Literature DB >> 3136295

Evolution of the secondary structures and compensatory mutations of the ribosomal RNAs of Drosophila melanogaster.

J M Hancock1, D Tautz, G A Dover.   

Abstract

This paper examines the effects of DNA sequence evolution on RNA secondary structures and compensatory mutations. Models of the secondary structures of Drosophila melanogaster 18S ribosomal RNA (rRNA) and of the complex between 2S, 5.8S, and 28S rRNAs have been drawn on the basis of comparative and energetic criteria. The overall AU richness of the D. melanogaster rRNAs allows the resolution of some ambiguities in the structures of both large rRNAs. Comparison of the sequence of expansion segment V2 in D. melanogaster 18S rRNA with the same region in three other Drosophila species and the tsetse fly (Glossina morsitans morsitans) allows us to distinguish between two models for the secondary structure of this region. The secondary structures of the expansion segments of D. melanogaster 28S rRNA conform to a general pattern for all eukaryotes, despite having highly divergent sequences between D. melanogaster and vertebrates. The 70 novel compensatory mutations identified in the 28S rRNA show a strong (70%) bias toward A-U base pairs, suggesting that a process of biased mutation and/or biased fixation of A and T point mutations or AT-rich slippage-generated motifs has occurred during the evolution of D. melanogaster rDNA. This process has not occurred throughout the D. melanogaster genome. The processes by which compensatory pairs of mutations are generated and spread are discussed, and a model is suggested by which a second mutation is more likely to occur in a unit with a first mutation as such a unit begins to spread through the family and concomitantly through the population. Alternatively, mechanisms of proofreading in stem-loop structures at the DNA level, or between RNA and DNA, might be involved. The apparent tolerance of noncompensatory mutations in some stems which are otherwise strongly supported by comparative criteria within D. melanogaster 28S rRNA must be borne in mind when compensatory mutations are used as a criterion in secondary-structure modeling. Noncompensatory mutation may extend to the production of unstable structures where a stem is stabilized by RNA-protein or additional RNA-RNA interactions in the mature ribosome. Of motifs suggested to be involved in rRNA processing, one (CGAAAG) is strongly overrepresented in the 28S rRNA sequence. The data are discussed both in the context of the forces involved with the evolution of multigene families and in the context of molecular coevolution in the rDNA family in particular.

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Year:  1988        PMID: 3136295     DOI: 10.1093/oxfordjournals.molbev.a040501

Source DB:  PubMed          Journal:  Mol Biol Evol        ISSN: 0737-4038            Impact factor:   16.240


  40 in total

1.  Integration of Bombyx mori R2 sequences into the 28S ribosomal RNA genes of Drosophila melanogaster.

Authors:  D G Eickbush; D D Luan; T H Eickbush
Journal:  Mol Cell Biol       Date:  2000-01       Impact factor: 4.272

2.  Intraspecific diversity of the 23S rRNA gene and the spacer region downstream in Escherichia coli.

Authors:  A I Antón; A J Martínez-Murcia; F Rodríguez-Valera
Journal:  J Bacteriol       Date:  1999-05       Impact factor: 3.490

3.  Nucleotide sequences of the internal transcribed spacers and 5.8S rRNA gene in Canella winterana (Magnoliales; Canellaceae).

Authors:  Y Suh; L B Thien; E A Zimmer
Journal:  Nucleic Acids Res       Date:  1992-11-25       Impact factor: 16.971

4.  Secondary structure of two regions in expansion segments ES3 and ES6 with the potential of forming a tertiary interaction in eukaryotic 40S ribosomal subunits.

Authors:  Gunnar Alkemar; Odd Nygård
Journal:  RNA       Date:  2004-03       Impact factor: 4.942

5.  Sequence and secondary structure of 5.8S rRNA in the tick, Ixodes scapularis.

Authors:  D M Wesson; F H Collins
Journal:  Nucleic Acids Res       Date:  1992-03-11       Impact factor: 16.971

6.  'Compensatory slippage' in the evolution of ribosomal RNA genes.

Authors:  J M Hancock; G A Dover
Journal:  Nucleic Acids Res       Date:  1990-10-25       Impact factor: 16.971

7.  rRNA genes from the lower chordate Herdmania momus: structural similarity with higher eukaryotes.

Authors:  B M Degnan; J Yan; C J Hawkins; M F Lavin
Journal:  Nucleic Acids Res       Date:  1990-12-11       Impact factor: 16.971

8.  Structure and Organization of the Engraulidae Family U2 snRNA: An Evolutionary Model Gene?

Authors:  Hicham Chairi; Laureana Rebordinos Gonzalez
Journal:  J Mol Evol       Date:  2015-04-03       Impact factor: 2.395

9.  Sequence variation within the rRNA gene loci of 12 Drosophila species.

Authors:  Deborah E Stage; Thomas H Eickbush
Journal:  Genome Res       Date:  2007-11-07       Impact factor: 9.043

10.  Molecular phylogeny of the subgenus Sophophora of Drosophila derived from large subunit of ribosomal RNA sequences.

Authors:  M Pélandakis; D G Higgins; M Solignac
Journal:  Genetica       Date:  1991       Impact factor: 1.082

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