The amphibian Xenopus laevis is the most primitive vertebrate in which
the major histocompatibility complex (MHC) has been defined at the bi
ochemical, functional, and molecular genetic levels. We previously des
cribed the isolation and characterization of cDNA clones encoding X. l
aevis MHC class II beta chains. In the present study, genomic clones e
ncoding class II beta chains were isolated from X. laevis homozygous f
or the MHC f haplotype, Three class II beta chain genes, designated Xe
la-DAB, Xela-DBB, and Xela-DCB, were identified. Sequence analysis of
these genes showed that Xela-DBB and Xela-DCB correspond to the previo
usly characterized cDNA clones F3 and F8, respectively, whereas Xela-D
AB encodes a third, hitherto unidentified class II beta chain of the M
HC f haplotype. As a representative of X. laevis class II beta chain g
enes, the Xela-DAB gene underwent detailed structural analysis. In add
ition, the nucleotide sequence of Xela-DABf cDNA clones was determined
. The Xela-DAB gene is made up of at least six exons, with an exon-int
ron organization similar to that of a typical mammalian class II beta
chain gene. The 5'-flanking region of the Xela-DAB gene contains trans
criptional control elements known as X1, X2, and Y, but lacks typical
TATA or CCAAT boxes. A notable feature of the X, laevis class II beta
chain genes is that the sizes of the introns are larger than those of
their mammalian counterparts. As assessed by northern blot analysis, t
he three class II beta chain genes had similar expression patterns, wi
th the highest level of transcription detected in the intestine. Ident
ification of the Xela-DAB, -DBB, and -DCB genes is consistent with our
previous observations, which suggested that the MHC of the tetraploid
frog X. laevis is diploidized at the genomic level and contains three
class II beta chain genes per haplotype that cross-hybridize to one a
nother under reduced stringency conditions.