RNase MRP and the RNA processing cascade in the eukaryotic ancestor

被引:31
|
作者
Woodhams, Michael D.
Stadler, Peter F.
Penny, David
Collins, Lesley J. [1 ]
机构
[1] Massey Univ, Allan Wilson Ctr Mol Ecol & Evolut, Palmerston North, New Zealand
[2] Univ Leipzig, Bioinformat Grp, Dept Comp Sci, D-04107 Leipzig, Germany
[3] Univ Leipzig, Interdisciplinary Ctr Bioinformat, D-04107 Leipzig, Germany
关键词
D O I
10.1186/1471-2148-7-S1-S13
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Background: Within eukaryotes there is a complex cascade of RNA-based macromolecules that process other RNA molecules, especially mRNA, tRNA and rRNA. An example is RNase MRP processing ribosomal RNA ( rRNA) in ribosome biogenesis. One hypothesis is that this complexity was present early in eukaryotic evolution; an alternative is that an initial simpler network later gained complexity by gene duplication in lineages that led to animals, fungi and plants. Recently there has been a rapid increase in support for the complexity-early theory because the vast majority of these RNA-processing reactions are found throughout eukaryotes, and thus were likely to be present in the last common ancestor of living eukaryotes, herein called the Eukaryotic Ancestor. Results: We present an overview of the RNA processing cascade in the Eukaryotic Ancestor and investigate in particular, RNase MRP which was previously thought to have evolved later in eukaryotes due to its apparent limited distribution in fungi and animals and plants. Recent publications, as well as our own genomic searches, find previously unknown RNase MRP RNAs, indicating that RNase MRP has a wide distribution in eukaryotes. Combining secondary structure and promoter region analysis of RNAs for RNase MRP, along with analysis of the target substrate ( rRNA), allows us to discuss this distribution in the light of eukaryotic evolution. Conclusion: We conclude that RNase MRP can now be placed in the RNA-processing cascade of the Eukaryotic Ancestor, highlighting the complexity of RNA-processing in early eukaryotes. Promoter analyses of MRP-RNA suggest that regulation of the critical processes of rRNA cleavage can vary, showing that even these key cellular processes ( for which we expect high conservation) show some species-specific variability. We present our consensus MRP-RNA secondary structure as a useful model for further searches.
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页数:13
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