Hendriks L, De Baere R, Van de Peer Y, Neefs J, Goris A, De Wachter R
Departement Biochemie, Universiteit Antwerpen (UIA), Belgium.
J Mol Evol. 1991 Feb;32(2):167-77. doi: 10.1007/BF02515389.
The complete small ribosomal subunit RNA (srRNA) sequence was determined for the red alga Porphyra umbilicalis and the basidiomycete Leucosporidium scottii, representing two taxa for which no srRNA sequences were hitherto known. These sequences were aligned with other published complete srRNA sequences of 58 eukaryotes. Evolutionary trees were reconstructed by a matrix optimization method from a dissimilarity matrix based on sections of the alignment that correspond to structurally conservative areas of the molecule that can be aligned unambiguously. The overall topology of the eukaryotic tree thus constructed is as follows: first there is a succession of early diverging branches, leading to a diplomonad, a microsporidian, a euglenoid plus kinetoplastids, an amoeba, and slime molds. Later, a nearly simultaneous radiation seems to occur into a number of taxa comprising the metazoa, the red alga, the sporozoa, the higher fungi, the ciliates, the green plants, plus some other less numerous groups. Because the red alga diverges late in the evolutionary tree, it does not seem to represent a very primitive organism as proposed on the basis of morphological and 5S rRNA sequence data. Asco- and basidiomycetes do not share a common ancestor in our tree as is generally accepted on the basis of conventional criteria. In contrast, when all alignment positions, rather than the more conservative ones, are used to construct the evolutionary tree, higher fungi do form a monophyletic cluster. The hypothesis that higher fungi and red algae might have shared a common origin has been put forward. Although the red alga and fungi seem to diverge at nearly the same time, no such relationship can be detected. The newly determined sequences can be fitted into a secondary structure model for srRNA, which is now relatively well established with the exception of uncertainties in a number of eukaryote-specific expansion areas. A specific structural model featuring a pseudoknot is proposed for one of these areas.
测定了红藻紫菜和担子菌斯科特利白冬孢酵母完整的小核糖体亚基RNA(srRNA)序列,这两个分类单元此前尚无srRNA序列。这些序列与其他已发表的58种真核生物的完整srRNA序列进行了比对。基于比对中对应于分子结构保守区域且可明确比对的片段构建的差异矩阵,通过矩阵优化方法重建了进化树。由此构建的真核生物树的总体拓扑结构如下:首先是一系列早期分化的分支,通向双滴虫、微孢子虫、眼虫加动基体、变形虫和黏菌。之后,似乎几乎同时辐射分化出多个分类单元,包括后生动物、红藻、孢子虫、高等真菌、纤毛虫、绿色植物以及其他一些数量较少的类群。由于红藻在进化树中分化较晚,它似乎并不像基于形态学和5S rRNA序列数据所提出的那样是一种非常原始的生物。在我们构建的树中,子囊菌和担子菌并不像基于传统标准普遍认为的那样有共同的祖先。相反,当使用所有比对位置而非更保守的位置来构建进化树时,高等真菌确实形成了一个单系类群。有人提出高等真菌和红藻可能有共同起源的假说。尽管红藻和真菌似乎几乎同时分化,但并未检测到这种关系。新测定的序列可以拟合到srRNA的二级结构模型中,除了一些真核生物特有的扩展区域存在不确定性外,该模型现在已经相对完善。针对其中一个区域提出了一个具有假结的特定结构模型。