Chapter 2 101D Flashcards
(98 cards)
How many chromosomes do humans inherit from each parent?
A. 23 total
B. 23 pairs
C. 46 pairs
D. 23 individual chromosomes
D. 23 individual chromosomes
Explanation: Each parent contributes 23 individual chromosomes, resulting in 46 total chromosomes in the child
How does a baby inherit its unique combination of DNA?
A. Through random mutations during development.
B. By inheriting one chromosome of each pair from each parent.
C. By receiving identical chromosomes from both parents.
D. By inheriting all 46 chromosomes from one parent.
B. By inheriting one chromosome of each pair from each parent.
Explanation: Each parent provides one chromosome from their 23 pairs, combining to form the child’s unique genetic makeup
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What is the genotype?
A. An organism’s observable physical characteristics.
B. The combination of genes an organism inherits from its parents.
C. The RNA surrounding the genes.
D. The environmental influences on an organis
B. The combination of genes an organism inherits from its parents.
Explanation: The genotype is the genetic makeup or combination of alleles an organism inherits.
What is the phenotype?
A. The genes an organism carries.
B. The physical expression of an organism’s genetic makeup.
C. The chromosomes passed down from parents.
D. The epigenetic modifications of DNA.
B. The physical expression of an organism’s genetic makeup.
Explanation: Phenotype refers to observable traits, such as eye color or height, which result from the genotype and environmental factors.
What role does epigenetics play in gene expression?
A. It determines the exact DNA sequence of an organism.
B. It influences how RNA surrounding genes modifies phenotypes.
C. It eliminates the need for environmental factors in development.
D. It only affects inherited genetic disorders.
B. It influences how RNA surrounding genes modifies phenotypes.
Explanation: Epigenetics studies how environmental factors and “non-junk” RNA can affect the expression of genes without altering the DNA sequence.
Which of the following is true about inherited genetic disorders?
A. All genetic disorders are dominant.
B. Most are recessive and require genes from both parents to be expressed.
C. They cannot be passed down from parents.
D. They only occur due to environmental factors
B. Most are recessive and require genes from both parents to be expressed.
Explanation: Recessive genetic disorders require two copies of the faulty gene (one from each parent) for the disorder to manifest
How can environmental factors influence genes through epigenetics?
A. They directly change the DNA sequence.
B. They affect how genes are expressed by modifying RNA or histones.
C. They replace inherited genes with new ones.
D. They only influence genes in the current generatio
B. They affect how genes are expressed by modifying RNA or histones.
Explanation: Environmental factors, including diet or stress, can alter gene expression through epigenetic mechanisms without changing the DNA sequence itself.
Which of the following best describes a chromosome abnormality?
A. A mutation in a single gene.
B. An error in the number or structure of chromosomes.
C. A temporary environmental effect on gene expression.
D. A normal variation in genetic inheritance
B. An error in the number or structure of chromosomes.
Explanation: Chromosome abnormalities involve missing, extra, or structurally altered chromosomes, such as in Down syndrome (trisomy 21).
Why are most recessive genetic disorders less likely to occur?
A. They require one faulty gene from only one parent.
B. They are influenced by environmental factors rather than inheritance.
C. They require two copies of the faulty gene, one from each parent.
D. They are eliminated by epigenetic changes during developmen
C. They require two copies of the faulty gene, one from each parent.
Explanation: Recessive disorders manifest only if an individual inherits the faulty gene from both parents, reducing their overall likelihood
. How do chromosomes contribute to the uniqueness of an individual?
A. Each chromosome is identical in all humans.
B. Chromosomes mix and match during reproduction, creating unique combinations.
C. Chromosomes only carry genes from the mother.
D. Each individual inherits all chromosomes unchanged from their parents
B. Chromosomes mix and match during reproduction, creating unique combinations.
Explanation: Genetic recombination during meiosis ensures each individual has a unique genetic makeup.
What is the relationship between genotype and phenotype?
A. Genotype is the physical expression of traits, while phenotype is the genetic code.
B. Genotype determines phenotype but does not always guarantee specific traits.
C. Phenotype influences genotype directly.
D. Phenotype is determined solely by environmental factors, not genetics
B. Genotype determines phenotype but does not always guarantee specific traits.
Explanation: Genotype refers to the genetic makeup, while phenotype is how these genes are expressed, influenced by both genotype and the environment.
What is epigenetics?
A. The study of genetic disorders.
B. The process by which environmental factors alter gene expression without changing DNA sequences.
C. The mixing of parental genes during reproduction.
D. The study of physical traits passed through generations
B. The process by which environmental factors alter gene expression without changing DNA sequences.
Explanation: Epigenetics focuses on how factors like diet and stress can modify gene expression through mechanisms such as RNA or histone modifications.
How can epigenetics influence future generations?
A. Only DNA mutations are passed down.
B. Environmental changes in one generation can permanently alter gene expression in subsequent generations.
C. Epigenetic changes do not affect inheritance.
D. Epigenetic effects are reset with each new generation
B. Environmental changes in one generation can permanently alter gene expression in subsequent generations.
Explanation: Epigenetic changes, such as methylation, can be inherited and influence gene expression across generations.
What distinguishes phenotype from genotype?
A. Phenotype is inherited, while genotype is not.
B. Phenotype is observable traits, while genotype is the genetic code.
C. Genotype is influenced by the environment, while phenotype is not.
D. Genotype determines all traits without environmental input.
B. Phenotype is observable traits, while genotype is the genetic code.
Explanation: Phenotype is how genetic traits are expressed outwardly, influenced by genotype and environmental factors.
What type of genetic disorder is most commonly inherited?
A. Dominant disorders requiring only one faulty gene.
B. Recessive disorders requiring faulty genes from both parents.
C. Chromosomal disorders caused by external factors.
D. Disorders caused solely by environmental influences.
B. Recessive disorders requiring faulty ( mutated) genes from both parents.
Explanation: Most inherited genetic disorders are recessive and require both parents to pass on the faulty gene.
cystic fibrosis and sickle cell anemia.
Dominant ones don’t survive
What is an example of a chromosomal abnormality?
A. A mutation in a single gene.
B. Down syndrome caused by an extra chromosome 21.
C. A disorder caused by a dominant allele.
D. An inherited recessive genetic disorder.
B. Down syndrome caused by an extra chromosome 21.
Explanation: Chromosomal abnormalities involve structural or numerical changes in chromosomes, such as trisomy 21 in Down syndrome.
What role does RNA play in epigenetics?
A. RNA determines the sequence of DNA.
B. RNA directly modifies DNA sequences.
C. RNA influences how genes are expressed, impacting phenotypes.
D. RNA eliminates the influence of environmental factors
C. RNA influences how genes are expressed, impacting phenotypes.
Explanation: RNA and other epigenetic factors helps the body use genetic instructions from DNA to make proteins
Why are recessive genetic disorders less common than dominant ones?
A. Recessive genes cannot be inherited.
B. Recessive disorders require two faulty alleles to be expressed.
C. Recessive disorders are more affected by the environment.
D. Recessive disorders only affect males.
B. Recessive disorders require two faulty alleles to be expressed.
Explanation: Both parents must contribute a faulty gene for a recessive disorder to manifest, making them less common.
What is an example of how epigenetics interacts with the environment?
A. A child inherits a genetic mutation.
B. Exposure to stress alters gene expression related to stress management.
C. A parent passes on their exact DNA sequence without modifications.
D. Genetic traits are unaffected by diet or environmental factors.
B. Exposure to stress alters gene expression related to stress management.
Explanation: Environmental factors, like stress, can lead to epigenetic changes, influencing how genes are expressed.
Which statement about phenotype is correct?
A. Phenotype is determined only by the genotype.
B. Phenotype results solely from environmental factors.
C. Phenotype is influenced by both genetic and environmental factors.
D. Phenotype and genotype are identical concepts.
C. Phenotype is influenced by both genetic and environmental factors.
Explanation: Phenotype reflects the expression of genes and their interaction with environmental influences.
What happens when an individual inherits one dominant allele for a genetic trait?
A. The trait will be expressed in the phenotype.
B. The trait will only be expressed if a recessive allele is also inherited.
C. The trait will not appear unless both alleles are dominant.
D. The trait is determined by environmental factors alon
A. The trait will be expressed in the phenotype.
Explanation: Dominant alleles only need one copy to be expressed in the phenotype
What causes chromosomal abnormalities?
A. Changes in environmental factors alone.
B. Errors during the formation of sex cells or early embryonic development.
C. External damage to the DNA sequence.
D. Mutations in a single recessive gene.
: B. Errors during the formation of sex cells or early embryonic development.
Explanation: Chromosomal abnormalities often occur due to issues during meiosis or early cell division, leading to missing or extra chromosomes.
What is the significance of studying epigenetics in prenatal development?
A. To identify how DNA changes during development.
B. To understand how environmental factors influence gene expression in utero.
C. To predict exact genetic outcomes for an individual.
D. To eliminate inherited genetic disorders.
B. To understand how environmental factors influence gene expression in utero.
Explanation: Epigenetics helps explain how prenatal environmental conditions, like nutrition or stress, can affect gene expression and influence development.
What is a mutation in the context of genetics?
A. A temporary change in DNA caused by environmental factors.
B. A permanent alteration in genes or chromosomes that affects an individual.
C. A reversible genetic change that does not influence traits.
D. A minor variation in phenotype unrelated to DNA change
B. A permanent alteration in genes or chromosomes that affects an individual.
Explanation: Mutations are permanent changes in DNA or chromosomes that can influence traits or health.