Molecular characterization of two ferritins of the scallop Argopecten purpuratus and gene expressions in association with early development, immune response and growth rate

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• 作者：Teodoro Coba de la Peñ ; a^a ; ^c ; ¹ ; Claudia B. Cá ; rcamo^a ; ^b ; ¹ ; Marí ; a I. Dí ; az^a ; ^b ; ^d ; Katherina B. Brokordt^a ; ^b ; Federico M. Winkler^a ; ^b ; ^{fwinkler@ucn.cl" class="auth_mail" title="E-mail the corresponding author}
• 关键词：Ferritin ; Argopecten purpuratus ; Iron homoeostasis ; Growth ; Development ; Immunity ; Apfer1 ; Apfer2
• 刊名：Comparative Biochemistry and Physiology Part B: Biochemistry and Molecular Biology
• 出版年：2016
• 出版时间：August 2016
• 年：2016
• 卷：198
• 期：Complete
• 页码：46-56
• 全文大小：2145 K

文摘

Ferritin is involved in several iron homoeostasis processes in molluscs. We characterized two ferritin homologues and their expression patterns in association with early development, growth rate and immune response in the scallop Argopecten purpuratus, a species of economic importance for Chile and Peru. Two ferritin subunits (Apfer1 and Apfer2) were cloned. Apfer1 cDNA is a 792 bp clone containing a 516 bp open reading frame (ORF) that corresponds to a novel ferritin subunit in A. purpuratus. Apfer2 cDNA is a 681 bp clone containing a 522 bp ORF that corresponds to a previously sequenced EST. A putative iron responsive element (IRE) was identified in the 5′-untranslated region of both genes. The deduced protein sequences of both cDNAs possessed the motifs and domains characteristic of functional ferritin subunits. Both genes showed differential expression patterns at tissue-specific and early development stage levels. Apfer1 expression level increased 40-fold along larval developmental stages, decreasing markedly after larval settlement. Apfer1 expression in mantle tissue was 2.8-fold higher in fast-growing than in slow-growing scallops. Apfer1 increased 8-fold in haemocytes 24 h post-challenge with the bacterium Vibrio splendidus. Apfer2 expression did not differ between fast- and slow-growing scallops or in response to bacterial challenge. These results suggest that Apfer1 and Apfer2 may be involved in iron storage, larval development and shell formation. Apfer1 expression may additionally be involved in immune response against bacterial infections and also in growth; and thus would be a potential marker for immune capacity and for fast growth in A. purpuratus.