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Late changes in spliceosomal introns define clades in vertebrate evolution
B Venkatesh1, Y Ning, S Brenner
1Marine Molecular Genetics Laboratory, Institute of Molecular and Cell Biology, 30 Medical Drive, Singapore 117609. mcbbv@imcb.nus.edu.sg
Summary
Spliceosomal introns gained by ray-finned fishes and lost in rhodopsin genes provide evolutionary markers. This study clarifies fish phylogeny, identifying bichirs as the earliest ray-finned fish lineage.
Area of Science:
- Evolutionary biology
- Genomics
- Phylogenetics
Background:
- The evolutionary history of spliceosomal introns, including their gain and loss, remains a contentious topic.
- Intron gain and loss events can serve as valuable phylogenetic markers if they are rare and unique occurrences.
Purpose of the Study:
- To investigate the phylogenetic distribution of specific spliceosomal introns in actinopterygian (ray-finned) fishes.
- To analyze intron pattern changes in the rhodopsin gene across fish evolution.
- To establish a robust intron-based cladogram for resolving complex ray-finned fish relationships.
Main Methods:
- Extensive survey of seven spliceosomal introns in Fugu genes compared to mammalian homologs.
- Investigation of intron patterns in the rhodopsin gene across various fish species.
- Construction of an intron-based cladogram to infer phylogenetic relationships.
Main Results:
- Seven spliceosomal introns were acquired by actinopterygian fishes at different evolutionary stages.
- Four introns present in the ancestral chordate rhodopsin gene were lost simultaneously in the common ancestor of ray-finned fishes.
- The intron-based cladogram resolved difficult phylogenetic relationships, positioning bichirs (Polypterus) as the sister group to all other extant ray-finned fishes.
Conclusions:
- Intron gain and loss events are significant evolutionary markers in ray-finned fishes.
- Intron patterns provide reliable data for constructing phylogenetic trees.
- This study clarifies the evolutionary position of bichirs within the ray-finned fish clade.