Analysis of the alternatively spliced isoforms of the human and mouse oct-1
genes, combined with their exon-intron structure, show a high level of evo
lutionary conservation between these two species; The differential expressi
on of several oct-1 isoforms was examined by reverse transcription-polymera
se chain reaction performed on the 3' region of the murine oct-1 cDNA. Vari
ations in the relative levels and patterns of expression of the isoforms we
re found among different tissues. Three novel isoforms originating from the
3'-distal region of oct-1, were isolated and sequenced: Two were derived f
rom testis, and one from myeloma cells. Splicing out of different exons as
revealed in the structure of these isoforms results in reading frameshifts
that presumably lead to the expression of shortened Oct-1 proteins, with di
stinct C-terminal tails. Altogether, six out of the eight known murine oct-
1 isoforms may have distinct C-termini, implying: that these multiple tails
have different functional roles in cellular differentiation and physiology
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