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Science 12 July 1996: Vol. 273. no. 5272, pp. 211 - 217 DOI: 10.1126/science.273.5272.211
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Research Articles
Transcription Processivity: Protein-DNA Interactions Holding
Together the Elongation Complex
Evgeny Nudler,
*
Ekaterina Avetissova,
Vadim Markovtsov,
Alex Goldfarb
The elongation of RNA chains during transcription
occurs in a ternary complex containing RNA polymerase (RNAP), DNA
template, and nascent RNA. It is shown here that elongating RNAP from
Escherichia coli can switch DNA templates by means of
end-to-end transposition without loss of the transcript. After the
switch, transcription continues on the new template. With the use of
defined short DNA fragments as switching templates, RNAP-DNA
interactions were dissected into two spatially distinct components,
each contributing to the stability of the elongating complex. The front
(F) interaction occurs ahead of the growing end of RNA. This
interaction is non-ionic and requires 7 to 9 base pairs of intact DNA
duplex. The rear (R) interaction is ionic and requires approximately
six nucleotides of the template DNA strand behind the active site and
one nucleotide ahead of it. The nontemplate strand is not involved.
With the use of protein-DNA crosslinking, the F interaction was mapped
to the conserved zinc finger motif in the NH2-terminus of
the  subunit and the R interaction, to the COOH-terminal catalytic
domain of the subunit. Mutational disruption of the zinc finger
selectively destroyed the F interaction and produced a salt-sensitive
ternary complex with diminished processivity. A model of the ternary
complex is proposed here that suggests that trilateral contacts in the
active center maintain the nonprocessive complex, whereas a front-end
domain including the zinc finger ensures processivity.
The authors are in the Public Health Research Institute, New York,
NY 10016, USA.
*
To whom correspondence should be addressed.
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