1995
DOI: 10.1111/j.0022-3646.1995.00970.x
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PHYLOGENETIC RELATIONSHIPS WITHIN THE COLONIAL VOLVOCALES (CHLOROPHYTA) INFERRED FROM rbcL GENE SEQUENCE DATA

Abstract: The chloroplast‐encoded large subunit of the ribulose‐1, 5‐bisphosphate carboxylase / oxygenase (rbcL) gene was sequenced from 20 species of the colonial Volvocales (the Volvacaceae, Goniaceae, and Tetrabaenaceae) in order to elucidate phylogenetic relationships within the colonial Volvocales. Eleven hundred twenty‐eight base pairs in the coding regions of the (rbcL) gene were analyzed by the neighbor‐joining (NJ) method using three kinds of distance estimations, as well as by the maximum parsimony (MP) method… Show more

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Cited by 115 publications
(98 citation statements)
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“…The method for sequencing the chloroplast gene (rbcL) for the large subunit of RuBisCO of two strains of Y. unicocca (Hasu-1 and NIES-870), E. unicocca UTEX 1221 and two aplanosporic strains (TKI-C-2 and 990601-IE-5) was essentially identical to that described previously (Nozaki et al, 1995(Nozaki et al, , 1997(Nozaki et al, , 2000(Nozaki et al, , 2002. The region sequenced corresponded to rbcL positions 31-1159 in Chlorella vulgaris Beijerinck (Yoshinaga et al, 1988;Wakasuagi et al, 1997).…”
Section: Molecular Phylogenetic Analysesmentioning
confidence: 88%
“…The method for sequencing the chloroplast gene (rbcL) for the large subunit of RuBisCO of two strains of Y. unicocca (Hasu-1 and NIES-870), E. unicocca UTEX 1221 and two aplanosporic strains (TKI-C-2 and 990601-IE-5) was essentially identical to that described previously (Nozaki et al, 1995(Nozaki et al, , 1997(Nozaki et al, , 2000(Nozaki et al, , 2002. The region sequenced corresponded to rbcL positions 31-1159 in Chlorella vulgaris Beijerinck (Yoshinaga et al, 1988;Wakasuagi et al, 1997).…”
Section: Molecular Phylogenetic Analysesmentioning
confidence: 88%
“…Nested RT-PCR using this cDNA yielded the partial fragment of GpMID; the primers used in the first PCR were the Seegene kit's 39-rapid amplification of the cDNA end (39-RACE) primer and dMT-dF3 (primers designed in this study are listed in Table 1); the primers used in the second PCR were dMT-dF3 and mt-R4 . The PCR reactions were carried out using TAKARA Taq polymerase (TAKARA, Osaka, Japan) using the cycling conditions described previously (Nozaki et al 1995). To determine the C terminus sequence of GpMID, 39-RACE was performed with the 39-RACE primer of the kit and GpMidF1.…”
Section: Experimental Organisms and Culture And Mating Methodsmentioning
confidence: 99%
“…Because it was unsuccessful to obtain rbcL gene sequences from zygotes of C. nivalis using previous published primers (Nozaki et al 1995(Nozaki et al , 1997 in the single-cell sequencing, specific primers newly designed (see Materials and methods) were used for single-cell sequencing of the zygotes. As a result, the partial sequences of rbcL gene (340-400 bp) were determined.…”
Section: Single-cell Sequencingmentioning
confidence: 99%