Abstract

The sarcolemmal associated proteins (SLAPs) are encoded by multiple mRNAs that are presumably generated by alternative splicing mechanisms. The amino acid sequence of the SLAP1 isoform exhibited 76% identity with TOP(AP), a topographically graded antigen of the chick visual system. The regions of coiled-coil structure including an 11-heptad acidic amphipathic alpha-helical segment was conserved with a major divergence in sequence noted in the hydrophobic C termini predicted to be transmembrane domains in the two polypeptides. The genomic organization of the 3' region of the SLAP gene indicated that SLAP1 and TOP(AP) are generated by alternative splicing mechanisms, which are conserved among mammalian and avian species. SLAP1/TOP(AP) were encoded by 11 exons distributed over a minimum of 35 kilobase pairs of continuous DNA; 9 of the exons were constitutively expressed, and 2 were alternatively spliced. The exons range in size from 60 to 321 base pairs, and the predicted functional domains within the polypeptides were encompassed by single exons. The introns vary from 0.2 to 10 kilobase pairs and conform to consensus dinucleotide splicing signals. Reverse transcriptase-polymerase chain reaction studies demonstrated that alternative exons (IV and X) of SLAP were expressed in a tissue-specific fashion and developmentally regulated. The alternatively spliced exon X, which encodes the putative transmembrane anchor in TOP(AP), and a constitutively expressed exon XI, which encodes the putative transmembrane domain in SLAP, were found to target these polypeptides to membrane structures. The presence and conservation of termination codons in exons X and XI render expression of the two SLAP1/TOP(AP) transmembrane domains mutually exclusive. These data reveal that TOP(AP) and SLAP are alternatively spliced products of a single gene that encodes a unique class of tail-anchored membrane proteins.

Highlights

  • The coiled-coil membrane proteins such as syntaxin, synaptobrevin, and epimorphin are believed to play diverse roles in cell function including membrane fusion, vesicle transport, and neurotransmitter release [1,2,3,4]

  • We undertook studies to determine the genomic organization of the 3Ј region of the SLAP gene, which revealed that mammalian SLAP1 and avian TOPAP are generated by alternative splicing mechanisms that are highly conserved among mammalian and avian species

  • Genomic Organization of the 3Ј Region of the SLAP Gene— Previous studies have identified three SLAP isoforms, SLAP1, SLAP2, and SLAP3, encoded by a single gene mapped to human chromosome 3p14.3–21.2

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Summary

Introduction

The coiled-coil membrane proteins such as syntaxin, synaptobrevin, and epimorphin are believed to play diverse roles in cell function including membrane fusion, vesicle transport, and neurotransmitter release [1,2,3,4]. The genomic organization of the 3؅ region of the SLAP gene indicated that SLAP1 and TOPAP are generated by alternative splicing mechanisms, which are conserved among mammalian and avian species.

Results
Conclusion
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