What are zygotic genes, and when are their gene products made?
14. Genetic Control of Development
Developmental Patterning Genes
- Open Question
- Open Question
Does the maternal genotype contain zygotic genes?
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Compare and contrast the specification of segmental identity in Drosophila with that of floral organ specification in Arabidopsis. What is the same in this process, and what is different?
- Open Question
List the main classes of zygotic genes. What is the function of each class of these genes?
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Actinomycin D is a drug that inhibits the activity of RNA polymerase II. In the presence of actinomycin D, early development in many vertebrate species, such as frogs, can proceed past the formation of a blastula, a hollow ball of cells that forms after early cleavage divisions, but development ceases before gastrulation (the stage at which cell layers are established). What does this tell you about maternal versus zygotic gene activity in early frog development?
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You observe that a particular gene is being transcribed during development. How can you tell whether the expression of this gene is under transcriptional or translational control?
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The homeotic mutation Antennapedia causes mutant Drosophila to have legs in place of antennae and is a dominant gain-of-function mutation. What are the properties of such mutations? How does the Antennapedia gene change antennae into legs?
- Open QuestionThe bicoid gene is a coordinate maternal–effect gene.If loss of bicoid function in the egg leads to lethality during embryogenesis, how are females homozygous for bicoid produced? What is the phenotype of a male homozygous for bicoid loss-of-function alleles?
- Open QuestionThe bicoid gene is a coordinate maternal–effect gene.A female that is homozygous for a loss-of-function bicoid allele is mated to a wild-type male. What are the phenotypes of their progeny?
- Open Question
The bicoid gene is a coordinate maternal–effect gene.
A female Drosophila heterozygous for a loss-of function bicoid allele is mated to a male that is heterozygous for the same allele. What are the phenotypes of their progeny? - Open Question
The Drosophila homeotic mutation spineless aristapedia (ssᵃ) results in the formation of a miniature tarsal structure (normally part of the leg) on the end of the antenna. What insight is provided by (ssᵃ) concerning the role of genes during determination?
- Open QuestionGiven that maternal Bicoid activates the expression of hunchback (see Figure 18.7), what would be the consequence of adding extra copies of the bicoid gene by transgenic means to a wild-type female with two copies, thus creating a female fly with three or four copies of the bicoid gene? How would hunchback expression be altered? What about the expression of other gap genes and pair-rule genes?
- Open Question
Embryogenesis and oncogenesis (generation of cancer) share a number of features including cell proliferation, apoptosis, cell migration and invasion, formation of new blood vessels, and differential gene activity. Embryonic cells are relatively undifferentiated, and cancer cells appear to be undifferentiated or dedifferentiated. Homeotic gene expression directs early development, and mutant expression leads to loss of the differentiated state or an alternative cell identity. M. T. Lewis [(2000). Breast Can. Res. 2:158–169] suggested that breast cancer may be caused by the altered expression of homeotic genes. When he examined 11 such genes in cancers, 8 were underexpressed while 3 were overexpressed compared with controls. Given what you know about homeotic genes, could they be involved in oncogenesis?
- Open QuestionWhat phenotypes do you expect in flies homozygous for loss-of-function mutations in the following genes: Krüppel, odd-skipped, hedgehog, and Ultrabithorax?
- Open Question
The specification of the anterior–posterior axis in Drosophila embryos is initially controlled by various gene products that are synthesized and stored in the mature egg following oogenesis. Mutations in these genes result in abnormalities of the axis during embryogenesis. These mutations illustrate maternal effect. How do such mutations vary from those produced by organelle heredity? Devise a set of parallel crosses and expected outcomes involving mutant genes that contrast maternal effect and organelle heredity.