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Book ChapterDOI

Visualization of RNA synthesis on chromosomes.

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TLDR
Structural aspects of the activity of specific genes are demonstrated here using representatives of both eukaryotic and prokaryotic cell types using the use of relatively simple techniques for isolating portions of active genomes.
Abstract
Publisher Summary The numerous electron microscope autoradiographic studies of eukaryotic cells show that RNA synthesis is localized in dispersed chromatin in both nucleolar and non-nucleolar compartments of the nucleus. Alternatively, autoradiography of thin sections of pulse-labeled bacteria shows the localization of RNA synthesis near the interface of the ribosome-containing areas of the cell and the nucleoid regions that contain most of the bacterial DNA. An example of the structural resolution of genetic activity obtainable by thin-sectioning methods is presented in this chapter. In none of the thin-section studies with either eukaryotic or prokaryotic cells, however, could a distinct genetic unit be resolved within the regions active in RNA synthesis. More recently, direct visualization of the fine structure of individual, active genes in both cell types has been accomplished through novel isolation techniques. This chapter discusses the current status of these studies. Structural aspects of the activity of specific genes are demonstrated here using representatives of both eukaryotic and prokaryotic cell types. In both cases, inherent characteristics of the cells permitted the use of relatively simple techniques for isolating portions of active genomes.

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Citations
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Journal ArticleDOI

In vivo dynamics of RNA polymerase II transcription

TL;DR: The systems approach, quantifying both polymerase and mRNA kinetics on a defined DNA template in vivo with high temporal resolution, opens new avenues for studying regulation of transcriptional processes in vivo.
Journal ArticleDOI

Structure and function of the cell envelope of gram-negative bacteria.

TL;DR: Annotation of structure of the gram-NEGATIVE CELL ENVELOPE, association of ENZYMES with SPECIFIC CELL WALL COMPONENTS, and mechanism of contact with wall components are described.
Journal ArticleDOI

Identification and characterization of the packaging proteins of core 40S hnRNP particles

TL;DR: The similarity in protein composition of core RNP particles from different cell types is consistent with a conserved particle structure and function in eucaryotes.
Journal ArticleDOI

Assembly of the nuclear transcription and processing machinery: Cajal bodies (coiled bodies) and transcriptosomes.

TL;DR: A model is presented in which pol I, pol II, and pol III transcriptosomes are assembled in the Cajal bodies before export to the nucleolus, to the B-snurposomes and eventually to the chromosomes (pol II), and directly to the chromosome (pol III).
Journal ArticleDOI

Ultrastructural aspects of oogenesis and oocyte growth in fish and amphibians.

TL;DR: Oogenesis, the early events of primary oocyte growth (meiotic arrest, synapsis, ribosomal gene duplication), and folliculogenesis can be seen to particular advantage in the germinal ridge of the syngnathan ovary.
References
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Journal ArticleDOI

Visualization of Nucleolar Genes

TL;DR: The presence of extrachromosomal nucleoli in amphibian oocytes has permitted isolation and electron microscopic observation of the genes coding for ribosomal RNA precursor molecules.
Journal ArticleDOI

Molecular characterization of ribonucleic acid from Escherichia coli ribosomes

TL;DR: The ribon nucleic acid from purified 30 s, 50 s and 70 s ribosomes of E. coli has been isolated by the phenol and detergent methods and it is suggested that they are heterogeneous; some contain one 23 s ribonucleic acid component, while others contain two 16 s units.
Journal ArticleDOI

A comparison of the ribosomal DNA's of Xenopus laevis and Xenopus mulleri: the evolution of tandem genes☆

TL;DR: It is concluded that a “correction” mechanism must operate to spread a mutation in one spacer sequence to the neighboring spacers faster than new changes arise in these genes.