Immunoglobulin genes are generated during differentiation of B lymphocytes by joining
gene segments. A mouse pre-B cell contains a functional immunoglobulin heavy-chain gene,
but no light-chain gene. Although there is only one heavy-chain locus, there are two lightchain
loci: κ and λ.It has been reported that κ loci in the germ-line configuration are never
(in man) or very rarely (in the mouse) present in cells with functionally rearranged λ-chain
genes. Two explanations have been proposed to explain this: (a) the ordered rearrangement
theory, which postulates that light-chain gene rearrangement in the pre-B cell is first
attempted at the κ locus, and that only upon failure to produce a functional κ chain is there
an attempt to rearrange the λ locus; and (b) the stochastic theory, which postulates that
rearrangement at the λ locus proceeds at a rate that is intrinsically much slower than that at
the κ locus. We show here that λ-chain genes are generated whether or not the κ locus has
lost its germ-line arrangement, a result that is compatible only with the stochastic theory.