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WorksheetsGA Bio EOC Review-SB2b
Total questions: 100
Worksheet time: 25hrs 0mins
The bacterium Agrobacterium tumefaciens infects plants, and a portion of its DNA is inserted into the plant’s chromosomes. This causes the plant to produce gall cells, which manufacture amino acids that the bacterium uses as food. This process is a natural example of
polyploidy.
genetic manipulation.
grafting.
hybridization.
Genetic engineering has produced goats whose milk contains proteins that can be used as medicines. This effect was produced by
mixing foreign genes into the milk.
injecting foreign genes into the goats’ udders.
inserting foreign genes into fertilized goat eggs.
genetically modifying the nutritional needs of the goats’ offspring.
Mutations within a DNA sequence are
natural processes that produce genetic diversity.
natural processes that always affect the phenotype.
unnatural processes that always affect the phenotype.
unnatural processes that are harmful to genetic diversity.
A substitution of thymine with adenine in one DNA codon causes a particular disorder. Which statement explains how the change in DNA leads to this disorder?
The deletion mutation prevents the production of the hemoglobin protein in the body.
The frameshift mutation prevents the production of several proteins found in the blood.
The insertion mutation causes extra hemoglobin proteins to attach to red blood cells.
The point mutation causes a different amino acid to be added to the hemoglobin protein.
A rare genetic condition causes dwarfism and immunodeficiencies. Which of the following is the most likely cause of this condition?
a parasitic infection
a mutation in DNA
a bacterial disease
an excess of ATP
Which of the following best describes the result of a mutation in an organism's DNA?
The mutation may produce a zygote.
The mutation may cause phenotypic change.
The mutation causes damage when it occurs.
The mutation creates entirely new organisms.
In phenylketonuria (PKU), an enzyme that converts one amino acid into another does not work properly. Which of the following is the most likely cause of this genetic condition?
an error in the transcription of the gene for the enzyme
a mutation in the DNA sequence that codes for the enzyme
an excess of the amino acids necessary to produce the enzyme
a structural variation in the amino acid modified by the enzyme
The box below contains a statement about mutations. In many cases throughout geologic history, if mutations in the genetic material of existing species had not occurred, new species would not have appeared. Which of the following conclusions about mutations in the DNA sequence of a gene is most consistent with the statement?
Mutations are always rapidly occurring.
Mutations are always beneficial.
Mutations are the only way new species arise.
Mutations are an important mechanism for the evolution of new species.
A hereditary muscular disease in horses causes abnormal opening and closing of the sodium ion channels in the muscle cells. Which of the following statements describes the most likely origin of this disease?
A virus evolved specifically to attack the muscle cells of horses.
Motor neurons near some of the muscle cells degenerated over time.
High levels of sodium in the blood irreversibly damaged the ion channels.
A mutation occurred in the gene coding for the sodium ion channel protein.
Huntington’s disease (HD) is a hereditary disease that destroys brain cells. In individuals with HD, the functioning of a specific protein is altered, and this leads to the disease’s effects. Which of the following is the most likely cause of the altered protein function in individuals with HD?
a mutation in the DNA sequence that codes for the protein
an increase in the amount of fat rather than protein in the diet
a decrease in the amount of glucose and amino acids in the blood
a structural abnormality in the endoplasmic reticulum of brain cells
During DNA replication, the wrong nucleotide was inserted in the DNA sequence. Which of the following terms describes this situation?
mutation
regeneration
transcription
translation
Crossing-over most commonly results in
new species
new populations
new combinations of genes
new numbers of chromosomes
What technology was made possible by the discovery of the structure of DNA?
organ transplants
antibiotic production
gene splicing
artificial fertilization
Scientists have altered crop plants to make them more resistant to insects and disease. Which of these processes makes it possible for scientists to alter plants?
natural selection
gene splicing
adaptation
chemosynthesis
Which of these is an environmental factor that causes damage to chromosomes?
acid rain
lead paint
methane gas
ultraviolet light
Which of these describes a mutation that can be inherited?
random breakage in a liver cell’s DNA
abnormal lung cells produced by toxins in smoke
a nitrogen base substitution in a gamete cell
ultraviolet radiation damage to skin cells
Which of these results when one nitrogen base replaces another in a segment of genetic material?
an enzyme substrate
a mutation
a feedback loop
an adaptation
A rare disorder is caused by changes in a gene. Parents of individuals with the disorder have only normal copies of this gene. Which of these most likely causes this disorder?
mitosis
gene splicing
mutation
natural selection
Certain plant crops are genetically engineered to grow faster and resist disease. These genetically engineered plant crops cannot reproduce because they have a “terminator” gene that keeps their seeds from sprouting. However, once the genetically engineered plant crops are planted outside, they may cross-pollinate with unaltered plant crops. The use of terminator genes is least likely to result in
increased costs for seeds
decreased varieties of food
terminator genes spreading to other crops
scientists being harmed from working with the terminator genes
In the laboratory, scientists remove the gene for insulin from human chromosomes. They insert the gene into the DNA of bacteria. This causes the bacteria to produce human insulin. The insulin is used to treat diabetes in humans. Which of these describes this process?
meiosis
fertilization
gene splicing
DNA fingerprinting
Two segments of DNA are shown in the diagram below. Normal thymine (T) is found in the old strand. It is replaced by an abnormal molecule (T*) in the new strand. The abnormal molecule (T*) binds to guanine (G) instead of binding to adenine (A). This is an example of
an adaptation
protein synthesis
a mutation
binary fission
Most bacteria do not have the ability to break down oil that is accidentally spilled into the ocean by tankers. However, scientists can insert a gene into the DNA of a bacterium to give it the ability to break down the oil. This technology is an example of
crossing-over
DNA replication
gene splicing
translation
When the segment of human DNA that codes for insulin production is inserted into bacterial DNA, the bacterium begins producing human insulin. Which of these best identifies the process by which human DNA is inserted into bacterial DNA?
gene splicing
crossing-over
mutation
cloning
Scientists can genetically alter corn so that it makes a protein that will harm a certain caterpillar that feeds on it. Which of the following is an advantage of producing this type of corn?
The corn will have a better color.
The corn will be able to resist insects.
The insects will reproduce more quickly.
The insects will become immune to the poison.
Risks of having genetic mutations are increased with excessive exposure to—
high air pressure.
high humidity.
ultraviolet rays.
oxygen.
Red blood cells contain the protein hemoglobin which aids in transportation of the respiratory gases. Most humans have a form of hemoglobin called hemoglobin A. Individuals with sickle cell anemia have a very similar form called hemoglobin S. This hemoglobin is slightly changed in shape and has a reduced ability to transport oxygen. It is the presence of hemoglobin S that results in the signs and symptoms of sickle cell anemia. Which of the following is the expected cause of the production of hemoglobin S?
Translocation of a chromosome
Deletion of part of a chromosome
Duplication of the hemoglobin A gene
A point mutation of the hemoglobin A gene
A botanist inserts a new gene sequence into a pink-flowering plant. He hopes that the genetically modified plant will now produce blue flowers. In nature, which of the following processes would result in this kind of change?
Grafting
Mutation
Photosynthesis
Transpiration
Which of the following chromosome pairs contain the above chromosomes after crossing over is complete?
A. [diagram]
B. [diagram]
C. [diagram]
D. [diagram]
The table shows a mutation in a DNA sequence. Original Sequence: GCA TAGT GCT ATA GCG ACT Mutated Sequence: GCA TTC CTA TAG CGA CT What is the result of this mutation during the translation process?
The translation process will fail to begin.
The mRNA will be translated at a faster rate than normal.
Everything after the mutation will be translated incorrectly.
Some of the proteins formed during translation will be unstable.
Which genetic abnormality can be identified through karyotyping?
point mutation
recessive allele
extra chromosome
sex-linked allele
Which would best allow a species to survive environmental changes?
similar physical features
low mutation rate
small population
genetic diversity
Which would most likely produce a mutation that is passed on to offspring?
radiation changing the DNA sequence in skin cells
a gamete with an extra chromosome forming
tobacco smoke altering the genes in lung cells
exposure to chemicals altering nerve cell function
Which will most likely cause variations to occur within a species?
competition
mutation
mutualism
predation
Instead of using chemicals to destroy some insects, scientists are now able to produce a type of corn that will repel insects. How are scientists able to produce this type of corn?
by not spraying the corn plants
by soaking corn seeds in insect spray
by changing the genetics of the corn plants
Which will most likely cause a gene to mutate?
water
radiation
soil
A mutation occurs in the genes that code for coat color in deer. Which change will most likely result from this mutation?
a change in the selection pressures acting on coat color
a change in the coat-color genes of deer predator species
an increase in coat-color diversity in the population
an increase in the number of genes for coat color in the population
This chart shows a list of messenger RNA codons. A strand of DNA with the sequence AAC AAG CCC undergoes a mutation, and the first A is changed to a C. How will this mutation affect the amino acid sequence?
One amino acid will change.
Two amino acids will change.
All of the amino acids will change.
The amino acids will remain the same.
Which of these would most likely cause a mutation?
the placement of ribosomes on the endoplasmic reticulum
the insertion of a nucleotide into DNA
the movement of transfer RNA out of the nucleus
the release of messenger RNA from DNA
One human disease is caused by a change in one codon in a gene from GAA to GUA. This disease is the result of
a mutation.
a meiosis error.
crossing-over.
polyploidy.
This segment of DNA has undergone a mutation in which three nucleotides have been deleted. A repair enzyme would replace them with
CGT.
GCA.
CTG.
GTA.
Radon is a radioactive gas that is sometimes present in homes. If radon is inhaled, its decay products are deposited in the lungs. Radioactive particles can penetrate cells and cause changes to the cells' DNA. These changes in DNA are an example of which of the following?
homeostasis
mitosis
mutation
transcription
People who inherit hemophilia type A are unable to make a protein required to clot blood. This disorder is directly related to which of the following?
A mutation in one gene
A chromosome that is duplicated
A gene that was incorrectly copied
A trait acquired from the environment
What is the mode of inheritance shown in the pedigree?
A. Autosomal dominant
B. Autosomal recessive
C. Sex-linked carried on the X chromosome
D. Sex-linked carried on the Y chromosome
The pedigree below shows the transmission of a disorder within a family. Which statement describes the offspring that would result if individual 1 has children with a woman that does not carry the allele for this disorder?
None of the daughters will inherit the allele for the disorder.
All of the sons will inherit the allele for the disorder.
All of the daughters will be affected by the disorder.
None of the sons will be affected by the disorder.
One of the dogs has progressive retinal atrophy, a condition that damages the retina. What are the genotypes of dog 1 and dog 2?
Dog 1 is aa and dog 2 is aa.
Dog 1 is aa and dog 2 is Aa.
Dog 1 is Aa and dog 2 is Aa.
Dog 1 is AA and dog 2 is Aa.
What is the genotype of individual 6?
XHXH
XHXb
XHY
XbY
How would overexposure to X-rays affect most animal cells?
It would increase cell specialization in organs.
It would change the sequence of DNA nucleotides in affected cells.
It would produce new nucleotides for DNA molecules.
It would cause an increase in red blood cell production.
A genetic mutation resulted in a change in the sequence of amino acids of a protein, but the function of the protein was not changed. Which statement best describes the genetic mutation?
It was a silent mutation that caused a change in the DNA of the organism.
It was a silent mutation that caused a change in the phenotype of the organism.
It was a nonsense mutation that caused a change in the DNA of the organism.
It was a nonsense mutation that caused a change in the phenotype of the organism.
Which stage in the diagram shows the separation of the original DNA molecule into two complementary strands?
A) Stage 1
B) Stage 2
C) Stage 3
D) None of the above
Fill in the blank: The letters __, __, __, and __ represent the four nucleotides in DNA.
A, T, C, and G
A, U, C, and G
A, T, U, and G
A, T, C, and U
After DNA replication, the result is two complete DNA molecules.
True
False
A partial DNA sequence for normal hemoglobin and a partial DNA sequence for sickle-cell anemia are shown below. G-G-A-C-T-T-C-T-T Normal hemoglobin G-G-A-C-A-T-C-T-T Sickle-cell anemia Based on the DNA sequences, sickle-cell anemia is caused by
a sex-linked trait
a dominant nucleotide
a mutation in the genetic code
an incomplete separation of chromosomes.
The chromosome numbered 1 through 22 are known as
ribosomes
lysosomes
centrosomes
autosomes
The preparation of these charts for individuals A and B is known as
microsurgery
karyotyping
blood typing
chemical screening.
Which genetic disorder in individual A is indicated by the number of chromosomes labeled 21?
phenylketonuria (PKU)
Tay-Sachs
sickle-cell anemia
Down's syndrome.
A change in the sequence of nitrogenous bases in DNA may result in
a gene mutation
sex linkage
polyploidy
nondisjunction.
A change that alters the base sequence in an organism's DNA is called a
synapsis
mutation
disjunction
replication.
Down syndrome is a genetic disorder caused by the presence of an extra chromosome number 21 in the body cells of humans. This extra chromosome most likely is a result of
mitotic cell division in the brain
development of an unfertilized egg
multiple allelic pairs of genes
nondisjunction during meiosis
Select the technique, chosen from the list below, that is best described by the statement shown. This technique involves the use of a photograph to study the homologous pairs of chromosomes of an individual in order to detect genetic disorders.
Chemical analysis of body fluids
Cloning
Genetic engineering
Karyotyping
Certain genetic disorders can be detected by preparing and studying an enlarged photograph of paired chromosomes from a cell. The preparation of this photograph is known as
genetic screening
karyotyping
genetic counseling
amniocentesis
The diagram shown represents a photographic enlargement of replicated chromosomes from a fetal cell. For which technique would this photograph be used to determine if the chromosomes of the fetus exhibit any genetic abnormalities?
cleavage
plasmolysis
chemosynthesis
karyotyping
Down syndrome in humans may result from
the presence of an extra chromosome in a zygote
the absence of a single chromosome in a zygote
a mutation of one gene in a zygote
failure of a chromosome to replicate in a zygote
X rays, formaldehyde and asbestos fibers are all similar in that they are
animal preservatives
used to treat diseases
used to diagnose diseases
mutagenic agents
The preparation of an enlarged photograph showing paired homologous chromosomes is known as
amniocentesis
blood screen
karyotyping
urine analysis
An analysis of chromosomes may show the loss of a portion of a chromosome. This type of chromosomal change is known as
nondisjunction
an addition
translocation
a deletion
The use of chemicals such as formaldehyde and asbestos has decreased because they have been
found to cause sterility in plants
replaced by more toxic chemicals
linked to uncontrolled meiotic cell division
found to increase the incidence of mutations
Select the term, chosen from the list below, that is best described by the statement shown. A photograph of paired human chromosomes is prepared.
Karyotyping
Cloning
Deletion
Translocation
Which genetic disorder is usually detected by analyzing a karyotype?
phenylketonuria
Tay-Sachs
Down syndrome
sickle-cell anemia
Select the genetic technique, chosen from the list below, that is best described by the statement shown. Enlarged photographs of homologous chromosomes are prepared for examination to detect chromosomal defects.
Screening
Karyotyping
Cloning
Genetic engineering
The diagram represents a
deletion
synapsis
karyotype
disjunction
The chromosomes are arranged to show
homologus pairs
tetrads
independent assortment
nucleotides
The individual from whom these chromosomes were taken is a
male
female
hermaphrodite
polyploid
This chromosomal arrangement indicates that the individual has
phenylketonuria
Down syndrome
sickle-cell anemia
Tay-Sachs disease
Substances that increase the chance of gene alterations are known as
mutagenic agents
genetic agents
chromosomal agents
adaptive agents
In humans, Down syndrome is often a result of the
disjunction of homologous chromosomes during meiotic cell divisions
nondisjunction of chromosome number 21 in one of the parents
combination of an egg and sperm, each carrying a recessive allele for this disorder
fusion of two 2n gametes during fertilization
Which phrase best describes a human with the chromosomes represented in the diagram shown?
a female who exhibits Down syndrome
a male who exhibits Down syndrome
a female who does not exhibit Down syndrome
a male who does not exhibit Down syndrome
The technique known as karyotyping is used to detect abnormalities in
chromosomes
ribosomes
blood and urine
amniotic fluid
The addition, removal, or substitution of nitrogenous bases in a DNA molecule may be caused by
mutagenic agents
cloning
vegetative propagation
nondisjunction
Mutations can be transmitted to the next generation only if they are present in
brain cells
sex cells
body cells
muscle cells
A karyotype is shown in the diagram. Information in this karyotype indicates that the individual is a
female with sickle-cell anemia
male with Tay-Sachs disease
female with Down syndrome
male with phenylketonuria
Genetic information is shown in the diagram. This type of diagram is used to
reveal chromosome disorders
determine the number of genes in a human genotype
detect sickle-cell anemia
correct the disorder known as PKU
The arrangement of chromosomes shown in the diagram is known as
a karyotype
a urine analysis
amniocentesis
blood typing
Examination of the diagram indicates that these are the chromosomes of a
female with Down syndrome
male with Down syndrome
female without Down syndrome
male without Down syndrome
The genetic disorder shown in the diagram most likely resulted from
crossing-over
nondisjunction
polyploidy
segregation
Which technique was used to organize the chromosomes as shown in the diagram?
screening
chromatography
karyotyping
grafting
For each phrase in the following question(s), select the genetic disorder that is most closely associated with that phrase. Changes in speech patterns and mental retardation due to the presence of an extra chromosome
Tay-Sachs
Phenylketonuria
Sickle-cell anemia
Down syndrome
A single change in the sequence of nitrogenous bases in a DNA molecule would most likely result in
crossing-over
polyploidy
nondisjunction of chromosomes
a gene mutation
The chromosomes of a person with a genetic disorder are shown in the diagram below. This genetic disorder resulted from
hybridization
nondisjunction
polyploidy
segregation
Question 40.
Question 41.
Question 42.
Question 43.
Question 44.
Question 45.
Question 46.
Question 47.
Question 48.
Question 49.
Question 50. (No question text or options provided.
Question 51.
