Murine heme oxygenase-2 (HO-2) cDNA sequences were determined through
the assembly of mouse expressed sequence tag (EST) sequences using the
rat NO-2 sequence as a template. The sequence analysis revealed two m
RNA isoforms, probably arising through alternative splicing, which dif
fered in their 5'-untranslated region (UTR), and were named HO-2a and
HO-2b. One EST sequence included an extended 3'-UTR and suggested ther
e may be a choice of poly-adenylation (poly-A) signal sequence. Revers
e transcriptase polymerase chain reaction (PCR) suggested that HO-2a m
RNA may be specifically expressed in the testis, while HO-2b mRNA was
present in all tissues analysed. Furthermore, HO-2a and HO-2b transcri
pts were both found to include the extended 3'-UTR, but these transcri
pts were detected only in the testis. Northern analysis of a greater r
ange of tissues confirmed the testis-specific expression of HO-2a mRNA
and suggested that the transcripts which included the extended 3'-UTR
were a small minority of the NO-2 mRNA population. These alternative
murine HO-2 transcripts suggest that mechanisms such as mRNA transport
, translational efficiency or mRNA turnover may be implicated in the r
egulation of HO-2 gene expression, most notably in the testis. (C) 199
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