2014
DOI: 10.1111/jeu.12161
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The Size of DNA Molecules and Chromatin Organization in the Macronucleus of the Ciliate Didinium nasutum (Ciliophora)

Abstract: Pulsed-field gel electrophoresis (PFGE) was applied to analyze the molecular karyotype of the ciliate Didinium nasutum. The data obtained indicate that D. nasutum belongs to the ciliate species with subchromosomal macronuclear genome organization. No short "gene-sized" DNA molecules were detected. Macronuclear DNAs formed a continuous spectrum from 50 kbp to approximately 1,000 kbp in size with a peak plateau between 250 and 400 kbp. The macronuclear DNA molecules were packed into chromatin bodies of 80-265 nm… Show more

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Cited by 6 publications
(5 citation statements)
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References 27 publications
(48 reference statements)
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“…S1 , Supplementary Material online). However, previous work using pulsed-field gel electrophoresis of total gDNA from D. nasutum did not report chromosomes <50 kb ( Popenko et al. 2015 ), which suggests that the nano-chromsomes may be present at relatively low copy numbers and/or that the retention of these chromosomes is strongly dependent on the DNA isolation approaches.…”
Section: Resultsmentioning
confidence: 89%
“…S1 , Supplementary Material online). However, previous work using pulsed-field gel electrophoresis of total gDNA from D. nasutum did not report chromosomes <50 kb ( Popenko et al. 2015 ), which suggests that the nano-chromsomes may be present at relatively low copy numbers and/or that the retention of these chromosomes is strongly dependent on the DNA isolation approaches.…”
Section: Resultsmentioning
confidence: 89%
“…However, our data indicate that the small size and the absence of typical chromosomes cannot be the only factors determining the inverted spatial organization of some ciliate nucleoli. Indeed, all three ciliate species studied here refer to the species with macronuclear DNA of subchromosomal size (Popenko et al, 1998(Popenko et al, , 2015Rautian and Potekhin, 2002). However, only in one of them we observed the unusual location of the fibrillar component and fibrillarin at the periphery of the nucleoli.…”
Section: Discussionmentioning
confidence: 99%
“…After 4 days the cells were collected by centrifugation, washed in distilled water and fixed in 2.5% glutaraldehyde. Aliquotes (80 mkL) of cell suspensions were centrifuged in the small centrifuge chambers onto freshly glow-discharged carbon-collodion electron microscopic grids at 2500 g for 20 min [64,65]. Specimens were briefly rinsed in distilled water, stained for 1 min in 1% aqueous uranyl acetate solution [66], air dried and studied on a JEM-100CX electron microscope (JEOL, Peabody, MA, USA) in Core Facility “UNIQEM Collection” of Federal Research Centre “Fundamentals of Biotechnology” of the Russian Academy of Sciences.…”
Section: Methodsmentioning
confidence: 99%