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PDBsum entry 1jzc
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Rna
7:1476-1485
(2001)
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PubMed id:
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A mutant viral RNA promoter with an altered conformation retains efficient recognition by a viral RNA replicase through a solution-exposed adenine.
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C.H.Kim,
C.C.Kao.
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ABSTRACT
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Brome mosaic virus (BMV) genomic minus-strand RNA synthesis requires an RNA
motif named stem-loop C (SLC). An NMR-derived solution structure of SLC was
reported by Kim et al. (Nature Struc Biol, 2000, 7:415-423) to contain three
replicase-recognition elements, the most important of which is a stable stem
with a terminal trinucleotide loop, 5'AUA3'. The 5'-most adenine of the triloop
is rigidly fixed to the stem helix by interactions that require the 3'-most
adenine, which is called a clamped adenine motif. However, a change of the 3'
adenine to guanine (5'AUG3') unexpectedly directed RNA synthesis at 130% of wild
type (Kim et al., Nature Struc Biol, 2000, 7:415-423). To understand how RNA
with the AUG mutation maintains interaction with the BMV replicase, we used NMR
and other biophysical techniques to elucidate the solution conformation of a
13-nt RNA containing the AUG triloop, called S-AUG. We found that S-AUG has a
drastically different loop conformation in comparison to the wild type, as
evidenced by an unusual C x G loop-closing base pair. Despite the conformational
change, S-AUG maintains a solution-exposed adenine similar to the clamped
adenine motif found in the wild type. Biochemical studies of the 5'AUG3' loop
with various substitutions in the context of the whole SLC construct confirm
that the clamped adenine motif exists in S-AUG remains a primary structural
feature required for RNA synthesis by the BMV replicase.
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Literature references that cite this PDB file's key reference
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PubMed id
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Reference
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O.Taxilaga-Zetina,
P.Pliego-Pastrana,
and
M.D.Carbajal-Tinoco
(2010).
Three-dimensional structures of RNA obtained by means of knowledge-based interaction potentials.
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Phys Rev E Stat Nonlin Soft Matter Phys,
81,
041914.
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G.Yi,
E.Letteney,
C.H.Kim,
and
C.C.Kao
(2009).
Brome mosaic virus capsid protein regulates accumulation of viral replication proteins by binding to the replicase assembly RNA element.
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RNA,
15,
615-626.
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G.Yi,
R.C.Vaughan,
I.Yarbrough,
S.Dharmaiah,
and
C.C.Kao
(2009).
RNA binding by the brome mosaic virus capsid protein and the regulation of viral RNA accumulation.
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J Mol Biol,
391,
314-326.
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K.Gopinath,
B.Dragnea,
and
C.Kao
(2005).
Interaction between Brome mosaic virus proteins and RNAs: effects on RNA replication, protein expression, and RNA stability.
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J Virol,
79,
14222-14234.
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M.Hema,
K.Gopinath,
and
C.Kao
(2005).
Repair of the tRNA-like CCA sequence in a multipartite positive-strand RNA virus.
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J Virol,
79,
1417-1427.
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T.Sakamoto,
A.Oguro,
G.Kawai,
T.Ohtsu,
and
Y.Nakamura
(2005).
NMR structures of double loops of an RNA aptamer against mammalian initiation factor 4A.
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Nucleic Acids Res,
33,
745-754.
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PDB codes:
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M.Hema,
and
C.C.Kao
(2004).
Template sequence near the initiation nucleotide can modulate brome mosaic virus RNA accumulation in plant protoplasts.
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J Virol,
78,
1169-1180.
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C.T.Ranjith-Kumar,
X.Zhang,
and
C.C.Kao
(2003).
Enhancer-like activity of a brome mosaic virus RNA promoter.
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J Virol,
77,
1830-1839.
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K.Sivakumaran,
M.Hema,
and
C.C.Kao
(2003).
Brome mosaic virus RNA syntheses in vitro and in barley protoplasts.
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J Virol,
77,
5703-5711.
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X.Zhang,
C.H.Kim,
K.Sivakumaran,
and
C.Kao
(2003).
Stable RNA structures can repress RNA synthesis in vitro by the brome mosaic virus replicase.
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RNA,
9,
555-565.
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The most recent references are shown first.
Citation data come partly from CiteXplore and partly
from an automated harvesting procedure. Note that this is likely to be
only a partial list as not all journals are covered by
either method. However, we are continually building up the citation data
so more and more references will be included with time.
Where a reference describes a PDB structure, the PDB
codes are
shown on the right.
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