2011
DOI: 10.1016/j.gene.2011.02.001
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Complex repeat structures and novel features in the mitochondrial genomes of the diatoms Phaeodactylum tricornutum and Thalassiosira pseudonana

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Cited by 71 publications
(61 citation statements)
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“…The homoplasmic nature of organelle genomes was consistent with the mitochondrial genome of allopolyploid yeast (Sipiczki, 2008). It should be noted that the mitochondrial genome assembly is incomplete, possibly due to the large inverted repeats commonly found in the mitochondrial genomes of diatoms (Oudot-Le Secq and Green, 2011). The sequenced region of the mitochondrial genome with no long repeat sequences is 38.6 kb, similar in size to the nonrepeat regions of the mitochondrial genomes of T. pseudonana (38.8 kb with 5.0-kb repeat region) and P. tricornutum (42.0 kb with 35.4-kb repeat region).…”
Section: Genome Sequencing and Assemblysupporting
confidence: 65%
“…The homoplasmic nature of organelle genomes was consistent with the mitochondrial genome of allopolyploid yeast (Sipiczki, 2008). It should be noted that the mitochondrial genome assembly is incomplete, possibly due to the large inverted repeats commonly found in the mitochondrial genomes of diatoms (Oudot-Le Secq and Green, 2011). The sequenced region of the mitochondrial genome with no long repeat sequences is 38.6 kb, similar in size to the nonrepeat regions of the mitochondrial genomes of T. pseudonana (38.8 kb with 5.0-kb repeat region) and P. tricornutum (42.0 kb with 35.4-kb repeat region).…”
Section: Genome Sequencing and Assemblysupporting
confidence: 65%
“…The three large tandem repeats are separated from each other within the repeat region by spacers (consisting of a C-A-A pattern). Interestingly, this direct repeat arrangement is strikingly similar to the larger (35 kb) repeat structure found in the diatom Phaeodactylum tricornutum [29]. The cryptophytes, Hemiselmis andersenii and Rhodomonas salina , and the chlorophytes Pedinomonas minor and Acutodesmus obliquus also contain large tandem repeat regions (>4 kb) that differ from the minimal repeat embellishment seen in most mitochondrial genomes of other algae.…”
Section: Resultsmentioning
confidence: 53%
“…Unfortunately, the use of short read, high throughput sequencing techniques do not easily facilitate solving these complex repeat structures. The first E. huxleyi mitochondrial genome published in 2004 [25], the stramenopile, Heterosigma akashiwo [30], as well as the diatoms Phaeodactylum tricornutum and Thalassiosira pseudonana [29] utilized fosmid sequencing, that supported assembly and primer walking for the resolution of longer repeats.…”
Section: Resultsmentioning
confidence: 99%
“…We were unable to bridge the final gap in both genomes, despite numerous attempts using different long-range PCR protocols under different conditions, buffer systems, and primers. This is most likely due to the presence of a large intervening sequence, as is common to other diatom mitochondrial genomes (for example the 35 kb insertion in P. tricornutum [29]), and/or to the presence of repetitive elements that may form complex secondary structures that inhibit PCR. Since all the other sequenced diatom mitochondrial genomes map as circular molecules [28], [29], it is likely that the D. baltica and K. foliaceum genomes share the same configuration.…”
Section: Resultsmentioning
confidence: 99%
“…Sequenced diatom mitochondrial genomes range from 43 to 77 kbp, have a circular map, and encode about 60 genes. While generally compact, they usually feature one large intergenic spacer composed of repetitive sequences (from nearly 5 kbp in the centric diatom Thalassiosira pseudonana and the araphid pennate diatom Synedra acus, to about 35 kbp in the raphid pennate diatom Phaeodactylum tricornutum) [28], [29]. In contrast, dinoflagellate mitochondria encode only three protein-coding genes (cox1, cox3 and cob) and many fragments of ribosomal RNA (rRNA), and these appear to be organised on multiple chromosomes that may be linear, and which are greatly expanded in number and include numerous incomplete copies or pseudogenes along with highly dispersed short or long stretches of non-coding and repetitive sequences [30][32].…”
Section: Introductionmentioning
confidence: 99%