Deck 2: Development of a Body Pattern
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Deck 2: Development of a Body Pattern
1
In humans, the pharyngeal arches develop into the
A) neural crest cells.
B) throat.
C) gills.
D) rhombomeres.
A) neural crest cells.
B) throat.
C) gills.
D) rhombomeres.
B
2
Which maternal factor in the Drosophila egg accumulates at the end of the embryo that will become the head?
A) Bicoid
B) Nanos
C) Caudal
D) Syncytium
A) Bicoid
B) Nanos
C) Caudal
D) Syncytium
A
3
If bicoid mRNA is injected into the middle of a bicoid-deficient Drosophila egg syncytium, the embryo will develop a
A) head at one end, a tail at the other, and another head in the middle.
B) head at one end, a tail at the other, and another tail in the middle.
C) tail at both ends and a head in the middle.
D) head at both ends and a tail in the middle.
A) head at one end, a tail at the other, and another head in the middle.
B) head at one end, a tail at the other, and another tail in the middle.
C) tail at both ends and a head in the middle.
D) head at both ends and a tail in the middle.
C
4
Which class of genes initially establishes the anterior-posterior axis of the body plan?
A) Pair-rule genes
B) Gap genes
C) Maternal polarity genes
D) Hox genes
A) Pair-rule genes
B) Gap genes
C) Maternal polarity genes
D) Hox genes
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5
Which class of genes directly influences the expression of pair-rule genes?
A) Realizator genes
B) Gap genes
C) Maternal polarity genes
D) Hox genes
A) Realizator genes
B) Gap genes
C) Maternal polarity genes
D) Hox genes
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6
Which is the first class of Drosophila regulatory genes to use cell-cell signaling across the membrane?
A) Pair-rule genes
B) Gap genes
C) Maternal polarity genes
D) Segment polarity genes
A) Pair-rule genes
B) Gap genes
C) Maternal polarity genes
D) Segment polarity genes
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7
Which statement regarding homeobox and Hox genes is true?
A) Every homeobox gene is a Hox gene.
B) Every transcription factor is a homeobox gene.
C) Every Hox gene is a homeobox gene.
D) Every transcription factor is a Hox gene.
A) Every homeobox gene is a Hox gene.
B) Every transcription factor is a homeobox gene.
C) Every Hox gene is a homeobox gene.
D) Every transcription factor is a Hox gene.
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8
Which set of genes shows colinearity?
A) Pair-rule genes
B) Gap genes
C) Hox genes
D) Segment polarity genes
A) Pair-rule genes
B) Gap genes
C) Hox genes
D) Segment polarity genes
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9
Hox genes in Drosophila are similar to Hox genes in vertebrates because they _______ in both organisms.
A) are located on one chromosome
B) show colinearity
C) have two complexes
D) developed by gene duplication and divergence
A) are located on one chromosome
B) show colinearity
C) have two complexes
D) developed by gene duplication and divergence
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10
Which segment in early human brain development contributes to the cerebellum?
A) Telencephalon
B) Rhombencephalon
C) Prosencephalon
D) Mesencephalon
A) Telencephalon
B) Rhombencephalon
C) Prosencephalon
D) Mesencephalon
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11
In normal vertebrate development, the hindbrain is distinguished from the forebrain and midbrain by the differential expression of
A) homeobox genes.
B) pair-rule genes.
C) maternal polarity genes.
D) Wnt1.
A) homeobox genes.
B) pair-rule genes.
C) maternal polarity genes.
D) Wnt1.
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12
The homeobox gene _______ is only expressed in the posterior portion of the midbrain and marks the boundary between midbrain and hindbrain.
A) engrailed
B) Gbx2
C) Wnt1
D) fibroblast growth factor
A) engrailed
B) Gbx2
C) Wnt1
D) fibroblast growth factor
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13
If scientists implant an acrylic bead infused with fibroblast growth factor into the middle of a developing chick embryo brain,
A) the brain will form an additional forebrain.
B) the embryo will die.
C) the brain will form an additional midbrain.
D) the brain will develop normally.
A) the brain will form an additional forebrain.
B) the embryo will die.
C) the brain will form an additional midbrain.
D) the brain will develop normally.
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14
As vertebrate development proceeds, the hindbrain becomes segmented into eight swellings called
A) rhombomeres.
B) rhombencephalons.
C) rhombiclips.
D) rhomboids.
A) rhombomeres.
B) rhombencephalons.
C) rhombiclips.
D) rhomboids.
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15
The structurally distinct swellings in the developing vertebrate hindbrain are demarcated by differential expression of
A) fibroblast growth factor.
B) ephrins.
C) bone morphogenetic protein.
D) retinoic acid.
A) fibroblast growth factor.
B) ephrins.
C) bone morphogenetic protein.
D) retinoic acid.
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16
Ephrins are _______ that affect gene expression by _______.
A) transcription factors; binding to DNA
B) proteins; binding to DNA
C) proteins; altering signaling pathways within the cell
D) transcription factors; altering signaling pathways within the cell
A) transcription factors; binding to DNA
B) proteins; binding to DNA
C) proteins; altering signaling pathways within the cell
D) transcription factors; altering signaling pathways within the cell
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17
Exposure to _______ prevents the posterior neural plate cells from becoming epithelial cells by making those cells _______ sensitive to BMP signaling.
A) FGF; less
B) Wnt; less
C) FGF; more
D) Wnt; more
A) FGF; less
B) Wnt; less
C) FGF; more
D) Wnt; more
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18
Which developmental signal is also a powerful teratogen?
A) Fibroblast growth factor
B) Wnt
C) Retinoic acid
D) Bone morphogenetic protein
A) Fibroblast growth factor
B) Wnt
C) Retinoic acid
D) Bone morphogenetic protein
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19
If a vertebrate embryo develops an enlarged posterior nervous system and little or no forebrain, what may have happened in development?
A) The embryo was over-exposed to fibroblast growth factor.
B) The embryo was over-exposed to retinoic acid.
C) The embryo was under-exposed to fibroblast growth factor.
D) The embryo was under-exposed to BMP.
A) The embryo was over-exposed to fibroblast growth factor.
B) The embryo was over-exposed to retinoic acid.
C) The embryo was under-exposed to fibroblast growth factor.
D) The embryo was under-exposed to BMP.
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20
The developmental signal _______ directs the development of the ventral portion of the spinal cord, and _______ directs the development of the dorsal portion of the spinal cord.
A) Sonic hedgehog; bone morphogenetic protein
B) retinoic acid; Sonic hedgehog
C) bone morphogenetic protein; Sonic hedgehog
D) Sonic hedgehog; retinoic acid
A) Sonic hedgehog; bone morphogenetic protein
B) retinoic acid; Sonic hedgehog
C) bone morphogenetic protein; Sonic hedgehog
D) Sonic hedgehog; retinoic acid
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21
Sonic hedgehog is secreted from the
A) neural tube.
B) ectoderm.
C) notochord.
D) roof plate.
A) neural tube.
B) ectoderm.
C) notochord.
D) roof plate.
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22
Bone morphogenetic protein is secreted from the
A) neural tube.
B) ectoderm.
C) notochord.
D) floor plate.
A) neural tube.
B) ectoderm.
C) notochord.
D) floor plate.
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23
An animal can be born with a single telencephalon and a single eye if _______ signaling is disrupted during development.
A) bone morphogenetic protein
B) Sonic hedgehog
C) fibroblast growth factor
D) retinoic acid
A) bone morphogenetic protein
B) Sonic hedgehog
C) fibroblast growth factor
D) retinoic acid
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24
If the anterior-posterior axis of the spinal cord is disrupted, what can you conclude happened in development?
A) Sonic hedgehog signaling was blocked
B) Sonic hedgehog signaling was increased
C) Bone morphogenetic protein signaling was increased
D) Homeobox genes were dysfunctional
A) Sonic hedgehog signaling was blocked
B) Sonic hedgehog signaling was increased
C) Bone morphogenetic protein signaling was increased
D) Homeobox genes were dysfunctional
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25
In the evolution of the human brain there were four crucial steps; which event was the first?
A) Social experience began to guide neural development
B) Sensory experience began to guide neural development
C) Cell-cell interactions began to determine cell fate
D) Electrical activity of neurons began to affect the fate of other cells
A) Social experience began to guide neural development
B) Sensory experience began to guide neural development
C) Cell-cell interactions began to determine cell fate
D) Electrical activity of neurons began to affect the fate of other cells
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26
Describe the possible reasons why embryonic structure across species is so similar.
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27
In insects, the early embryo consists of a single cell with one continuous cytoplasm containing many nuclei. How can those nuclei become different types of cells if they all started out in the same cytoplasm?
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28
Refer to the graph.
Where is the highest concentration of hunchback protein expressed in the Drosophila embryo, and how do the antagonistic actions of maternal polarity genes bicoid and nanos result in sharper boundaries of hunchback gene expression?

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29
What is the relationship between Hox genes and realizator genes? How is their function different?
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30
What is a potential benefit of a random mutation that leads to a duplication in a gene?
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31
Refer to the figure.
A normal wild-type mouse is shown in (A), a mutant mouse with enlarged rostral cortex centers is shown in (B), and a mutant mouse with enlarged caudal cortical centers is shown in (C). What specific mutations might (B) and (C) have?

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32
In vertebrate nervous system development, what system is responsible for sharpening the homeobox gene expression boundaries between rhombomeres? How does this system work with respect to what the key players are, where they are located, how they interact, and how they influence gene expression and rhombomere boundaries? What does this mean for the fate of the cells that make up each rhombomere?
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33
What four factors in the vertebrate neurula direct cells to take on a fate appropriate for the caudal end of the animal? What two characteristics do these factors share?
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34
In vertebrate nervous system development, what would happen to the neural tube if the notochord was removed? What would happen if a second notochord was transplanted to another part of the neural tube? What does this suggest about the function of the notochord?
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35
How is it that the body can randomly assign cells to a particular fate based solely on where they are located, and how is this accomplished?
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