ArticleCurrent genetics2009
Identification of transcribed and persistent variants of the psbA gene carried by plastid minicircles in a dinoflagellate.
Article in Current genetics, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.
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Who cites it
4 citing papers in PubMed.
- Interpreting the complexities of the plastid genome in dinoflagellates: a mini-review of recent advances.Plant molecular biology · 2024Review
- Small Genomes and Big Data: Adaptation of Plastid Genomics to the High-Throughput Era.Biomolecules · 2019Review
- Plastid Transcript Editing across Dinoflagellate Lineages Shows Lineage-Specific Application but Conserved Trends.Genome biology and evolution · 2018Article
- Genome-wide transcript profiling reveals the coevolution of plastid gene sequences and transcript processing pathways in the fucoxanthin dinoflagellate Karlodinium veneficum.Molecular biology and evolution · 2014Article
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Authors and funding
4 authors.
Funding
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Abstract
Plastid genomes of the peridinin-containing dinoflagellates are composed of a limited number of genes that are contained separately on small circular molecules (minicircles). It has been shown that occasionally aberrant minicircles are generated, but they are usually small and contain little coding information. In this study, we discovered multiple variants, a putative "gene family", of the gene psbA in the plastid minicircles of the dinoflagellate Alexandrium tamarense, which have persisted for almost 3 years in culture. Each variant, like the ordinary psbA, existed on distinct minicircles of similar size (5-6 kb). These psbA variants retained all, or almost all, the coding sequence of the ordinary gene, and all four were transcribed and edited after transcription, even though they could not encode the entire protein due to intervening or translocated sequences. Repeat elements were generally found in the relatively large non-coding region of these minicircles. Each psbA variant might have been generated by DNA recombination and/or replication slippage, as for previously reported aberrant minicircles. The fact that these minicircles are transcribed, individually edited and maintained in the genome suggests that they are functionally important, although their precise roles remain unclear.
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