Bio 4 Flashcards
(99 cards)
Which of the following best describes Mendel’s key contribution to genetics?
A) Inheritance is a blending process of parental traits.
B) Genes are passed down from generation to generation through dominant and recessive inheritance.
C) Inheritance follows the pattern of multiple alleles without any influence from the environment.
D) Inheritance is determined solely by environmental factors.
Answer: B) Genes are passed down from generation to generation through dominant and recessive inheritance.
Explanation: Mendel’s experiments demonstrated that traits are inherited through genes, which exist in pairs and are inherited according to specific laws of dominance and recessiveness. His work refuted the idea of blending inheritance
What is the primary distinction between dominant and recessive genes?
A) Dominant genes are only expressed in the homozygous condition.
B) Recessive genes can be expressed even when paired with a dominant gene.
C) Dominant genes show their effect in both homozygous and heterozygous conditions.
D) Recessive genes are more likely to be inherited than dominant genes.
Answer: C) Dominant genes show their effect in both homozygous and heterozygous conditions.
Explanation: Dominant genes exhibit their traits whether the individual is homozygous or heterozygous for that gene, while recessive genes show their effects only in the homozygous condition.
If a man and a woman both carry one dominant gene for PTC tasting (T) and one recessive gene for low sensitivity (t), what is the probability that their child will be homozygous for the recessive gene (tt)?
A) 25%
B) 50%
C) 75%
D) 0%
Answer: A) 25%
Explanation: Each parent contributes one allele to the child. The probability of inheriting the recessive allele (t) from both parents is 25%, resulting in a child who is homozygous recessive (tt).
Which of the following is an example of a sex-limited gene?
A) Gene for red-green color vision deficiency.
B) Gene for height.
C) Gene for breast size in women.
D) Gene for eye color.
Answer: C) Gene for breast size in women.
Explanation: A sex-limited gene is present in both sexes but is active mainly in one sex. The gene for breast size in women is an example because it is activated by female sex hormones.
How do sex-linked genes typically affect males and females differently?
A) Males are more likely to be affected by X-linked recessive traits because they only have one X chromosome.
B) Females are more likely to be affected by X-linked recessive traits because they have two X chromosomes.
C) Both males and females are equally likely to express X-linked recessive traits.
D) Males cannot be affected by X-linked recessive traits.
Answer: A) Males are more likely to be affected by X-linked recessive traits because they only have one X chromosome.
Explanation: Since males have only one X chromosome, if they inherit a recessive gene on their X chromosome, they will express the associated trait. Females, with two X chromosomes, need two copies of the recessive allele to express the trait.
Which of the following best describes the genetic code that translates DNA into proteins?
A) The order of bases in RNA determines the amino acid sequence in proteins.
B) The order of bases in DNA directly determines the protein sequence.
C) Only messenger RNA (mRNA) is involved in translating DNA into proteins.
D) Proteins are synthesized directly from DNA without the need for RNA
Answer: A) The order of bases in RNA determines the amino acid sequence in proteins.
Explanation: The process of translation involves mRNA, which is transcribed from DNA. The sequence of bases in the mRNA determines the sequence of amino acids in the resulting protein.
Which of the following is a key feature of sex-linked genes on the X chromosome?
A) They are only passed down from father to daughter.
B) They always show dominant inheritance patterns.
C) Males are more likely to be affected by X-linked recessive genes due to the presence of a single X chromosome.
D) X-linked genes only affect female offspring.
Answer: C) Males are more likely to be affected by X-linked recessive genes due to the presence of a single X chromosome.
Explanation: Males, having only one X chromosome, are more vulnerable to X-linked recessive disorders because they lack a second X chromosome to potentially mask the recessive allele.
How does the environment influence gene expression according to modern genetics?
A) The environment has no impact on gene expression.
B) The environment can alter the expression of a gene but not its underlying genetic code.
C) Genes can only be expressed if the environmental conditions are exactly controlled.
D) Environmental factors determine the inheritance pattern of a gene
Answer: B) The environment can alter the expression of a gene but not its underlying genetic code.
Explanation: Environmental factors can influence how genes are expressed, but they do not alter the DNA sequence itself. This means gene expression can vary based on external conditions.
Which of the following scenarios correctly demonstrates the inheritance of a sex-linked trait?
A) A male inherits a gene for color vision deficiency from his mother and expresses the condition.
B) A female inherits a gene for color vision deficiency from one parent and expresses the condition.
C) A male inherits a dominant gene for color vision from his father and expresses normal vision.
D) A female inherits the gene for color vision deficiency from both parents and expresses normal vision.
Answer: A) A male inherits a gene for color vision deficiency from his mother and expresses the condition.
Explanation: Males inherit their X chromosome from their mother and their Y chromosome from their father. If they inherit a recessive X-linked gene for color vision deficiency, they will express the condition because they only have one X chromosome.
Which of the following statements best explains why most point mutations are not beneficial in evolutionary terms?
A. Mutations always disrupt protein synthesis entirely.
B. Evolution has already optimized gene sequences, making most mutations detrimental.
C. Mutations only occur in non-coding DNA.
D. Mutations are typically reversed by natural cellular repair mechanisms.
Answer: B
Explanation: Evolution has had extensive time to select advantageous gene variants, so most mutations disrupt finely-tuned genetic functions. However, rare beneficial mutations—such as those seen in the FOXP2 gene—can have significant evolutionary impact.
Which type of mutation is most likely to result in schizophrenia or neurological disorders, according to current research?
A. Silent point mutations
B. Frameshift mutations caused by insertion
C. Microduplications and microdeletions
D. Substitutions in mitochondrial DNA
Answer: C
Explanation: Microduplications and microdeletions—changes affecting small chromosome segments—have been linked to several brain-related conditions, including some forms of schizophrenia.
Epigenetic modifications can be passed to the next generation. Which of the following findings best supports this claim?
A. Histone modifications are always reset during fertilization.
B. Rats conditioned to fear a sound have offspring that also fear it.
C. Mice exposed to specific odors produced offspring with increased sensitivity to that odor.
D. Red blood cells show unique patterns of gene expression.
Answer: C
Explanation: The study with mice conditioned to fear an odor, where their offspring also displayed heightened sensitivity, supports the concept of transgenerational epigenetic inheritance.
How does the addition of acetyl groups to histones influence gene expression?
A. It tightens DNA winding, silencing the gene.
B. It loosens DNA from histones, enhancing gene expression.
C. It causes RNA to degrade prematurely.
D. It recruits methyl groups to promote transcription.
Answer: B
Explanation: Acetylation of histone tails relaxes the grip of histones on DNA, allowing genes to become more accessible for transcription, thus increasing their expression.
Which scenario exemplifies an epigenetic change rather than a genetic mutation?
A. A base pair substitution in the FOXP2 gene.
B. A duplication of a chromosome segment during meiosis.
C. Increased gene expression due to social isolation.
D. A deletion of a tumor suppressor gene.
Answer: C
Explanation: Epigenetics refers to changes in gene expression without altering the DNA sequence. Social isolation alters the expression of hundreds of genes, fitting the epigenetic definition.
What does “heritability” measure?
A) The influence of prenatal nutrition on behavior
B) The extent to which genes contribute to individual differences in a trait
C) The impact of environment on personality
D) The ability to pass a trait to the next generation
Answer: B
Explanation: Heritability refers to how much of the variation in a trait across individuals in a population is due to genetic differences—not about whether a trait is inherited at all.
What are “virtual twins”?
A) Twins born via IVF
B) Identical twins raised in different environments
C) Unrelated children of the same age raised together from infancy
D) Cloned siblings with shared DNA
Answer: C
Explanation: Virtual twins are genetically unrelated but grow up in the same environment—similarities point to environmental effects, while differences can highlight genetic ones.
Which trait has not shown significant heritability in studies?
A) Neuroticism
B) Childhood misbehavior
C) Religious affiliation
D) Cognitive performance
Answer: C
Explanation: While most behaviors show some heritability, religious affiliation is heavily shaped by environment, family, and culture rather than genetics.
Why can heritability estimates differ between populations?
A) Genes evolve rapidly in different regions
B) Environmental differences can mask or amplify genetic influences
C) People in one region may lie on surveys
D) Twin studies are unreliable outside the U.S.
Answer: B
Explanation: If environments vary widely, genetics may play a smaller role; if environments are more uniform, genetic effects become more visible.
What is one major limitation of genome-wide association studies (GWAS)?
A) They only study twins
B) They ignore environmental factors
C) They test thousands of genes, increasing the risk of false positives
D) They are outdated and rarely used
Answer: C
Explanation: Because GWAS tests many genes simultaneously, there’s a higher chance of finding misleading links by coincidence—especially in small or diverse samples.
What does the condition PKU illustrate about heritability?
A) Genetic conditions are always untreatable
B) A heritable trait can still be modified by environment
C) Environmental changes have no impact on genetic disorders
D) It only affects people of Asian descent
Answer: B
Explanation: PKU is a genetic disorder, but it can be managed through diet, showing that even high-heritability traits can be altered by environmental interventions.
Which dietary substance must people with PKU strictly avoid?
A) Gluten
B) Lactose
C) Phenylalanine
D) Caffeine
Answer: C
Explanation: PKU prevents proper metabolism of phenylalanine, which builds up to toxic levels and harms brain development unless it’s restricted from the diet.
According to behavioral genetics, what is true of most psychological traits?
A) They are entirely shaped by the environment
B) They are caused by a single gene
C) They are influenced by many genes, each with small effects
D) They show no genetic influence
Answer: C
Explanation: Most traits in psychology show moderate heritability, typically due to the combined effect of many genes rather than any one major gene.
Which of the following best illustrates how a gene can influence behavior indirectly?
A. A gene directly stimulates aggression through amygdala activation.
B. A gene influences a person’s height, which leads to basketball success and time spent practicing.
C. A gene changes dopamine production, altering mood.
D. A gene expresses only in neurons, changing reaction times.
Correct Answer: B
Explanation: The gene influences height, which leads to a behavior (playing basketball) due to environmental reinforcement. This is an example of indirect influence through changing the environment.
Why does the idea of Lamarckian evolution not align with modern biology?
A. It supports natural selection, which contradicts genetic inheritance.
B. It requires that acquired traits change gene sequences, which they do not.
C. It ignores the role of mutation in evolution.
D. It assumes traits are lost over time due to environmental pressures.
Correct Answer: B
Explanation: Lamarckian evolution wrongly suggests that traits acquired in one’s lifetime (e.g., muscle growth) can be passed to offspring. Modern biology shows acquired traits do not alter genes.