We have devised a scheme that facilitates rapid screening for duplicat
ions of essential loci. Our scheme takes advantage of the lev-1(x22) m
utation, which confers resistance in a recessive fashion to the potent
anthelmintic levamisole. We have tested our methodology by recovering
two gamma ray induced duplications of let-56, the first essential gen
e to the left of unc-22. One of the duplications is attached to the fo
urth chromosome. The other duplication is attached to the X chromosome
. This duplication contains a functional copy of the unc-22 gene, as w
ell as functional copies of several essential loci adjacent to unc-22.
Results we have obtained during analysis of this duplication are comp
atible with the notion that the copy of the unc-22 gene located on the
duplication is subject to X chromosome dosage compensation.