Gupta R S
Department of Biochemistry, McMaster University, Hamilton, Ontario, Canada.
Mol Biol Evol. 1995 Nov;12(6):1063-73. doi: 10.1093/oxfordjournals.molbev.a040281.
The heat shock protein (Hsp) sequences, because of their ubiquity and high degree of conservation, provide useful models for phylogenetic analysis. In this paper I have carried out a global alignment of all available sequences (a total of 31) for the 90-kD heat shock protein (Hsp90) family. The minimum amino acid identity that is seen between presently known Hsp90 homologs is about 40% over the entire length, indicating that it is a highly conserved protein. Based on the alignment, a number of signature sequences that either are distinctive of the Hsp90 family or that distinguish between the cytosolic and the endoplasmic reticular forms of Hsp90 have been identified. Detailed phylogenetic analyses based on Hsp90 sequences reported here strongly indicate that the cytosolic and the endoplasmic reticulum (ER) resident forms of Hsp90 constitute paralogous gene families which arose by a gene duplication event that took place very early in the evolution of eukaryotic cells. A minimum of two additional gene duplication events, which took place at a later time, are required to explain the presence of two different forms of Hsp90 that are found in fungi and vertebrate species. In a consensus neighbor-joining bootstrap tree based on Hsp90 sequences, plants and animals species grouped together 989 times of 1,000 (a highly significant score), indicating a closer relationship between them as compared to fungi. A closer affiliation of plant and animal species was also observed in the maximum-parsimony tree, although the relationship was not significantly supported by this method. A survey of the recent literature on this subject indicates that depending on the protein sequence and the methods of phylogenetic analysis, the animal species are indicated as closer relatives to either plants or fungi with significant statistical support for both topologies. Thus the relationship among the animal, plant, and fungi kingdoms remains an unresolved issue at the present time.
热休克蛋白(Hsp)序列因其普遍性和高度保守性,为系统发育分析提供了有用的模型。在本文中,我对90-kD热休克蛋白(Hsp90)家族的所有可用序列(共31个)进行了全局比对。目前已知的Hsp90同源物之间在全长范围内的最小氨基酸同一性约为40%,这表明它是一种高度保守的蛋白质。基于该比对,已鉴定出一些Hsp90家族特有的或区分Hsp90胞质形式和内质网形式的特征序列。基于本文报道的Hsp90序列进行的详细系统发育分析强烈表明,Hsp90的胞质形式和内质网(ER)驻留形式构成了旁系同源基因家族,它们是由真核细胞进化早期发生的基因复制事件产生的。为了解释在真菌和脊椎动物物种中发现的两种不同形式的Hsp90的存在,至少还需要另外两次较晚发生的基因复制事件。在基于Hsp90序列的一致邻接法自展树中,植物和动物物种在1000次中有989次聚在一起(得分非常显著),这表明它们之间的关系比与真菌的关系更密切。在最大简约树中也观察到植物和动物物种有更紧密的联系,尽管这种方法对这种关系的支持并不显著。对近期关于该主题的文献调查表明,根据蛋白质序列和系统发育分析方法,动物物种被表明与植物或真菌是更亲近的亲属,两种拓扑结构都有显著的统计支持。因此,动物、植物和真菌界之间的关系目前仍然是一个未解决的问题。