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首页> 外文期刊>Journal of Molecular Evolution >Complex patterns of plastid 16S rRNA gene evolution in nonphotosyntheticgreen algae
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Complex patterns of plastid 16S rRNA gene evolution in nonphotosyntheticgreen algae

机译:非光合绿藻中质体16S rRNA基因进化的复杂模式

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This study provides a phylogenetic/comparative approach to deciphering the processes underlying the evolution of plastid rRNA genes in genomes under relaxed functional constraints. Nonphotosynthetic green algal taxa that belong to two distinct classes, Chlorophyceae (Polytoma) and Trebouxiophyceae (Prototheca), were investigated. Similar to the situation described previously for plastid 16S rRNA genes in nonphotosynthetic land plants, nucleotide substitution levels, extent of structural variations, and percentage AT values are increased in nonphotosynthetic green algae compared to their closest photosynthetic relatives. However, the mutational processes appear to be different in many respects. First, with the increase in AT content, more transversions are noted in Polytoma and holoparasite angiosperms, while more transitions characterize the evolution of the 16S rDNA sequences in Prototheca. Second, although structural variations do accumulate in both Polytoma and Prototheca (as well as holoparasitic plastid 16S rRNAs), insertions as large as 1.6 kb characterize the plastid 16S rRNA genes in the former, whereas significantly smaller indels (not exceeding 24 bp) seem to be more prevalent in the latter group. The differences in evolutionary rates and patterns within and between lineages might be due to mutations in replication/repair-related genes; slipped-strand mispairing is likely the mechanism responsible for the expansion of insertions in Polytoma plastid 16S rRNA genes.
机译:这项研究提供了一种系统发生/比较方法,以破译功能松弛的基因组中质体rRNA基因的进化过程。研究了属于两个不同类别的非光合绿色藻类群,即绿藻科(Polytoma)和千藻科(Prototheca)。与之前在非光合陆地植物中的质体16S rRNA基因描述的情况类似,与光合最接近的藻类相比,非光合绿色藻类的核苷酸取代水平,结构变异程度和AT百分比增加。但是,突变过程似乎在许多方面都不同。首先,随着AT含量的增加,在多发瘤和全寄生的被子植物中发现了更多的转化,而更多的转化则表征了Prototheca中16S rDNA序列的进化。其次,尽管在多发瘤和Prototheca(以及全寄生质体16S rRNA)中都确实积累了结构变异,但前者中质体16S rRNA基因的特征是高达1.6 kb的插入,而似乎较小的插入缺失(不超过24 bp)在后一组中更为普遍。谱系内部和谱系之间进化速率和模式的差异可能是由于复制/修复相关基因的突变所致。滑链错配可能是造成多瘤质体16S rRNA基因插入扩展的机制。

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