Endo Hirotoshi, Takagi Yasuaki, Ozaki Noriaki, Kogure Toshihiro, Watanabe Toshiki
Department of Marine Bioscience, Ocean Research Institute, The University of Tokyo, Tokyo, Japan.
Biochem J. 2004 Nov 15;384(Pt 1):159-67. doi: 10.1042/BJ20041052.
The DD4 mRNA of the penaeid prawn Penaeus japonicus was shown previously to be expressed in the epidermis adjacent to the exoskeleton specifically during the post-moult period, when calcification of the exoskeleton took place. The encoded protein possessed a Ca2+-binding site, suggesting its involvement in the calcification of the exoskeleton. In the present study, an additional ORF (open reading frame) of 289 amino acids was identified at the 5' end of the previous ORF. The newly identified part of the encoded protein included a region of approx. 120 amino acids that was highly rich in glutamate residues, and contained one or more Ca2+-binding sites. In an immunohistochemical study, signals were detected within calcified regions in the endocuticular layer of the exoskeleton. Bacterially expressed partial segments of the protein induced CaCO3 crystallization in vitro. Finally, a reverse transcription-PCR study showed that the expression was limited to an early part of the post-moult period, preceding significant calcification of the exoskeleton. These observations argue for the possibility that the encoded protein, renamed crustocalcin (CCN), promotes formation of CaCO3 crystals in the exoskeleton by inducing nucleation.
先前研究表明,日本对虾的DD4 mRNA在蜕皮后外骨骼钙化期间,于紧邻外骨骼的表皮中特异性表达。其编码蛋白具有一个Ca2+结合位点,提示其参与外骨骼钙化过程。在本研究中,在前一个开放阅读框的5'端鉴定出一个额外的289个氨基酸的开放阅读框。新鉴定出的编码蛋白部分包含一个约120个氨基酸的区域,该区域谷氨酸残基高度富集,且含有一个或多个Ca2+结合位点。在免疫组织化学研究中,在外骨骼内皮层的钙化区域检测到信号。该蛋白的细菌表达部分片段在体外诱导了CaCO3结晶。最后,逆转录-PCR研究表明,该基因表达仅限于蜕皮后早期,即外骨骼显著钙化之前。这些观察结果支持这样一种可能性,即该编码蛋白(重新命名为甲壳钙蛋白,CCN)通过诱导成核作用促进外骨骼中CaCO3晶体的形成。