Nuclear pre-mRNA compartmentalization: trafficking of released transcripts to splicing factor reservoirs
Jazyk angličtina Země Spojené státy americké Médium print
Typ dokumentu časopisecké články, práce podpořená grantem
Grantová podpora
Wellcome Trust - United Kingdom
PubMed
10679009
PubMed Central
PMC14788
DOI
10.1091/mbc.11.2.497
Knihovny.cz E-zdroje
- MeSH
- biologický transport MeSH
- buněčné jádro genetika metabolismus ultrastruktura virologie MeSH
- DNA řízené RNA-polymerasy antagonisté a inhibitory metabolismus MeSH
- DNA virů genetika metabolismus MeSH
- elektronová mikroskopie MeSH
- fluorescenční mikroskopie MeSH
- genetická transkripce genetika MeSH
- genom virový MeSH
- heterogenní jaderné ribonukleoproteiny MeSH
- introny genetika MeSH
- jaderné proteiny metabolismus MeSH
- konfokální mikroskopie MeSH
- lidé MeSH
- messenger RNA genetika metabolismus MeSH
- nádorové buňky kultivované MeSH
- plazmidy genetika MeSH
- prekurzory RNA genetika metabolismus MeSH
- ribonukleoproteiny metabolismus MeSH
- RNA virová genetika metabolismus MeSH
- serin-arginin sestřihové faktory MeSH
- spliceozomy genetika metabolismus ultrastruktura MeSH
- virové geny genetika MeSH
- virus Epsteinův-Barrové genetika MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- DNA řízené RNA-polymerasy MeSH
- DNA virů MeSH
- heterogenní jaderné ribonukleoproteiny MeSH
- jaderné proteiny MeSH
- messenger RNA MeSH
- prekurzory RNA MeSH
- ribonukleoproteiny MeSH
- RNA virová MeSH
- serin-arginin sestřihové faktory MeSH
- SRSF2 protein, human MeSH Prohlížeč
In the present study, the spatial organization of intron-containing pre-mRNAs of Epstein-Barr virus (EBV) genes relative to location of splicing factors is investigated. The intranuclear position of transcriptionally active EBV genes, as well as of nascent transcripts, is found to be random with respect to the speckled accumulations of splicing factors (SC35 domains) in Namalwa cells, arguing against the concept of the locus-specific organization of mRNA genes with respect to the speckles. Microclusters of splicing factors are, however, frequently superimposed on nascent transcript sites. The transcript environment is a dynamic structure consisting of both nascent and released transcripts, i.e., the track-like transcript environment. Both EBV sequences of the chromosome 1 homologue are usually associated with the track, are transcriptionally active, and exhibit in most cases a polar orientation. In contrast to nascent transcripts (in the form of spots), the association of a post-transcriptional pool of viral pre-mRNA (in the form of tracks) with speckles is not random and is further enhanced in transcriptionally silent cells when splicing factors are sequestered in enlarged accumulations. The transcript environment reflects the intranuclear transport of RNA from the sites of transcription to SC35 domains, as shown by concomitant mapping of DNA, RNA, and splicing factors. No clear vectorial intranuclear trafficking of transcripts from the site of synthesis toward the nuclear envelope for export into the cytoplasm is observed. Using Namalwa and Raji cell lines, a correlation between the level of viral gene transcription and splicing factor accumulation within the viral transcript environment has been observed. This supports a concept that the level of transcription can alter the spatial relationship among intron-containing genes, their transcripts, and speckles attributable to various levels of splicing factors recruited from splicing factor reservoirs. Electron microscopic in situ hybridization studies reveal that the released transcripts are directed toward reservoirs of splicing factors organized in clusters of interchromatin granules. Our results point to the bidirectional intranuclear movement of macromolecular complexes between intron-containing genes and splicing factor reservoirs: the recruitment of splicing factors to transcription sites and movement of released transcripts from DNA loci to reservoirs of splicing factors.
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Formation of nuclear splicing factor compartments is independent of lamins A/C
Prespliceosomal assembly on microinjected precursor mRNA takes place in nuclear speckles