ライフサイエンスコーパス: polyadenylated mRNA

1 ion factors, mRNA binding proteins, and most polyadenylated mRNA.

2 form lacking it, eIF4G-1a(DM), but only with polyadenylated mRNA.

3 lly activate the translation of a capped and polyadenylated mRNA.

4 SG-PB docking, and impaired preservation of polyadenylated mRNA.

5 amyxoviruses produce capped, methylated, and polyadenylated mRNAs.

6 , similar to the mechanism of translation of polyadenylated mRNAs.

7 ns two sets of histone genes that encode non-polyadenylated mRNAs.

8 etween 3' end formation of histone mRNAs and polyadenylated mRNAs.

9 istone genes that encode histone variants as polyadenylated mRNAs.

10 turbing the overall cellular distribution of polyadenylated mRNAs.

11 stone H1 genes encodes detectable amounts of polyadenylated mRNAs.

12 ion-dependent histone mRNAs and encodes only polyadenylated mRNAs.

13 minators in this system, producing truncated polyadenylated mRNAs.

14 association even in yeast cells deficient in polyadenylated mRNA and/or Rpl46.

15 Both genes encode polyadenylated mRNAs and are highly expressed in vegetat

16 Polyadenylated mRNAs and replication-dependent histone m

17 mplexes-one specifically crafted to generate polyadenylated mRNAs and the other to generate nonpolyad

18 Since PABP1 binds to all polyadenylated mRNAs, and is involved in translation ini

19 requires shortened/no poly(A)-tail targets; polyadenylated mRNAs are partially activated upon PAIP2

20 During heat shock, most polyadenylated mRNAs are retained in the nucleus, wherea

21 Together, these results suggest that polyadenylated mRNAs can enter P-bodies, and an mRNP com

22 ate of labeling of rp mRNA relative to total polyadenylated mRNA changed very little after stimulatio

23 f the maize cell line P3377.5' capped and 3' polyadenylated mRNA constructs containing the firefly ge

24 All polyadenylated mRNAs contain sequence of variable length

25 the prototype VZV genome isomer, expresses a polyadenylated mRNA containing a splice within the 3' un

26 PABPC1 antagonizes uridylation of polyadenylated mRNAs, contributing to the specificity fo

27 Genes encoding polyadenylated mRNAs depend on their poly(A) signals for

28 Genes encoding polyadenylated mRNAs depend on their poly(A) signals for

29 synthesized during replication is a 0.8-kb, polyadenylated mRNA encoding the hepatitis delta antigen

30 the antigenome, and (iii) the less abundant polyadenylated mRNA for the small delta protein.

31 of target mRNAs produce diagnostic uncapped, polyadenylated mRNA fragments.

32 d of the genome followed by 5'-capped and 3'-polyadenylated mRNAs from internal genes by a stop-start

33 xon 2 resulting in the production of a small polyadenylated mRNA (HTTexon1) that encodes the highly p

34 stem-loop, the H1c gene expresses a longer, polyadenylated mRNA in differentiated cells, although in

35 We demonstrate that hos1 mutants accumulate polyadenylated mRNA in the nucleus and that the circadia

36 crete set of pathways for the degradation of polyadenylated mRNAs in eukaryotic cells have been descr

37 They are expressed as polyadenylated mRNAs in fibroblasts differentiated in vi

38 of this system, including the prevalence of polyadenylated mRNAs in the bacterium, are still poorly

39 t the M3 protein is encoded by an unspliced, polyadenylated mRNA initiating at bp 7294 and terminatin

40 We established that this polyadenylated mRNA is 0.8 kb in length and its 5' end b

41 adaptors that flag alternatively spliced and polyadenylated mRNA isoforms as cargo ready for the cyto

42 roteins (sFlt1s) produced from alternatively polyadenylated mRNA isoforms.

43 ssed in terminally differentiated tissues as polyadenylated mRNAs, likely serving as replacement hist

44 eta-lactamase family generate the 3' ends of polyadenylated mRNAs, nonpolyadenylated histone mRNAs, a

45 n-independent histones, which are encoded by polyadenylated mRNAs, persists outside of S phase.

46 otein factors necessary for 3' processing of polyadenylated mRNA precursors are well known.

47 Transcription termination for genes encoding polyadenylated mRNAs requires a functional poly(A) signa

48 are needed for the translation of capped or polyadenylated mRNA, respectively.

49 ause mtDNA is transcribed and processed into polyadenylated mRNAs reverse transcription coupled to PC

50 f genomic RNA replication and positive-sense polyadenylated mRNA(s) were synthesized.

51 t did not stimulate translation of uncapped, polyadenylated mRNA suggested additional Pab1p-dependent

52 er half of human genes produce alternatively polyadenylated mRNAs, suggesting that regulated polyaden

53 he oligo(dT)-primed reverse transcription of polyadenylated mRNA templates used to generate EST cDNA

54 its exact complement (the antigenome), and a polyadenylated mRNA that acts as a template for the smal

55 principally to a genomic region producing a polyadenylated mRNA that encodes a protein.

56 elongs to the picornavirus superfamily, is a polyadenylated mRNA that is naturally uncapped and yet i

57 nt splicing of exon 1 HTT results in a short polyadenylated mRNA that is translated into an exon 1 HT

58 erminal portion of DUX4 and (iii) capped and polyadenylated mRNAs that contain the double-homeobox do

59 alone caused an increase in the synthesis of polyadenylated mRNA, the majority of which was due to a

60 inserted gene into the predicted subgenomic polyadenylated mRNA was demonstrated by Northern (RNA) b

61 bed exclusively in testis, where the spliced polyadenylated mRNA was detected.

62 About 70% of total polyadenylated mRNA was in the polysome fraction in all

63 The ratio of cytoplasmic to nuclear polyadenylated mRNA was increased in the presence of SM,

64 ated in vitro and also when m(7)G-capped and polyadenylated mRNA was transiently transfected into 293

65 Polyadenylated mRNAs were captured by oligo-dT primers a

66 s the genomic RNA to produce five capped and polyadenylated mRNAs with the 5'-terminal structure 7mGp