Chen Bin, Zhong Daibin, Monteiro Antónia
School of Life Sciences, Southwest University, Chongqing 400715, P.R. China.
BMC Genomics. 2006 Jun 17;7:156. doi: 10.1186/1471-2164-7-156.
HSP90 proteins are essential molecular chaperones involved in signal transduction, cell cycle control, stress management, and folding, degradation, and transport of proteins. HSP90 proteins have been found in a variety of organisms suggesting that they are ancient and conserved. In this study we investigate the nuclear genomes of 32 species across all kingdoms of organisms, and all sequences available in GenBank, and address the diversity, evolution, gene structure, conservation and nomenclature of the HSP90 family of genes across all organisms.
Twelve new genes and a new type HSP90C2 were identified. The chromosomal location, exon splicing, and prediction of whether they are functional copies were documented, as well as the amino acid length and molecular mass of their polypeptides. The conserved regions across all protein sequences, and signature sequences in each subfamily were determined, and a standardized nomenclature system for this gene family is presented. The proeukaryote HSP90 homologue, HTPG, exists in most Bacteria species but not in Archaea, and it evolved into three lineages (Groups A, B and C) via two gene duplication events. None of the organellar-localized HSP90s were derived from endosymbionts of early eukaryotes. Mitochondrial TRAP and endoplasmic reticulum HSP90B separately originated from the ancestors of HTPG Group A in Firmicutes-like organisms very early in the formation of the eukaryotic cell. TRAP is monophyletic and present in all Animalia and some Protista species, while HSP90B is paraphyletic and present in all eukaryotes with the exception of some Fungi species, which appear to have lost it. Both HSP90C (chloroplast HSP90C1 and location-undetermined SP90C2) and cytosolic HSP90A are monophyletic, and originated from HSP90B by independent gene duplications. HSP90C exists only in Plantae, and was duplicated into HSP90C1 and HSP90C2 isoforms in higher plants. HSP90A occurs across all eukaryotes, and duplicated into HSP90AA and HSP90AB in vertebrates. Diplomonadida was identified as the most basal organism in the eukaryote lineage.
The present study presents the first comparative genomic study and evolutionary analysis of the HSP90 family of genes across all kingdoms of organisms. HSP90 family members underwent multiple duplications and also subsequent losses during their evolution. This study established an overall framework of information for the family of genes, which may facilitate and stimulate the study of this gene family across all organisms.
热休克蛋白90(HSP90)是一类重要的分子伴侣,参与信号转导、细胞周期调控、应激管理以及蛋白质的折叠、降解和运输。HSP90已在多种生物中被发现,这表明它们古老且保守。在本研究中,我们调查了所有生物界32个物种的核基因组以及GenBank中所有可用序列,并探讨了所有生物中HSP90基因家族的多样性、进化、基因结构、保守性和命名。
鉴定出12个新基因和一种新型HSP90C2。记录了它们的染色体定位、外显子剪接以及是否为功能性拷贝的预测,还有其多肽的氨基酸长度和分子量。确定了所有蛋白质序列中的保守区域以及每个亚家族的特征序列,并提出了该基因家族的标准化命名系统。原核生物HSP90同源物HTPG存在于大多数细菌物种中,但不存在于古细菌中,它通过两次基因复制事件进化为三个谱系(A组、B组和C组)。没有一个细胞器定位的HSP90是早期真核生物内共生体的产物。线粒体TRAP和内质网HSP90B分别在真核细胞形成的早期从类厚壁菌门生物中的HTPG A组祖先独立起源。TRAP是单系的,存在于所有动物界和一些原生生物物种中,而HSP90B是并系的,存在于所有真核生物中,但一些真菌物种似乎已经丢失了它。HSP90C(叶绿体HSP90C1和定位未确定的SP90C2)和胞质HSP90A都是单系的,并且通过独立的基因复制从HSP90B起源。HSP90C仅存在于植物界,并在高等植物中复制为HSP90C1和HSP90C2异构体。HSP90A存在于所有真核生物中,并在脊椎动物中复制为HSP90AA和HSP90AB。双滴虫目被确定为真核生物谱系中最基部的生物。
本研究首次对所有生物界的HSP90基因家族进行了比较基因组研究和进化分析。HSP90家族成员在进化过程中经历了多次复制以及随后的丢失。本研究为该基因家族建立了一个总体信息框架,这可能有助于并促进对所有生物中该基因家族的研究。