Genetics MCAT Biology Diagnostic Exam 2B Flashcards
A researcher has a population of flies with either white (r) or red eyes (R). A white-eyed female is mated with a red-eyed male. All resultant female flies have red eyes and all the males have white eyes. If two flies from the F1 generation are mated, which of the following would NOT be observed?
A. Exactly half the female F2 flies are pure-breeding.
B. 75% of the F2 offspring will have red eyes, and 25% will have white eyes.
C. Some of the F2 males could have white-eyed daughters, and others cannot.
D. 50% of the F2 female flies are carriers.
B. If the eye-color trait is being inherited differently in males and females, it must be a sex-linked trait. Since both females and males are affected, it must be an X-linked trait. The white-eyed female in the original cross must be XrXr and the male is XRY. All female F1 flies are XRXr (red-eyed) and males are XrY (white-eyed). If these two mate (XRXr × XrY), the F1 offspring will be 25% XRXr (red-eyed females that carry the white-eye allele; choice D would be observed and can be eliminated), 25% XrXr (pure-breeding white-eyed females; choice A would be observed and can be eliminated), 25% XRY (red-eyed males that cannot produce white-eyed daughters) and 25% XrY (white-eyed males that can produce white-eyed daughters; choice C would be observed and can be eliminated). Note that half the F2 generation has red eyes and half has white eyes (choice B would NOT be observed and is the correct answer choice).
Concepts tested
Genetics: Mendelian Genetics/Probability
The nuclear envelope makes the interior of the nucleus continuous with what other membrane-bound organelle?
A. Lysosome
B. Golgi complex
C. Endoplasmic reticulum
D. Mitochondria
C. The nuclear envelope subdivides the nucleus and is composed of two lipid bilayers. While the outer side faces the cytoplasm, the inner side faces the interior of the nucleus and is continuous with the endoplasmic reticulum (choice C is correct). The lysosome, Golgi complex, and mitochondria are fully distinct from the nucleus (choices A, B, and D are wrong).
Concepts tested
Cell Biology: Cellular Organelles and Structures
typical viral genome:
A. is made of several linear DNA molecules, wrapped around histone proteins.
B. is a circular DNA molecule with one origin of replication.
C. can be made of DNA or RNA, and can be double- or single-stranded.
D. typically contains more thymine and adenine than guanine and cytosine.
C. Choice A describes a typical eukaryotic genome and choice B describes a typical prokaryotic genome (both choices are wrong). Choice C is a true statement, and the correct answer choice. Since viral genomes are so variable, there is no reason to believe choice D is true.
Concepts tested
Microbiology: Viruses and Subviral Particles
Which of the following accurately describes the structure of a bacterium?
A. A circular single-stranded DNA genome is located in the cytoplasm.
B. 80S ribosomes can generate multiple peptide chains using one polycistronic mRNA template.
C. Transcription and translation can occur simultaneously, as both occur in the cytoplasm and no post-transcriptional modification is required.
D. Aquaporin proteins in the plasma membrane protect against the osmotic pressure gradient generated by the cell wall.
C. Choice C is a true statement and the correct answer choice. The bacterial genome is a circular, double-stranded DNA molecule (choice A is wrong). While many peptide chains can be made from a polycistronic mRNA, this is done by a 70S ribosome in bacteria. The eukaryotic ribosome is 80S (choice B is wrong). The peptidoglycan cell wall prevents lysis due to osmotic pressure, but doesn’t generate osmotic pressure gradients (choice D is wrong). Many eukaryotic cells have aquaporin water channels in the plasma membrane to facilitate osmosis.
Concepts tested
Microbiology: Bacteria
A researcher is tracking two traits in a family. One trait is consistently passed from affected mothers to all offspring. The other trait passes from affected fathers to 0% of sons but 100% of daughters. The respective two traits are mostly likely:
A. autosomal recessive and Y-linked.
B. autosomal dominant and X-linked recessive.
C. mitochondrial and X-linked recessive.
D. mitochondrial and X-linked dominant.
D. All humans receive their mitochondrial genome from their mother’s egg, so mitochondrial traits are passed from mothers to all offspring (choices A and B can be eliminated). If the trait does not pass from fathers to sons, it is likely X-linked. X-linked recessive traits can be masked by a mother’s dominant X chromosome in female offspring. If the trait is showing up in all of their daughters, it is most likely an X-linked dominant trait (choice C can be eliminated and choice D is correct). In this case, when a father passes this X chromosome to a daughter, the allele for this trait is expressed phenotypically.
Concepts tested
Genetics: Mendelian Genetics/Probability
All of the following could help prevent cancer EXCEPT:
overexpression of the Ras protooncogene.
activation of initiator caspases upon cellular oxidative damage.
p53 activation in response to accelerated progression through the cell cycle.
A. I only
B. I and II only
C. II and III only
D. I and III only
A. Item I would not help prevent cancer: overexpression of protooncogenes would push the cell inappropriately into cell division (choice C can be eliminated). Item II could help prevent cancer: initiator caspases start the apoptotic pathway when cells are dividing inappropriately (choice B can be eliminated). Item III could help prevent cancer: p53 is a tumor suppressor gene that when active can halt progression through the cell cycle or can trigger apoptosis (choice D can be eliminated and choice A is correct).
Concepts tested
Cell Biology: Cancer
The ability to taste phenylthiocarbamide depends on genetics. Humans with the dominant allele taste phenylthiocarbamide as very bitter and make up about 70% of the population. The allele that leads to phenylthiocarbamide being tasteless:
A. is recessive and occurs at a frequency of 0.55.
B. is dominant and occurs at a frequency of 0.70.
C. is recessive and occurs at a frequency of 0.84.
D. is epistatic and occurs at a frequency of 0.30.
A. Since the ability to taste phenylthiocarbamide is dominant we will assign it an allele frequency of p. From the equation for genotype frequency (p2 + 2pq + q2 = 1), individuals who have this trait will make up p2 + 2pq of the population, which the question states is 70%, or 0.70. The recessive allele leads to tasteless phenylthiocarbamide (choices B and D can be eliminated) and occurs at a frequency of q, so individuals who cannot taste phenylthiocarbamide occur at a frequency of q2. Since the question stem tells you p2 + 2pq = 0.70, q2 = 1 – 0.70 = 0.30, and q would be the square root of this number, or approximately 0.55 (choice A is correct and choice C is wrong).
Concepts tested
Genetics: Hardy-Weinberg
Staphylococcus aureus is a facultative anaerobic Gram-positive bacterium. This organism has a:
A. thick peptidoglycan cell wall and can use oxygen when it is present.
B. thin peptidoglycan cell wall and dies in the presence of oxygen.
C. thick peptidoglycan cell wall and will never perform aerobic cellular respiration or oxidative phosphorylation.
D. thin peptidoglycan cell wall and can perform fermentation and utilize an electron transport chain.
A. Gram-positive bacteria have a thick peptidoglycan cell wall (choices B and D are wrong). Facultative anaerobes can survive without oxygen, but will use it if it is present (choice A is correct and choice C is wrong). Obligate anaerobes die in the presence of oxygen, and tolerant anaerobes will survive in oxygen but will not use it.
Concepts tested
Microbiology: Bacteria
The sodium-potassium ATPase moves three sodium ions out of the cell and two potassium ions into the cell at the cost of one ATP molecule. In the absence of ion leak channels, the ATPase would make the cytoplasm:
A. hypertonic to the extracellular environment.
B. isotonic to the extracellular environment.
C. hypotonic to the extracellular environment.
D. hyperosmotic to the extracellular environment.
C. Since the ATPase moves more ions out of the cell than in, and since in the absence of leak channels these ions have no way to cross the cell membrane, the cytoplasm would ultimately become hypotonic, meaning it has less particles when compared to the extracellular environment (choice C is correct). Hypertonic (or hyperosmotic) would mean that the cytoplasm had more particles than the extracellular environment (choices A and D are wrong), and isotonic would mean they had the same number of particles (choice B is wrong).
Concepts tested
Cell Biology: Osmosis/Diffusion/Colligative Properties
Animal viruses differ from prokaryotic viruses in that they:
A. can enter a host cell without specificity for a receptor macromolecule.
B. usually enter the host via membrane-fusion or endocytosis.
C. secrete lysozyme to facilitate entry into the host cell.
D. always bind a receptor on the surface of the host cell, then inject the genomic material into the cytoplasm.
B. All viruses are very particular about the specifics of their host cell. This specificity comes from the requirement of a virus to bind a host cell receptor, to allow viral entry (choice A is wrong). Receptor binding allows a prokaryotic virus to inject its genome into the host cell (choice D applies to bacterial viruses and can be eliminated). In contrast, animal viruses usually enter the host cell via membrane-fusion (where the envelope of the virus fuses with the host plasma membrane) or endocytosis (choice B is correct). In both cases, receptor binding is still required, and the viral genome is uncoated after entry into the host. Lysozyme is an example of a late gene for prokaryotic viruses, and facilitates viral exit at the end of a lytic cycle. It is not used for viral entry, and in any case, does not apply to animal viruses (choice C is wrong).
Autophagy in lysosomes is responsible for:
A. destroying excess secretory products.
B. degrading nonfunctional cellular components.
C. detoxifying cellular waste products.
D. phosphorylating secretory proteins.
B. Autophagy refers to the process by which the cell degrades worn out cellular components (choice B is correct). Excess secretory products are also destroyed in the lysosomes, but by the process of crinophagy (choice A is wrong). Peroxisomes detoxify waste products (choice C is wrong), and post-translational modification of proteins (such as phosphorylation) is the job of the endoplasmic reticulum and the Golgi complex (choice D is wrong).
Concepts tested
Cell Biology: Cellular Organelles and Structures
Which of the following is an example of secondary active transport?
A. Na+-glucose cotransporter
B. Ligand-gated ion channel
C. K+ leak channel
D. Na+/K+ ATPase
A. In secondary active transport, energy is used to establish an electrochemical gradient, and that gradient then provides the driving force to move other molecules against their concentration gradient. The use of energy is one step removed from the molecule movement, hence the designation of “secondary.” The Na+-glucose cotransporter moves glucose against its gradient as Na+ moves down its gradient. The Na+ gradient is established by the Na+/K+ ATPase, a primary active transporter (uses ATP directly, choice D is wrong). Ligand-gated ion channels are opened by the binding of a ligand to a receptor; movement of the ion then occurs passively down its gradient (choice B is wrong). K+ leak channels are an example of facilitated diffusion; K+ moves across the membrane, down its gradient, through the channel (choice C is wrong).
Concepts tested
Cell Biology: The Cell Membrane
Map distances can be calculated by:
A. sequencing a chromosome.
B. calculating recombination frequencies.
C. determining the length of a chromosome.
D. elucidating the ploidy of a cell.
B. Recombination frequency gives a measure of map distances between genes on the same chromosome (choice B is correct). While sequencing a chromosome can determine how many base pairs apart the genes are, it will not give map unit information directly (choice A is wrong). Determining the length of a chromosome or the ploidy of the cell will give no additional information on map distance (choices C and D are not relevant and can be eliminated).
Concepts tested
Genetics: Linked Genes
Warkany syndrome is a perinatal lethal disease caused by nondisjunction. Which of the following is another name for Warkany syndrome?
A. 1p36 deletion syndrome
B. Chromosome 8 trisomy syndrome
C. Alpha-galactosidase A deficiency
D. Congenital hypothyroidism
B. Nondisjunction is a meiotic anaphase separation defect. It leads to too many or too few chromosomes (also known as aneuploidy) in gametes and resultant zygotes. Trisomy is when a cell contains three copies of a given chromosome, instead of two, and is an example outcome of nondisjunction (choice B is correct). There is no reason to believe that aneuploidy would result in the loss of a portion of a chromosome (choice A is incorrect), an enzymatic deficiency (choice C is incorrect) or thyroid hormone deficiency (choice D is incorrect).
Concepts tested
Cell Biology: Mitosis/Meiosis
Hemophilia is an X-linked recessive trait in humans. If a carrier female mates with the hemophiliac male, what is the probability they will have a daughter who does NOT have hemophilia?
A. 0.75
B. 0.5
C. 0.25
D. 0.125
C. If we assign D = normal and d = hemophiliac, the cross in the question stem is XDXd × XdY. If the offspring is female, she will receive the Xd chromosome from her father, and the probability of this is 0.5. To have a normal phenotype, she must receive the XD chromosome from her mother, and the probability of this is 0.5. Overall, the probability of having a normal daughter is (0.5)(0.5) = 0.25, (choice C is correct).
Concepts tested
Genetics: Mendelian Genetics/Probability