Alternative spliced variants of the alpha-methylacyl-CoA racemase gene and their expression in prostate cancer

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• 作者：Mubiru ; James N. ; Shen-Ong ; Grace L. ; Valente ; Anthony J. ; Troyer ; Dean A.
• 关键词：Prostate cancer ; Alternative splicing ; Racemase ; Fumarate hydratase ; Peroxisome ; Mitochondria ; AMACR ; alpha-methylacyl-CoA racemase ; 5&prime ; -RACE ; 5&prime ; rapid amplification of cDNA ends ; PSA ; prostate-specific antigen ; MMLV ; Moloney murine leukemia vi
• 刊名：Gene
• 出版年：2004
• 出版时间：February 18, 2004
• 年：2004
• 卷：327
• 期：1
• 页码：89-98
• 全文大小：771 K

文摘

Alpha-methyacyl-CoA racemase (AMACR), a mitochondrial and peroxisomal enzyme essential in lipid metabolism, is overexpressed in prostate cancer. Two different AMACR transcripts (designated IA and IIA), each derived from five exons, have been reported. AMACR IA, the most abundant form, encodes a 382-amino acid protein (M_w 42 kDa, pI 6.07). AMACR IIA contains an alternative fifth exon that has extensive homology to the human fumarate hydratase (FH) and encodes a 288-amino acid protein (M_w 32 kDa, pI 9.6). Here we report additional variants of IA and IIA whereby the transcripts lack exon 3 and are designated as IB (M_w 22 kDa, pI 10.31) and IIB (M_w 31 kDa, pI 9.44). Due to a frameshift, the alternative fifth exon in the IIA transcript encodes a polypeptide that differs from FH. In contrast, the IIB transcript, generated as a result of the dual alternative splicing events, encodes a polypeptide homologous with a highly conserved region of FH. We also identified a shorter variant form of IIA (IIAs, M_w 28 kDa, pI 9.65), which lacks the 5′ half of the alternative fifth exon. The carboxy termini of all five gene products differ as a result of the alternative splicing events. In prostate tumor tissues that overexpressed AMACR, both the A and B forms were overexpressed, suggesting coregulation. Only the predominant AMACR IA has an acidic pI and contains the previously identified peroxisomal targeting signal (PTS1) peptide, while the other four variants are basic proteins that lack the peroxisomal targeting signal peptide. These observations have implications for the cellular localization and function of these AMACR variants.