Subject(s)
DNA Replication , RNA, Ribosomal/genetics , Sea Urchins/genetics , Animals , Chromosome Mapping , DNA, Satellite/genetics , Genes , Genes, RegulatorSubject(s)
Genes , RNA, Ribosomal/genetics , Transcription, Genetic , Xenopus/genetics , Animals , Base Sequence , Cell Nucleolus/metabolism , Chromosomal Proteins, Non-Histone/metabolism , DNA Topoisomerases, Type I/metabolism , Female , Guanosine Triphosphate/metabolism , Methylation , Oocytes/metabolism , RNA Polymerase I/metabolismABSTRACT
Many repeating units of Drosophila melanogaster rDNA contain a DNA sequence within the gene for 28S rRNA that does not code for rRNA. This sequence has been called the ribosomal insertion [Wellauer, P. K. & Dawid, I. B. (1977) Cell 10, 193-212]. We report here that members of the same sequence family occur outside the ribosomal locus. "Non-rDNA insertion DNA" was separated from rDNA by density gradient centrifugation, and sequences homologous to the ribosomal insertion were detected by hybridization with restriction endonuclease fragments derived from a cloned rDNA repeating unit. Pure insertion sequences from cloned rDNA separated from main band DNA and behaved like a component with high G + C content. Non-rDNA components hybridizing to the insertion also separated from main band DNA but less so than pure insertion sequences, suggesting that non-rDNA insertion sequences are linked to DNA of different nucleotide composition. Restriction endonuclease analysis of non-rDNA insertion DNA showed many fragments of different sizes. The patterns obtained were similar in embryonic, larval, pupal, and adult DNA and DNA from cultured cells (Schneider cell line 3). Non-rDNA insertion sequences account for about 0.2% of the genome or about 400 kbases of DNA per haploid complement.
Subject(s)
Cell Nucleolus/analysis , DNA/genetics , Ribosomes/analysis , Animals , Base Sequence , DNA Replication , DNA Restriction Enzymes , Drosophila melanogaster , HydrolysisSubject(s)
DNA/analysis , Genes , RNA, Ribosomal/biosynthesis , Animals , Base Sequence , DNA Restriction Enzymes , XenopusSubject(s)
DNA, Viral , Transcription, Genetic , Bacterial Proteins , Coliphages , DNA Restriction Enzymes , DNA, Circular/metabolism , DNA, Viral/metabolism , DNA-Directed RNA Polymerases/metabolism , Escherichia coli/enzymology , Haemophilus influenzae/enzymology , Microscopy, Electron , Nucleic Acid Conformation , Streptomyces/enzymology , Viral ProteinsABSTRACT
We studied RNA synthesis in vitro from closed-circular lambda DNA molecules with varying degrees of superhelicity. The four circular templates examined had 0, -50, -110, and -160 superhelical turns under the conditions of the transcription assay. We found that the total amount of RNA synthesis increases as the template acquires more negative superhelical turns. This increased transcription results from more frequent initiation of RNA chains. Transcription of circular DNA with no superhelical turns appears to mimic RNA synthesis in vivo more closely than transcription from either highly superhelical or linear DNA with regard to two criteria: preferential transcription of the region corresponding to early genes and sensitivity to repression by lambda cI protein. We suggest that the physical basis for the increased initiation of RNA chains from superhelical DNA is the fact that unwinding events are energetically favored on a DNA molecule with negative superhelical turns. Possible general mechanisms are: (a) RNA polymerase must unwind the DNA duplex as a prelude to initiation; (b) the DNA itself must assume a new conformation at the promoter site which requires an unwinding of the DNA duplex.