Learn Extracted exam questions AP Biology 2023 Free Response
2023 Free Response
Source PDF on the left, extracted YAML on the right. Compare numbering, marks, options and text.
In eukaryotic microorganisms, the PHO signaling pathway regulates the expression of certain genes. These genes, Pho target genes, encode proteins involved in regulating phosphate homeostasis. When the level of extracellular inorganic phosphate (Pi) is high, a transcriptional activator Pho4 is phosphorylated by a complex of two proteins, Pho80-Pho85. As a result, the Pho target genes are not expressed. When the level of extracellular Pi is low, the activity of the Pho80-Pho85 complex is inhibited by another protein, Pho81, enabling Pho4 to induce the expression of these target genes. A simplified model of this pathway is shown in Figure 1.
[Figure 1, two panels side by side, showing a simplified model of the regulation of expression of Pho target genes. Panel A - "High-Phosphate Environment": An oval labeled "Pho81" sits above and unconnected to the rest of the diagram. A rectangle divided into two boxes labeled "Pho80" and "Pho85" sits above a horizontal arrow. The arrow points from a triangle labeled "Pho4" to another triangle labeled "Pho4" with a circled "P" attached (phosphorylated Pho4). Below the arrow, a curved arrow goes from "ATP" to "ADP", indicating ATP is consumed to phosphorylate Pho4. Below that, a DNA double helix is drawn (labeled "DNA") leading into an X-shaped region labeled "Pho Target Genes" (genes not being transcribed). Panel B - "Low-Phosphate Environment": An oval labeled "Pho81" sits above a "T"-shaped inhibition symbol (flat bar) pointing down to the "Pho80 | Pho85" rectangle, indicating Pho81 inhibits the Pho80-Pho85 complex. Below that, a triangle labeled "Pho4" (unphosphorylated) has a downward arrow to a bent arrow ("promoter" symbol) pointing into the DNA/"Pho Target Genes" region, indicating Pho4 activates transcription. From the Pho Target Genes region, a diagonal arrow labeled "Pho Target Gene mRNAs" points up and to the right to another diagonal arrow labeled "Proteins Encoded by Pho Target Genes".]
Figure 1. A simplified model of the regulation of expression of Pho target genes in (A) a high-phosphate (high-Pi) environment and (B) a low-phosphate (low-Pi) environment
To study the role of the different proteins in the PHO pathway, researchers used a wild-type strain of yeast to create a strain with a mutant form of Pho81 (pho81mt) and a strain with a mutant form of Pho4 (pho4mt). In each of these mutant strains, researchers measured the activity of a particular enzyme, APase, which removes phosphates from its substrates and is encoded by PHO1, a Pho target gene (Table 1). They then determined the level of PHO1 mRNA relative to that of the wild-type yeast strain, which was set to 10.
TABLE 1. APase ACTIVITY AND RELATIVE AMOUNTS OF PHO1 mRNA IN WILD-TYPE AND MUTANT STRAINS OF YEAST IN HIGH- AND LOW-PHOSPHATE ENVIRONMENTS
| Yeast Strain | Mutation | APase Activity in High-Pi Environment (mU/mL/OD$_{600}$) $\pm 2\text{SE}_{\bar{x}}$ | APase Activity in Low-Pi Environment (mU/mL/OD$_{600}$) $\pm 2\text{SE}_{\bar{x}}$ | Relative Amounts of PHO1 mRNA in High-Pi Environment $\pm 2\text{SE}_{\bar{x}}$ | Relative Amounts of PHO1 mRNA in Low-Pi Environment $\pm 2\text{SE}_{\bar{x}}$ |
|---|---|---|---|---|---|
| Wild-type | None | $0.5 \pm 0.1$ | $17.3 \pm 0.9$ | $0.1 \pm 0.0$ | $10 \pm 2.0$ |
| pho81mt | Nonfunctional Pho81 | $0.4 \pm 0.1$ | $0.6 \pm 0.1$ | $0.7 \pm 0.2$ | $0.9 \pm 0.8$ |
| pho4mt | Nonfunctional Pho4 | $0.5 \pm 0.0$ | $0.8 \pm 0.2$ | $0.6 \pm 0.4$ | $0.3 \pm 0.1$ |
Describe the effect that the addition of a charged phosphate group can have on a protein that would cause the protein to become inactive. Explain how a signal can be amplified during signal transduction in a pathway such as the PHO signaling pathway.
Based on Table 1, identify a dependent variable in the researchers' experiment. Justify the researchers' using the wild-type strain for the creation of the mutant strains. Justify the researchers' using mutant strains in which only a single component of the pathway was mutated in each strain.
Based on the data in Table 1, identify the yeast strain and growth conditions that lead to the highest relative amount of PHO1 mRNA. Calculate the percent change in APase activity in wild-type yeast cells in a high-Pi environment compared with that of wild-type cells in a low-Pi environment.
In a follow-up experiment, researchers created a strain of yeast with a mutation that resulted in a nonfunctional Pho85 protein. Based on Figure 1, predict the effects of this mutation on PHO1 expression in the mutant strain in a high-Pi environment. Provide reasoning to justify your prediction.
Elevated levels of $\text{CO}_2$ increase the rate of photosynthesis and growth in plants. Scientists studying the mechanisms involved in these increases examined a variety of species and found that when plants are exposed to elevated levels of $\text{CO}_2$, there is an increase in the number of chloroplasts per cell. To investigate whether the elevated levels of $\text{CO}_2$ have a similar effect on the number of mitochondria in plant cells, the scientists then selected six of these species to quantify the number of mitochondria per cell when the plants were exposed to both normal and elevated levels of $\text{CO}_2$ (Table 1).
TABLE 1. AVERAGE NUMBER OF MITOCHONDRIA IN PLANTS EXPOSED TO NORMAL AND ELEVATED LEVELS OF $\text{CO}_2$
| Species | Mitochondria at Normal $\text{CO}_2$ (per 100 $\mu\text{m}^2$ of cell area) $\pm 2\text{SE}_{\bar{x}}$ | Mitochondria at Elevated $\text{CO}_2$ (per 100 $\mu\text{m}^2$ of cell area) $\pm 2\text{SE}_{\bar{x}}$ |
|---|---|---|
| 1 | $1.0 \pm 0.10$ | $1.6 \pm 0.10$ |
| 2 | $0.4 \pm 0.05$ | $0.9 \pm 0.08$ |
| 3 | $0.5 \pm 0.07$ | $0.9 \pm 0.10$ |
| 4 | $0.3 \pm 0.03$ | $0.6 \pm 0.06$ |
| 5 | $0.7 \pm 0.06$ | $1.5 \pm 0.22$ |
| 6 | $1.3 \pm 0.15$ | $2.4 \pm 0.22$ |
Describe the role of the inner mitochondrial membrane in cellular respiration.
Using the template in the space provided for your response, construct an appropriately labeled graph that represents the data in Table 1. Determine which species show(s) a difference in the number of mitochondria between normal and elevated levels of $\text{CO}_2$.
Based on the data in Table 1, describe the relationship between the level of $\text{CO}_2$ and the average number of mitochondria per unit area of a cell.
The leaves of a particular plant species are typically green, but scientists notice a plant in which the leaves have white stripes. They determine that the stripes result from a mutation in mitochondrial DNA that interferes with the development of chloroplasts. The scientists crossed plants using pollen from the plant with white-striped leaves and ovules from a plant with green leaves. Predict the phenotype(s) of the leaves of offspring produced from this cross. Provide reasoning to justify your prediction. Explain why plants with the same genotype are able to differ in the structure and/or number of certain organelles in response to changes in atmospheric levels of $\text{CO}_2$.
Sand lances of the genus Ammodytes are small fish that function as keystone organisms in several coastal ecosystems. These sand lances are prey fish that support organisms at higher trophic levels. Scientists performed experiments to examine how sand lance populations are likely to be affected by the rising temperatures and $\text{CO}_2$ levels associated with climate change.
Sand lance embryos typically develop and mature into adult fish at low temperatures (approximately $5^{\circ}\text{C}$) and stable, low $\text{CO}_2$ levels (approximately 400 $\mu\text{atm}$). Over the course of two years, the scientists measured the survival rate of sand lance embryos allowed to develop and mature in a laboratory at three different temperatures, $5^{\circ}\text{C}$, $7^{\circ}\text{C}$, and $10^{\circ}\text{C}$, with the level of $\text{CO}_2$ maintained at 400 $\mu\text{atm}$, 1,000 $\mu\text{atm}$, and 2,100 $\mu\text{atm}$ for each temperature.
Describe the effect of increased biodiversity on the resilience of an ecosystem in a changing environment.
Justify the scientists' selecting $5^{\circ}\text{C}$ as the lowest temperature and 400 $\mu\text{atm}$ as the lowest $\text{CO}_2$ level in their study of sand lance embryo survival.
State a null hypothesis for the experiment.
The scientists claim that a reduction in the population size of the Ammodytes sand lances will affect the stability of the entire coastal ecosystem. Provide reasoning to support the scientists' claim.
Noncyclic electron flow and cyclic electron flow are two major pathways of the light-dependent reactions of photosynthesis. In noncyclic electron flow, electrons pass through photosystem II, then components of a chloroplast electron transport chain, and then photosystem I before finally reducing $\text{NADP}^+$ to NADPH. In cyclic electron flow, electrons cycle through photosystem I and some components of the electron transport chain (Figure 1).
[Figure 1, an energy diagram of electron flow during the light-dependent reactions, with a vertical axis labeled "Energy of Electrons" (arrow pointing up, no numeric scale). At the bottom, "H$_2$O" has an arrow labeled "2e$^-$" pointing up into an oval labeled "Photosystem II", with a side arrow from the same point going to "1/2 O$_2$". From "Photosystem II", a solid vertical arrow rises to an oval labeled "Primary e$^-$ Acceptor". A dashed arrow descends from "Primary e$^-$ Acceptor" down to a rectangle labeled "Cytochrome Complex"; from the Cytochrome Complex a bolt symbol points down labeled "Energy for ATP Synthesis". A dashed arrow continues from the Cytochrome Complex down-and-right to an oval labeled "Photosystem I". From "Photosystem I", a solid vertical arrow rises to another oval labeled "Primary e$^-$ Acceptor" (top of diagram). A heavy curved arrow labeled "Cyclic" loops from this top "Primary e$^-$ Acceptor" back down to the "Cytochrome Complex", representing cyclic electron flow. From the top "Primary e$^-$ Acceptor", a dashed arrow also goes down-and-right to a diamond labeled "Ferredoxin", from which a curved arrow leads to "NADP$^+$" and then to "NADPH".]
Figure 1. The pathways of noncyclic and cyclic (heavy arrows) electron flow. The cytochrome complex is a component of the electron transport chain between the two photosystems.
Describe the role of chlorophyll in the photosystems of plant cells.
Based on Figure 1, explain why an increase in the ratio of NADPH to $\text{NADP}^+$ will cause an increase in the flow of electrons through the cyclic pathway.
Using rice plants, scientists examined the effect of a mutation that results in the loss of the protein CRR6. CRR6 is a part of the photosystem I complex, and its absence reduces the activity of photosystem I. Predict the effect of the mutation on the rate of biomass (dry weight) accumulation.
Justify your prediction in part (c).
Ruminants are hoofed animals, including cattle and sheep, that have a unique four-chambered stomach specialized to digest tough, fiber-filled grasses. Researchers studying ruminants are investigating the morphological and molecular characteristics of different ruminant families in order to determine the evolutionary relationships among the families. Cladograms of several ruminant families were constructed based on morphological data (Figure 1A) and molecular data (Figure 1B). Table 1 shows a sample of the morphological characteristics present in each family used to construct the cladogram in Figure 1A.
[Figure 1, two cladograms labeled A and B, each showing six ruminant family names (Tragulidae, Giraffidae, Bovidae, Moschidae, Antilocapridae, Cervidae) at branch tips connected by a tree of internal nodes/branch points, with a shared basal branch line running to the lower left. Panel A ("Cladogram of six ruminant families based on morphological data"): from left to right along the tips, the branch order is Tragulidae, Giraffidae, Bovidae, Moschidae, Antilocapridae, Cervidae. Giraffidae branches off first (closest to the base) from a node shared with (Bovidae, Moschidae, Antilocapridae, Cervidae); Bovidae and Moschidae share a nearer common node together, forming a pair; that pair's node then joins with a node leading to Antilocapridae and Cervidae, which themselves diverge from a shared node closer to the tips. Panel B ("Cladogram of six ruminant families based on molecular data"): from left to right along the tips, the branch order is Tragulidae, Giraffidae, Antilocapridae, Bovidae, Moschidae, Cervidae. Giraffidae and Antilocapridae share a nearer common node together, forming a pair; Bovidae and Moschidae share a separate nearer common node together, forming another pair; these two pairs then join at a shared internal node closer to the base; Cervidae diverges separately, joining nearer the base of the tree.]
Figure 1. Cladogram of six ruminant families based on (A) morphological data and (B) molecular data
TABLE 1. MORPHOLOGICAL CHARACTERISTICS FOUND IN EACH RUMINANT FAMILY
| Characteristic Number | Morphological Characteristic | Tragulidae | Giraffidae | Bovidae | Moschidae | Antilocapridae | Cervidae |
|---|---|---|---|---|---|---|---|
| 1 | Extra tooth material | X | X | ||||
| 2 | Third stomach | X | X | X | X | X | |
| 3 | Double opening for tear ducts | X | X |
Describe how a scientist would use a comparison of the DNA sequences of different organisms to suggest the most likely evolutionary relationship among the organisms.
Based on Figure 1, explain why Bovidae is likely to be more closely related to Moschidae than it is to Giraffidae.
Using the template in the space provided for your response, represent the point(s) at which characteristic 1, listed in Table 1, evolved by marking "X" on the line(s) of the cladogram in the correct location(s).
Based on Figure 1A, explain why a characteristic found only in the Cervidae and Bovidae families is more likely evidence of convergent evolution than it is of common ancestry.
Housekeeping genes encode proteins involved in universally important processes such as transcription, translation, and glycolysis. Because these genes appear to be expressed in all cells at constant levels, the expression of housekeeping genes is often used as a control when comparing how the expression of other genes varies under different conditions.
Researchers studying the effect of pesticides on declining bee populations wanted to determine whether the expression of four housekeeping genes (GAPDH, RPL32, RPS5, and TBP-AF) was in fact constant in bees across different variables. The researchers collected samples of mRNA for each of the four genes and compared how their expression varied across the developmental stage of the bee, the sex of the bee, and the cell type from which the sample was taken. The mRNA from the samples was reverse transcribed to produce DNA copies of each gene. PCR was then used to amplify the DNA, and the Cq value was determined. The Cq value is the number of PCR cycles needed to produce a specified number of DNA copies. A high Cq value for a sample indicates the gene was expressed at a low level.
To analyze whether any of the examined variables affected expression of the housekeeping genes, researchers examined the range of Cq values for each gene in response to each variable. Genes with a wide range of Cq values were determined to be affected by the variable, while genes with a narrow range of Cq values were determined to be unaffected by the variable.
[Figure 1, a box-and-whisker plot with the y-axis labeled "Cq Value" ranging from 16 to 32 (gridlines at 16, 20, 24, 28, 32) and the x-axis labeled "Variable Examined", divided by dashed vertical lines into three groups: "Developmental Stage", "Sex", and "Cell Types". Each group contains four box plots, one per gene, per the legend: open square = GAPDH, filled black square = RPL32, gray square = RPS5, hatched/crosshatched square = TBP-AF. Developmental Stage group: GAPDH box spans roughly 15.5-19.5 (median ~17.5); RPL32 box spans roughly 16.5-18.5 (median ~17.5); RPS5 box spans roughly 15.5-18 (median ~16.5); TBP-AF box spans roughly 19.5-22 (median ~20.5). Sex group: GAPDH box spans roughly 17-18.5 (median ~17.5); RPL32 box spans roughly 16.5-18.5 (median ~17.5); RPS5 box spans roughly 15.5-17 (median ~16); TBP-AF box spans roughly 19.5-21.5 (median ~20.5). Cell Types group: GAPDH box spans roughly 17.5-31.5 (median ~20.5), the widest range of all boxes shown; RPL32 box spans roughly 16.5-26 (median ~18.5); RPS5 box spans roughly 16.5-25.5 (median ~18); TBP-AF box spans roughly 21-32 (median ~23).]
Figure 1. The effect of developmental stage, sex, and cell type on the Cq value of four housekeeping genes
Based on the data in Figure 1, identify the gene that had the lowest median Cq value when bees of different developmental stages were compared.
The Cq value is inversely proportional to the amount of mRNA from that gene in the starting sample. Based on the data in Figure 1, identify the gene that has the lowest level of gene expression regardless of variable.
The scientists investigated the effect of pesticides on the expression of other genes in one cell type of a group of bees containing males and females of the same developmental stage. They hypothesized that TBP-AF would serve as the best control gene for this experiment. Use the data to evaluate their hypothesis.
Explain how expression of a gene such as GAPDH can vary from one cell type to another within the same bee.