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

1 nserved domains, YonO is a highly processive 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 thesis typical of the three major eukaryotic DNA-dependent RNA polymerases.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

55 DNA-dependent RNA polymerase (RNAP) accomplishes multipl

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

88 A DNA-dependent RNA polymerase was purified to homogeneity

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

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