory of biological evolution
C) law of independent assortment
D) particulate theory of inheritance
E) law of segregation
C) law of independent assortment
Which situation below would violate the law of independent assortment, as understood by Mendel?
A. Combining certain alleles of different genes results in a plant that grows poorly.
B. A mutant gene can prevent pod formation altogether, thus preventing expression of the round or wrinkled pea alleles.
C. A plant breeder is able to create a true-breeding line that combines the alleles for white flowers and wrinkled peas.
D. A gene for petal color does not affect the expression of a gene for petal number.
E. A gene for leaf shape is linked to a gene for petal number nearby on the same chromosome, so their alleles usually segregate together.
A gene for leaf shape is linked to a gene for petal number nearby on the same chromosome, so their alleles usually segregate together.
Dosage compensation offsets the problem associated with differences in the number of ________ chromosomes in many species.
A. autosome
B. somatic
C. sex
D. nuclear
C. sex
How many Barr bodies would an individual with a XXY genotype possess?
A. 1
B. 2
C. 0
A. 1
In a Z-W system, which is considered to be the homogametic sex?
A) males
B) females
A) males
During sexual reproduction, gametes are made that contain ______ amount of genetic material as a somatic cell in the organism.
A) the same
B) twice the
C) half the
D) A quarter of the
C) half the
Polydactyly in humans is an example of __________.
A. incomplete dominance
B. gene dosage
C. incomplete penetrance
D. sex-limited inheritance
E. codominance
C. incomplete penetrance
A heterozygote possesses a phenotype that is intermediate between the homozygous dominant and homozygous recessive phenotypes. This is most likely an example of ________.
A. sex-influenced inheritance
B. incomplete dominance
C. lethal alleles
D. gene dosage
B. incomplete dominance
In human blood groups, the fact that an individual can have an AB blood type is an example of ___________.
A) incomplete penetrance
B) temperature-sensitive conditional allele
C) codominance
D) sex-influenced trait
E) incomplete dominance
C) codominance
In overdominance, the _______ genotype is beneficial over the _______ genotypes.
A. homozygous recessive; homozygous dominant
B. heterozygous; homozygous
C. homozygous; heterozygous
D. homozygous dominant; homozygous recessive
E. incomplete dominant; codominant
B. heterozygous; homozygous
For a certain trait, a heterozygous individual has a selective advantage over a homozygous dominant or homozygous recessive individual. This is called ________.
A.codominance
B.incomplete dominance
C.multiple allele systems
D.overdominance
E.incomplete penetrance
D.overdominance
Genes that are not required for survival, but are likely to be beneficial to the organism, are called _________.
A. lethal alleles
B. conditional lethal alleles
C. essential genes
D. nonessential genes
E. semilethal alleles
D. nonessential genes
The alleles that cause Huntington disease in humans are an example of ____________.
A) essential genes
B) nonessential genes
C) semilethal alleles
D) lethal alleles
E) sex linked allele
D) lethal alleles
The symbiotic relationship where one organism lives inside another species is called
A. heteroplasmy.
B. cytoplasmic inheritance.
C. endosymbiosis.
D. exosymbiosis.
E. genomic imprinting.
C. endosymbiosis.
Which of the following is primarily responsible for the maternal effect?
A) nurse cells
B) oocytes
C) sperm cells
D) placenta
A) nurse cells
G and g are dominant and recessive alleles, respectively, for a gene. If a mating of a gg female with a Gg male resulted in offspring that all have the recessive phenotype, this would most likely be an example of
A. a recessive lethal gene.
B. a maternal effect gene.
C. imprinting which results in silencing of the maternal alleles.
D. environmental influence on phenotype.
B. a maternal effect gene.
In maternal effect, the _____ of the mother determines the _______ of the offspring.
A) phenotype, genotype
B) genotype, phenotype
C) rRNA, tRNA
D) imprinting, genotype
B) genotype, phenotype
What controls the coiling of shells in snail offspring?
A) father’s phenotype
B) mother’s genotype
C) mother’s phenotype
D) father’s genotype
C) mother’s phenotype
In genomic imprinting, erasure of DNA methylation occurs in the
A) chloroplasts.
B) cells destined to become gametes.
C) mitochondria.
D) somatic cells of the embryo.
B) cells destined to become gametes.
What is the molecular mechanism for imprinting a gene?
A. methylation
B. nitration
C. phosphorylation
D. acetylation
A. methylation
To determine the genotype of a pea plant with purple flowers it was crossed with a pea plant with white flowers. Half of the offspring exhibited the dominant purple flower while the other half had white flowers. What was the genotype of the parental pea plant with the purple flowers?
A. can’t be determined
B. homozygous recessive
C. heterozygous
D. homozygous dominant
C. heterozygous
The failure of chromosomes to separate during anaphase is called __________.
A. nondisjunction
B. synapsis
C. epistasis
D. maternal effect
A. nondisjunction
Trisomy 8 usually leads to the early miscarriage of a fetus. However, adult individuals have been found with cells that have three copies of chromosome 8 in them. How can this be?
A. The trisomic 8 adults likely have a mosaic region with trisomy 8.
B. This individual must be triploid.
C. The trisomic cells underwent complete nondisjunction.
D. The trisomic cells underwent a meiotic nondisjunction.
A. The trisomic 8 adults likely have a mosaic region with trisomy 8.
Two genes that are located on the same chromosome are said to be _____.
A. linked
B. recombinant
C. parental-like
D. nonparental-like
A. linked
Another name for a chromosome is a _______, since it contains genes that are often inherited together.
A. linkage group
B. crossing over group
C. genetic recombinant
D. bivalent
A. linkage group
Which of the following defines gene linkage?
A. Two or more genes that are physically connected on a chromosome.
B. Genes that are transmitted to the next generation as a group.
C. The process by which genetic information is exchanged between homologous chromosomes.
D. All of these choices are correct.
E. Both two or more genes that are physically connected on a chromosome and genes that are transmitted to the next generation as a group.
E. Both two or more genes that are physically connected on a chromosome and genes that are transmitted to the next generation as a group.
In humans, there are _______ autosomal linkage groups, plus an X and Y chromosome linkage group.
A. 23
B. 46
C. 92
D. 22
D. 22
Which of the following is not one of the properties of gene linkage that Morgan obtained from his experiments?
A. Genes that are on the same chromosome are always transmitted together as a unit.
B. Crossing over exchanges pieces of chromosomes and creates new allele combinations.
C. Genes that are on the same chromosome may be inherited together.
D. The likelihood of crossing over occurring between two genes is dependent on the distance of the genes from one another.
A. Genes that are on the same chromosome are always transmitted together as a unit.
The formula p^2 + 2pq + q^2 = 1 is associated with which of the following
A. calculations of heterozygosity
B. Hardy-Weinberg equilibrium
C. calculations of recombination frequencies
D. degrees of freedom
E. None of these choice are correct
B. Hardy-Weinberg equilibrium
In the equation p2 + 2pq + q2 = 1, what does the term 2pq represent?
A) the genotypic frequency of homozygous recessive individuals
B) the genotypic frequency of homozygous dominant individuals
C) the genotypic frequency of heterozygous individuals
D) the sum of the phenotypic frequencies in the population
E) None of these choices are correct.
C) the genotypic frequency of heterozygous individuals
Natural selection occurs when
A) humans breed certain individuals with the most desirable phenotypes.
B) the genotype of an individual does not determine whether or not is has reproductive success.
C) individuals whose phenotypes are best suited for environmental conditions have lower reproductive success but live longer.
D) individuals whose phenotypes are best suited for environmental conditions have higher reproductive success and contribute more alleles to the next generation.
D) individuals whose phenotypes are best suited for environmental conditions have higher reproductive success and contribute more alleles to the next generation.
Select the definition of genetic drift.
A. Changes in genome size in a species due to random mutations
B. Changes in genotype frequencies in a population due to new mutations
C. Changes in allele frequencies in a population due to migration
D. Changes in allele frequencies in a population due to random fluctuations
D. Changes in allele frequencies in a population due to random fluctuations
The mechanism that results in a change in allele frequencies due to random processes is known as?
A. genetic drift
B. natural selection
C. migration
D. non random mating
A. genetic drift
A _______ translocation occurs when a piece of one chromosome is attached to another chromosome.
A. balanced
B. complex
C. simple
D. reciprocal
C. simple
Which of the following generally has the least effect on the phenotype of the individual who carries it?
A. Robertsonian translocation
B. unbalanced translocation
C. balanced translocation
D. All of these choices are equally detrimental to the phenotype
C. balanced translocation
A phenotypically normal person is having fertility issues. They consult a geneticist. Their karyotype shows they have 45 chromosomes. Which of the following is the most likely cause of their chromosome abnormality?
A. Inversion
B. Robertsonian translocation
C. Partial deletion
D. Balanced translocation
B. Robertsonian translocation
A translocation cross may occur in an individual which has which of the following?
A) reciprocal translocation
B) unbalanced translocation
C) simple translocations
D) All of these choices are correct.
A) reciprocal translocation
The term _______ refers to genetic differences between members of the same species.
A. chromosomal variation
B. chromosomal deletions
C. genetic variation
D. polyploidy
C. genetic variation
A loss of an internal portion of a chromosome is called a(n) __________.
A) terminal deficiency
B) interstitial deletion
C) reciprocal translocation
D) gene duplication
B) interstitial deletion
Given the following sequence of genes on a chromosome, determine what change in chromosome structure occurred. The asterisk (*) indicates the centromere.
Before: A B C D * E F G H
After: A C D * E F G H
A. interstitial deletion
B. terminal deletion
C. gene duplication
D. recombination
A. interstitial deletion
Given the following sequence of genes on a chromosome, determine what change in
chromosome structure occurred. The asterisk (*) indicates the centromere.
Before: A B C D * E F G H
After: A B G F E * D C H
A) reciprocal translocation
B) pericentric inversion
C) paracentric inversion
D) gene duplication
E) None of the answers are correct.
B) pericentric inversion
Inversion loops can occur in which of the following?
A. reciprocal translocations
B. paracentric inversions
C. pericentric inversions
D. gene duplications
E. both paracentric inversions and pericentric inversions
E. both paracentric inversions and pericentric inversions
Calculate the narrow sense heritability for a grandparent-grandchild relationship when the observed correlation coefficient is 0.2.
A. 0.8
B. 2.5
C. 0.4
D. 1.25
A. 0.8
Calculate the narrow-sense heritability of height between aunts and nieces if the observed phenotypic correlation coefficient is 0.1
A. 2.5
B. 0.25
C. 4
D. 0.4
D. 0.4