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Question 1: You want to identify genes on chromosome 2 that control the size of eyes in flies.
Flies can survive without eyes. You have balancers for chromosome 2: CyO (recessive lethal,
dominant curly wings) and DTS (dominant temperature sensitive).
Propose a screen:
Step 1: mutagenize males (+/+). This doesn't matter, but usually we mutagenize male. What are
the next steps?
Question 2: You want to identify genes on the X chromosome that control the size of the eyes
in flies. Flies can survive without eyes. You have balancers for the X chromosome: FM6, which
has dominant Bar eye phenotype, and FM0, which has dominant yellow body phenotype.
Propose a screen:
Step 1: mutagenize female (X+/X+) - This accelerates the screen step. What are the next steps?
Question 3: You want to identify maternal effect genes on chromosome 2 (for example, genes
that regulate mRNA deposition from mother's follical cells into eggs). Often time, when you
disrupt a maternal effect gene, the embryos will die during development.
Propose a screen:
Step 1: mutagenize males (+/+). This doesn't matter, but usually we mutagenize male. What are
the next steps?
Compare and contrast the three examples:
1) In which of the screens above, will you find mutants whose mutation is in non-essential
zygotic genes?
2) In which of the screens above, will you find mutants whose mutation is in X-linked
genes? In this case, should you mutagenize males or females?
3) In which of the screens above, will you find mutants whose mutation is in maternal effect
genes? What is the difference between this screen and the screen in question 1?
How would you deduce the complementation groups if you have two heterozygous flies, one
heterozygous for b1 and the other, heterozygous for b2?