Ultrastructural analysis of nucleolar transcription in cells microinjected with 5-bromo-UTP

被引:69
作者
Cmarko, D
Verschure, PJ
Rothblum, LI
Hernandez-Verdun, D
Amalric, F
van Driel, R
Fakan, S
机构
[1] Univ Lausanne, Ctr Electron Microscopy, CH-1005 Lausanne, Switzerland
[2] Univ Amsterdam, EC Slater Inst Biochem Res, NL-1081 TV Amsterdam, Netherlands
[3] Penn State Univ, Coll Med, Weis Ctr Res, Danville, PA 17822 USA
[4] Univ Paris 07, Inst Jacques Monod, F-75251 Paris, France
[5] Inst Pharmacol & Biol Struct, F-31077 Toulouse, France
关键词
D O I
10.1007/s004180050437
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
In situ sites of nucleolar transcription in cells microinjected with 5-bromo-UTP (BrUTP) were visualized at an ultrastructural level. After injection the cells were maintained for 4-90 min at 37 degrees C, fixed, and embedded in LR White resin. Postembedding immunoelectron microscopic visualization with colloidal gold has been used for localizing both Br-labeled precursor incorporated into pre-rRNA and different nucleolar transcription or processing factors. This high resolution approach allowed us to identify significant signal as early as after 4-min incubation periods following BrUTP microinjection. It revealed the dense fibrillar component (DFC) as being the first nucleolar compartment labeled with anti-bromodeoxyuridine antibody. Moreover, RNA polymerase I, nucleolar transcription factor UBF, and fibrillarin were also detected almost exclusively in this same nucleolar compartment. From 30 min onward, following microinjection, Br-labeled rRNA occurred also in the granular component. The results indicate that the DFC is the site of pre-rRNA transcription and of initial steps of pre-rRNA processing. Moreover, it demonstrates that BrUTP microinjection followed by postembedding detection of Br-labeled RNA is a useful technique for high resolution studies of structure-function associations in the nucleolus.
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收藏
页码:181 / 187
页数:7
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