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Evolution of Nucleotide Punctuation Marks: From Structural to Linear Signals
Nawal El Houmami1, Hervé Seligmann1
1URMITE, Aix Marseille Université UM63, CNRS 7278, IRD 198, INSERM 1095, IHU - Méditerranée Infection Marseille, France.
Frontiers in Genetics
|April 12, 2017
Summary
Nucleotide signals evolved from multi- to unidimensional structures, transitioning from transcription to translation. The natural circular code X in human mitochondrial RNAs regulates frameshifts in both processes, supporting this evolutionary hypothesis.
Area of Science:
- Molecular Biology
- Evolutionary Biology
- Genetics
Background:
- Nucleotide synthesis signals (DNA replication, RNA transcription) may have evolutionary links to translation.
- Evolutionary transitions might involve signals combining primary and secondary nucleotide structures.
- Mitochondrial replication initiation provides a potential model for this evolutionary scenario.
Purpose of the Study:
- To propose an evolutionary hypothesis for nucleotide synthesis signals.
- To investigate the dual role of signals in transcription and translation.
- To analyze the function of the natural circular code X in human mitochondrial RNAs.
Main Methods:
- Comparative analysis of nucleotide sequences in mitochondrial RNAs (delRNAs) and other mitochondrial genome regions.
- Examination of homopolymer triplet distribution in delRNAs.
- Analysis of the natural circular code X's role in frameshift regulation.
Main Results:
- delRNAs exhibit a 2x higher frequency of homopolymer triplets compared to other mitochondrial regions.
- The natural circular code X (20 specific codons) is implicated in regulating frameshifts during both transcription and translation.
- Observations support the hypothesis that translational signals originated from transcriptional signals.
Conclusions:
- The natural circular code X demonstrates a dual role in transcription and translation, confirming its evolutionary origin from transcriptional signals.
- The findings support the hypothesis that signals evolved from multi- to unidimensional structures and were transferred from transcription to translation.
- Mitochondrial replication initiation serves as a valid model for this evolutionary pathway.