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Vol. 14, Issue 3, 1255-1267, March 2003
Institute of Genetics, University of Nottingham,
Nottingham NG7 2UH, United Kingdom
We have examined the localization and targeting of the RNA
polymerase II (pol II) transcription elongation factor TFIIS in amphibian oocyte nuclei by immunofluorescence. Using a novel antibody against Xenopus TFIIS the major sites of immunostaining
were found to be Cajal bodies, nuclear organelles that also contain pol
II. Small granular structures attached to lampbrush chromosomes were also specifically stained but the transcriptionally active loops were
not. Similar localization patterns were found for the newly synthesized
myc-tagged TFIIS produced after injection of synthetic transcripts into the cytoplasm. The basis of the rapid and preferential targeting of TFIIS to Cajal bodies was investigated by examining the
effects of deletion and site-specific mutations. Multiple regions of
TFIIS contributed to efficient targeting including the domain required
for its binding to pol II. The localization of TFIIS in Cajal bodies,
and in particular the apparent involvement of pol II binding in
achieving it, offer further support for a model in which Cajal bodies
function in the preassembly of the transcriptional machinery. Although
our findings are therefore consistent with TFIIS playing a role in
early events of the transcription cycle, they also suggest that this
elongation factor is not generally required during transcription in oocytes.
Corresponding author. E-mail address:
garry.morgan{at}nottingham.ac.uk.
*
Present address: Department of Biochemistry, University of
Bristol, School of Medical Sciences, Bristol BS8 1TD, UK.
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