scholarly journals Fractionation of nucleic acids from Penicillium chrysogenum and associated ribonucleic acid viruses by selective exclusion and retention in agarose gels

1974 ◽  
Vol 139 (1) ◽  
pp. 157-162 ◽  
Author(s):  
S. L. Petrović ◽  
B. D. Šumonja ◽  
R. B. Vasiljević

Double-stranded nucleic acids from a strain of Penicillium chrysogenum containing RNA viruses were isolated by agarose-gel filtration, and separated into DNA and double-stranded RNA fractions by agarose-gel chromatography in 2.5m-NaCl. The DNA fraction contained less than 1% alkali-labile polynucleotides, and sedimented homogeneously at 8–10S in alkaline sucrose gradients. In CsCl gradients it tended to band in the density region of 1.66–1.72g/ml. It had a `melting' temperature (Tm) of 75°C in 0.015m-NaCl–0.0015m-trisodium citrate, corresponding to 51.5mol% of G+C. The double-stranded RNA fraction did not contain detectable DNA. It could not band in CsCl up to a density of 1.78g/ml, and mainly consisted of a 14–15S RNA species with a Tm of 88.5°C in the above solvent, and a G+C content of 49.3 mol%.

2019 ◽  
Vol 94 (1) ◽  
Author(s):  
Yuxin Ma ◽  
Armelle Marais ◽  
Marie Lefebvre ◽  
Sébastien Theil ◽  
Laurence Svanella-Dumas ◽  
...  

ABSTRACT Metagenomic studies have indicated that the diversity of plant viruses was until recently far underestimated. As important components of ecosystems, there is a need to explore the diversity and richness of the viruses associated with plant populations and to understand the drivers shaping their diversity in space and time. Two viral sequence enrichment approaches, double-stranded RNA (dsRNA) and virion-associated nucleic acids (VANA), have been used and compared here for the description of the virome of complex plant pools representative of the most prevalent plant species in unmanaged and cultivated ecosystems. A novel bioinformatics strategy was used to assess viral richness not only at the family level but also by determining operational taxonomic units (OTU) following the clustering of conserved viral domains. A large viral diversity dominated by novel dsRNA viruses was detected in all sites, while a large between-site variability limited the ability to draw a clear conclusion on the impact of cultivation. A trend for a higher diversity of dsRNA viruses was nevertheless detected in unmanaged sites (118 versus 77 unique OTUs). The dsRNA-based approach consistently revealed a broader and more comprehensive diversity for RNA viruses than the VANA approach, whatever the assessment criterion. In addition, dissimilarity analyses indicated both approaches to be largely reproducible but not necessarily convergent. These findings illustrate features of phytoviromes in various ecosystems and a novel strategy for precise virus richness estimation. These results allow us to reason methodological choices in phytovirome studies and likely in other virome studies where RNA viruses are the focal taxa. IMPORTANCE There are today significant knowledge gaps on phytovirus populations and on the drivers impacting them but also on the comparative performance-methodological approaches for their study. We used and compared two viral sequence enrichment approaches, double-stranded RNAs (dsRNA) and virion-associated nucleic acids (VANA), for phytovirome description in complex pools representative of the most prevalent plant species in unmanaged and cultivated ecosystems. Viral richness was assessed by determining operational taxonomic units (OTU) following the clustering of conserved viral domains. There is some limited evidence of an impact of cultivation on viral populations. These results provide data allowing us to reason the methodological choices in virome studies. For researchers primarily interested in RNA viruses, the dsRNA approach is recommended because it consistently provided a more comprehensive description of the analyzed phytoviromes, but it understandably underrepresented DNA viruses and bacteriophages.


1977 ◽  
Vol 55 (8) ◽  
pp. 904-907 ◽  
Author(s):  
Alan Pater ◽  
Mary M. Pater

In dilute solutions, proteins and nucleic acids from the extremely halophilic bacterium Halobacterium cutirubrum remain soluble in 2.38 M ammonium sulphate and bind firmly to unsubstituted agarose gel columns. These macromolecules are clearly separated during elution with a decreasing salt concentration gradient.


1990 ◽  
Vol 68 (9) ◽  
pp. 1898-1902 ◽  
Author(s):  
W. K. Kim ◽  
W. Mauthe ◽  
G. Hausner ◽  
G. R. Klassen

An efficient method for the extraction of DNA and RNA from fungi is described. Urediosporelings and sporidia of two basidiomycete species and mycellia from several species of Ascomycetes and Oomycetes were homogenized in a lysis buffer containing sodium dodecyl sulfate followed by cetyltrimethylammonium bromide extraction of carbohydrates in 1.4 M NaCl, leaving nucleic acids in the supernatant. After chloroform – isoamyl alcohol extraction of proteins, nucleic acids were precipitated with ethanol. Total nucleic acids prepared in this way contained nuclear, ribosomal, and mitochondrial DNA as well as double-stranded and single-stranded RNA. DNA was eluted from agarose gels and digested with endonucleases, labelled by nick translation, and used for hybridization without nonspecific background signal. A method is also described for RNase digestion of single-stranded and double-stranded RNA in agarose gels. Key words: DNA extraction, double-stranded RNA, cetyltrimethylammonium bromide, sodium dodecyl sulfate.


1972 ◽  
Vol 27 (03) ◽  
pp. 610-618 ◽  
Author(s):  
H Graeff ◽  
R von Hugo

SummaryThe observation of fibrinogen derivatives with a molecular weight higher than the parent molecule in human cases of DIC initiated the present methodological study. These derivatives were identified by the following methods : 2.5 M β-alanine precipitation of the plasma samples, PAA gel electrophoresis, intra gel immunoprecipitation and agarose gel chromatography. In the plasma of a patient with severe eclampsia and laboratory signs of DIC two derivatives with a molecular weight higher than that of fibrinogen were identified according to their relative electrophoretic mobilities: 0.18 and 0.28 × 10−5 cm2/V × sec (fibrinogen: 0.43 × 10−5 cm2/V × sec). Electrophoretic studies in the presence of 5 M urea indicated that the 0.28 derivative is a complex probably formed by fibrinogen and a fibrin monomer.


Viruses ◽  
2021 ◽  
Vol 13 (3) ◽  
pp. 361
Author(s):  
Rui-Zhu Shi ◽  
Yuan-Qing Pan ◽  
Li Xing

The RNA helicase A (RHA) is a member of DExH-box helicases and characterized by two double-stranded RNA binding domains at the N-terminus. RHA unwinds double-stranded RNA in vitro and is involved in RNA metabolisms in the cell. RHA is also hijacked by a variety of RNA viruses to facilitate virus replication. Herein, this review will provide an overview of the role of RHA in the replication of RNA viruses.


Sign in / Sign up

Export Citation Format

Share Document