ライフサイエンスコーパス: RNA transport

1 otein complex links microtubule polarity and RNA transport.

2 y oocyte, distinct from nurse-cell-to-oocyte RNA transport.

3 dimerizes the motor and activates processive RNA transport.

4 onal transport that are required for vegetal RNA transport.

5 of OsTudor-SN and GFP, suggesting a role in RNA transport.

6 s a dsRNA binding domain that contributes to RNA transport.

7 ng roles for these kinesin motors in vegetal RNA transport.

8 causes inhibition of host transcription and RNA transport.

9 the Vg1 RNP is remodeled during cytoplasmic RNA transport.

10 eviously, and that viral infection may alter RNA transport.

11 ermediate RNA-binding states of THOC2 during RNA transport.

12 s associate with localized RNAs to carry out RNA transport.

13 rvous system, was used as a probe for axonal RNA transport.

14 hat dsRNA binding to SID-1 ECD is related to RNA transport.

15 C and L are unable to stimulate Rev-mediated RNA transport.

16 A-binding motif of HDAg are required for the RNA-transporting activity of HDAg.

17 -binding motifs was sufficient to confer the RNA-transporting activity.

18 ioning trial changes the amount of antiNOS-2 RNA transported along the axon.

19 cellular Rev-like proteins to facilitate HIV RNA transport and efficient translation.

20 d participation of kinesin motors in vegetal RNA transport and identified a direct role for Xenopus k

21 identified: distinct cis-acting elements for RNA transport and localization have been characterized i

22 t parameters that can define the dynamics of RNA transport and localization.

23 oskeletal-associated RNA binding protein, in RNA transport and localization.

24 in live cells and spatiotemporal analysis of RNA transport and localization.

25 TR-dependent particle serves as a marker for RNA transport and localization.

26 , containing the RTS, is sufficient for both RNA transport and localization.

27 es may be the destination of retrotransposon RNA transport and may be degradation or sequestration si

28 editing, mRNA splicing, pre-rRNA processing, RNA transport and RNA decay, scanning is facilitated by

29 idues that is dispensable for its effects on RNA transport and splicing.

30 o a newly emerging role in compartmentalized RNA transport and translation in neuronal dendrites.

31 nded repeat RNAs interact with the messenger RNA transport and translation machinery, causing transpo

32 le genes, initiation of DNA replication, and RNA transport and translation.

33 ative splice site selection, RNA processing, RNA transport, and chromosome maintenance reflect its ab

34 ular motors implicated in vesicular traffic, RNA transport, and mechanochemical coupling of the actin

35 adation processes interact with translation, RNA transport, and other cellular processes.

36 n RNA-binding protein required for dendritic RNA transport, and other RNA-binding proteins was confir

37 sible roles in transcription termination and RNA transport are discussed.

38 hat control directionality during asymmetric RNA transport are not yet clear.

39 est that these compounds affect Rev-mediated RNA transport by different mechanisms.

40 and suggest that Rev proteins activate viral RNA transport by providing export ribonucleoproteins wit

41 In this paper, we ask how dendritic RNA transport can be regulated in a manner that is infor

42 approach is based on the characterization of RNA transport complexes carried by molecular motor kines

43 l localized mRNAs, we immunoprecipitated the RNA transport components She2p, She3p, and Myo4p and per

44 valent to those produced using a combination RNA transport (CTE and Rev-Rev response element)-based p

45 Exogenous ZBP1 can rescue the RNA transport deficits, but the axonal growth deficit is

46 Rev NES function and may play a role in RRE RNA transport during HIV infection.

47 The factors that mediate microtubule-based RNA transport during the late pathway have been elusive.

48 with these mutations decrease SID-1-mediated RNA transport efficiency, providing evidence that dsRNA

49 We demonstrate here that the minimal RNA transport element (musD transport element) of musD c

50 We previously identified an RNA transport element (RTE), present in a subclass of ro

51 ained within a 247-nucleotide fragment named RNA transport element (RTE), which was able to promote r

52 nodeficiency virus (SIV) by the constitutive RNA transport element CTE of the simian type D retroviru

53 ian/Mason-Pfizer monkey retroviruses and the RNA transport element found in rodent intracisternal A-p

54 his work constitutes the first example of an RNA transport element requiring such structural motifs t

55 esults implicate a novel role in cytoplasmic RNA transport for this family of nuclear RNA-binding pro

56 ive element is required mainly for efficient RNA transport from the nucleus to the cytoplasm.

57 These studies indicate that the RNA transport function of eIF4E could contribute to leuk

58 RNA transport granules deliver translationally repressed

59 nd translation factors conveyed in dendritic RNA transport granules, including the purine-rich elemen

60 y similar but not identical to physiological RNA transport granules.

61 ed with MS, we identified Staufen-containing RNA-transporting granules and Ro ribonucleoprotein compl

62 t RNAs are recruited into Staufen-containing RNA-transporting granules in the presence of A3G.

63 ) RNA-protein complexes that include Staufen RNA-transporting granules.

64 Importantly, the minimal RTE able to promote RNA transport has key structural features which are pres

65 identified in dendrites and axons; however, RNA transport in axons remains poorly understood.

66 y reveals an unanticipated widespread use of RNA transport in budding yeast.

67 protein synthesis in dendritic microdomains, RNA transport in dendrites is thought to be underlying l

68 -protein interactions and activity-inducible RNA transport in dendrites.

69 Here we analyzed axonal RNA transport in goldfish Mauthner neurons in vivo.

70 part of the element is essential to mediate RNA transport in microinjected Xenopus laevis oocyte nuc

71 chnology to demonstrate their importance for RNA transport in neurons.

72 tified as cytoskeletal elements required for RNA transport in oligodendrocytes.

73 Here we have examined dendritic RNA transport in sympathetic neurons in primary culture,

74 o further analyze the mechanisms involved in RNA transport, in situ hybridization and autoradiography

75 Full-length HIV-1 RNA transport is further complicated when group-specific

76 These results suggest that prolamine RNA transport is initiated in the nucleus to form a zipc

77 or theme that emerges from recent studies of RNA transport is that specific signals mediate the trans

78 Thus, vegetal RNA transport occurs through a multistep pathway with a

79 s show that OsTudor-SN is a component of the RNA transport particle, and may control storage protein

80 These prolamine RNA transport particles generally move unidirectionally

81 rice plants expressing GFP-tagged prolamine RNA transport particles showed co-localization of OsTudo

82 ssembly and composition of ribonucleic acid (RNA)-transporting particles for asymmetric messenger RNA

83 s, requiring the assembly of motor-dependent RNA-transport particles.

84 We find here that in a key dendritic RNA transport pathway (exemplified by BC1 RNA, a dendrit

85 ation do not travel through a CRM1-dependent RNA transport pathway.

86 dicate that there are at least two regulated RNA transport pathways as well as a constitutive pathway

87 esult from molecular competition in neuronal RNA transport pathways.

88 ate inhibition of src splicing and unspliced RNA transport, point mutations in the upstream and downs

89 over rates, the phosphorylation of the yeast RNA transport protein Npl3 by its natural protein kinase

90 transduction, starch and sucrose metabolism, RNA transport, protein processing in endoplasmic reticul

91 odular domain structure reminiscent of other RNA transport proteins where one region of the molecule

92 tin modifying, intracellular trafficking and RNA transport proteins.

93 ple molecular processes, including splicing, RNA transport, RNA stability, and translation.

94 godendrocytes that binds specifically to the RNA transport sequence; and microtubules and kinesin hav

95 equires a 21-nucleotide sequence, termed the RNA transport signal (RTS), in the 3' UTR of MBP mRNA.

96 a and muscle, we have identified a consensus RNA transport signal in transitin mRNA that is absent fr

97 uggest that the MPMV element mimics cellular RNA transport signals and mediates RNA export through in

98 c localization also occurs in the absence of RNA transport, suggesting the existence of redundant pro

99 onaute-containing complexes, and induced NCL RNA transport to PBs.

100 absence of She2 increases the efficiency of RNA transport to the bud.

101 ence of replication, deltaAg facilitates HDV RNA transport to the nucleoplasm and helps redirect host

102 (i) IEX-1 RNA transported to the cytoplasm after 1 h of infection

103 of a variety of cellular processes including RNA transport, transcription, apoptosis, vesicular traff

104 l clouds which designates one of them as the RNA transport vehicle.

105 nergy sensor and negatively regulates poly(A)RNA transport via deacetylating a poly(A)-binding protei

106 on defect is due to complex effects on viral RNA transport, viral RNA half-life, and virus particle a

107 RTE-mediated RNA transport was CRM1 independent, and RTE did not show

108 Furthermore, RNA transport was shown to be stage dependent for both V

109 o examine the effect of Gag protein on HIV-1 RNA transport, we analyzed the cytoplasmic HIV-1 RNA mov

110 mechanistic basis for understanding directed RNA transport within the cytoplasm.