Literature DB >> 9056409

Quantitative digital analysis of diffuse and concentrated nuclear distributions of nascent transcripts, SC35 and poly(A).

F S Fay1, K L Taneja, S Shenoy, L Lifshitz, R H Singer.   

Abstract

Digital imaging microscopy was used to analyze the spatial distribution and levels of newly synthesized RNA in relation to steady-state poly(A) RNA and to the splicing factor SC35. Transcription was monitored over time after microinjection of BrUTP and was detected using antibodies. Poly(A) RNA was detected with probes directly conjugated to fluorochromes, allowing direct detection of the hybrids. Objective methods were used to determine genuine signal. A defined threshold level to separate signal from noise was established for each nucleus. The nucleolus was used to determine poly(A) and SC35 background and the juxtanuclear cytoplasm was used for the BrUTP background. The remaining signal was segmented into high (concentrated) and low (diffuse) levels. Surprisingly, for all probes examined, most of the signal was not in concentrated areas, but rather was diffusely spread throughout the nucleoplasm. A minority (20-30%) of the SC35 signal was in concentrated areas ("speckles") and the rest was dispersed throughout the nucleoplasm. In addition, the concentrated areas had a mean intensity only twice the average. The amount and significance of the colocalization of the diffuse, or concentrated, areas of SC35 [or poly(A)] with BrUTP incorporation were analyzed. The image from one probe was translated with respect to the other in three dimensions to compare colocalization with random alignments. Both poly(A) and SC35 were found to have low colocalization with the total BrU signal. Sites of transcription were determined using an algorithm to find maxima of BrUTP signal within clusters. From 849 to as many as 3888 sites per nucleus were detected. A rim of hybridization to poly(A) coinciding with the nuclear envelope was eliminated by actinomycin treatment, suggesting that these transcripts were exiting from the nucleus. These results emphasize the importance of utilizing the full dynamic range of the image before drawing conclusions as to the distribution of nuclear components.

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Year:  1997        PMID: 9056409     DOI: 10.1006/excr.1996.3460

Source DB:  PubMed          Journal:  Exp Cell Res        ISSN: 0014-4827            Impact factor:   3.905


  48 in total

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Authors:  M N Szentirmay; M Sawadogo
Journal:  Nucleic Acids Res       Date:  2000-05-15       Impact factor: 16.971

2.  Nuclear pre-mRNA compartmentalization: trafficking of released transcripts to splicing factor reservoirs.

Authors:  I Melcák; S Cermanová; K Jirsová; K Koberna; J Malínský; I Raska
Journal:  Mol Biol Cell       Date:  2000-02       Impact factor: 4.138

3.  Dynamics and three-dimensional localization of ribosomal RNA within the nucleolus.

Authors:  M Thiry; T Cheutin; M F O'Donohue; H Kaplan; D Ploton
Journal:  RNA       Date:  2000-12       Impact factor: 4.942

4.  Linear 2' O-Methyl RNA probes for the visualization of RNA in living cells.

Authors:  C Molenaar; S A Marras; J C Slats; J C Truffert; M Lemaître; A K Raap; R W Dirks; H J Tanke
Journal:  Nucleic Acids Res       Date:  2001-09-01       Impact factor: 16.971

5.  The functional architecture of the nucleus as analysed by ultrastructural cytochemistry.

Authors:  Stanislav Fakan
Journal:  Histochem Cell Biol       Date:  2004-08-05       Impact factor: 4.304

6.  Nascent RNA synthesis in the context of chromatin architecture.

Authors:  Nicolas Sadoni; Daniele Zink
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Journal:  Nat Methods       Date:  2012-06-28       Impact factor: 28.547

Review 8.  Organization of transcription.

Authors:  Lyubomira Chakalova; Peter Fraser
Journal:  Cold Spring Harb Perspect Biol       Date:  2010-07-28       Impact factor: 10.005

Review 9.  Gene positioning.

Authors:  Carmelo Ferrai; Inês Jesus de Castro; Liron Lavitas; Mita Chotalia; Ana Pombo
Journal:  Cold Spring Harb Perspect Biol       Date:  2010-05-19       Impact factor: 10.005

10.  A practical guide to evaluating colocalization in biological microscopy.

Authors:  Kenneth W Dunn; Malgorzata M Kamocka; John H McDonald
Journal:  Am J Physiol Cell Physiol       Date:  2011-01-05       Impact factor: 4.249

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