ライフサイエンスコーパス: DNA-dependent RNA polymerase

1 es at promoters, DNA regions recognized by a DNA-dependent RNA polymerase.

2 lates transcription through interaction with DNA-dependent RNA polymerase.

3 ichia coli DnaG primase is a single-stranded DNA-dependent RNA polymerase.

4 nserved domains, YonO is a highly processive DNA-dependent RNA polymerase.

5 cription machineries, including five nuclear DNA-dependent RNA polymerases.

6 ogy to the catalytic centers of multisubunit DNA-dependent RNA polymerases.

7 thesis typical of the three major eukaryotic DNA-dependent RNA polymerases.

8 ellular transcription catalyzed by all three DNA-dependent RNA polymerases.

9 ryotes, giving rise to 2 of the 3 eukaryotic DNA-dependent RNA polymerases.

10 other primases, shares limited homology with DNA-dependent RNA polymerases.

11 sms of initiation by other RNA-dependent and DNA-dependent RNA polymerases.

12 ogous to the recognition of DNA promoters by DNA-dependent RNA polymerases.

13 ogous to the recognition of DNA promoters by DNA-dependent RNA polymerases.

14 RNA can be synthesized in vitro using phage DNA-dependent RNA-polymerases.

15 These RNAs are synthesized by host DNA-dependent RNA polymerase acting as an RNA-dependent

16 and Mg2+ and was resistant to inhibitors of DNA-dependent RNA polymerases (actinomycin D, alpha-aman

17 the template and substrate specificity of a DNA-dependent RNA polymerase and a DNA ligase to act as

18 zed by RB69 DNA-dependent DNA polymerase, T7 DNA-dependent RNA polymerase and HIV reverse transcripta

19 The additional detection of the viral DNA-dependent RNA polymerase and intermediate and late t

20 ere associated with nascent DNA, as were the DNA-dependent RNA polymerase and intermediate- and late-

21 intermediate genes, respectively, the viral DNA-dependent RNA polymerase, and an unmapped factor sed

22 lmodulin, minichromosome maintenance factor, DNA-dependent RNA polymerase, and pre-rRNA processing pr

23 beta and beta' subunits of Escherichia coli DNA-dependent RNA polymerase are highly conserved throug

24 Escherichia coli and yeast DNA-dependent RNA polymerases are shown to mediate effic

25 ely for the beta- and beta'-like subunits of DNA-dependent RNA polymerase, are organized in an operon

26 ely, for the beta and beta'-like subunits of DNA-dependent RNA polymerase, are organized in an operon

27 eir activity, and increases the occupancy of DNA-dependent RNA polymerases at MIR promoters, suggesti

28 ht to influence the rate of transcription by DNA-dependent RNA polymerases, but the influence of DNA

29 Mechanistically, termination by all DNA-dependent RNA polymerases can be reduced to two step

30 , and recent results identify a diversity of DNA-dependent RNA polymerase complexes operating in maiz

31 , beta', and sigma(70) subunits of bacterial DNA-dependent RNA polymerases (DdRp), combined with sequ

32 ication systems have evolved to use cellular DNA-dependent RNA polymerase for primer synthesis.

33 Phage T7 RNA polymerase is the only DNA-dependent RNA polymerase for which we have a high-re

34 he amino terminus of the largest subunits of DNA-dependent RNA polymerases from bacteria, archaea, an

35 zed that a dominant-negative mutation in the DNA-dependent RNA polymerase gene would inhibit transcri

36 The properties of DNA-dependent RNA polymerases have been studied since th

37 e arisen as a result of mutations within the DNA-dependent RNA polymerase holoenzyme.

38 erase (Pol IV) in addition to the well-known DNA-dependent RNA polymerases I, II, and III.

39 Cellular DNA-dependent RNA polymerase II (pol II) has been postul

40 minal domain (CTD) of the largest subunit of DNA-dependent RNA polymerase II (RNAP II) is composed of

41 of the gene encoding the largest subunit of DNA-dependent RNA polymerase II (RPB1) from the pelobion

42 Analyses of an expanded alignment of DNA-dependent RNA polymerase II largest subunit sequence

43 ns can arise from errors made either by host DNA-dependent RNA polymerase II or by HIV-1 reverse tran

44 ane-associated transcription system in which DNA-dependent RNA polymerase II, which colocalizes with

45 oters of genes encoding miRNAs (MIR) and the DNA-dependent RNA polymerase II.

46 on RNA polymerase IV (PolIV), a homologue of DNA-dependent RNA polymerase II.

47 STVd), replicate in the nucleus by utilizing DNA-dependent RNA polymerase II.

48 omain (CTD) of the largest subunit (RPB1) of DNA-dependent RNA polymerase II.

49 al purification led to the identification of DNA-dependent RNA polymerase III (Pol-III) as the enzyme

50 is mediated by a virus-encoded multisubunit DNA-dependent RNA polymerase in conjunction with early-,

51 Prokaryotic primase, a DNA-dependent RNA polymerase, is a target of interest fo

52 In Arabidopsis (Arabidopsis thaliana), DNA-dependent RNA polymerase IV (Pol IV) is required for

53 These mutations affect two subunits of the DNA-dependent RNA polymerase IV (Pol IV), which is essen

54 Further analysis showed that DNA-dependent RNA polymerase IV (Pol IV)-dependent smRNA

55 RNA POLYMERASE2, and the largest subunit of DNA-DEPENDENT RNA POLYMERASE IV, with the largest subuni

56 ing and splicing in the context of two other DNA-dependent RNA polymerases, mammalian RNAP III and ba

57 ck of extensive sequence similarity to other DNA-dependent RNA polymerases, mini-vRNAP is related to

58 All eukaryotes have three nuclear DNA-dependent RNA polymerases, namely, Pol I, II, and II

59 in vivo, the initiation of RNA synthesis by DNA-dependent RNA polymerases occurs using NTPs alone.

60 no acid peptide inhibitor active against the DNA-dependent RNA polymerase of Gram negative bacteria.

61 are biochemically undefined: the presumptive DNA-dependent RNA polymerases Pol IV and Pol V and the p

62 Eukaryotes express at least three nuclear DNA dependent RNA polymerases (Pols).

63 Eukaryotes express at least three nuclear DNA-dependent RNA polymerases (Pols) responsible for syn

64 All eukaryotes possess three DNA-dependent RNA polymerases, Pols I-III, while land pl

65 In DNA-dependent RNA polymerases, reactions of RNA synthesi

66 In plants, two atypical DNA-dependent RNA polymerases, RNA polymerase IV (Pol IV

67 DNA-dependent RNA polymerase (RNAP) accomplishes multipl

68 How DNA-dependent RNA polymerase (RNAP) acts on bacterial ce

69 cteria, and particularly the Firmicutes, the DNA-dependent RNA polymerase (RNAP) complex contains an

70 The single subunit DNA-dependent RNA polymerase (RNAP) from bacteriophage T

71 rapid two-column purification procedure, the DNA-dependent RNA polymerase (RNAP) from the thermophile

72 The three-dimensional structure of DNA-dependent RNA polymerase (RNAP) from thermophilic Th

73 Bacterial DNA-dependent RNA polymerase (RNAP) has subunit composit

74 RNA synthesis, carried out by DNA-dependent RNA polymerase (RNAP) in a process called

75 iple sequence alignments of the multisubunit DNA-dependent RNA polymerase (RNAP) large subunits, incl

76 During transcription initiation by DNA-dependent RNA polymerase (RNAP) promoter DNA has to

77 The DNA-dependent RNA polymerase (RNAP) subunits A', A", B',

78 Archaea are prokaryotes with a single DNA-dependent RNA polymerase (RNAP) that is homologous t

79 gene expression machinery, such as bacterial DNA-dependent RNA polymerase (RNAP), has never been repo

80 some strains of Escherichia coli and targets DNA-dependent RNA polymerase (RNAP).

81 is, this protein was identified as bacterial DNA-dependent RNA polymerase (RNAP).

82 All multisubunit DNA-dependent RNA polymerases (RNAP) are zinc metalloenz

83 nisms) ensuring fidelity of transcription by DNA-dependent RNA polymerases (RNAPs) is not fully under

84 lypeptide loop conserved in all multisubunit DNA-dependent RNA polymerases (RNAPs) that extends into

85 code IIV3-053L, a protein with similarity to DNA-dependent RNA polymerase subunit 7; IIV3-044L, a put

86 nase (G3PDH), heat-shock protein 60 (HSP60), DNA-dependent RNA polymerase subunit II (RPB2), and necr

87 DNA-dependent RNA polymerase subunits of Group I, which

88 These components include the following: DNA-dependent RNA polymerase subunits rpo147, rpo132, rp

89 Multi-subunit DNA-dependent RNA polymerases synthesize all classes of

90 Structural studies of the T7 bacteriophage DNA-dependent RNA polymerase (T7 RNAP) have shown that t

91 fornica nuclear polyhedrosis virus encodes a DNA-dependent RNA polymerase that is required for transc

92 otes requires the activity of DNA primase, a DNA-dependent RNA polymerase that lays short RNA primers

93 tably, our results suggest that QDE-1 is the DNA-dependent RNA polymerase that produces aRNAs.

94 genomic duplication depends on primase, the DNA-dependent RNA polymerase that synthesizes de novo th

95 The SP6 primase is a DNA-dependent RNA polymerase that synthesizes short olig

96 ms depends on the activity of DNA primase, a DNA-dependent RNA polymerase that synthesizes short RNA

97 fornica nuclear polyhedrosis virus encodes a DNA-dependent RNA polymerase that transcribes viral late

98 c analyses indicate roles for plant-specific DNA-dependent RNA polymerases that generate small RNAs,

99 ular organisms is performed by multisubunit, DNA-dependent RNA polymerases that synthesize RNA from D

100 hus extending the capability of the cellular DNA-dependent RNA polymerases to utilizing RNA as templa

101 Poxviruses encode a multisubunit DNA-dependent RNA polymerase (vRNAP) that carries out vi

102 Bacteriophage N4 encapsidates a 3500-aa-long DNA-dependent RNA polymerase (vRNAP), which is injected

103 In contrast to other DNA-dependent RNA polymerases, vRNAP initiates transcrip

104 A single subunit DNA-dependent RNA polymerase was identified and purified

105 A DNA-dependent RNA polymerase was purified to homogeneity

106 Among them, the largest subunits of the DNA-dependent RNA polymerase were transferred between 2

107 lymerase II (Pol II) is a well-characterized DNA-dependent RNA polymerase, which has also been report

108 Ternary complexes of DNA-dependent RNA polymerase with its DNA template and n