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(Received for publication, April 17, 1997, and in revised form, July 14, 1997)
From the Department of Biological Chemistry, Faculty of
Pharmaceutical Sciences, Teikyo University, Sagamiko,
Kanagawa 199-01, Japan
Galectins are a family of soluble
-galactoside-binding lectins distributed in both vertebrates and
invertebrates and, more recently, found also in fungus. The 32-kDa
galectin isolated from the nematode Caenorhabditis elegans
(Hirabayashi, J., Satoh, M., and Kasai, K. (1992) J. Biol.
Chem. 267, 15485-15490) was the first "tandem repeat-type"
galectin, containing two homologous carbohydrate-binding sites. Here,
we report the structure of the nematode 32-kDa galectin gene. Physical
mapping by yeast artificial chromosome polytene filter hybridization
revealed that the 32-kDa galectin gene is located on chromosome II.
Analysis of the transcript (1.4 kilobases) showed the presence at its
5
-end of a 22-nucleotide trans-spliced leader sequence
(SL1). The entire genomic structure spanning >5 kilobase pairs (kbp),
including the 5
-noncoding region, two intervening sequences (introns 1 and 2), and the 3
-noncoding region, was completely determined by the
combination of genomic polymerase chain reaction and conventional
colony hybridization. Intron 1 was relatively long (2.4 kbp) and was
found to be inserted after the ninth codon (TAC) from the initiation
codon. This position proved to be almost homologous to the conserved
first intron insertion position in the vertebrate galectin genes
(i.e. genes of mammalian galectin-1, -2, and -3 and chick
14-kDa galectin). On the other hand, intron 2 was much shorter (0.6 kbp), and it was inserted into the central region of the second
carbohydrate-binding site. Although such an insertion pattern has never
been observed in the vertebrate galectin genes, it seems to be common
in C. elegans tandem repeat-type galectin genes, as
predicted by the C. elegans genome project (Coulson, A.,
and the C. elegans Genome Consortium (1996) Biochem.
Soc. Trans. 24, 289-291). Based on extensive sequence comparison, the origin and molecular evolution of the tandem
repeat-type galectins are discussed.
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