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1.
Mol Biol Cell ; 18(2): 394-403, 2007 Feb.
Article in English | MEDLINE | ID: mdl-17108330

ABSTRACT

Pre-rRNA synthesis and processing are key steps in ribosome biogenesis. Although recent evidence in yeast suggests that these two processes are coupled, the nature of their association is unclear. In this report, we analyze the coordination between rDNA transcription and pre-rRNA processing in mammalian cells. We found that pol I transcription factor UBF interacts with pre-rRNA processing factors as analyzed by immunoprecipitations, and the association depends on active rRNA synthesis. In addition, injections of plasmids containing the human rDNA promoter and varying lengths of 18S rDNA into HeLa nuclei show that pol I transcription machinery can be recruited to rDNA promoters regardless of the product that is transcribed, whereas subgroups of pre-rRNA processing factors are recruited to plasmids only when specific pre-rRNA fragments are produced. Our observations suggest a model for sequential recruitment of pol I transcription factors and pre-rRNA processing factors to elongating pre-rRNA on an as-needed basis rather than corecruitment to sites of active transcription.


Subject(s)
DNA, Ribosomal/genetics , Pol1 Transcription Initiation Complex Proteins/metabolism , RNA Precursors/metabolism , RNA Processing, Post-Transcriptional , RNA, Ribosomal/metabolism , Transcription, Genetic , Dactinomycin/pharmacology , HeLa Cells , Humans , Plasmids/genetics , Pol1 Transcription Initiation Complex Proteins/analysis , Promoter Regions, Genetic , RNA, Small Nucleolar/metabolism , Ribonuclease, Pancreatic/pharmacology , Transcription, Genetic/drug effects
3.
J Microsc ; 112(2): 169-82, 1978 Mar.
Article in English | MEDLINE | ID: mdl-650676

ABSTRACT

A chamber for introducing, fracturing and coating frozen biological samples has been developed as an attachment to the sepcimen chamber of a scanning electron microscope. Together with a eucentric-tilt cold-stage, this chamber constitutes a complete system for viewing fractured biological surfaces of the type normally only seen by replica techniques. An air-lock on the chamber accepts a transfer module to allow insertion of the frozen sample without frost build-up. Fracturing is carried out with a precisely adjustable cooled knife under a 10--100X binocular microscope. The sample can tilt and rotate while being coated with carbon or metals evaporated from rechargeable sources introduced through the air-lock. Cooling in the chamber is provided by a cylindrical copper tank filled with liquid nitrogen. The chamber has its own LN2 trapped high vacuum system. After preparation the sample can be placed directly into the SEM through an isolation valve. The cold-stage utilizes a Joule-Thomson refrigerator. The sample can be kept below 103 K at all times though there are provisions for heating it in the fracturing and cold-stage positions. A system of controls, sensors and interlocks simplifies the operation of the system.


Subject(s)
Freeze Fracturing/instrumentation , Microscopy, Electron, Scanning , Animals , Blood Cells/ultrastructure , Epithelium/ultrastructure , Kidney Tubules, Proximal/ultrastructure , Mice , Plants/ultrastructure
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