Xi Yang, Obara Masanobu, Ishida Yuji, Ikeda Shino, Yoshizato Katsutoshi
Laboratory of Developmental Biology and Hiroshima University 21st Century COE Program for Advanced Radiation Casualty Medicine, Department of Biological Science, Hiroshima University, 1-3-1 Kagamiyama, Higashihiroshima, Japan.
Gene. 2007 Aug 15;398(1-2):94-102. doi: 10.1016/j.gene.2007.01.040. Epub 2007 May 6.
Cytoglobin (Cygb), a recently discovered vertebrate cytoplasmic heme-binding globin, is considered to be in a clade with vertebrate myoglobin (Mb), which is exclusively distributed in the cytoplasm of cardiac and skeletal muscles as an oxygen storage protein. GenBank databases (NCBI and JGI) and gene synteny analyses showed the absence of the Mb gene (mb) in two anuran amphibians, Xenopus laevis and X. tropicalis. Here we conducted comparative studies on the gene expression and tissue distribution of Cygb and Mb in anuran and reptilian tissues. Cygb and Mb genes were cloned from a reptile, iguana (Iguana iguana). Two types of cygb (cygb-1 and -2) were cloned, with lengths of 1066 and 1034 bp, and 196 and 193 amino acid residues, respectively. Their nucleotide and amino acid sequence identities were 90 and 87%, respectively. The Mb gene covered 1416 bp with an open reading frame of 465 bp, giving rise to a 154 amino acid protein. The distal ligand-binding histidine at E7, the proximal heme-binding histidine at F8, and the phenylalanine residue at CD1 were conserved in Mb and Cygb. The nucleotide and amino acid sequence identity of I. iguana cygb-1 and cygb-2 against X. laevis cygb were approximately 67% and 65%, respectively. RT-PCR demonstrated that X. laevis cygb was uniquely expressed in the heart and skeletal muscles, and faintly in the liver and spleen, which was quite contrasted with Iguana and the other vertebrates, where mb is exclusively expressed in the heart and skeletal muscles. Immunohistochemical analyses showed the distribution of Cygb in the cytoplasm of skeletal muscle cells. Interestingly, Cygb in the heart was localized in the nuclei. Considering the absence of mb in the Anura, we hypothesize that Cygb in muscle cells of anurans compensates for the lack of Mb for the storage and intracellular transportation of oxygen.
细胞珠蛋白(Cygb)是一种最近发现的脊椎动物细胞质血红素结合珠蛋白,被认为与脊椎动物肌红蛋白(Mb)同属一个进化枝,肌红蛋白作为一种氧储存蛋白仅分布于心肌和骨骼肌的细胞质中。GenBank数据库(NCBI和JGI)以及基因共线性分析表明,在两种无尾两栖动物非洲爪蟾和热带爪蟾中不存在肌红蛋白基因(mb)。在此,我们对无尾两栖动物和爬行动物组织中细胞珠蛋白和肌红蛋白的基因表达及组织分布进行了比较研究。从一种爬行动物鬣蜥(Iguana iguana)中克隆了细胞珠蛋白和肌红蛋白基因。克隆出了两种类型的细胞珠蛋白(cygb - 1和 - 2),长度分别为1066和1034 bp,氨基酸残基数分别为196和193个。它们的核苷酸和氨基酸序列同一性分别为90%和87%。肌红蛋白基因覆盖1416 bp,开放阅读框为465 bp,产生一个154个氨基酸的蛋白质。在肌红蛋白和细胞珠蛋白中,E7位的远端配体结合组氨酸、F8位的近端血红素结合组氨酸以及CD1位的苯丙氨酸残基是保守的。鬣蜥的cygb - 1和cygb - 2与非洲爪蟾细胞珠蛋白的核苷酸和氨基酸序列同一性分别约为67%和65%。逆转录 - 聚合酶链反应(RT - PCR)表明,非洲爪蟾细胞珠蛋白仅在心脏和骨骼肌中表达,在肝脏和脾脏中表达较弱,这与鬣蜥和其他脊椎动物形成鲜明对比,在这些动物中肌红蛋白仅在心脏和骨骼肌中表达。免疫组织化学分析显示细胞珠蛋白分布于骨骼肌细胞的细胞质中。有趣的是,心脏中的细胞珠蛋白定位于细胞核中。考虑到无尾目动物中不存在肌红蛋白基因,我们推测无尾目动物肌肉细胞中的细胞珠蛋白可弥补肌红蛋白在氧储存和细胞内运输方面的缺失。