Sequence complexity of nuclear RNA from 2-acetylaminofluorene-induced rat hepatomas and host cirrhotic liver. 1982

G E Austin, and R J Russo, and G H Moyer

The sequence complexities of nuclear of RNAs from 2-acetylaminofluorene-induced rat hepatomas and host cirrhotic livers were compared in RNA-driven and host cirrhotic livers were compared in RNA-driven hybridization experiments using iodinated single-copy DNa as a probe. Normal liver nuclei RNA hybridized to 10.0 +/- 0.3+ (mean +/- S.D.) of the DNA, indicating an RNA sequence complexity of 3.8 x 10(8) nucleotides. Although nuclear RNAs from cirrhotic livers displayed a greater variation between animals, the mean values for percent DNA hybridized (9.5 +/- 2.0%) and RNA sequence complexity (3.6 x 10(8) nucleotides) for 5 cirrhotic livers examined did not differ significantly from normal. Analysis of nuclear RNAs from 10 tumors, 8 of which were classified as moderately to well differentiated histologically, revealed a level of hybridization (9.5 +/- 1.8%) and a mean value of RNA sequence complexity (3.6 x 10(8) nucleotides) that were almost identical with those for normal liver. Variation in the complexity amont tumors was slightly less than that among cirrhotic liver RNAs. These results suggest that while growth characteristics, biochemical properties, and physiology are known to vary between hepatomas and normal or cirrhotic liver tissue, there is no substantial or consistent difference in the RNA sequence complexity of chemically-induced hepatoma cells compared with normal or chemically-induced cirrhotic liver.

UI MeSH Term Description Entries
D008106 Liver Cirrhosis, Experimental Experimentally induced chronic injuries to the parenchymal cells in the liver to achieve a model for LIVER CIRRHOSIS. Hepatic Cirrhosis, Experimental,Cirrhoses, Experimental Liver,Cirrhosis, Experimental Liver,Experimental Liver Cirrhoses,Experimental Liver Cirrhosis,Liver Cirrhoses, Experimental,Experimental Hepatic Cirrhosis
D008114 Liver Neoplasms, Experimental Experimentally induced tumors of the LIVER. Hepatoma, Experimental,Hepatoma, Morris,Hepatoma, Novikoff,Experimental Hepatoma,Experimental Hepatomas,Experimental Liver Neoplasms,Hepatomas, Experimental,Neoplasms, Experimental Liver,Experimental Liver Neoplasm,Liver Neoplasm, Experimental,Morris Hepatoma,Novikoff Hepatoma
D008297 Male Males
D009693 Nucleic Acid Hybridization Widely used technique which exploits the ability of complementary sequences in single-stranded DNAs or RNAs to pair with each other to form a double helix. Hybridization can take place between two complimentary DNA sequences, between a single-stranded DNA and a complementary RNA, or between two RNA sequences. The technique is used to detect and isolate specific sequences, measure homology, or define other characteristics of one or both strands. (Kendrew, Encyclopedia of Molecular Biology, 1994, p503) Genomic Hybridization,Acid Hybridization, Nucleic,Acid Hybridizations, Nucleic,Genomic Hybridizations,Hybridization, Genomic,Hybridization, Nucleic Acid,Hybridizations, Genomic,Hybridizations, Nucleic Acid,Nucleic Acid Hybridizations
D011919 Rats, Inbred Strains Genetically identical individuals developed from brother and sister matings which have been carried out for twenty or more generations or by parent x offspring matings carried out with certain restrictions. This also includes animals with a long history of closed colony breeding. August Rats,Inbred Rat Strains,Inbred Strain of Rat,Inbred Strain of Rats,Inbred Strains of Rats,Rat, Inbred Strain,August Rat,Inbred Rat Strain,Inbred Strain Rat,Inbred Strain Rats,Inbred Strains Rat,Inbred Strains Rats,Rat Inbred Strain,Rat Inbred Strains,Rat Strain, Inbred,Rat Strains, Inbred,Rat, August,Rat, Inbred Strains,Rats Inbred Strain,Rats Inbred Strains,Rats, August,Rats, Inbred Strain,Strain Rat, Inbred,Strain Rats, Inbred,Strain, Inbred Rat,Strains, Inbred Rat
D004273 DNA, Neoplasm DNA present in neoplastic tissue. Neoplasm DNA
D000818 Animals Unicellular or multicellular, heterotrophic organisms, that have sensation and the power of voluntary movement. Under the older five kingdom paradigm, Animalia was one of the kingdoms. Under the modern three domain model, Animalia represents one of the many groups in the domain EUKARYOTA. Animal,Metazoa,Animalia
D001483 Base Sequence The sequence of PURINES and PYRIMIDINES in nucleic acids and polynucleotides. It is also called nucleotide sequence. DNA Sequence,Nucleotide Sequence,RNA Sequence,DNA Sequences,Base Sequences,Nucleotide Sequences,RNA Sequences,Sequence, Base,Sequence, DNA,Sequence, Nucleotide,Sequence, RNA,Sequences, Base,Sequences, DNA,Sequences, Nucleotide,Sequences, RNA
D012313 RNA A polynucleotide consisting essentially of chains with a repeating backbone of phosphate and ribose units to which nitrogenous bases are attached. RNA is unique among biological macromolecules in that it can encode genetic information, serve as an abundant structural component of cells, and also possesses catalytic activity. (Rieger et al., Glossary of Genetics: Classical and Molecular, 5th ed) RNA, Non-Polyadenylated,Ribonucleic Acid,Gene Products, RNA,Non-Polyadenylated RNA,Acid, Ribonucleic,Non Polyadenylated RNA,RNA Gene Products,RNA, Non Polyadenylated
D015073 2-Acetylaminofluorene A hepatic carcinogen whose mechanism of activation involves N-hydroxylation to the aryl hydroxamic acid followed by enzymatic sulfonation to sulfoxyfluorenylacetamide. It is used to study the carcinogenicity and mutagenicity of aromatic amines. 2-Acetamidofluorene,Fluoren-2-ylacetamide,2-AAF,2-Fluorenylacetamide,AAF, Aminofluorene,Acetylaminofluorene,N-2-Fluorenylacetamide,N-Acetyl-2-Aminofluorene,2 Acetamidofluorene,2 Acetylaminofluorene,2 Fluorenylacetamide,Aminofluorene AAF,Fluoren 2 ylacetamide,N 2 Fluorenylacetamide,N Acetyl 2 Aminofluorene

Related Publications

G E Austin, and R J Russo, and G H Moyer
January 1969, Cancer research,
G E Austin, and R J Russo, and G H Moyer
December 1967, Die Naturwissenschaften,
G E Austin, and R J Russo, and G H Moyer
October 1979, The Biochemical journal,
G E Austin, and R J Russo, and G H Moyer
December 1976, Biochimica et biophysica acta,
G E Austin, and R J Russo, and G H Moyer
January 1971, Israel journal of medical sciences,
G E Austin, and R J Russo, and G H Moyer
January 1968, European journal of biochemistry,
G E Austin, and R J Russo, and G H Moyer
December 1975, Cancer research,
G E Austin, and R J Russo, and G H Moyer
January 1967, Voprosy onkologii,
G E Austin, and R J Russo, and G H Moyer
March 1977, Biulleten' eksperimental'noi biologii i meditsiny,
Copied contents to your clipboard!