Bailly Xavier, Vanin Stefano, Chabasse Christine, Mizuguchi Kenji, Vinogradov Serge N
Station Biologique de Roscoff, 29680, Roscoff, France.
BMC Evol Biol. 2008 Sep 2;8:244. doi: 10.1186/1471-2148-8-244.
Hemerythrins, are the non-heme, diiron binding respiratory proteins of brachiopods, priapulids and sipunculans; they are also found in annelids and bacteria, where their functions have not been fully elucidated.
A search for putative Hrs in the genomes of 43 archaea, 444 bacteria and 135 eukaryotes, revealed their presence in 3 archaea, 118 bacteria, several fungi, one apicomplexan, a heterolobosan, a cnidarian and several annelids. About a fourth of the Hr sequences were identified as N- or C-terminal domains of chimeric, chemotactic gene regulators. The function of the remaining single domain bacterial Hrs remains to be determined. In addition to oxygen transport, the possible functions in annelids have been proposed to include cadmium-binding, antibacterial action and immunoprotection. A Bayesian phylogenetic tree revealed a split into two clades, one encompassing archaea, bacteria and fungi, and the other comprising the remaining eukaryotes. The annelid and sipunculan Hrs share the same intron-exon structure, different from that of the cnidarian Hr.
The phylogenomic profile of Hrs demonstrated a limited occurrence in bacteria and archaea and a marked absence in the vast majority of multicellular organisms. Among the metazoa, Hrs have survived in a cnidarian and in a few protostome groups; hence, it appears that in metazoans the Hr gene was lost in deuterostome ancestor(s) after the radiata/bilateria split. Signal peptide sequences in several Hirudinea Hrs suggest for the first time, the possibility of extracellular localization. Since the alpha-helical bundle is likely to have been among the earliest protein folds, Hrs represent an ancient family of iron-binding proteins, whose primary function in bacteria may have been that of an oxygen sensor, enabling aerophilic or aerophobic responses. Although Hrs evolved to function as O2 transporters in brachiopods, priapulids and sipunculans, their function in annelids remains to be elucidated. Overall Hrs exhibit a considerable lack of evolutionary success in metazoans.
血红细胞素是腕足动物、鳃曳动物和星虫动物中与非血红素、二价铁结合的呼吸蛋白;在环节动物和细菌中也有发现,但其功能尚未完全阐明。
在43种古生菌、444种细菌和135种真核生物的基因组中搜索假定的血红细胞素,发现它们存在于3种古生菌、118种细菌、几种真菌、一种顶复门生物、一种异叶类、一种刺胞动物和几种环节动物中。约四分之一的血红细胞素序列被鉴定为嵌合趋化基因调节因子的N端或C端结构域。其余单结构域细菌血红细胞素的功能仍有待确定。除了氧气运输外,环节动物中血红细胞素的可能功能还包括镉结合、抗菌作用和免疫保护。贝叶斯系统发育树显示分为两个进化枝,一个包含古生菌、细菌和真菌,另一个包含其余的真核生物。环节动物和星虫动物的血红细胞素具有相同的内含子-外显子结构,不同于刺胞动物的血红细胞素。
血红细胞素的系统基因组图谱表明其在细菌和古生菌中出现的情况有限,在绝大多数多细胞生物中明显缺失。在后生动物中,血红细胞素在一种刺胞动物和少数原口动物类群中得以保留;因此,后生动物中血红细胞素基因似乎在辐射对称/两侧对称动物分化后的后口动物祖先中丢失。几种蛭纲血红细胞素中的信号肽序列首次表明其可能定位于细胞外。由于α-螺旋束可能是最早的蛋白质折叠结构之一,血红细胞素代表了一个古老的铁结合蛋白家族,其在细菌中的主要功能可能是作为氧气传感器,实现需氧或厌氧反应。尽管血红细胞素在腕足动物、鳃曳动物和星虫动物中进化为氧气转运蛋白,但其在环节动物中的功能仍有待阐明。总体而言,血红细胞素在后生动物中进化成功的程度相当低。