The major splice variant of human 5-aminolevulinate synthase-2 contributes significantly to erythroid heme biosynthesis

• Published in: The international journal of biochemistry & cell biology 2004-02, Vol.36 (2), p.281-295
• Main Authors: Cox, Timothy C, Sadlon, Timothy J, Schwarz, Quenten P, Matthews, Christopher S, Wise, Phillip D, Cox, Liza L, Bottomley, Sylvia S, May, Brian K
• Format: Article
• Language: English
• Subjects: 5-Aminolevulinate synthase; 5-Aminolevulinate Synthetase - biosynthesis; 5-Aminolevulinate Synthetase - genetics; Alternative Splicing; Amino Acid Sequence; Animals; Base Sequence; Catalysis; Catalytic activity; Codon; COS Cells; Electrophoresis, Polyacrylamide Gel; Erythrocytes - metabolism; Exons; Genetic Vectors; Green Fluorescent Proteins; Heme - biosynthesis; Hemoglobins - chemistry; Humans; Luminescent Proteins - metabolism; Microscopy, Fluorescence; Mitochondria - metabolism; Mitochondrial import; Molecular Sequence Data; Polymerase Chain Reaction; Protein Isoforms; Protein Structure, Tertiary; Reticulocytes - metabolism; Ribonucleases - metabolism; RNA, Messenger - metabolism; Signal sequence; Splice variant; Subcellular Fractions - metabolism; Succinate-CoA Ligases - chemistry; Two-Hybrid System Techniques
• ISSN: 1357-2725; 1878-5875
• DOI: 10.1016/S1357-2725(03)00246-2

The initial step of the heme biosynthetic pathway in erythroid cells is catalyzed by an erythroid-specific isoform of 5-aminolevulinate synthase-2 (ALAS2). Previously, an alternatively spliced mRNA isoform of ALAS2 was identified although the functional significance of the encoded protein was unknown. We sought to characterize the contribution of this ALAS2 isoform to overall erythroid heme biosynthesis. Here, we report the identification of three novel ALAS2 mRNA splice isoforms in addition to the previously described isoform lacking exon 4-derived sequence. Quantitation of these mRNAs using ribonuclease protection experiments revealed that the isoform without exon 4-derived sequence represents ∼35–45% of total ALAS2 mRNA while the newly identified transcripts together represent ∼15%. Despite the significant amounts of these three new transcripts, their features indicate that they are unlikely to substantially contribute to overall mitochondrial ALAS2 activity. In contrast, in vitro studies show that the major splice variant (lacking exon 4-encoded sequence) produces a functional enzyme, albeit with slightly reduced activity and with affinity for the ATP-specific, beta subunit of succinyl CoA synthase, comparable to that of mature ALAS2. It was also established that the first 49 amino acids of the ALAS2 pre-protein are necessary and sufficient for translocation across the mitochondrial inner membrane and that this process is not affected by the absence of exon 4-encoded sequence. We conclude that the major splice isoform of ALAS2 is functional in vivo and could significantly contribute to erythroid heme biosynthesis and hemoglobin formation.