The metallothionein genes of Mytilus galloprovincialis: Genomic organization, tissue expression and evolution

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• 作者：Serena Aceto ; ^a ; ^{serena.aceto@unina.it} ; Giulia Formisano^a ; Francesca Carella^a ; Gionata De Vico^a ; Luciano Gaudio^a
• 关键词：Metallothionein genes ; Mytilus galloprovincialis ; Real-Time PCR ; Introns ; Molecular evolution
• 刊名：Marine Genomics
• 出版年：2011
• 出版时间：March 2011
• 年：2011
• 卷：4
• 期：1
• 页码：61-68
• 全文大小：1258 K

文摘

Recently, increasing interest has been directed to the study of metallothioneins (MTs), which are small proteins that are able to bind metal ions. The induction of MT synthesis after exposure to metal or other environmental contaminants in a large number of aquatic invertebrates makes these proteins good biomarkers in water monitoring programs. Within bivalves, the species Mytilus galloprovincialis and Mytilus edulis represent model organisms for these types of studies, as well as for molecular studies regarding the expression and characterization of MT encoding genes.

In the present paper, we focused on the genomic characterization, evolutionary, and tissue-expression analyses of the MT-10, MT-10 Intronless, and MT-20 genes in M. galloprovincialis. The comparison of the genomic sequences showed the presence of long nucleotide stretches within the introns of the MT genes that are conserved between M. galloprovincialis and M. edulis. These non-coding conserved sequences may contain regulatory motifs. Real-Time RT-PCR experiments revealed that, at the basal conditions, the MT-10 and MT-10 Intronless genes are expressed at levels considerably higher than the MT-20 gene, mainly in the digestive gland and gill tissue. The strong induction of the MT-20 gene expression detected in a field-collected sample is associated with the up-regulation of both the MT-10 and MT-10 Intronless genes. Evolutionary analysis revealed signals of localized positive selection that, together with the tissue-expression data, support a possible functional diversification between the MTs encoded by the MT-10 and MT-10 Intronless genes.