
The mouse S‐antigen gene
Author(s) -
TSUDA Masahiko,
KIKUCHI Takanobu,
YAMAKI Kunihiko,
SHINOHARA Toshimichi
Publication year - 1991
Publication title -
european journal of biochemistry
Language(s) - English
Resource type - Journals
eISSN - 1432-1033
pISSN - 0014-2956
DOI - 10.1111/j.1432-1033.1991.tb21053.x
Subject(s) - gene , antigen , biology , genetics
We have characterized a gene for mouse S‐antigen and compared its sequence with that of corresponding human and two recently published Drosophila S‐antigen genes. The mouse S‐antigen gene was approximately 50 kbp in length and consisted of 16 exons and 15 introns. The length of most exons was less than 100 bp and the smallest one was only 10 bp. In contrast, the length of most introns was larger than 2 kbp and the gene consisted of 97% intron and 3% exon. Both splice sites for donor and accepter were in good agreement with the GT/AG rule. S‐antigen genes in human and mouse were highly conserved. In contrast, genes for the Drosophila 49‐kDa arrestin homolog and arrestin consist of three introns and four exons and two introns and three exons, respectively. The 5′‐flanking region of the mouse S‐antigen gene, approximately 1.0 kbp long, had no regulatory elements for transcription such as the TATA, CAAT and GC boxes, while a Drosophila arrestin gene has TATA and CAAT boxes. Interestingly, the 5′‐flanking region of the mouse gene had promoter activity in an in vitro transcription assay using a nuclear extract of rat brain. A major transcription start site was found at 387 bp upstream from the translation start codon ATG in mouse. From our results, and those of others, we suggest that the S‐antigen gene has evolved from a comman ancestor gene by either insertion or deletion of introns. Such an alteration of gene structure may have played a role in the evolution of the S‐antigen.