The human immunoglobulin lambda-like (IGLL) genes, which are homologou
s to the human immunoglobulin lambda (IGL) light chain genes, are expr
essed only in pre-B cells and are involved in B cell development. Thre
e IGLL genes, 14.1, 16.1, and 16.2 are present in humans as opposed to
one, lambda5 (Igll), found in the mouse. To precisely map the locatio
n of the human IGLL genes in relation to each other and to the human I
GL gene locus, at 22q11.1-2, a somatic cell hybrid panel and pulsed fi
eld gel electrophoresis (PFGE) were used. Hybridization with a lambda-
like gene-specific DNA probe to somatic cell hybrids revealed that the
se genes reside on 22q11.2 between the breakpoint cluster region (BCR)
and the Ewing sarcoma breakpoint at 22q12 and that gene 161 was locat
ed distal to genes 14.1 and 16.2. Gene 14.1 was found by PFGE to be pr
oximal to 16.2 by at least 30 kilobases (kb). A 210 kb Not I fragment
containing genes 14.1 and 16.2 is adjacent to a 400 kb Not I fragment
containing the BCR locus, which is just distal to the IGL-C (IGL const
ant region) genes. We have determined that the IGLL genes 14.1 and 16.
2 are approximately 670 kb and 690 to 830 kb distal, respectively, to
the 3'-most IGL-C gene in the IGL gene locus, IGL-C7. We thus show the
first physical linkage of the IGL and the IGLL genes, 14.1 and 16.2.
We discuss the relevance of methylation patterns and CpG islands to ex
pression, and the evolutionary significance of the IGLL gene duplicati
ons. Consistent with the GenBank nomenclature, these human IGLL genes
will be referred to as IGLL1 (14.1), IGLL2 (16.2), and IGLL3 (16.1), r
eflecting their position on chromosome 22, as established by this repo
rt.