Cryptic tRNAs in chaetognath mitochondrial genomes. (June 2016)

• Record Type: Journal Article
• Authors: Barthélémy, Roxane-Marie; Seligmann, Hervé
• Is Part Of: Computational biology and chemistry. Volume 62(2016)
• Page Start: 119
• Page End: 132
• Publication Date: 2016-06
• Subjects: tRNA -- Chaetognatha -- Cryptic tRNA -- Overlap coding -- tRNA misloading; Chemistry -- Data processing -- Periodicals; Biology -- Data processing -- Periodicals; Biochemistry -- Data processing; Biology -- Data processing; Molecular biology -- Data processing; Periodicals; Electronic journals; 542.85
• DOI: 10.1016/j.compbiolchem.2016.04.007
• Languages: English
• ISSNs: 1476-9271

Abstract

Highlights: Chaetognath mitogenomes exhibit more than one tRNA-like sequence as previously suggested. 16S rRNA genes appear as chaetognath tRNA nurseries. TRNA pairs seem templated by sense-antisense strands as previously suggested for multifunctional ribosomal-like protogenomes. Abstract: The chaetognaths constitute a small and enigmatic phylum of little marine invertebrates. Both nuclear and mitochondrial genomes have numerous originalities, some phylum-specific. Until recently, their mitogenomes seemed containing only one tRNA gene ( trnMet ), but a recent study found in two chaetognath mitogenomes two and four tRNA genes. Moreover, apparently two conspecific mitogenomes have different tRNA gene numbers (one and two). Reanalyses by tRNAscan-SE and ARWEN softwares of the five available complete chaetognath mitogenomes suggest numerous additional tRNA genes from different types. Their total number never reaches the 22 found in most other invertebrates using that genetic code. Predicted error compensation between codon-anticodon mismatch and tRNA misacylation suggests translational activity by tRNAs predicted solely according to secondary structure for tRNAs predicted by tRNAscan-SE, not ARWEN. Numbers of predicted stop-suppressor (antitermination) tRNAs coevolve with predicted overlapping, frameshifted protein coding genes including stop codons. Sequence alignments in secondary structure prediction with non-chaetognath tRNAs suggest that the most likely functional tRNAs are in intergenic regions, as regular mt-tRNAs. Due to usually short intergenic regions, generally tRNA sequences partially overlap with flanking genes. Some tRNA pairs seem templated by sense-antisense strands. Moreover, 16S rRNA genes, but not 12S rRNAs, appear as tRNA nurseries, as previously suggested for multifunctional ribosomal-like protogenomes.