2004
DOI: 10.1055/s-2004-820888
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Phylogenetic Position of Endosymbiotic Green Algae in Paramecium bursaria Ehrenberg from Japan

Abstract: Endosymbiotic green algae of Japanese Paramecium bursaria were phylogenetically analyzed based on DNA sequences from the ribosomal DNA operon (18S rDNA, ITS1, 5.8S rDNA, and ITS2). Phylogenetic trees constructed using 18S rDNA sequences showed that the symbionts belong to the Chlorella sensu stricto (Trebouxiophyceae) group. They are genetically closer to the C. vulgaris Beijerinck group than to C. kessleri Fott et Nováková as proposed previously. Branching order in C. vulgaris group was unresolved in 18S rDNA… Show more

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Cited by 46 publications
(36 citation statements)
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“…Smith) Hinda´k and D. palatina Schmidle (formerly Scenedesmaceae) and Micractinium pusillum Fresenius (formerly Micractiniaceae). On the other hand, Hoshina et al (2004) have discussed the phylogenetic position of endosymbiotic green algae in Paramecium bursaria Ehrenberg. These algae would be genetically closer to the C. vulgaris group than to the (at that time) P. kessleri group.…”
Section: Discussionmentioning
confidence: 99%
“…Smith) Hinda´k and D. palatina Schmidle (formerly Scenedesmaceae) and Micractinium pusillum Fresenius (formerly Micractiniaceae). On the other hand, Hoshina et al (2004) have discussed the phylogenetic position of endosymbiotic green algae in Paramecium bursaria Ehrenberg. These algae would be genetically closer to the C. vulgaris group than to the (at that time) P. kessleri group.…”
Section: Discussionmentioning
confidence: 99%
“…Polymerase chain reaction (PCR) was carried out to amplify SSU to ITS rDNA by using the primer pairs SR-1/SR-9 [22], SR-6 [22]/SR-12 k [23], INT-4 F [24]/ITS4 [25] and INT-4 F/HLR-3R [23]. PCR products were purified with NucleoSpin Gel and PCR Clean-up (Macherey-Nagel, Düren, Germany), and were directly sequenced by using the Operon DNA sequencing service (Operon Biotechnology, Tokyo).…”
Section: Methodsmentioning
confidence: 99%
“…Whole P. bursaria DNA extracts were used to amplify both host SSU rDNA and photobiont SSU rDNA. Host targeting PCR was performed with the primer pair SR-1 (universal [27])/Paramecium800R (host specific [6]), and algae targeting PCR was also performed with CHspeRmaeF (trebouxiophyte specific [6])/INT-5R (trebouxio- phyte specific [5]) for the photobiont. The PCR product of the host DNA was purified via Quantum Prep PCR Kleen Spin Columns (Bio-Rad, CA) and directly sequenced.…”
Section: Dna Extraction Amplification and Sequencingmentioning
confidence: 99%