2000
DOI: 10.2307/1542872
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Biogeography of two species of Symbiodinium (Freudenthal) inhabiting the intertidal sea anemone Anthopleura elegantissima (Brandt)

Abstract: We have analyzed the genetic profiles of dinoflagellate populations obtained from the Pacific coast sea anemone Anthopleura elegantissima (Brandt) at collection sites from Washington to California. Genetic differences within the symbiont populations of California anemones have been uncovered by restriction length polymorphism (RFLP) analysis of the small subunit (SSU) and large subunit (LSU) ribosomal RNA genes, and by denaturing gradient gel electrophoresis (DGGE) of the internal transcribed spacer region 2 (… Show more

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Cited by 334 publications
(293 citation statements)
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“…DNA was extracted from each sample using an organic extraction protocol ). The ITS-2 region was amplified from each sample using the Symbiodinium-specific primers 'ITSintfor2' and 'ITS2clamp' (LaJeunesse & Trench 2000) with the following profile: an initial denaturing step of 94°C for 3 min, followed by 35 cycles of 1 min at 94°C, 1 min at 58°C, and 1 min at 74°C, followed by a single cycle of 7 min at 74°C. Products were electrophoresced on 1.2% agarose gels to check for amplification success.…”
Section: Methodsmentioning
confidence: 99%
“…DNA was extracted from each sample using an organic extraction protocol ). The ITS-2 region was amplified from each sample using the Symbiodinium-specific primers 'ITSintfor2' and 'ITS2clamp' (LaJeunesse & Trench 2000) with the following profile: an initial denaturing step of 94°C for 3 min, followed by 35 cycles of 1 min at 94°C, 1 min at 58°C, and 1 min at 74°C, followed by a single cycle of 7 min at 74°C. Products were electrophoresced on 1.2% agarose gels to check for amplification success.…”
Section: Methodsmentioning
confidence: 99%
“…Symbiodinium types were identified from three cores of each colony by sequencing the internal transcribed spacer-2 region of ribosomal DNA (ITS2 rDNA). This gene was amplified using the primers ITSintfor2 and ITS2clamp [36], and products were separated by denaturing gradient gel electrophoresis using a CBS scientific system (35-75% denaturing gradient). Dominant bands were excised, reamplified and sequenced in both directions using BIGDYE TERMINATOR v. 3.1 cycle sequencing kit and an APPLIED BIOSYSTEMS 3130XL GENETIC ANALYZER.…”
Section: (E) Symbiont Identificationmentioning
confidence: 99%
“…All DNA samples from the investigations of Toller et al (2001) were extracted as per their protocols. All field samples were initially screened using denaturing gradient gel electrophoresis (DGGE) of ITS2 PCR amplifications (LaJeunesse & Trench, 2000). Bands diagnostic of the resulting ITS fingerprint were excised, eluted, re-amplified and directly sequenced as described by LaJeunesse (2002).…”
Section: Genetic Analysesmentioning
confidence: 99%