ライフサイエンスコーパス: precursor RNA

1 inct miRNAs that are transcribed in a common precursor RNA.

2 BF1 and UBF2 are splice variants of a common precursor RNA.

3 repressing alternative splicing of the viral precursor RNA.

4 on of mtDNA entails multi-step maturation of precursor RNA.

5 becomes associated with complexes containing precursor RNA.

6 ing from processing of a circularly permuted precursor RNA.

7 ngle gene and the same alternatively spliced precursor RNA.

8 romoter and transcribed into a monocistronic precursor RNA.

9 splicing of multiple products from a single precursor RNA.

10 he complex correctly processes the 3'-end of precursor RNA.

11 RNAs from dsRNA as well as synthetic miR167b precursor RNAs.

12 ecessary and sufficient for processing miRNA precursor RNAs.

13 to liberate stable 3' fragments from various precursor RNAs.

14 nvolving trans-splicing of two discontinuous precursor RNAs.

15 reveal the existence of four different psbH precursor RNAs.

16 t Pol II inactivated splicing of this set of precursor RNAs and addition of recombinant CTD restored

17 drives transcription of both pachytene piRNA precursor RNAs and the mRNAs for core piRNA biogenesis f

18 the 5' splice site, cross-linking of U2AF to precursor RNA, and assembly of the active spliceosome, s

19 lated in extract, became associated with the precursor RNA, and stimulated the association of U1 snRN

20 th in its processed form and as a repetitive precursor RNA, and this inhibition is linked to the self

21 60 S precursor RNAs are co-precipitated with NOG1.

22 Group II introns are usually removed from precursor RNAs as lariats comprised of a circular compon

23 smaller amount is associated with unspliced precursor RNA, as expected from the role of the protein

24 occurs by reverse transcription of unspliced precursor RNA at a break in double-strand DNA made by an

25 o the sustained elevation of miR-155 and its precursor RNA, BIC.

26 Unlike most introns, which are removed from precursor RNAs by the spliceosome in two sequential but

27 ing introns catalyze their own excision from precursor RNAs by way of a two-step transesterification

28 ernative splicing of a single neosynthesized precursor RNA can result in production of different prot

29 re we show that in splicing reactions with a precursor RNA containing a 3'-sulphur substitution at th

30 We conclude that a common precursor RNA containing both let-7 and miR-125 is induc

31 pair defines the 5'-exon/intron boundary of precursor RNAs containing group I introns.

32 tivated in vitro polyadenylation cleavage of precursor RNAs containing the CT/CGRP exon 4 poly(A) sit

33 eaves two phosphodiester bonds within folded precursor RNAs during intron removal, producing the func

34 ectly to a subset of mitochondrial tRNAs and precursor RNA encoded in L-strand mtDNA.

35 t for the observed increase in nuclear P450R precursor RNA, followed by a decrease back to basal tran

36 nd clusters and block production of putative precursor RNAs from both strands of the major 42AB dual-

37 response elements in the promoter of the LAT precursor RNA; (iii) ATF3 is induced nearly 100-fold in

38 Although p62 is bound to unspliced precursor RNA in position to initiate cDNA synthesis in

39 s occurs soon after the synthesis of its 47S precursor RNA in the nucleolus before cleavage to smalle

40 ted disruption of PTB interaction with FGFR1 precursor RNA in vivo by an antisense oligonucleotide al

41 Prp18 is dispensable for splicing of precursor RNAs in which the interval between the branch

42 ila melanogaster a developmentally regulated precursor RNA is cleaved by an RNA interference-like mec

43 In strains where Rrp3 is depleted, 35S precursor RNA is improperly processed.

44 espire well; this phenotype implies that COB precursor RNA is translated efficiently.

45 The maturase bound rapidly to the precursor RNA (kon approximately 3 x 10(9) M(-1) min(-1)

46 plausible mechanism by which RNA itself (or precursor RNA-like polymers) can be synthesized nonenzym

47 ory pathways, the endonuclease Dicer cleaves precursor RNA molecules to produce microRNAs (miRNAs) an

48 nce and results in accumulation of unspliced precursor RNAs of dimeric tRNA(Ser)-tRNA(Met)i, suggesti

49 II-mediated transcription of a single common precursor RNA (pri-miRNA) encoding both mature miRNAs.

50 First, only half of the precursor RNA self-cleaved.

51 We further determined the size of CopepodSL precursor RNA (slRNA; 108-158 nt) through genomic analys

52 ed from either the 5' or 3' ends of the same precursor RNA strand, are increased in the hippocampus f

53 the overall binding isotherm of Cbp2 for the precursor RNA, suggesting that contacts critical for act

54 An HDV antigenomic ribozyme precursor RNA that included the upstream poly(A) process

55 They are processed from longer precursor RNAs that fold into stem-loop structures by th

56 The proteins bind specifically to unspliced precursor RNA to promote splicing, and then remain assoc

57 ding transcription and cleavage of the miRNA precursor RNAs, to generate a mature miRNA, which is tho

58 The gene that produces the precursor RNA transcript to the three largest structural

59 -splicing introns catalyze autoexcision from precursor RNA transcripts by a mechanism strikingly simi

60 nad5 requires the assembly of three distinct precursor RNAs via trans-splicing reactions, and the acc

61 ate transcription of gene pieces, joining of precursor RNAs via trans-splicing, and RNA editing by su

62 NA for viral protein synthesis and as virion precursor RNA (vpRNA) for encapsidation remains an impor

63 uclear extracts if, and only if, the assayed precursor RNA was recognized via exon definition, i.e.,

64 Rlp7p-depleted cells accumulate the 27SA(3) precursor RNA, which is normally the major substrate (85

65 ific splicing factor that binds to unspliced precursor RNA with a K(d) of </=0.12 pM at 30 degrees C.

66 By comparing intron precursor RNAs with long ( approximately 300 nt) and sho