IBO 2020 - Theory Exam 1
IBO 2020 - Theory Exam 1
IBO 2020 - Theory Exam 1
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All IBO examination questions are published under the following Creative Commons license:
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CC BY-NC-SA (Attribution-NonCommercial-ShareAlike) -
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1
General instructions for theoretical examinations
Exam 1
• Date: August 12th 2020
• Total time of Exam 1 is 3 hours. Follow the instruction by Jury members of your country.
• Exam 1 consists of 50 questions.
• Each correct answer scores 1 marks, each incorrect or missing answer score 0 marks.
3
Biochemistry
Q1
The citric acid cycle is central to metabolism, for the supply energy and various key compounds. In citric acid
cycle, the enzyme aconitase catalyzes the reversible conversion between citrate and isocitrate. In this reaction,
OH group at C3 and H group at C4 of citrate are removed as water, thereafter a water molecule is added back
in a reverse manner to generate isocitrate (Figure 1). However, OH group is never added at C2.
aconitase
citrate isocitrate
Figure 1
4
Biochemistry
Q2
The figure 1 illustrated below shows oxygen consumption (respiration) in aqueous suspension of intact animal
mitochondria with additions of ADP or chemical compounds (dinitrophenol (DNP) or N,N'-
dicyclohexylcarbodiimide (DCCD)). The suspension already contains respiratory substrates, oxygen, and
inorganic phosphate.
O2 concentration
Time Time
Figure 1. Oxygen consumption of mitochondria in suspension. Identical aliquots of ADP were added in both
experiments.
5
Biochemistry
Q3
When carbon isotopes (13C and 12C) are analyzed, plants can be categorized into two groups (Figure 1), based
on the isotope fractionation (d13C, equation 1). This is because of the slight differences in molecular mass
between 13CO2 and 12CO2, although there are no known chemical differences between them. In photosynthesis,
two types of carboxylase enzymes fix carbon from CO2 in the two groups, provided that CO2 is converted to
H2CO3 by an enzyme carbonic anhydrase.
Reaction 1: C3H5O6P + H2CO3 → C4H4O5 + H3PO4 (C4 plants)
Reaction 2: C5H12O11P2 + CO2 + H2O → 2 C3H7O7P (C3 plants)
sample
(equation 1)
standard
Sample: a plant material Standard: the reference represents the typical carbon on the Earth
group 2 group 1
Frequency
Figure 1 Distribution of the carbon isotope fractionation (d13C value) of various plants.
6
Cell Biology
Q.4
Centrifugation is one of the most important biochemical techniques in the separation and purification of
biomolecules and organelles. The sedimentation speed (v) of specimens during centrifugal operation is
proportional to the applied acceleration rate (gc), as shown in equation (1).
𝑣 = 𝑆 × 𝑔! . (1)
S in the equation is called the sedimentation coefficient and is determined by the ratio between the
centrifugal force applied to the object in the solvent (numerator) versus a parameter reflecting the magnitude
of viscous resistance against sedimentation (denominator), as shown in equation (2).
7
Cell Biology
Q5
ATP is an important energy source for maintaining normal membrane potential in nerve cells. Figure 1 shows
the result of an experiment demonstrating Na+ efflux from an isolated squid giant nerve axon after injecting a
buffer solution (artificial cytoplasm) that contains radioactive 24Na+.
Efflux rate of 24Na+ (relative value)
Time [min]
Figure 1 Investigation of the efflux rate of radioisotope 24Na from a squid giant axon to the external solution
(seawater). At 0 min, a buffer solution containing 24Na+ was injected into the giant axon. For 100-190 min, the
external seawater was replaced with a solution (seawater) containing 0.2 mM DNP (dinitrophenol), an uncoupler
of oxidative phosphorylation.
8
Cell Biology
Q6
For the growth of plants, the supply of nutrient inorganic ions is essential. A certain crop was grown in two
different soils (X, Y). The concentrations of nutrients (potassium ions and chloride ions) in each type of soil
are shown in the table. The estimated cytosolic concentrations of each ion in the root epidermal cells of this
crop are also shown. When the membrane potential of the epidermal cell is −150 mV, how is each ion
transported into the cell?
Ion movement is determined by electrical and concentration gradients. The membrane potential which
would counterbalance the concentration gradient is given by the Nernst equilibrium potential equation:
60 Ci
E = − ——— log ——— (mV)
z Co
9
Cell Biology
Q7
"Secondary metabolism" in microorganisms and plants is not essential for their survival, but is a metabolic
process that plays an important role depending on species or in environmental adaptation. Many secondary
metabolites accumulated by plants, such as nicotine and caffeine, play a role in resistance to damage from
herbivorous insects.
Glucosinolate, which is accumulated in the leaves of Arabidopsis thaliana, is a repellent for herbivorous
insects (Helicoverpa armigera). The leaves of the wild type (Wild) and the leaves of the mutant (Mutant)
incapable of synthesizing glucosinolate are arranged as shown in Figure 1.
% Choice
10
Cell Biology
Q8
Isoetes howelli is an amphibious plant that can live in both aerial and submerged conditions. In a completely
submerged condition in shallow fresh water, Isoetes howelli shows characteristic metabolism; CO2 is fixed to
malate in a certain time period and released in another period to be used in photosynthetic carbon assimilation.
This metabolism is not seen in the aerial condition. There shall be a strong photosynthetic competition in
daytime between Isoetes howelli and other photosynthetic organisms.
11
Genetics
Q9
Both eukaryotes and prokaryotes have a common feature that mRNA starts translation at the AUG codon.
Eukaryotic mRNA is usually a monocistron that encodes only one protein, whereas prokaryotic mRNA is often
a polycistron that encodes multiple proteins. The following experiments were performed to investigate the
mechanism of the AUG codon that initiates translation. Post-translation decomposition need not be considered.
(1) For several operons of Escherichia coli, the promoter was replaced with a yeast promoter and introduced
into yeast cells. Although all full-length mRNAs were transcribed for all operons, some operons translated only
the first gene correctly, while other operons did not translate any genes.
(2) The promoters derived from E. coli were ligated to cDNAs obtained by removing introns from several yeast
genes and introduced into the E. coli host. Full-length mRNA was transcribed for all operon genes, but there
was little translation of any genes.
From these experiments, it is considered that the AUG codon that initiates the translation of Escherichia coli
and yeast is determined through the following mechanism.
12
Genetics
Q10
There are four types of bases used for RNA – A, C, G and U – while for DNA there are four types of bases, A,
C, G, and T. I wondered why thymine T could only be used for DNA and looked closely at the base-pairing
pattern (Figure 1).
It is reported that the mutant strain of the certain gene in Escherichia coli sometimes incorporates dUTP in
place of thymine to include bases in the DNA strand. This frequently results in a new mutation. In a chemistry
lecture, I learned that compounds such as bases could undergo chemical changes (mainly hydrolytic
02
deamination) by reacting with certain water molecules even under in vivo conditions.
H
N O H N
N N H
R
N
R
N N
Ribose
Riboseoror
N H O R Deoxyribose
Deoxyribose
Guanine H
Guanine Cytosine
Cytosine
H
N N H O CH3 O
N N H N H N
R
N N N
O R O R
Adenine
Adenine Thymine
Thymine Uracil
Uracil
Figure 1
13
Genetics
Q11
For the three heritable features, Alfa, Baker, and Charlie, pedigree analysis was performed on pedigree A,
pedigree B, and pedigree C, respectively, and the results in Figure 1 were obtained.
Family A 03
A1 A2
male female
male female
A3 A4 A5 A6 A7 A8 no
no trait
trait
trait
trait
Family B Family C
B1 B2 C1 C2
B3 B4 B5 B6 B7 B8 C3 C4 C5 C6 C7 C8
B9 B10 B11 B12 B13 B14 C9 C10 C11 C12 C13 C14
Figure 1
A subsequent detailed analysis revealed that all of the inheritance patterns of Alfa, Baker, and Charlie were
due to recessive alleles on the autosome.
14
Genetics
Q12
In Escherichia coli. the rutA - G gene cluster activates when pyrimidine is decomposed and used as a nitrogen
source. The rutA - G genes constitute a single rut operon, and a single Prut promoter regulates the expression.
The expression of the Prut promoter is regulated by a RutR repressor using uracil as an inducer.
15
Genetics
Q13
Bacteria regulate gene expression through transcription factors that sense environmental changes in order to
adapt to the ever-changing environment. One transcription factor often controls multiple genes. Since the
expression of a gene consumes energy, the selection of the gene group to be expressed is important for the
survival strategy of the bacterium. It is often observed that bacteria move vigorously in search of nutrients in
the aquatic environment, while bacteria in biofilms rarely move.
16
Genetics
Q14
With the advancement of DNA research, various technologies have been developed, and it has become important
to select appropriate research methods according to one’s research purpose. Among the research methods M1
to M7, mark (T) if it is appropriate as the method that provides the most direct information on the following
research purpose A – D, and mark (F) if it is inappropriate.
Research methods
(M1) DNA microarray
(M2) Quantitative RT-PCR
(M3) CRISPR-Cas9 method
(M4) In situ hybridization
(M5) Reproductive cloning
(M6) Construction of iPS cell
(M7) Metagenome analysis
Purpose of research
A. To examine the site where a specific gene is expressed in a mouse tissue, it is appropriate to perform (M4).
52
B. To analyze the expression level of a specific gene in maple leaves, it is appropriate to perform (M2).
53
C. To search the Bacillus subtilis genome for genes the expression of which is induced when the nitrogen source
is depleted. (M1) 54
D. To identify microbial species from microbial communities thriving in compost. (M7) 55
17
Genetics
Q15
The seed germination of plants is mainly controlled by the action of two plant hormones called gibberellin and
abscisic acid. Gibberellin promotes germination and abscisic acid suppresses germination. Through the actions
of these two plant hormones, plant seeds are regulated so that germination is induced in an appropriate
environment.
In plants, gibberellin is biosynthesized from a molecule called geranylgeranyl diphosphate. Geranylgeranyl
diphosphate is converted into ent-kaurene through the action of ent-kaurene synthase. ent-Kaurene is then
converted into gibberellin through the action of several enzymes such as GA20 oxidase. Biosynthetic
intermediates such as ent-kaurene do not have germination-inducing activity (Figure 1).
On the other hand, abscisic acid is biosynthesized from carotenoid pigments. Abscisic acid is converted into 8'-
hydroxyabscisic acid by an oxidase called CYP707A. Seeds of Arabidopsis mutants lacking the gene encoding
CYP707A were observed to have significantly delayed germination as compared to seeds of wild-type plants.
In addition, the germination of the seeds of plants in which the CYP707A gene was overexpressed were
promoted more than the wild-type seeds. In this experiment, the administered compounds play a similar function
of endogenous hormones.
(suppress germination)
ent-kaurene synthase
CYP707A
ent-kaurene
8’-hydroxyabscisic acid
GA20 oxidase
gibberellin
Figure 1
(promote germination)
18
B. When a mutant lacking the ent-kaurene synthase gene is treated with ent-kaurene, germination is
promoted. 57
C. ent-Kaurene treatment to a mutant lacking the gene encoding GA20-oxidase promotes germination.
58
D. 8'-Hydroxyabscisic acid has a stronger germination-inhibiting activity than abscisic acid. 59
19
Genetics
Q16
Part of the sequence of vector A, which is for protein expression using Escherichia coli as a host, is shown. It
was planned to express a plant-derived gene X using vector A. Vector A is a plasmid vector that expresses a
protein fused to the N-terminus His-tag, which enables efficient purification of the expressed protein. As
shown in Figure 1, translation of the protein occurs from the start codon immediately before the His tag with
six consecutive His residues. The DNA sequences of the 5’ and 3’ regions of gene X are shown in Figure 2.
We planned to clone gene X using restriction enzyme sites, EcoRI, SmaI, or SalI in vector A. When the gene
X is amplified by PCR, a fragment with a restriction enzyme site at the end can be amplified using the primer
with a restriction enzyme site. Since the restriction enzyme site is not recognized if it is located at the end of
the DNA fragment, three “Cs” were also attached in addition to the restriction enzyme site.
For example, in order to add the EcoRI site to 5’-XXXXXXXXXX----, the primer is designed as below.
5’-CCCGAATTCXXXXXXXXXX----,
14
Start codon
--- ATA CAT ATG GCA CAT CAC CAC CAC CAT CAC TCC GCG GCT CTT GAA GTC CTC TTT CAG GGA
--- TAT GTA TAC GCA GTA GTG GTG GTG GTA GTG AGG CGC CGA GAA CTT CAG GAG AAA GTC CCT
CCC GGG TAC CAG GAT CCG AAT TCT GTA CAG GCC TTG GCG CGC CCG ACG TCC GTC GAC AAG CTT---
GGG CCC ATG GTC CTA GGC TTA AGA CAT GTC CGG AAC CGC GCG GGC TGC AGG CAG CTG TTC GAA---
Start codon
ATG AAG TTA TTG AGC AAT AGT CTA ATG TTC CTT CCT CTG CTG GCT TTG GCT ---
TAC TTC AAT AAC TCG TTA TCA GAT TAC AAG GAA GGA GAG GAC CGA AAC CGA ---
--- TCT TCC TTC CTC AAG GGA ACA CTG CAC CAT CCA TCA TAT GCT TCG TCT TGA
--- AGA AGG AAG GAG TTC CCT TGT GAC GTG GTA GGT AGT ATA CGA AGC AGA ACT
Stop codon
Figure 2. DNA sequence of the gene X showing 5’ region and 3’ region: 1566 base pair
20
Choose true if the primer is a correct one to use, if not, choose false.
A. Forward primer( : the start codon)
5'-CCC GAA TTC ATG AAG TTA TTG AGC AAT A-3' 60
EcoRI site
B. Forward primer( : the start codon)
5'- CCC CCC GGG ATG AAG TTA TTG AGC AAT A-3' 61
SmaI site
C. Reverse primer( : the stop codon)
5'-CCC GTC GAC TCA AGA CGA AGC ATA TGA T-3' 62
SalI site
D. Reverse primer( : the stop codon)
5'-CCC AAG CTT GTA GGT AGT ATA CGA AGC AGA ACT -3' 63
HindⅢ site
21
Genetics
Q17
In recent years, a genome editing technology called the CRISPR-Cas9 method has been widely used for biology
research. In the CRISPR-Cas9 method, an enzyme called Cas9 is guided to the target gene by forming a complex
with a guide RNA with a sequence complementary to a part of the target gene. Then, Cas9 cleaves the double-
stranded DNA of the target gene specifically with its activity of cleaving double-stranded DNA. Cas9 recognizes
a 3-base sequence (NGG) called PAM sequence and cuts the DNA strand 3 to 4 bases upstream of PAM. The
15
cleaved DNA chain is repaired by the DNA repair system, but at that time, a few bases are frequently deleted
or inserted.
The CRISPR-Cas9 method was applied by targeting the region close to the translation start codon of the most
upstream exon of a gene encoding enzyme A of a certain animal. The base sequence of the target region was
determined for each of the four mutants obtained (Figure 1).
Original
Originalsequence
sequence TA TCT TAC ATG ATC CTA CAA GTA CCT TAC GCT CGG CAG GAA G
Mutant 1
Mutant TAT CTT ACA TGA TCC TAC AAG TAC CTT ACA GCT CGG CAG GAA G
Mutant
Mutant 2 TAT CTT ACA TGA TCC TAC AAG TAC CTT GCT CGG CAG GAA G
Mutant
Mutant 3 TA TCT TAC ATG ATC CTA CAA GTA CCT GCT CGG CAG GAA G
Mutant
Mutant 4
4 TA TCT TAC ATG ATC CTA CAA GTA CCT TAA CTC GCT CGG CAG GAA G
Figure 1
22
Genetics
Q18
The tryptophan operon (trp operon) of E. coli is transcriptionally regulated by a repressor that is activated by
the binding of tryptophan. The active form repressor binds to the operator sequence located between the
promoter and the transcription initiating point and blocks the RNA polymerase. There is another expression
control system called the attenuator linked to transcription and translation in the trp operon.
Between the operator sequence and the trpE gene, which is the first structural gene of the trp operon, there are
four sequences of about 15 bases called Region 1-4 (Figure 1). Region 1 and Region 2, and Region 3 and Region
17
4 have complementary sequences, respectively. When these regions are transcribed as mRNA, they are paired
with each other and form stem-loop structures (Figure 2). Furthermore, the sequences of Region 2 and Region
17
3 are also complementary, so a stem loop structure can be formed.
Leader Peptide
Leader Peptide
Leader sequence
Leader sequence Region
Region1 1
Region 22
Region
Region 33
Region
trpE gene
Region 1 : Region 2, Region 3: Region 4 ; complementary
Region 2 : Region 3 ;complementary
Region 44
Region
trpEDCBA
Leader sequence Region 1 encodes short peptide mRNA
containing two tryptophan residue (Trp)
Figure 1
A short peptide of 14 amino acids containing two tryptophan codons called a leader peptide is encoded in Region
1 (Figure 1).
If the trp operon mRNA is not translated at the same time as it is transcribed by RNA polymerase, Region 1 and
Region 2 of mRNA, and Region 3 and Region 4 pair with each other to form stem loop structures, respectively.
In this case, a consecutive U bases is located immediately after Region 4. Since the form in which U bases
continue immediately after the stem loop structure functions as a transcription termination signal in the
23
procaryote, the RNA polymerase is released and the transcription is terminated(Figure 2).
No ribosome
Transcription
termination signal
Figure 2
When the translation of the leader sequence occurs at the same time as the transcription of the mRNA, the
ribosome can translate the mRNA with the stem loop structure, but the transcription also ends by forming the
stem loop structure of Region 3 and Region 4.
Trp rich
Leader Peptide:
completed
Transcription
termination signal
Transcription stops
Trp depleted
Leader Peptide:
not completed
Transcription continues
Figure 3
24
When tryptophan is deficient, it takes time to translate the Trp codons in the leader sequence, and the ribosome
temporarily stays in Region 1. The mRNA transcribed during that time will be paired with Region 2 and Region
3 to form a stem loop structure. In this case, since Region 4 does not pair, a transcription termination signal is
not formed, and RNA polymerase continues transcription of the trpEDCBA operon encoding the downstream
Trp biosynthetic enzymes (Figure 3).
25
Animal biology
Q19
Glucagon is secreted from pancreatic A-cells and works as a signal via receptors (GLR) on the cells of target
tissues. The amount of GLR expressed on cell surfaces is important in determining the magnitude of the
response to glucagon in each target tissue. Figure 1 shows the amount of GLR mRNA in different rat tissues. In
the data shown here, the glucagon receptor is not detected in brain tissue, but recent reports have revealed that
it is present even in a very small amount, e.g., in the hypothalamus.
Liver
Adipose tissue
Kidney
Spleen
Ovary
Pancreatic islets
Thymus
Stomach
Adrenal glands
Small intestine
Thyroid
Muscle
Brain(whole)
Figure 1 Relative abundance of GLR (glucagon receptor) mRNA in rat tissue. * indicates less than detectable level.
26
Animal biology
Q20
Metabolic Concentration Output power Expected speed Exercise duration
substrate [mM] [W] [m/s] [s]
ATP 8 6400 27 2-4
CP 26 6000 25 10-17
Glycogen 90 1640 6.7
>6000
Fat 7-25 1100 4.6
Table 1. Types of metabolic substrate and its concentration as an energy source in human muscle cells. The
predicted values of output power produced by the muscle tissue, the expected speed at which the athlete ran
with that power, and the duration of exercise are shown when only the respective energy sources were used.
CP indicates creatine phosphate.
27
Animal biology
Q21
Huntington's disease (HD) is a genetic disorder characterized by devastating degeneration of nerve
tissues that progresses with age. Huntingtin (HTT) is known to be the causative protein of HD. Near
the transcriptional initiation point of HTT gene, there is a sequence containing repeated CAG
(corresponding to glutamine), which are usually between 9 to 35 repeats in healthy individuals.
These repeats are 35 to 75 in HD-population. The symptoms of HD tend to appear at a younger age
and are more severe when there are an increased number of CAG repeats.
Recently, scientists in France have revealed that HTT plays an important role in maintaining neuronal fast
axonal transport (FAT, Figure 1). By careful observations with fluorescence microscopy, they first showed that
HTT was co-localized with motor proteins (kinesin and dynein) that are involved in FAT. HTT was also shown
to be co-localized with synaptic vesicles, as well as with glyceraldehyde-3-phosphate dehydrogenase (GAPDH).
Interestingly, HTT was not found with mitochondria that were transported by FAT. Next, using cultured neurons,
they investigated the effects of oligomycin, an inhibitor of ATP production in mitochondria, and iodoacetate
acid, an inhibitor of GAPDH activity (Table 1). Furthermore, when HTT expression was suppressed by RNAi
treatment, only the FAT of synaptic vesicles, not that of mitochondria, was significantly reduced. These results
indicate that HTT was solely involved in FAT of synaptic vesicles.
Cell body
Nerve axon
Distribution [%]
Figure 1 Fast axonal transport (FAT) in nerve cells. a, active transportation of synaptic vesicles and mitochondria
outward to the nerve ends is called anterograde FAT (aFAT). Transportation in the opposite inward direction is called
retrograde FAT (rFAT). Measured velocity and its distribution (%) is shown in b.
28
Synaptic vesicles Mitochondria
aFAT 2.3 + 0.1 2.2 + 0.2 0.3 + 0.1 0.9 + 0.1 0.3 + 0.1 1.0 + 0.1
rFAT -1.9 + 0.1 -1.9 + 0.2 -0.2 + 0.1 -1.2 + 0.1 -0.4 + 0.2 -1.0 + 0.1
Table 1 Effects of oligomycin and iodoacetate on the velocity [μm/s] of anterograde (aFAT) and retrograde
(rFAT) transportation. In the experiments to determine FAT velocity with iodoacetate, pyruvate was included to
maintain ATP production by mitochondria. Control experiments were carried out in a buffer medium without
inhibitors. Under all experimental conditions, ATP/ADP ratio in axons was maintained >80%.
29
Animal biology
Q22
Animals living in deserts like kangaroo rats achieve the ability to sustain themselves on a limited supply of
water through incredibly well adapted kidney. To remove waste without losing water, species have developed
mechanisms to concentrate their urine. There are two types of nephrons that concentrate urine, a type with a
short Henle loop located in the renal cortex (cortex: C) and a type with a long Henle loop located near the renal
medulla (juxtamedullary: JM). The ratio of these two types of nephrons differs depending on the animal. The
table shows the habitat of each animal species and the urea concentration in urine. The graph plots the
juxtamedullary-cortex ratio (the number of JM type loop/the number of C type loop) in each animal species.
30
Animal biology
Q23
A researcher recorded neurotransmitter responses from a neurosecretory neuron in the hypothalamus. Gamma-
aminobutyric acid (GABA) is well-known as the neurotransmitter at most inhibitory synapses in the brain. The
researcher found that the application of GABA to this neuron induced more action potentials (Figure 1). Then,
the researcher measured GABA-induced chloride current responses of the neuron under various experimentally
controlled membrane potentials (from -50 to 0 mV at 10mV steps; Figure 2). They also plotted maximum current
amplitudes (current differences before and after the GABA application) against membrane potentials (Figure 3).
A downward deflection of a current trace is referred to as an inward current and reflects the movement of Cl-
ions out of the cell (Figure 4). Table 1 shows the intra- and extracellular concentrations and the equilibrium
potentials of sodium, potassium, and chloride ions calculated by Nernst’s equation.
GABA
Membrane potential (mV)
2 sec.
Figure 1
GABA
Current (pA)
Figure 2 Figure 3
31
Concentration (mM) Equilibrium
+ Current
Cl- Ion
Inner Outer
Potential
(mV)
GABA Na+ 15 150 58
K+ 140 7 -75
Figure 4
Table 1
Indicate whether each of the following statements is true or false.
A. When the membrane potential was -10 mV, the application of GABA induced the depolarization of the
recorded neuron. 88
B. The equilibrium potential of chloride ions was more positive (less negative) than the resting membrane
potential of the recorded neuron. 89
C. Under the presence of tetrodotoxin (pufferfish toxin that blocks the generation of action potentials), the
higher concentration of GABA depolarized the neuron more positively than 0mV. 90
D. The researcher recorded other neurons. The neurons hyperpolarized their membrane potentials by GABA.
If the resting membrane potential of both neurons are the same, intracellular chloride ion concentration of
the hyperpolarized neurons is lower than those of the neurons observed in Figure 1-4. 91
32
Animal biology
Q24
In the African clawed frog, Xenopus laevis, the mode of cell division shifts from cleavage to somatic cell
division, which has interphase, at the 12th cleavage after fertilization. This is called the mid-blastula transition
(MBT).
Microinjection of mRNA of genes that are required for nuclear membrane formation at one-cell stage results
in the increase of the nuclear size, but cell size does not change compared with a control embryo. In this
experiment, MBT occurs earlier than the 12th cleavage (Figure 1, left). Conversely, when the nuclear size is
artificially reduced, the cell size does not again change but MBT occurs later than the 12th cleavage (Figure 1,
right). Note: These treatments do not alter the time required for each cleavage.
Figure 1
33
Animal biology
Q25
In a Xenopus embryo, the dorsal-ventral axis is determined through cortical rotation after fertilization. On the
dorsal side of an embryo, the Spemann-Mangold organizer is necessary to determine the body plan of the
embryo. When the organizer formation is inhibited, a head defect occurs in embryos. On the other hand, the
head is enlarged when the organizer region expands.
β-catenin (β-cat) and GSK3β are involved in organizer formation. The table below shows the results of
phenotype of tadpoles microinjected with β-cat, GSK3β, an DN β-cat (β-catenin inhibition factor), and DN
GSK3β (GSK3β inhibition factor) into the dorsal or ventral side of the embryo.
34
Animal biology
Q26
Animals possess mechanisms for maintaining their body temperature within permissible levels. For example,
they show various responses to changes in room temperature. In addition, animals’ body shapes are optimized
to adapt to various climate changes, and their behaviors also regulate their body temperature.
35
Animal biology
Q27
A researcher aimed to induce undifferentiated cells by expressing multiple genes in human fibroblasts. They
focused on 24 genes that were identified as highly expressed in embryonic stem (ES) cells. It was found that
when all 24 genes were simultaneously introduced in fibroblasts, the colony formation characteristics of
undifferentiated cells occurs. Next the researchers tried to find the minimum set of genes that induce
undifferentiated cells. The graph shows the colony formation when 23 genes except one were introduced into
fibroblast cells.
Number of colonies
All
Gene number excluded from 24 genes
(“All” on the X axis shows that the 24 genes are all introduced.)
36
Animal biology
Q28
Immature lymphocyte B cells differentiate in an area of the peripheral lymph organ called the embryo center.
Myeloma cells are tumor cells that produce one type of mature immunoglobulin. mRNAs for full-length or only
3 'half of the immunoglobulin light chain gene were purified from a myeloma cell and were radioisotope-labeled.
Genomic DNA fragments obtained from either the embryo center or myeloma cells were digested with a
restriction enzyme and size fractionated by agarose electrophoresis. These DNA were hybridized with
radiolabeled mRNA, and radiation was measured after the removal of unhybridized mRNA (the experimental
flow is shown in Figure 1). The results are shown in Figure 2.
Myeloma
cell mRNA RI labeling
preparation
Figure 1
Radiation (counts per min.)
DNA mRNA
myeloma Full length
myeloma 3’end half
embryo Full length
embryo 3’end half
37
Indicate whether the sentences below are correct or incorrect.
A. The immunoglobulin light chain gene contained in the embryo center cells is shorter than that in the myeloma
cells. 109
B. The running distance depends on the length of DNA hybridized with mRNA. 110
C. The nucleotide sequence of DNA region hybridized with 3'-end mRNA is different between the myeloma-
derived DNA and the embryo center-derived DNA. 111
D. The full-length immunoglobulin light chain mRNA isolated from myeloma cells contains sequences from
two different parts of the DNA genome of the embryo center cells. 112
38
Plant biology
Q29
In order to prevent an excess water loss, stomata respond rapidly to changes in humidity. Transpiration rate per
unit leaf area represents the speed of water loss from the plant body. It is proportional to the diffusion rate of
water vapor (dwater), the water vapor concentration difference across the leaf epidermis (Δw), and the relative
stomatal aperture. Figure 1 shows relative stomatal apertures in normal air and in Helox air (79:21 mixture of
He and O2 with the appropriate concentrations of water vapor and CO2 added). Relative stomatal apertures were
measured in normal air (Air) and in Helox air under three different Δw conditions: the same Δw as that in normal
air (Helox), 2/3 of the normal air Δw (Helox2/3), and 1/2.33 of the normal air Δw (Helox1/2.33). dwater in Helox air
is 2.33 times higher than that in normal air, while Helox air does not affect any other factors of transpiration.
Note that water vapor diffuses only though the stomata and that the water vapor concentration inside the leaf is
always saturated.
Relative stomatal aperture
39
Plant biology
Q30
When tomato leaves are wounded, the expression of protease inhibitor genes is induced and protease inhibitor
proteins accumulate in the leaves. This response contributes to defense against insect herbivory as the protease
inhibitor proteins suppress the digestive function of insects. Since this response occurs not only in damaged
leaves but also in undamaged leaves, it is assumed that some mobile molecules transmit wound signals over
long distances.
Jasmonate and systemin, a signaling peptide composed of 18 amino acids, are involved in wound-induced
expression of protease inhibitor genes. Indeed, neither systemin-insensitive mutant (spr1), jasmonate
biosynthesis-deficient mutant (spr2), nor jasmonate-insensitive mutant (jai1) show expression of protease
inhibitor genes after wounding.
To investigate the roles of jasmonate and systemin in the long-distance signaling, experiments with grafts
between wild-type and mutant plants were conducted. Leaves of the stock were subjected to wounding and then
the expression of protease inhibitor genes were assayed, both in damaged leaves of the stock and in undamaged
leaves of the scion (Figure 1). The results are summarized in Table 1.
undamaged
scion leaf
graft
damaged
leaf
stock wounding
40
Table 1
Genotype Expression of protease inhibitor genes
stock scion stock scion
wild type spr1 + +
spr1 wild type – –
wild type spr2 + +
spr2 wild type – –
wild type jai1 + –
jai1 wild type – +
41
Plant biology
Q31
Strigolactone (SL) is a plant hormone that controls shoot branching. In Arabidopsis thaliana, several
SL-related mutants, such as max1, max2, and max4, which have loss-of-function mutations in the genes
MAX1, MAX2, and MAX4, respectively, have been isolated. While MAX2 encodes a key component of
the SL receptor complex, MAX1 and MAX4 each encode an enzyme for SL biosynthesis (Figure 1);
MAX4 for the production of the SL precursor carlactone (CL), and MAX1 for the conversion of CL into
SL. Grafting experiments using these mutants and the wild type (WT) were conducted, and the number
of shoot branches were counted (Figure 2 & 3). In this experiment, neither mRNAs nor proteins of the
MAX genes were found to move across the grafting junction.
Carotenoid
Shoot
scion Shoot
scion
Grafting
Carlactone (CL)
Root- Root-
stock stock
Strigolactone (SL)
Figure 1.
Figure 2.
Biosynthetic pathway of strigolactone
Schematic illustration of grafting experiments
Number of shoot branches
shoot scion
Genotype of
rootstock
42
Indicate whether each of the following statements is true or false.
A. The MAX2 gene mainly functions in the root. 121
B. SL is synthesized both in the root and shoot. 122
C. CL, the substrate of MAX1, is transported between the root and shoot in either direction. 123
D. If a shoot scion of max4 is grafted on a rootstock of max2, shoot branching will be normal. 124
43
Plant biology
Q32
Zinc (Zn) and iron (Fe) are both micronutrients for plants. Plants obtain Zn and Fe ions from soil through the
root system, and transport them to the shoot. Plant culture media usually contains low concentrations of these
micronutrients. Half-strength MS medium, a typical plant culture medium, contains 15 μM Zn2+ and 50 μM
Fe2+.
Although micronutrients are essential for plant growth, at excess concentrations they inhibit plant growth. To
examine the inhibitory effects of excess micronutrients, Arabidopsis thaliana plants were grown on half-
strength MS media, supplemented with additional Zn2+ and/or Fe2+.
Additional Zn2+(μM) Additional
Fe2+(μM)
Relative dry weight (%)
Additional Fe2+(μM)
Additional Zn2+(μM)
Additional Zn2+(μM)
44
Plant biology
Q33
While snapdragon normally has bilateral flowers, flowers of its mutant defective in gene G lose bilateral
symmetry and have radial symmetry, thereby indicating that gene G confers bilateral symmetry to the flower.
In the inflorescence of wild-type sunflower, the outer region has ligulate florets, whereas the inner region has
tubular florets (Figure 1). Variants x, y, and z of sunflower have DNA insertions in gene G’, a sunflower
orthologue of the gene G from snapdragon (Figure 2). As a result of these insertions, variant x has only ligulate
florets over the entire inflorescence, and variants y and z have only tubular florets over the entire inflorescence.
Ligulate Tubular
Figure 1 Ligulate and tubular florets of sunflower
Intron
Exon 1 Exon 2
45
Plant biology
Q34
Fragaria chiloensis is a stolon*-bearing perennial herb that grows on coastal sand dunes. In coastal sand
dunes, nitrogen-fixing shrubs often create small patches of lower photon flux density (PFD) but higher soil
nitrogen availability. The presence of such patches frequently makes a difference in the resource availability
between stolon-connected ramets**. To examine effects of stolon connection, researchers compared the
growth of connected ramets and severed ramets; one ramet in each pair was provided with high PFD but a low
level of soil nitrogen, and the other ramet was provided with low PFD but a high level of soil nitrogen (Figure
1). As a result, combined dry biomass of connected ramets was 54% higher than that of severed ramets.
*Stolon: a stem that grows along the soil surface and forms buds and roots at the nodes for clonal propagation.
**Ramet: an individual unit of a clonal colony.
connected
severed
46
Plant biology
Q35
Soil salinity (NaCl) affects the growth of plants. As the increase of osmotic pressure induced by soil salinity
reduces the ability of plants to take up water and minerals, soil salinity elicits osmotic stress. Additionally,
because cytosolic Na+ interferes with the activities of metabolic enzymes, soil salinity also elicits ionic stress.
Thus, NaCl elicits two primary effects on plant cells, which both trigger a signaling cascade that start with the
elevation of the intracellular Ca2+ concentration ([Ca2+]i). In contrast, sorbitol, a sugar alcohol often used as an
osmoticum, elicits only osmotic stress because sorbitol is non-ionic. x and y are mutants of Arabidopsis
isolated as defective in NaCl-induced increases in [Ca2+]i. Figure 1 illustrated below shows the dose-
dependent [Ca2+]i increases induced by NaCl or sorbitol in the seedlings of the wild type (WT) and mutants x
and y.
Figure 1
47
Q36
Following is a description regarding a population of a diploid organism, species A, with a special focus on the
locus C that is involved in body color.
Based on the given information, indicate whether each of the following statements is true or false.
A. Information: Species A consists of two color morphs, black and yellow, controlled by a single locus C: the
allele CB for the black type and the allele CY for the yellow type.
Statement: If the allele CB is completely dominant to the allele CY and the frequency of the yellow type
individuals is 9%, the genotype frequency of CBCB is about 70%. Note that the population is assumed to be
under Hardy-Weinberg equilibrium. 141
B. Information: When the body colors of ten species belonging to the same genus with species A were examined,
they were all yellow.
Statement: In this case, the body color of the ancestral species A just after splitting from these closely related
species must have been yellow under a parsimony principle. 142
C. Information: A small portion of individuals in the population of species A was isolated due to diastrophism
(large-scale deformation of Earth's crust) and formed a new population A’.
Statement: The drastic inter-generation changes of allele frequency of locus C in population A’ can be best
explained by natural selection. 143
D. Information: A slightly deleterious mutation with exactly the same effect on the fitness of an individual
independently occurred in both the small population A’ and the larger parental population A.
Statement: The fixation probability of this mutation is the same in both populations. 144
48
Evolution
Q37
The following figure is a phylogenetic tree of ECP and EDN genes in primates. EDN shows strong ribonuclease
activity. By contrast, ECP shows strong anti-bacterial function, although its ribonuclease activity is weak.
1/0
0/0 Human
Human
6/0 2/1
Chimpanzee
Chimpanzee
1/2 2/1
Gorilla
Gorilla
ECP
33/3 17/2
Orangutan
Orangutan
15/5
Macaque
Macaque
0/2
X 0/0 Human
Human
7/3 1/1
Chimpanzee
Chimpanzee
3/5 1/2
Gorilla
Gorilla
8/3 5/5
Orangutan
Orangutan
EDN
21/13
Macaque
Macaque
36/16
Tamarin
Tamarin
Figure 1. A molecular phylogenetic tree of ECP and EDN genes in primates based on amino-acid sequences.
The numerator and denominator along each branch show the numbers of nonsynonymous and synonymous
nucleotide substitutions (substitutions that cause and do not cause amino-acid changes), respectively. Branch
length is not proportional to sequence divergence nor time.
49
Evolution
Q38
Following is the phylogenetic tree based on the amino-acid sequences of all opsin genes in the human and
zebrafish genomes.
Zebrafish MWS1
Zebrafish MWS2
Zebrafish MWS3
Zebrafish MWS4
Zebrafish RH
Human RH
Zebrafish SWS
I Zebrafish UVS
Human SWS
Zebrafish LWS1
Zebrafish LWS2
I Human LWS
Human MWS
Figure 1. A phylogenetic tree based on the amino-acid sequences of all opsin genes in the human and zebrafish
genomes. LWS: Long Wavelength Sensitive opsin, MWS: Middle Wavelength Sensitive opsin, SWS: Short
Wavelength Sensitive opsin, UVS: Ultra Violet Sensitive opsin, RH: Rhodopsin type opsin. Branch length is
not proportional to sequence divergence nor time.
Indicate whether each of the following statements is true or false under a parsimony principle.
A. In the phylogenetic tree, zebrafish SWS is most closely related to RH. 149
B. The common ancestor of the human and zebrafish had four opsin genes in the genome. 150
C. The opsin gene at node I was supposed to encode an LWS. 151
D. The zebrafish has acquired five opsin genes after splitting from the human. 152
E. The human has lost two opsin genes after splitting from the zebrafish. 153
F. The common ancestor of the human and zebrafish did not have any SWS in the genome. 154
50
Evolution
Q39
The Peromyscus polionotus inhabits the mainland of the Florida peninsula (Figure 1 ④) and has a dark-colored
coat (Figure 1). In contrast, P. polionotus, inhabiting the light-colored sandy coastal dunes (Figure 1 ①-③),
which are estimated to be 6,000 years old, has a lighter-colored coat (Figure 1). These mice show obvious
differences in color patterns according to their habitat. The researchers compared the melanocortin 1 receptor
gene (MC1R), a key gene for melanogenesis, and revealed the existence of two alleles, of which 65th amino acid
residue is R or C, among these mice populations.
(pmol/mg)
(logM)
Figure 1 Figure 2
Figure 1. (left) Four localities of habitat of P. polionotus in the Florida peninsula. (right) Cartoons represent the
color patterns of the mice in each locality. Pie charts indicate the frequencies of the R allele (black) and C allele
(white). n indicates the number of individuals surveyed.
Figure 2. Plot of the cAMP response to the MSH (melanocyte stimulating hormone) stimulation for MC1R
expressing cultured cells. The X and Y axis indicate the concentration of the MSH and cAMP, respectively. The
MC1R proteins encoded by R or C alleles were examined in this experiment.
51
Evolution
Q40
Pundamilia pundalilia and P. nyererei are a closely related sister species pair of cichlids in Lake Victoria. These
two species are distinct in male nuptial body colors, in that the former and latter are blue and red, respectively.
By contrast, the females of the two species are not distinct, both possessing cryptic body coloration. P.
pundamilia and P. nyererei inhabit shallow and deep environments, respectively. The light component in Lake
Victoria is oriented to be blue (short wavelength) in shallow and red (long wavelength) in deep environments.
The opsin protein of the two species are shifted to the same wavelength of their habitat light components. In
addition, inter-species hybridization occurs under the specific light condition, where red and blue lights cannot
be distinguished.
52
Evolution
Q41
Molecular phylogenetics is a powerful tool for inferring phylogenetic relationships among extant species. The
following are methodological statements on molecular phylogenetics.
53
Evolution
Q42
Figure 1 shows the evolution of cetaceans. Studies using stable isotopes indicate that Pakicetus and
Amburocetus ate freshwater fish, while Remingtonocetus, Miacetus and Basirosaurus ate seawater fish. Indhyus
was, like most extant artiodactyls, a terrestrial herbivorous animal.
70 60 50 40 30 20 10 0 (MYA)
Odontoceti(AQ)
Odontoceti (AQ)
Mysticeti (AQ)
Mysticeti (AQ)
CE
CETACEA
†
Basirosaurus (AQ)
TACEA
†
Miacetus (AM)
†
Remingtonocetus (AM)
† Archaeoceti
Archaeoceti
Amburocetus (AM)
†
Pakicetus (AM)
†
ARTIODACTYLA
Indhyus (TE)
ARTIODACTYLA
hippopotamus (AM)
hippopotamus (AM)
cow (TE)
cow (TE)
pig (TE)
pig (TE)
camel (TE)
camel (TE)
Figure 1. A phylogenetic tree of cetaceans and artiodactyls. Extinct fossil species are shown with†. All extant
cetaceans are classified into two subfamilies: Mysticeti (baleen whales, which do not possess enamel-based
teeth but possess baleen plates) and Odontoceti (toothed whales, which possess teeth). The lifestyle (AQ: aquatic,
AM: amphibious, TE: terrestrial) of each group is also shown. Lifestyles of fossil species are inferred based on
morphological characteristics. MYA: million years ago
Judging ONLY from this phylogenetic tree, indicate whether each of the following statements is true or
false.
A. Under the maximum-parsimony criterion, the most recent common ancestor of the hippopotamus and
modern cetaceans is amphibious. 167
B. There were no fully-aquatic cetaceans 50 MYA. 168
C. Based on these studies, the evolutionary scenario of cetaceans is speculated as follows: 1. becoming
54
carnivorous, 2. becoming fully aquatic, 3. invasion to oceanic environments, 4. divergence into baleen
whales and toothed whales. 169
D. The enamelin gene, which encodes an essential protein for the formation of teeth enamel, was lost during
the evolution of cetaceans before 35 MYA. 170
55
Evolution
Q43
Proteins encoded by Hox genes share a 60-amino-acid DNA-binding motif, the homeodomain. In the fruit fly
Drosophila melanogaster genome, eight Hox genes are assembled in one cluster on the same chromosome
(Figure 1A). The segmental expression pattern of Hox genes along the anterior-posterior axis of the fruit fly
embryo shows collinearity with the gene order on the chromosome (Figure 1B). Fruit flies normally possess a
pair of wings that develop from the second thoracic segment (T2) of the embryo, and a pair of balance organs
(halteres) that develop from the third thoracic segment (T3). When the gene expression of Ubx gene is lost by
mutations, T3 transform into T2 and two pairs of wings are formed. Beetles and grasshoppers have two pairs of
wings although the most anterior segment of the UBX protein expression of their embryos is found in T3, the
same as that of the wild fruit fly (Figure 1C).
A
C Fruitfly
Fruit fly Beetle
Beetle Grasshopper
Grasshopper
lab pb Dfd Scr Antp Ubx abdA AbdB
T2 T3
B
lab
pb Scr
Antp
Dfd Ubx
abdA AbdB
Figure 1. (A) Eight Hox genes on the fruit fly genome: lab, pb, Dfd, Scr, Antp, Ubx, abd-A, and Abd-B. (B)
Segmental expression pattern of the Hox genes in the fruit fly embryo. Anterior is the left. The expression
patterns for each gene are illustrated by labels that correspond to (A). Arced bars shown below indicate the range
of the expression of each gene. (C) Schematic drawings for UBX protein expression in three species of embryos.
Anterior is up. Red arrows indicate the boundary between T2 and T3. Area with gene expression is painted dark.
57
Evolution
Q44
Three-spined stickleback Gasterosteus aculeatus are widely distributed in both marine and freshwater areas
across the world. Adaptive radiation has led to morphological differences between marine and freshwater
populations. Of such differences, all of the marine population have a pair of pelvic spines that evolved from the
pelvic skeleton, while some freshwater populations of various localities have lost their spines (Figure 1). Genetic
analyses revealed that the causative genomic region for this pelvic difference is located around the Pitx1 gene.
This Pitx1 plays an important role in the development of the ventral spine, thymus, and neuromast. Although
the amino acid sequences of Pitx1 transcripts are identical in both populations, the expression patterns of Pitx1
in the pelvic fin buds of embryos are different: Pitx1 is expressed in the marine population (purple), while it is
not in the freshwater population (Figure 1 insets).
Marine Freshwater
Figure 1. Ventral view of marine (left) and freshwater (right) sticklebacks, showing the presence/absence of
pelvic spines (shown by dark blue). Anterior is to up. (Boxes) Magnified ventral view of stickleback embryos
showing Pitx1 expressions in the pelvic fin buds.
58
Ecology
Q45
Density dependence is the fundamental process governing the population dynamics of organisms. The graph
below describes per capita (per-individual) birth rate and death rate as a function of population density in two
types of species (I and II).
Birth rate
Per capita growth rate
Birth rate
Death rate
Death rate
59
Ecology
Q46
An animal’s territory is an exclusive area defended by an individual to keep resources, such as food, and mates.
Territory is different from home range, because home range simply represents an area over which an animal
regularly moves and may overlap with those of neighboring animals of the same species. The size of the territory
is determined by the cost and benefit obtained from the area, in a way that maximizes the net benefit gain of
individual animals. The graph below shows how cost and benefit change with the size of the territory.
Benefit
Benefit or cost
Cost
Territory size
60
Ecology
Q47
An experiment was conducted to examine the relative effect of pollinators during the night and in the daytime
on the reproductive success of golden rod flowers. Pollinators cannot visit the bagged flowers. The figure shows
the number of viable seeds produced (mean ± standard deviation) by flowers that were not bagged (1), those
bagged during the night (2), those bagged in the daytime (3), those bagged during both day and night (4), and
those that underwent enforced pollination by an experimenter (5).
Daytime Nighttime
Number of seeds produced
61
Ecology
Q48
Mosquitos are vectors for transmitting human diseases, and the application of insecticides to water bodies is
occasionally conducted to control mosquito populations. In a mosquito population, there are two alleles of a
locus that affect susceptibility to pesticides, (s): susceptible, and (r): resistant. The resistance is completely
recessive. The table below shows the change in the number of individuals with different genotypes before (Pre-
1990), during (1990-2000; shown by an arrow), and after (2005-2015) pesticide application.
62
Ecology
Q49
Scientists monitored the number of individuals for ant species in a 5 hectare plot of land for 50 years. The below
figures represent the dominance rank of observed species in terms of their abundance, that is, the number of
individuals for each species. Each open circle represents the value for each species. Note that the most abundant
species is given rank 1.
Species A Species A
Abundance
Species A
63
Ecology
Q50
Understanding how plant species richness affects community biomass production is important for biodiversity
and ecosystem conservation. In a grassland, scientists created 72 experimental plots (1 m2 each) with different
numbers of vascular plant species (from 1 to 10 species), with species combinations assembled randomly. Both
local light and soil conditions were similar among the plots before establishing vegetation. After three years of
this experiment, they harvested aboveground vegetation to measure aboveground biomass in each plot. The
figure shows the relationship between species richness (number of species) and the dry weight of aboveground
biomass (kg m-2) of plant communities in each plot. The line indicates the linear relationship obtained from the
least square regression.
Aboveground biomass (kg m )
-2
Species richness
64