Abstract

BackgroundGroup I introns are found in the nuclear small subunit ribosomal RNA gene (SSU rDNA) of some species of the genus Porphyra (Bangiales, Rhodophyta). Size polymorphisms in group I introns has been interpreted as the result of the degeneration of homing endonuclease genes (HEG) inserted in peripheral loops of intron paired elements. In this study, intron size polymorphisms were characterized for different Porphyra spiralis var. amplifolia (PSA) populations on the Southern Brazilian coast, and were used to infer genetic relationships and genetic structure of these PSA populations, in addition to cox2-3 and rbcL-S regions. Introns of different sizes were tested qualitatively for in vitro self-splicing.ResultsFive intron size polymorphisms within 17 haplotypes were obtained from 80 individuals representing eight localities along the distribution of PSA in the Eastern coast of South America. In order to infer genetic structure and genetic relationships of PSA, these polymorphisms and haplotypes were used as markers for pairwise Fst analyses, Mantel's test and median joining network. The five cox2-3 haplotypes and the unique rbcL-S haplotype were used as markers for summary statistics, neutrality tests Tajima's D and Fu's Fs and for median joining network analyses. An event of demographic expansion from a population with low effective number, followed by a pattern of isolation by distance was obtained for PSA populations with the three analyses. In vitro experiments have shown that introns of different lengths were able to self-splice from pre-RNA transcripts.ConclusionThe findings indicated that degenerated HEGs are reminiscent of the presence of a full-length and functional HEG, once fixed for PSA populations. The cline of HEG degeneration determined the pattern of isolation by distance. Analyses with the other markers indicated an event of demographic expansion from a population with low effective number. The different degrees of degeneration of the HEG do not refrain intron self-splicing. To our knowledge, this was the first study to address intraspecific evolutionary history of a nuclear group I intron; to use nuclear, mitochondrial and chloroplast DNA for population level analyses of Porphyra; and intron size polymorphism as a marker for population genetics.

Highlights

  • Group I introns are found in the nuclear small subunit ribosomal RNA gene (SSU rDNA) of some species of the genus Porphyra (Bangiales, Rhodophyta)

  • The smallest introns were amplified from Porphyra spiralis var. amplifolia (PSA)-V population (616 bp) and the largest introns were amplified from PSA-A, PSA-I, PSA-L and PSA-T populations (1054-8 bp; Table 3)

  • Population structure of Porphyra spiralis var. amplifolia could be assigned by homing endonuclease genes (HEG) degeneration, not by cox2-3 and rbcL-S regions

Read more

Summary

Introduction

Group I introns are found in the nuclear small subunit ribosomal RNA gene (SSU rDNA) of some species of the genus Porphyra (Bangiales, Rhodophyta). Size polymorphisms in group I introns has been interpreted as the result of the degeneration of homing endonuclease genes (HEG) inserted in peripheral loops of intron paired elements. Group I introns belong to a family of RNAs with catalytic activities These ribozymes are mobile elements inserted within coding sequences of nuclear rDNA, chloroplast and mitochondrial genomes of some eukaryotes; and less frequently within coding sequences of eubacteria, phages and viruses. Size polymorphisms in group I introns have been described [2,3,4,5] and are occasionally generated by the insertion of a mobile element such as homing endonuclease genes (HEG) in peripheral loops of intron paired elements P1, P2, P6, P8 and P9 [4,6]. Homing endonucleases were described for fungi, protists, bacteria and viruses, but with unknown function for the hosts [6]

Methods
Results
Discussion
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call