a. Bindin | ||
b. Vitelline envelope | ||
c. Cortical granules | ||
d. Dynein |
a. Bindin | ||
b. Vitelline envelope | ||
c. Cortical granules | ||
d. Dynein |
a. The activation of egg metabolism | ||
b. The primary binding of sperm to the zona pellucida | ||
c. The secondary binding of sperm to the zona pellucida | ||
d. The absorption of nutrients into the egg's cytoplasm |
a. The activation of egg metabolism | ||
b. The slow reaction to prevent polyspermy | ||
c. The fast reaction to prevent polyspermy | ||
d. The binding of sperm and egg |
a. Hertwig and Fol | ||
b. Leeuwenhoek | ||
c. Aristotle | ||
d. Both B and C |
a. It is most important in species with external fertilization. | ||
b. It involves chemicals that have powerful effects at very low concentrations. | ||
c. It involves chemicals that are present in sperm at higher and higher doses as they mature. | ||
d. It involves the creation of a concentration gradient. |
a. The blood vessels of chicks form before the heart. | ||
b. The intestinal tube forms by the folding of tissue that was once flat. | ||
c. Each generation organisms are created anew. | ||
d. Embryonic organs develop from different tissues than their adult counterparts. |
a. Fertilization occurs as a fusion of a sperm and an egg. | ||
b. Cleavage occurs through either the entire egg dividing into smaller cells or a small portion of the egg dividing and forming the embryo. | ||
c. All animals, even mammals, derive from eggs. | ||
d. The intestinal tube forms by the folding of tissue that was once flat. |
a. Calcium | ||
b. Sodium | ||
c. Potassium | ||
d. Hydrogen |
a. Yes, because you will ensure that these proteins are able to function properly in binding sperm to the egg. | ||
b. No, because these proteins are only marginally involved in chemoattraction and will not affect fertilization success. | ||
c. No, because while you might increase fertilization success, you will block the egg's ability to prevent polyspermy. | ||
d. Yes, because you will ensure that the cumulus does not thicken too early in fertilization. |
a. Vertebrate embryos in their early stages of development are difficult to tell apart. | ||
b. As the embryos of "higher" (more recently evolved) vertebrate species develop, they resemble the adult stages of various ancestral forms. | ||
c. Early vertebrate embryos all have the same type of skin, only later growing scales, hair, or feathers. | ||
d. Vertebrate embryos resemble one another early in development but later do not resemble other species, only their own. |
a. RNA processing | ||
b. Post-translational modification | ||
c. Transcription | ||
d. Translation |
a. RNA processing | ||
b. Post-translational modification | ||
c. Transcription | ||
d. Translation |
a. RNA processing | ||
b. Post-translational modification | ||
c. Transcription | ||
d. Translation |
a. Promoters | ||
b. Enhancers | ||
c. Transcription factors | ||
d. Introns |
a. Pax6 works in combination with Sox2 to allow the transcription of the gene in the appropriate tissues. | ||
b. The lens gene is transcribed but is prevented from transport into the cytoplasm; it remains in the nucleus until it is degraded. | ||
c. The gene is stabilized in cells fated to become the lens by the addition of a longer poly(A) tail. | ||
d. The enzyme deltaEF1 phosphorylates the otherwise-inactive crystalline-lens protein, after it has been translated. |
a. Northern blot | ||
b. Making a quail-chick chimera | ||
c. In situ hybridization | ||
d. PCR |
a. Northern blot | ||
b. Making a quail-chick chimera | ||
c. In situ hybridization | ||
d. PCR |
a. Genetic knockout | ||
b. Insertion via retroviral vector | ||
c. Making a transgenic mouse | ||
d. Antisense RNA |
a. Northern blot | ||
b. Making a quail-chick chimera | ||
c. In situ hybridization | ||
d. PCR |
a. Genetic knockout | ||
b. Insertion via retroviral vector | ||
c. In situ hybridization | ||
d. PCR |
a. Genetic knockout | ||
b. Insertion via retroviral vector | ||
c. In situ hybridization | ||
d. PCR |
a. Autonomous | ||
b. Syncytial | ||
c. Semelparous | ||
d. Conditional |
a. Autonomous | ||
b. Syncytial | ||
c. Semelparous | ||
d. Conditional |
a. Sea urchins | ||
b. Amphibians | ||
c. Birds | ||
d. Mammals |
a. It serves as a buffer, preventing cells below it from affecting cells above it. | ||
b. It has no function and occurs as a byproduct of the cleavage process. | ||
c. It induces the formation of the blastopore. | ||
d. It forms the gut in later development. |
a. Veg1 | ||
b. β-catenin | ||
c. Veg2 | ||
d. Micromeres |
a. During early cleavage, stored maternal proteins and mRNAs control development, and virtually no activity is undergone by the zygote's genome. | ||
b. Division occurs without any increase in the volume of the cell. | ||
c. The initiation of cleavage is inhibited by MPF. | ||
d. All of the above |
a. It provides nutrients for developing embryos. | ||
b. It helps determine the pattern and distribution of cleavage. | ||
c. It inhibits cleavage. | ||
d. None of the above |
a. Compaction | ||
b. Rotational cleavage | ||
c. Early activation of the zygotic genome | ||
d. Asynchronous cell division |
a. The animal pole | ||
b. The vegetal pole | ||
c. Neither has yolk | ||
d. Both have the same amount of yolk |
a. Your eggs undergo meroblastic cleavage. | ||
b. Your eggs divide at a slower rate than those with a great deal of yolk. | ||
c. Your young go through a larval stage in which they eat a great deal. | ||
d. Your eggs undergo discoidal cleavage. |
a. Autonomous | ||
b. Syncytial | ||
c. Semelparous | ||
d. Conditional |
a. Frog and avian gastrulation events are nearly identical. | ||
b. Mammalian gastrulation events are very similar to avian and reptilian events in spite of their eggs no longer having large amounts of yolk. | ||
c. Gastrulation events in amphibians are initiated by the same cell signals that are used in sea-urchin gastrulation. | ||
d. Gastrulation in birds goes through stages that reiterate the development of all earlier vertebrate groups. |
a. Involution | ||
b. Ingression | ||
c. Delamination | ||
d. Epiboly |
a. Involution | ||
b. Ingression | ||
c. Delamination | ||
d. Epiboly |
a. Involution | ||
b. Ingression | ||
c. Delamination | ||
d. Epiboly |
a. Invagination | ||
b. Involution | ||
c. Ingression | ||
d. Epiboly |
a. Blastocoel | ||
b. Cytotrophoblast | ||
c. Archenteron | ||
d. Epiblast |
a. The primitive groove, because it provides the opening through which cells migrate into the blastocoel. | ||
b. The scatter factor, because it defines the dorsal portion of the embryo. | ||
c. The germinal crescent, because it initiates gastrulation. | ||
d. There is no avian equivalent to the frog blastopore because of their different patterns of cleavage and gastrulation. |
a. Sea urchins | ||
b. Frogs | ||
c. Birds and mammals | ||
d. Mammals |
a. It is the point at which gastrulation is initiated. | ||
b. The cells opposite it will become the blastopore. | ||
c. It induces the necessary movement of the egg cytoplasm. | ||
d. It marks the future dorsal portion of the embryo. |
a. VegT | ||
b. Sonic hedgehog | ||
c. Distal | ||
d. Cortical cytoplasm |
a. Ectoderm | ||
b. Mesoderm | ||
c. Endoderm | ||
d. Neural crest |
a. Nanos | ||
b. Caudal | ||
c. Gurken | ||
d. Bicoid |
a. Two normal frog embryos | ||
b. One normal frog embryo and one mass of tissue | ||
c. One conjoined-twin frog embryo | ||
d. A mutant, non-viable embryo |
a. Two normal frog embryos | ||
b. One normal frog embryo and one mass of tissue | ||
c. One conjoined-twin frog embryo | ||
d. A mutant, non-viable embryo |
a. Two normal frog embryos | ||
b. One normal frog embryo and one mass of tissue | ||
c. One conjoined-twin frog embryo | ||
d. A mutant, non-viable embryo |
a. Left-right axis formation | ||
b. Dorsal-ventral axis formation | ||
c. Anterior-posterior axis formation | ||
d. Specification of the ectoderm |
a. Block the factors that inhibit ectoderm from developing into its "default fate" | ||
b. Overexpress the inhibitory factors within the organizer (e.g. follistatin, chordin) | ||
c. Block the factors that inhibit BMP4 expression | ||
d. Both A and B |
a. It is specified but not determined. | ||
b. It is composed of the dorsal-most vegetal cells. | ||
c. It induces the organizer. | ||
d. It occurs opposite the point of sperm entry. |
a. Both rely upon gradients of proteins and mRNAs to induce appropriate structures in appropriate regions along the anterior-posterior axis. | ||
b. Both have homeotic genes whose expression patterns control the development of regions of the body. | ||
c. Both form their anterior-posterior axis after dorsal-ventral axis formation has been induced. | ||
d. All of the above |
a. pH | ||
b. Nanos | ||
c. Gravity | ||
d. β-catenin |
a. Transplanting the dorsal lip of the blastopore from an untreated embryo to the same site on a treated embryo | ||
b. Transplanting the dorsal-most blastomeres from an untreated embryo to the same site on a treated embryo | ||
c. Rotating the embryo 180 degrees before the 32-cell stage | ||
d. Either A or B would allow you to rescue the embryo. |
a. Both are influenced by the asymmetric expression of the genes iv and inv. | ||
b. Both are influenced by the presence of a nodal gene on the left side of the embryo which activates pitx2. | ||
c. In both, right-side structures are initiated by the activation of snail, and left-side structures are initiated by the activation of pitx2. | ||
d. In both, left-right axis patterning is initiated by the presence of Noggin and Cerberus proteins. |
a. The AER | ||
b. BMP | ||
c. Retinoic acid (RA) | ||
d. Noggin |
a. Pax6 expression is not downregulated in the center of the brain. | ||
b. The migration of ectoderm to the developing face is not initiated. | ||
c. Hox gene constellations in the head are not expressed. | ||
d. The gradient of TGF-β proteins in the face is not established. |
a. Upside-down digits | ||
b. Development of hind-limb structures in forelimb area | ||
c. Webbing and/or no separation of digits | ||
d. Absence of distal limb structures |
a. Upside-down digits | ||
b. Development of hind-limb structures in forelimb area | ||
c. Webbing and/or no separation of digits | ||
d. Absence of distal limb structures |
a. Upside-down digits | ||
b. Development of hind-limb structures in forelimb area | ||
c. Webbing and/or no separation of digits | ||
d. Absence of distal limb structures |
a. Upside-down digits | ||
b. Development of hind-limb structures in forelimb area | ||
c. Webbing and/or no separation of digits | ||
d. Absence of distal limb structures |
a. Autonomous development | ||
b. Pluripotency | ||
c. Differentiation | ||
d. Syncytial development |
a. Paraxial mesoderm | ||
b. Intermediate mesoderm | ||
c. Neural crest | ||
d. Lateral-plate mesoderm |
a. Paraxial mesoderm | ||
b. Intermediate mesoderm | ||
c. Neural crest | ||
d. Lateral-plate mesoderm |
a. Mesonephros | ||
b. Metanephros | ||
c. Pronephros | ||
d. Germinativum |
a. Chorion | ||
b. Archenteron | ||
c. Blastocoel | ||
d. Coelom |
a. Juvenile hormone (JH) | ||
b. 20-hydroxyecdysone | ||
c. Imaginal discs | ||
d. Pupae |
a. Juvenile hormone (JH) | ||
b. 20-hydroxyecdysone | ||
c. Imaginal discs | ||
d. Pupae |
a. Juvenile hormone (JH) | ||
b. 20-hydroxyecdysone | ||
c. Imaginal discs | ||
d. Pupae |
a. The fly would develop as a fertile female. | ||
b. The fly would develop as a fertile male. | ||
c. The fly would develop as a sterile male. | ||
d. The fly would develop as a sterile female. |
a. The mammal would develop as a fertile female. | ||
b. The mammal would develop as a fertile male. | ||
c. The mammal would develop as a sterile male. | ||
d. The mammal would develop as a sterile female. |
a. Drosophila fruit-flies | ||
b. Mammals | ||
c. Most turtles and all crocodilians | ||
d. Crepidula fornicata snails |
a. A pollutant that blocks the transcription of Sry | ||
b. A pollutant that blocks the action of aromatase | ||
c. A pollutant that mimics Sox9 | ||
d. A pollutant that mimics Sex-lethal (Sxl) |
a. Epimorphosis, hydra | ||
b. Epimorphosis, newts | ||
c. Compensatory regeneration, liver | ||
d. Morphallaxis, newts |
a. Epimorphosis, hydra | ||
b. Epimorphosis, newts | ||
c. Compensatory regeneration, liver | ||
d. Morphallaxis, hydra |
a. It involves a reorganization of virtually every organ. | ||
b. It relies on a threshold response with different tissues responding to different concentrations of hormones. | ||
c. It can be inhibited by the removal of the pancreas. | ||
d. The hormones involved in it primarily regulate gene transcription. |
a. Juvenile hormone (JH) | ||
b. 20-hydroxyecdysone | ||
c. Thyroxine | ||
d. PTTH |
a. Turtle eggs must be raised at a fluctuating temperature in order to develop functioning gonads; these turtles were all sterile. | ||
b. The high temperature inactivated the transcription factors involved in initiating gonadal development from the turtles' X and Y chromosomes. | ||
c. The high temperatures stimulated the hormonal induction of female sex development; the turtles were fertile but all female. | ||
d. The turtles' gonads developed normally, but the constant temperature prevented the hormonal induction of secondary sex characteristics, and they could not display mating behaviors. |
a. Duplication and divergence | ||
b. Co-option | ||
c. Dissociation (allometry) | ||
d. Dissociation (heterochrony) |
a. Duplication and divergence | ||
b. Co-option | ||
c. Dissociation (allometry) | ||
d. Dissociation (heterochrony) |
a. Duplication and divergence | ||
b. Co-option | ||
c. Dissociation (allometry) | ||
d. Dissociation (heterochrony) |
a. Physical | ||
b. Phyletic | ||
c. Morphogenetic | ||
d. Heterochronic |
a. Physical | ||
b. Phyletic | ||
c. Morphogenetic | ||
d. Heterochronic |
a. It suggests that there has been a leap in complexity from invertebrates to vertebrates. | ||
b. The formation of the central nervous system and the limb are examples of pathways that exhibit it. | ||
c. When pathways exhibit it, it suggests that there has been only one way in which a particular development process has ever evolved. | ||
d. It occurs in pathways that not only involve the same proteins but use them for the same function. |
a. Pax6 | ||
b. Hox genes | ||
c. Tinman | ||
d. Dax1 |
a. Macroevolutionary events can be studied and explained by examining microevolution. | ||
b. The evolution of complex structures like the eye is more easily understood when the processes of Pax6 pathways, modularity, and correlated progression are explained. | ||
c. The environment, as well as genotype, influences an individual's phenotype, and development is the means through which this relationship is mediated. | ||
d. Homologous genes have been found in very disparate, distantly related organisms. |
a. The early stage, because changes during that time will dramatically alter the embryo and create non-viable phenotypes. | ||
b. The early stage, because changes during that time are reversed or halted by developmental-repair factors. | ||
c. The middle stage, because changes during that time will affect processes of global induction and organogenesis. | ||
d. The late stage, because changes during that time will only disrupt the normal development of tissues that have already been differentiated. |
a. Organisms that display modular growth are those that are still in existence today, while those without it only exist in the fossil record. | ||
b. Because portions of the body are somewhat independent from one another, changes can alter one portion without affecting the entire organism. | ||
c. Because dramatic evolutionary changes can only occur when several modules are altered, genes that are expressed globally are the likeliest evolutionary candidates. | ||
d. Modularity is what allows for the sequestration of imaginal discs and the evolution of metamorphosis in insects. |
a. Physical | ||
b. Phyletic | ||
c. Morphogenetic | ||
d. Heterochronic |
a. An increase in the number of water fleas (Daphnia) with large head helmets | ||
b. A higher rate of early hatching in treefrog embryos | ||
c. A reduction in the number of insects entering diapause | ||
d. A change in the number of parthenogenetic vs. sexual aphids |
a. Snails exhibiting "imposex" | ||
b. Frogs exhibiting sex abnormalities | ||
c. Salmon exhibiting an inability to develop from parr (freshwater form) to smolt (saltwater form) | ||
d. Birds exhibiting beak abnormalities and soft eggshells |
a. Snails exhibiting "imposex" | ||
b. Frogs exhibiting sex abnormalities | ||
c. Salmon exhibiting an inability to develop from parr (freshwater form) to smolt (saltwater form) | ||
d. Birds exhibiting beak abnormalities and soft eggshells |
a. They would all be female. | ||
b. They would not develop functional abdomens. | ||
c. They would have a small sac behind their mantle, but it would not function as a light organ. | ||
d. They would have neither a light organ nor a sac designed to house one. |
a. In persistent ponds, tadpoles grow at faster rates and metamorphose sooner. | ||
b. In ponds that begin drying up, tadpoles metamorphose into larger juveniles. | ||
c. In ponds that begin drying up, tadpoles increase their assimilation efficiency of algae to speed up metamorphosis. | ||
d. In persistent ponds, tadpoles grow at normal rates with only a single phenotype and metamorphose later. |
a. Overcrowding | ||
b. Increasing water temperature | ||
c. Decreasing oxygen concentration | ||
d. Proximity to bottom (increasing shallowness) |
a. Retinoic acid (RA). | ||
b. Quinine. | ||
c. Ethanol (alcohol). | ||
d. Caffeine. |
a. Molts (from instar to instar vs. to pupa or eclosion) | ||
b. The development of queen bees and ants | ||
c. The development of short-winged or long-winged morphs in locusts | ||
d. The switch between parthenogenetic and sexual forms in female aphids |
a. The development of eyespots in different morphs of African butterflies | ||
b. The development of queen bees and ants | ||
c. The development of light-winged and dark-winged morphs of Pieris and Colias butterflies (the cabbage whites and sulphurs) | ||
d. The switch between parthenogenetic and sexual forms in female aphids |
a. These traits are caused by the presence of trout predators. | ||
b. These traits are heritable. | ||
c. Chub with these traits are eaten less. | ||
d. Both A and C |
a. Snails exhibiting "imposex" | ||
b. Frogs exhibiting sex abnormalities | ||
c. Salmon exhibiting an inability to develop from parr (freshwater form) to smolt (saltwater form) | ||
d. Birds exhibiting beak abnormalities and soft eggshells |