Semaphorins were initially described as a family of repulsive guidance
molecules in embryonal development. Their basic structure consists of
an N-terminal signal sequence, the defining semaphorin domain of appr
oximately 500 amino acids, an Ig-like domain, and a variable carboxy-t
erminus. We recently described a viral semaphorin homologue encoded by
the alcelaphine herpesvirus type 1. Less conserved, truncated homolog
ues were also identified in poxviruses. Here we describe new human and
murine semaphorin homologues. The respective genes were cloned and se
quenced, and they were termed H-Sema-L and M-Sema-L (HGMW-approved sym
bols SEMAL and Semal, respectively). A multiply spliced mRNA of 3.2 kb
is expressed in human placenta, spleen, thymus, and gonadal tissue. H
-Sema-L maps to chromosome 15q22.3-q23 and M-Sema-L to the homologous
locus 9A3.3-B in the mouse genome. The expression patterns and the pre
sence of related genes in large DNA viruses suggest that this new sema
phorin has a relevant function in the immune system. (C) 1998 Academic
Press