Visualization of the Nucleolus Using Ethynyl Uridine

被引:10
作者
Dvorackova, Martina [1 ]
Fajkus, Jiri [1 ,2 ,3 ]
机构
[1] Masaryk Univ, Mendel Ctr Plant Genom & Prote, Cent European Inst Technol, Brno, Czech Republic
[2] Masaryk Univ, Natl Ctr Biomol Res, Fac Sci, Lab Funct Genom & Prote, Brno, Czech Republic
[3] Acad Sci Czech Republ, Inst Biophys, Brno, Czech Republic
关键词
nucleolus; nucleus; transcription; Arabidopsis thaliana; click iT; DENSE FIBRILLAR COMPONENTS; RIBOSOMAL-RNA; ACTINOMYCIN-D; TRANSCRIPTION SITES; NASCENT RNA; TERMINAL ALKYNES; DNA-REPLICATION; CLICK CHEMISTRY; CHRISTMAS TREES; CELL NUCLEOLUS;
D O I
10.3389/fpls.2018.00177
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Thanks to recent innovative methodologies, key cellular processes such as replication or transcription can be visualized directly in situ in intact tissues. Many studies use so-called click iT chemistry where nascent DNA can be tracked by 5-ethynyl-2'-deoxyuridine (EdU), and nascent RNA by 5-ethynyl uridine (EU). While the labeling of replicating DNA by EdU has already been well established and further exploited in plants, the use of EU to reveal nascent RNA has not been developed to such an extent. In this article, we present a protocol for labeling of nucleolar RNA transcripts using EU and show that EU effectively highlights the nucleolus. The method is advantageous, because the need to prepare transgenic plants expressing fluorescently tagged nucleolar components when the nucleolus has to be visualized can be avoided.
引用
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页数:8
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共 62 条
[1]  
Bernhard W, 1966, Natl Cancer Inst Monogr, V23, P13
[2]  
BEVEN AF, 1995, J CELL SCI, V108, P509
[3]   SIMULTANEOUS IMMUNOELECTRON MICROSCOPIC VISUALIZATION OF PROTEIN B23 AND C23 DISTRIBUTION IN THE HELA-CELL NUCLEOLUS [J].
BIGGIOGERA, M ;
FAKAN, S ;
KAUFMANN, SH ;
BLACK, A ;
SHAPER, JH ;
BUSCH, H .
JOURNAL OF HISTOCHEMISTRY & CYTOCHEMISTRY, 1989, 37 (09) :1371-1374
[4]   Nuclear organization and dynamics of transcription sites in rat sensory ganglia neurons detected by incorporation of 5′-fluorouridine into nascent RNA [J].
Casafont, I. ;
Navascues, J. ;
Pena, E. ;
Lafarga, M. ;
Berciano, M. T. .
NEUROSCIENCE, 2006, 140 (02) :453-462
[5]   Chromosome-specific NOR inactivation explains selective rRNA gene silencing and dosage control in Arabidopsis [J].
Chandrasekhara, Chinmayi ;
Mohannath, Gireesha ;
Blevins, Todd ;
Pontvianne, Frederic ;
Pikaard, Craig S. .
GENES & DEVELOPMENT, 2016, 30 (02) :177-190
[6]   Visualization of nascent transcripts on Drosophila polytene chromosomes using BrUTP incorporation [J].
Chang, WY ;
Winegarden, NA ;
Paraiso, JP ;
Stevens, ML ;
Westwood, JT .
BIOTECHNIQUES, 2000, 29 (05) :934-936
[7]  
Chen M, 2004, ACTA PHARMACOL SIN, V25, P902
[8]   Simultaneous localization of transcription and early processing markers allows dissection of functional domains in the plant cell nucleolus [J].
de Cárcer, G ;
Medina, FJ .
JOURNAL OF STRUCTURAL BIOLOGY, 1999, 128 (02) :139-151
[9]   Analysis of Termination of Transcription Using BrUTP-strand-specific Transcription Run-on (TRO) Approach [J].
Dhoondia, Zuzer ;
Tarockoff, Ricci ;
Alhusini, Nadra ;
Medler, Scott ;
Agarwal, Neha ;
Ansari, Athar .
JOVE-JOURNAL OF VISUALIZED EXPERIMENTS, 2017, (121)
[10]   DNA replication initiation patterns and spatial dynamics of the human ribosomal RNA gene loci [J].
Dimitrova, Daniela S. .
JOURNAL OF CELL SCIENCE, 2011, 124 (16) :2743-2752