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Updated: Apr 25, 2026

An Integrated Approach for Microprotein Identification and Sequence Analysis
Published on: July 12, 2022
An evolutionary preserved intergenic spacer in gadiform mitogenomes generates a long noncoding RNA.
Tor Erik Jørgensen, Ingrid Bakke, Anita Ursvik
1Marine Genomics group, Faculty of Biosciences and Aquaculture, University of Nordland, Bodø, Norway. Steinar.Johansen@uit.no.
The T-P spacer in gadiform mitogenomes is evolutionarily conserved due to a long noncoding RNA, likely enhancing stability and protein binding. This finding sheds light on mitochondrial genome organization and function in fish.
Area of Science:
- Mitochondrial genomics
- Evolutionary biology
- Noncoding RNA research
Background:
- Vertebrate mitogenomes typically lack extensive intergenic sequences.
- The biological roles of intergenic spacers between tRNA(Thr) and tRNA(Pro) genes (T-P spacers) in gadiforms remain largely unknown.
Purpose of the Study:
- To characterize the T-P spacer in European hake (Merluccius merluccius) mitogenomes.
- To investigate the evolutionary presence and function of T-P spacers across diverse gadiform species.
- To elucidate the potential role of T-P spacers in mitochondrial gene expression and regulation.
Main Methods:
- Mitochondome sequencing and characterization.
- Phylogenetic analysis of T-P spacer sequences across 32 gadiform species.
- Intraspecific variation analysis in Atlantic cod (Gadus morhua) using 225 specimens.
- Mito-transcriptome pyrosequencing to identify noncoding RNAs.
Main Results:
- A complex T-P spacer (223-532 bp) was identified in Merluccius merluccius.
- T-P spacers are evolutionarily conserved across 8 families and 28 genera of gadiforms, with complexity correlating with phylogenetic relationships.
- An abundant H-strand specific long noncoding RNA (lncRNA) was detected in Atlantic cod, with the T-P spacer forming its 5' region.
Conclusions:
- The T-P spacer is evolutionarily preserved in gadiform mitogenomes due to a gain of function via a lncRNA.
- The T-P spacer likely enhances the stability of the H-strand specific lncRNA through hairpin structures and protein binding sites.
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