4.6 Article

Shell Biosynthesis and Pigmentation as Revealed by the Expression of Tyrosinase and Tyrosinase-like Protein Genes in Pacific Oyster (Crassostrea gigas) with Different Shell Colors

Journal

MARINE BIOTECHNOLOGY
Volume 23, Issue 5, Pages 777-789

Publisher

SPRINGER
DOI: 10.1007/s10126-021-10063-2

Keywords

Tyr; Typ-2; Crassostrea gigas; Pigmentation; Biosynthesis

Funding

  1. National Natural Science Foundation of China [31772843, 31972789]
  2. Earmarked Fund for Agriculture Seed Improvement Project of Shandong Province [2020LZGC016]
  3. Industrial Development Project of Qingdao City [20-3-4-16-nsh]

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Through extensive multi-omics data mining, two key tyrosinase genes involved in shell pigmentation were identified in Pacific oyster Crassostrea gigas, with distinct expression patterns in black and white shell color oysters. The study suggests that Tyr gene may be involved in shell pigmentation, while Typ-2 gene plays critical roles in both the formation of shell prismatic layer and shell pigmentation. Typ-2 gene is also likely to be involved in the initial non-calcified shell of trochophores.
The widely recognized color polymorphisms of molluscan shell have been appreciated for hundreds of years by collectors and scientists, while molecular mechanisms underlying shell pigmentation are still poorly understood. Tyrosinase is a key rate-limiting enzyme for the biosynthesis of melanin. Here, we performed an extensive multi-omics data mining and identified two tyrosinase genes, including tyrosinase and tyrosinase-like protein 2 (Tyr and Typ-2 respectively), in the Pacific oyster Crassostrea gigas, and investigated the expression patterns of tyrosinase during adults and embryogenesis in black and white shell color C. gigas. Tissue expression analysis showed that two tyrosinase genes were both specifically expressed in the mantle, and the expression levels of Tyr and Typ-2 in the edge mantle were significantly higher than that in the central mantle. Besides, Tyr and Typ-2 genes were black shell-specific compared with white shell oysters. In situ hybridization showed that strong signals for Tyr were detected in the inner surface of the outer fold, whereas positive signals for Typ-2 were mainly localized in the outer surface of the outer fold. In the embryos and larvae, the high expression of Tyr mRNA was detected in eyed-larvae, while Typ-2 mRNA was mainly expressed at the trochophore and early D-veliger. Furthermore, the tyrosinase activity in the edge mantle was significantly higher than that in the central mantle. These findings indicated that Tyr gene may be involved in shell pigmentation, and Typ-2 is more likely to play critical roles not only in the formation of shell prismatic layer but also in shell pigmentation. In particular, Typ-2 gene was likely to involve in the initial non-calcified shell of trochophores. The work provides valuable information for the molecular mechanism study of shell formation and pigmentation in C. gigas.

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