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1 ulting from rapid binding of the promoter to T7 RNA polymerase.
2 vitro run-off RNA synthesis is bacteriophage T7 RNA polymerase.
3 (Gly) to glyQS leader RNA generated by phage T7 RNA polymerase.
4 stream of -17 in transcription regulation of T7 RNA polymerase.
5 tochondria that we had engineered to contain T7 RNA polymerase.
6 h transcription by Escherichia coli and then T7 RNA polymerase.
7 siRNAs are siRNAs produced by bacteriophage T7 RNA polymerase.
8 the second resembles the specificity loop of T7 RNA polymerase.
9 nscription under the T7 class II promoter by T7 RNA polymerase.
10 anscription by both RNA polymerase II and by T7 RNA polymerase.
11 cultivated with human cells transfected with T7 RNA polymerase.
12 range of temperature and salinity than does T7 RNA polymerase.
13 ressed in the cytoplasm of cultured cells by T7 RNA polymerase.
14 or transcription of nucleosomal templates by T7 RNA polymerase.
15 in baby hamster kidney cells that expressed T7 RNA polymerase.
16 a new part for this function: a split intein T7 RNA polymerase.
17 ed antibody raised against the C-terminus of T7 RNA polymerase.
18 ngent for Syn5 RNA polymerase as compared to T7 RNA polymerase.
19 us locations within the promoter element for T7 RNA polymerase.
20 increase in fluorescence upon binding to the T7 RNA polymerase.
21 g low concentrations of ribonucleotides than T7 RNA polymerase.
22 in which we repositioned gene 1, coding for T7 RNA polymerase.
23 inant vaccinia virus (MVA-T7) that expressed T7 RNA polymerase.
24 understand the interaction of promoter with T7 RNA polymerase.
25 se is 24 degrees C, much lower than that for T7 RNA polymerase.
26 scherichia coli using pTara as the source of T7 RNA polymerase.
27 y kidney cells that constitutively expressed T7 RNA polymerase.
28 with a vaccinia virus recombinant expressing T7 RNA polymerase.
29 hymena group I intron using a mutant form of T7 RNA polymerase.
30 with a vaccinia virus recombinant expressing T7 RNA polymerase.
31 ro transcription of linearized plasmids with T7 RNA polymerase.
32 in the cytoplasm of mouse OST7-1 cells using T7 RNA polymerase.
33 rmediates during transcription initiation by T7 RNA polymerase.
34 of the mtRNAP closely resembles that of the T7 RNA polymerase.
35 BSRT7-5 cells, which constitutively express T7 RNA polymerase.
36 ducing RNA transcripts of various lengths by T7 RNA polymerase.
37 es by in vitro transcription reactions using T7 RNA polymerase.
38 initially transcribing abortive complexes in T7 RNA polymerase.
40 placing the template strand correctly in the T7 RNA polymerase active site upon promoter melting for
41 nucleic acid scaffolds that, when mixed with T7 RNA polymerase, allow the formation of functional tra
42 thesis using in vitro transcription by phage T7 RNA polymerase allows preparation of milligram quanti
43 protein expression 5- to 10-fold compared to T7 RNA polymerase alone while enhancing reovirus rescue
44 wnian motion and transcription elongation of T7 RNA polymerase along aligned DNA molecules bound to s
45 T7 gene 3.5 that affect its interaction with T7 RNA polymerase, also reduce the interference with T7
51 and RNA-primed DNA "bubble" constructs with T7 RNA polymerase and by initiating transcription at pro
52 ould be generated following transcription by T7 RNA polymerase and cleavage by hepatitis delta virus
54 cs between single molecules of bacteriophage T7 RNA polymerase and DNA, as a function of tension.
56 ugates inhibited transcription elongation by T7 RNA polymerase and eukaryotic RNA polymerase II from
58 ese data show that O(6)-meG partially blocks T7 RNA polymerase and human RNA polymerase II elongation
61 an layer of the cell wall, but it also binds T7 RNA polymerase and inhibits transcription, and it sti
64 of DNA templates, in vitro transcription by T7 RNA polymerase and kit-based purification provides a
68 was due to a combination of mutations in the T7 RNA polymerase and other genes expressed at the same
69 of the analogues is readily incorporated by T7 RNA polymerase and produces fully active transcripts
70 control the expression of both bacteriophage T7 RNA polymerase and recombinant gene(s) of interest.
71 hymine glycol on transcription elongation by T7 RNA polymerase and RNA polymerase II from rat liver.
73 scription system was applied, which utilizes T7 RNA polymerase and template DNAs that are either mode
74 d d5SICS:dNaM are selectively transcribed by T7 RNA polymerase and that the efficiency of d5SICS:dNaM
75 e (nA) and 2-thiouracil (sU) are taken up by T7 RNA polymerase and that the resulting RNA possesses r
76 atch and dialysis mode) under the control of T7 RNA polymerase and to other environments where transc
78 xtracted from these cells was amplified with T7 RNA polymerase and used to hybridize a microarray con
79 tude larger binding constant between DNA and T7 RNA polymerase, and five to six times larger rate con
80 cap analogue was an efficient substrate for T7 RNA polymerase, and the mRNA transcribed, with a poly
82 d strand blocked transcription elongation by T7 RNA polymerase approximately 50% of the time but did
83 ter linkages; both Klenow DNA polymerase and T7 RNA polymerase are found to synthesize complementary
84 ng in vitro transcription of longer repeats, T7 RNA polymerase arrests in the promoter distal end of
85 experimental system that uses bacteriophage T7 RNA polymerase as a probe for aspects of nucleosome t
86 he case for phage polymerases, as used here (T7 RNA polymerase), as well as RNA polymerases in bacter
87 etic studies, we propose that a fast form of T7 RNA polymerase binds promoter double-stranded DNA by
88 y shown to increase the thermal tolerance of T7 RNA polymerase can increase the activity of mutants w
89 with a biotin tag, have been prepared using T7 RNA polymerase-catalyzed transcription of synthetic D
91 Transcription initiation as catalyzed by T7 RNA polymerase consists primarily of promoter binding
94 in the thumb subdomain (residues 335-408) of T7 RNA polymerase decrease elongation complex stability
95 from the initial, promoter-bound complex of T7 RNA polymerase describes the very beginning of the in
96 hypernegative supercoiling of plasmid DNA by T7 RNA polymerase did not require anchoring of DNA to th
97 nst a d(tC-A) base pair only by factors <10, T7 RNA polymerase discriminates against tC-A base pair f
98 Based on the recent crystal structure of the T7 RNA polymerase-DNA complex, we propose that the large
101 M1 was expressed by using the vaccinia virus T7 RNA polymerase-driven overexpression system, in our n
103 also made in vivo in uninfected cells when a T7 RNA polymerase-driven transient-transfection system w
106 slippage synthesis, this study reveals that T7 RNA polymerase elongation complexes containing only a
110 cription, T7 lysozyme, does not compete with T7 RNA polymerase for RNA cross-linking, implying that t
111 initiation by affecting both the affinity of T7 RNA polymerase for the promoter and the efficiency of
112 During the early stages of transcription, T7 RNA polymerase forms an unstable initiation complex t
113 polymerase-driven minigenome system in which T7 RNA polymerase from an expression plasmid drove expre
114 e sliding and transcription by bacteriophage T7 RNA polymerase from the nucleosomal template, but not
116 e constructed in which the ecdysone promoter-T7 RNA polymerase gene had been integrated intact, as de
117 here that the pET system, in which the phage T7 RNA polymerase gene is expressed via lac operon contr
118 ible and glucose-repressible expression of a T7 RNA polymerase gene that has been integrated with an
119 , in which a lambdaDE3 prophage containing a T7 RNA polymerase gene under the control of lacUV5 promo
123 n alternative and facile delivery system for T7 RNA polymerase has been devised and constructed.
127 lve non-equivalent mechanisms, as mutants of T7 RNA polymerase have been identified that fail to reco
129 hnique, termed immuno-detection amplified by T7 RNA polymerase (IDAT) that is capable of monitoring p
130 With the linear amplification ability of T7 RNA polymerase, IDAT represents a significant improve
131 the present study the gene for bacteriophage T7 RNA polymerase, implanted with a eukaryotic nuclear l
133 As of PaV RNAs 1 and 2 were cotranscribed by T7 RNA polymerase in baby hamster kidney cells that expr
134 a single protein having the expected size of T7 RNA polymerase in immunoblots of cell extracts probed
135 rigins contain T7 promoters, but the role of T7 RNA polymerase in initiating replication is not under
136 These results highlight the malleability of T7 RNA polymerase in recognizing its promoter element an
137 nstrates that halted elongation complexes of T7 RNA polymerase in the absence of termination signals
138 nucleosomes, and transcription was done with T7 RNA polymerase in the presence of a negatively coiled
140 sphate (tCTP) and tested it as substrate for T7 RNA polymerase in transcription reactions, a convenie
142 the polyprotein and transfected the derived T7 RNA polymerase in vitro transcripts into FRhK-4 cells
143 oncentration, Hlp represses transcription by T7 RNA polymerase in vitro whereas the individual N- and
149 current study strongly supports a model for T7 RNA polymerase in which initial bubble collapse from
153 here that transcription by the bacteriophage T7 RNA polymerase increases the deamination of cytosine
154 ce with similar kinetics upon binding to the T7 RNA polymerase, indicating that the TATA sequence bec
161 In contrast, nascent pre-mRNA synthesized by T7 RNA polymerase is quantitatively assembled into the n
164 is conjugated to an antibody (Ab), and then T7 RNA polymerase is used to amplify RNA from the double
171 We also observe binding and transcription by T7 RNA polymerases on single combed T7 DNA molecules wit
172 removed from RNA substrates transcribed from T7 RNA polymerase or delivered directly to the cytoplasm
173 ally inhibited DNA transcription mediated by T7 RNA polymerase or human RNA polymerase II in vitro an
174 DNA transcription mediated by single-subunit T7 RNA polymerase or multisubunit human RNA polymerase I
175 ing transcription mediated by single-subunit T7 RNA polymerase or multisubunit human RNA polymerase I
176 to examine the fidelity of transcription by T7 RNA polymerase past an adenine residue adducted at th
180 reverse transcription with oligo(dT) with a T7 RNA polymerase promoter (T7dT) on the 5' end, and sub
181 y assembling five cDNA fragments between the T7 RNA polymerase promoter and the autocatalytic hepatit
182 st, capsid did not inhibit expression from a T7 RNA polymerase promoter construct, suggesting that th
186 PLP-1 domain in Escherichia coli by using a T7 RNA polymerase promoter system or as a maltose-bindin
187 plasmid vector directly downstream from the T7 RNA polymerase promoter, and capped RNA transcripts d
188 s NP, P, and L proteins under control of the T7 RNA polymerase promoter, were transfected into A549 c
190 ase of the T7 promoter is inhibited when the T7 RNA polymerase-promoter interaction is strengthened.
191 that open complex formation in bacteriophage T7 RNA polymerase:promoter binary complexes is thermodyn
192 specific stabilizing interactions, of the 17 T7 RNA polymerase promoters in the phage genome, 15 begi
193 translated in HeLa cells when transcribed by T7 RNA polymerase provided by a recombinant vaccinia vir
194 ed from cotransfected plasmids driven by the T7 RNA polymerase provided by the recombinant vaccinia v
195 e synthesized by in vitro transcription with T7 RNA polymerase, providing an economical alternative t
198 mid with pTara provides a low-cost method of T7 RNA polymerase-regulated expression that can be fine-
199 o I, bcTopo IIIalpha), have been cloned into T7 RNA polymerase-regulated plasmid expression vectors a
201 ins of AMPV/CO, into cells stably expressing T7 RNA polymerase resulted in the recovery of infectious
202 nscription complexes formed by bacteriophage T7 RNA polymerase reveal a nucleotide-addition cycle dri
206 orm a functional open complex, bacteriophage T7 RNA polymerase (RNAP) binds to its promoter DNA and i
207 Recent work showed that the single-subunit T7 RNA polymerase (RNAP) can generate misincorporation e
211 n vitro transcription of the kan gene by the T7 RNA polymerase (RNAP) in the presence of AID and a ge
214 We have characterized the roles of the phage T7 RNA polymerase (RNAP) thumb subdomain and the RNA bin
215 stability is a kinetic mechanism that allows T7 RNA polymerase (RNAP) to achieve promoter specificity
216 ted a series of plasmid templates that allow T7 RNA polymerase (RNAP) to be halted at defined interva
217 mplex (EC), the single-subunit bacteriophage T7 RNA polymerase (RNAP) undergoes dramatic conformation
219 omplex (IC) to an elongation complex (EC) in T7 RNA polymerase (RNAP), we used nucleic acid-protein c
220 acts as a partial block to the bacteriophage T7 RNA polymerase (RNAP), which allows nucleotide incorp
224 template that contains promoters for T3 and T7 RNA polymerases (RNAPs) in opposing orientations, and
225 of bound target by quantifying DNA tails by T7 RNA polymerase runoff transcription and real-time pol
227 this system, we found that transcription by T7 RNA polymerase strikingly induced the formation of hy
230 s in mammalian cells were investigated using T7 RNA polymerase-synthesized small interfering RNA and
232 We found that siRNAs synthesized from the T7 RNA polymerase system can trigger a potent induction
233 of transcription in the model bacteriophage T7 RNA polymerase system, the simplest possible reaction
236 nd single guide RNAs (sgRNAs) produced using T7 RNA polymerase (T7 RNAP) efficiently edit the Plasmod
240 in vitro transcription system with purified T7 RNA polymerase (T7 RNAP) or rat liver RNAP II, we cha
241 To address this, we modified bacteriophage T7 RNA polymerase (T7 RNAP) to create a library of trans
243 ake messenger RNA transcripts, bacteriophage T7 RNA polymerase (T7 RNAP) undergoes a transition from
244 sed on co-delivery of mRNA(A64) encoding for T7 RNA polymerase (T7 RNAP) with a T7-driven plasmid, pr
245 l interest, T7 RNA polymerase (T7RP) and the T7 RNA polymerase-T7 lysozyme complex (T7RPL) in forms s
247 On the basis of their recently described T7 RNA polymerase-T7 promoter crystal structure, Cheetha
250 al4, (ii) transcription by the bacteriophage T7 RNA polymerase (T7RNAP), and (iii) FLP-mediated site-
251 approaches that may be of general interest, T7 RNA polymerase (T7RP) and the T7 RNA polymerase-T7 ly
252 ubstitute was a more effective substrate for T7 RNA polymerase than 5-(2-mercaptoethyl)uridine tripho
253 otein trans-splicing, yielding a full-length T7 RNA polymerase that can transcribe genes via a T7 pro
255 ed an unusual type of termination signal for T7 RNA polymerase that requires a conserved 7-base pair
256 re by providing examples of (i) selection of T7 RNA polymerases that recognize orthogonal promoters a
258 Unlike the salt-sensitive bacteriophage T7 RNA polymerase, this marine RNA polymerase requires 1
260 nt translation of viral transcripts, we used T7 RNA polymerase to express constructs engineered with
261 ence functional) by DNA polymerase, allowing T7 RNA polymerase to generate a target-dependent RNA sig
264 rt of the upstream binding energy is used by T7 RNA polymerase to melt the downstream initiation regi
268 ast 100-fold more efficient than that from a T7 RNA polymerase transcript with the same sequence.
269 ed by these genes were overexpressed using a T7 RNA polymerase transcription (pET102/D-TOPO) system i
270 ese stereoisomers on RNA synthesis, in vitro T7 RNA polymerase transcription assays were performed us
271 the non-template strand reduces the yield of T7 RNA polymerase transcription by more than an order of
272 Here, we photo-cross-linked the RNA in a T7 RNA polymerase transcription complex and mapped a maj
273 aracterize the transitions that occur in the T7 RNA polymerase transcription complex during initiatio
274 ur picture of the functional architecture of T7 RNA polymerase transcription complexes remains incomp
275 e sequences on transcription we have studied T7 RNA polymerase transcription of G-rich sequences in v
281 ation complex to an elongation complex (EC), T7 RNA polymerase undergoes major conformational changes
283 ity in a simplified model system, by using a T7 RNA polymerase variant capable of transcribing nuclei
285 tem also enables the continuous evolution of T7 RNA polymerase variants capable of initiating transcr
289 quence preference in start site selection by T7 RNA polymerase was investigated by using a series of
290 and open complex formation in bacteriophage T7 RNA polymerase was investigated using 2-aminopurine (
293 Here, using a purified in vitro system with T7 RNA polymerase, we show that increased distance betwe
296 strate here that the P266L point mutation in T7 RNA polymerase, which shows dramatically reduced abor
297 lular synthesis of the LCMV MG was driven by T7 RNA polymerase whose expression was also mediated by
298 emplate encoding the initial sequence GGGA., T7 RNA polymerase will synthesize a 'ladder' of poly-G R
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