Abstract

Amelogenin, the major enamel matrix protein in tooth development, has been demonstrated to play a significant role in tooth enamel formation. Previous studies have identified the alternative splicing of amelogenin in many mammalian vertebrates as one mechanism for amelogenin heterogeneous expression in teeth. While amelogenin and its splicing forms in mammalian vertebrates have been cloned and sequenced, the amelogenin gene, especially its splicing forms in non-mammalian species, remains largely unknown. To better understand the mechanism underlying amelogenin evolution, we previously cloned and characterized an amelogenin gene sequence from a squamate, the green iguana. In this study, we employed RT-PCR to amplify the amelogenin gene from the black spiny-tailed iguana Ctenosaura similis teeth, and discovered a novel splicing form of the amelogenin gene. The transcript of the newly identified iguana amelogenin gene (named C. Similis-T2L) is 873 nucleotides long encoding an expected polypeptide of 206 amino acids. The C. Similis-T2L contains a unique exon denominated exon X, which is located between exon 5 and exon 6. The C. Similis-T2L contains 7 exons including exon 1, 2, 3, 5, X, 6, and 7. Analysis of the secondary and tertiary structures of T2L amelogenin protein demonstrated that exon X has a dramatic effect on the amelogenin structures. This is the first report to provide definitive evidence for the amelogenin alternative splicing in non-mammalian vertebrates, revealing a unique exon X and the splicing form of the amelogenin gene transcript in Ctenosaura similis.

Highlights

  • As the major enamel matrix protein in tooth development, amelogenin has been demonstrated to play a significant role in tooth enamel formation [1,2,3]

  • We further report the identification of a novel amelogenin splicing form consisting of 7 exons with a unique exon X in the black spiny-tailed iguana Ctenosaura similis

  • We have demonstrated the heterogeneous amelogenin expression in the black spiny-tailed iguana tooth organs using western blot and immunohistochemistry, discovered for the first time the alternative splicing of amelogenin gene in non-mammalian vertebrate by employing RT-PCR and sequencing analysis

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Summary

Introduction

As the major enamel matrix protein in tooth development, amelogenin has been demonstrated to play a significant role in tooth enamel formation [1,2,3]. It has been reported that mammalian amelogenin exhibits heterogeneity in tooth organs with different isoforms playing different roles in enamel formation [4,7,9,10,11,12,18,19,20,21]. Mammalian amelogenin and its alternative splicing forms have been characterized, splicing forms of amelogenin gene and their functions in non-mammalian species remain largely unknown. To explore the mechanism underlying the enamel microstructure difference among mammalian and nonmammalian vertebrates, and amelogenin evolution, we previously cloned a full-length amelogenin gene and characterized the enamel formation in tooth organs from green iguana. We further report the identification of a novel amelogenin splicing form consisting of 7 exons with a unique exon X in the black spiny-tailed iguana Ctenosaura similis

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