2009
DOI: 10.1099/ijs.0.65855-0
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Caryotricha minuta (Xu et al., 2008) nov. comb., a unique marine ciliate (Protista, Ciliophora, Spirotrichea), with phylogenetic analysis of the ambiguous genus Caryotricha inferred from the small-subunit rRNA gene sequence

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Cited by 16 publications
(16 citation statements)
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“…Since the monophyly of the Armophorea is questionable and the phylogenetic affinities are variable (Shin et al , 2000; Miao et al , 2009a,b; Vd’acny et al , 2010), we broadly sampled ciliophoran 18S sequences to include representatives of all recognized ciliate classes (Lynn, 2008). One hundred and ninety-five ciliate 18S rDNA sequences, including 44 armophorean sequences, were downloaded from the NCBI database (Table S1) and assembled for multiple alignment.…”
Section: Methodsmentioning
confidence: 99%
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“…Since the monophyly of the Armophorea is questionable and the phylogenetic affinities are variable (Shin et al , 2000; Miao et al , 2009a,b; Vd’acny et al , 2010), we broadly sampled ciliophoran 18S sequences to include representatives of all recognized ciliate classes (Lynn, 2008). One hundred and ninety-five ciliate 18S rDNA sequences, including 44 armophorean sequences, were downloaded from the NCBI database (Table S1) and assembled for multiple alignment.…”
Section: Methodsmentioning
confidence: 99%
“…In the past, the armophoreans were classified as heterotrichs based on their morphology (Corliss, 1979). However, phylogenetic analyses of the 18S-rDNA (Embley et al , 1995; Hirt et al , 1995; van Hoek et al , 1998; Shin et al , 2000; Affa’a et al , 2004; Gong et al , 2009; Miao et al , 2009a,b; Vd’acny et al , 2010) and of histone H4 and α-tubulin data (Israel et al , 2002; Katz et al , 2004) have all grouped these organisms outside the Heterotrichea Stein, 1859, and within the Intramacro-nucleata Lynn, 1996. Hence, Armophorea is now considered as a molecular class, sometimes referred to as a “riboclass”, for which morphological synapomorphies are unknown (Lynn, 2008).…”
Section: Introductionmentioning
confidence: 99%
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“…SSU rRNA coding regions were amplified by PCR according to Miao et al [13], using two primers complementary to the 5′ and 3′ termini of eukaryotic 16S-like rRNA genes [14]. The full-length PCR products were purified by agarose gel electrophoresis, cloned in the pUCm-T vector (Sangon, Toronto, ON, Canada), and sequenced on both strands by the Takara sequencing facility, Shanghai, China.…”
Section: Samples Dna Extraction and Amplification And Sequencing Ofmentioning
confidence: 99%