We recently isolated a human SART3 (hSART3) gene encoding a tumor-rejection
antigen recognized by HLA-A2402-restricted cytotoxic T lymphocytes (CTLs),
The hSART3 was also found to exist as an RNA-binding nuclear protein of un
known biological function. In this study, we cloned and analyzed the homolo
gous mouse SART3 (mSART3) gene in order to understand better the function o
f hSART3, and to aid in establishing animal models of specific immunotherap
y. The cloned 3586-bp cDNA encoded a 962-amino acid polypeptide with high h
omology to hSART3 (80% or 86% identity at the nucleotide or protein level,
respectively). Nonapeptides recognized by the HLA-A2402-restricted CTLs and
all of the RNA-binding motifs were conserved between hSART3 and mSART3. Th
e mSART3 mRNA was ubiquitously expressed in normal tissues, with low level
expression in the liver, heart, and skeletal muscle. It was widely expresse
d in various organs from as early as day 7 of gestation. mSART3 was mapped
to chromosome 5, a syntenic region for human chromosome 12q23-24, and its g
enomic DNA extended over 28-kb and consisted of 19 exons, This information
should be important for studies of the biological functions of the SART3 pr
otein and for the establishment of animal models of specific cancer immunot
herapy.