Literature DB >> 26723232

Translation of mitochondrial swinger RNAs according to tri-, tetra- and pentacodons.

Hervé Seligmann1.   

Abstract

Transcriptomes and proteomes include RNA and protein fragments not matching regular transcription/translation. Some 'non-canonical' mitochondrial transcripts match mitogenomes after assuming one among 23 systematic exchanges between nucleotides, producing swinger RNAs (nine symmetric, X↔Y, example C↔T; 14 asymmetric, X→Y→Z→X, example A→T→G→A) in GenBank's EST database. Here, reanalyzes of (a) public human mitochondrial transcriptome data (Illumina: RNA-seq) allowed to detect mitochondrial swinger RNAs for all 23 exchanges and (b) independent public human mitochondrial trypsinized proteomic mass spectrometry data allowed to detect peptides predicted from translation of parts of swinger-transformed mitogenomes covered by detected swinger reads. RNA-seq and previous EST swinger transcript data converge. Swinger RNA translation frequently inserts various amino acids at stop codons. Swinger RNA-peptide associations exist also for peptides matching systematically frameshifting translation, peptides entirely coded by tetra- and pentacodons (regular codons expanded by silent mononucleotides at 4th, and silent dinucleotides at 4th and 5th position(s), respectively). Swinger peptides differ from regular mitochondrial proteins: not membrane embedded, reflect warmer, anaerobic, low resource conditions, reminding a free-living ancestor. Tetra- and pentacoded peptides associate with low, high GC contents, respectively, suggesting expanded codon translations associate with thermic stresses. Results confirm experimentally predicted swinger, tetra- and pentacoded mitochondrial peptides, increasing mitogenomic coding density.
Copyright © 2015 Elsevier Ireland Ltd. All rights reserved.

Entities:  

Keywords:  Expanded anticodon; Frameshift; Mass spectrometry; Non-canonical RNA; Swinger DNA polymerization; Systematic nucleotide exchange; Transcription

Mesh:

Substances:

Year:  2015        PMID: 26723232     DOI: 10.1016/j.biosystems.2015.11.009

Source DB:  PubMed          Journal:  Biosystems        ISSN: 0303-2647            Impact factor:   1.973


  7 in total

1.  More Pieces of Ancient than Recent Theoretical Minimal Proto-tRNA-Like RNA Rings in Genes Coding for tRNA Synthetases.

Authors:  Jacques Demongeot; Hervé Seligmann
Journal:  J Mol Evol       Date:  2019-04-05       Impact factor: 2.395

2.  Bijective codon transformations show genetic code symmetries centered on cytosine's coding properties.

Authors:  Hervé Seligmann
Journal:  Theory Biosci       Date:  2017-11-16       Impact factor: 1.919

3.  Unbiased Mitoproteome Analyses Confirm Non-canonical RNA, Expanded Codon Translations.

Authors:  Hervé Seligmann
Journal:  Comput Struct Biotechnol J       Date:  2016-10-05       Impact factor: 7.271

4.  Genetic Code Optimization for Cotranslational Protein Folding: Codon Directional Asymmetry Correlates with Antiparallel Betasheets, tRNA Synthetase Classes.

Authors:  Hervé Seligmann; Ganesh Warthi
Journal:  Comput Struct Biotechnol J       Date:  2017-08-12       Impact factor: 7.271

5.  Transcripts with systematic nucleotide deletion of 1-12 nucleotide in human mitochondrion suggest potential non-canonical transcription.

Authors:  Ganesh Warthi; Hervé Seligmann
Journal:  PLoS One       Date:  2019-05-23       Impact factor: 3.240

6.  Chimeric Translation for Mitochondrial Peptides: Regular and Expanded Codons.

Authors:  Hervé Seligmann; Ganesh Warthi
Journal:  Comput Struct Biotechnol J       Date:  2019-08-23       Impact factor: 7.271

7.  Chimeric mitochondrial peptides from contiguous regular and swinger RNA.

Authors:  Hervé Seligmann
Journal:  Comput Struct Biotechnol J       Date:  2016-06-29       Impact factor: 7.271

  7 in total

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