Summary information and primary citation
- PDB-id
-
7eh2;
DSSR-derived features in text and
JSON formats
- Class
- transcription-DNA-RNA
- Method
- X-ray (3.34 Å)
- Summary
- Thermus thermophilus transcription initiation complex
containing a template-strand pyrimidine at position tss-2
and gpg RNA primer
- Reference
-
Skalenko KS, Li L, Zhang Y, Vvedenskaya IO, Winkelman JT,
Cope AL, Taylor DM, Shah P, Ebright RH, Kinney JB, Zhang
Y, Nickels BE (2021): "Promoter-sequence
determinants and structural basis of primer-dependent
transcription initiation in Escherichia coli ."
Proc.Natl.Acad.Sci.USA, 118.
doi: 10.1073/pnas.2106388118.
- Abstract
- Chemical modifications of RNA 5'-ends enable
"epitranscriptomic" regulation, influencing multiple
aspects of RNA fate. In transcription initiation, a large
inventory of substrates compete with nucleoside
triphosphates for use as initiating entities, providing an
ab initio mechanism for altering the RNA 5'-end. In
<i>Escherichia coli</i> cells, RNAs with a
5'-end hydroxyl are generated by use of dinucleotide RNAs
as primers for transcription initiation, "primer-dependent
initiation." Here, we use massively systematic transcript
end readout (MASTER) to detect and quantify RNA 5'-ends
generated by primer-dependent initiation for
∼4<sub>10</sub> (∼1,000,000) promoter sequences
in <i>E. coli</i> The results show
primer-dependent initiation in <i>E. coli</i>
involves any of the 16 possible dinucleotide primers and
depends on promoter sequences in, upstream, and downstream
of the primer binding site. The results yield a consensus
sequence for primer-dependent initiation,
Y<sub>TSS-2</sub>N<sub>TSS-1</sub>N<sub>TSS</sub>W<sub>TSS+1</sub>,
where TSS is the transcription start site,
N<sub>TSS-1</sub>N<sub>TSS</sub> is
the primer binding site, Y is pyrimidine, and W is A or T.
Biochemical and structure-determination studies show that
the base pair (nontemplate-strand base:template-strand
base) immediately upstream of the primer binding site
(Y:R<sub>TSS-2</sub>, where R is purine) exerts
its effect through the base on the DNA template strand
(R<sub>TSS-2</sub>) through interchain base
stacking with the RNA primer. Results from analysis of a
large set of natural, chromosomally encoded
<i>E</i> <i>coli</i> promoters
support the conclusions from MASTER. Our findings provide a
mechanistic and structural description of how TSS-region
sequence hard-codes not only the TSS position but also the
potential for epitranscriptomic regulation through
primer-dependent transcription initiation.