Search bioRxiv⌕ Search

Biology subjects

Bendich, A. J.

Publications and source records attributed to Bendich, A. J..

2 recordsLinked to original sources

Introns are derived from transposons

Introns and transposons exhibit many similar features, but the connections between them have yet to be firmly established. Group I introns have commonalities with DNA transposons, while group II introns share many features with retrotransposons. Here, we report the results of an analysis of 214 introns (including group I, group II, group III, twintrons, spliceosomal, and archaeal introns) from members of seven major taxa (within Eukarya, Bacteria, and Archaea) that all have direct repeats at or near both exon/intron borders, indicating that they were inserted via transposition events. Border sequence analysis indicates that after splicing, most mature transcripts would be functionally compromised because they do not restore the DNA sequence information before intron insertion. Transposons and introns thus appear to be members of a diverse assemblage of parasitic mobile genetic elements that secondarily may benefit their host cell and have expanded greatly in eukaryotes from their presumed prokaryotic ancestors. Author SummaryIntrons are found in all domains of life. While they are limited in prokaryotes, they have greatly expanded in number and diversity in eukaryotes. We found direct repeat sequences at or near both exon/intron borders for all 214 introns analyzed among eukaryotes, bacteria, and archaea. We infer that all introns were inserted into genes via transposon-like mechanisms and are members of a large family of mobile genetic elements.

evolutionary biology↗

Ribosomal intergenic spacers are filled with transposon remnants

Eukaryotic ribosomal DNA (rDNA) comprises tandem units of highly-conserved coding genes separated by rapidly-evolving spacer DNA. The spacers of all 12 species examined were filled with short direct repeats (DRs) and multiple long tandem repeats (TRs), completing the rDNA maps that previously contained unannotated and inadequately studied sequences. The external transcribed spacers also were filled with DRs and some contained TRs. We infer that the spacers arose from transposon insertion, followed by their imprecise excision, leaving short DRs characteristic of transposon visitation. The spacers provided a favored location for transposon insertion because they occupy loci containing hundreds to thousands of gene repeats. The spacers primary cellular function may be to link one rRNA transcription unit to the next, whereas transposons flourish here because they have colonized the most frequently-used part of the genome. Author SummaryThe DNA loci containing the ribosomal RNA genes (the rDNA) in eukaryotes are puzzling. The sections encoding the rRNA are so highly conserved that they can be used to assess evolutionary relationships among diverse eukaryotes, yet the rDNA sequences between the rRNA genes (the intergenic spacer sequences; IGS) are among the most rapidly evolving in the genome, including varying within and between species and between individuals of a species, and within cells of an individual. Here we report the presence of large numbers of direct repeats (DRs) throughout the IGSs of a diverse set of organisms. Parasitic DNA and RNA elements often leave short DRs when they are excised resulting in "molecular scars" in the DNA. These "scars" are absent from the coding sections of the rDNA repeats, indicating that the IGSs have long been targets for integration of these parasitic elements that have been eliminated from the coding sections by selection. While these integration events are mostly detrimental to the organism, occasionally they have caused beneficial changes in eukaryotes, thus allowing both the parasites and the hosts to survive and co-evolve.

evolutionary biology↗