ライフサイエンスコーパス: RNA transport

1 otein complex links microtubule polarity and RNA transport.

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

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

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

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

6 dimerizes the motor and activates processive RNA transport.

7 onal transport that are required for vegetal RNA transport.

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

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

10 causes inhibition of host transcription and RNA transport.

11 the Vg1 RNP is remodeled during cytoplasmic RNA transport.

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

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

14 rvous system, was used as a probe for axonal 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 s for inducible and reversible bidirectional RNA transport along microtubules via motor proteins, fac

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

20 rodegenerative diseases, establishing failed RNA transport and associated processes as a unifying pat

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

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

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

24 including cell compartmentalization through RNA transport and localization, supporting catalytic pro

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

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

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

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

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

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

31 iated with diverse biological processes like RNA transport and metabolism, sterol metabolism, chromos

32 s involved in protein synthesis, protein and RNA transport and osteoclast formation and are validated

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

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

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

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

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

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

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

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

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

42 The neuronal RNA transport apparatus, composed of cis-acting RNA regu

43 In this review, we deconstruct the RNA transport apparatus, exploring each constituent's ro

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

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

46 ovides not only an unprecedented view of HIV RNA transport but also illuminates how CRM1 can recogniz

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

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

49 Thus, ANXA11 mediates neuronal RNA transport by tethering RNA granules to actively-tran

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

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

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

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

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

55 are required for pre-mRNA processing and for RNA transport, degradation and translation into protein,

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

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

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

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

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

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

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

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

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

65 Long-distance RNA transport enables local protein synthesis at metabol

66 Lupus anti-BC abs effectively compete with RNA transport factor heterogeneous nuclear ribonucleopro

67 SLE anti-BC abs effectively compete with RNA transport factor heterogeneous nuclear ribonucleopro

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

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

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

71 RNA transport granules deliver translationally repressed

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

73 in stress granules, P bodies, and messenger RNA transport granules, we have developed and applied a

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

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

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

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

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

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

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

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

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

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

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

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

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

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

88 Here, we present a mechanism for RNA transport in which RNA granules "hitchhike" on movin

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

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

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

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

93 role for TMEM106B core filaments in impaired RNA transport, local translation, and endolysosomal func

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

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

96 These prolamine RNA transport particles generally move unidirectionally

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

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

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

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

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

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

103 esult from molecular competition in neuronal RNA transport pathways.

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

105 al SARS-CoV-2 structural events - e.g. viral RNA transport portals, virus assembly intermediates, vir

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

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

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

109 tin modifying, intracellular trafficking and RNA transport proteins.

110 a reveal how Nxf2 might have evolved from an RNA transport receptor into a cotranscriptional silencin

111 Mutations in protein complexes that control RNA transport result in aberrant endosperm with shrunken

112 carbon metabolism, glycolysis, spliceosome, RNA transport, RNA binding, transcription, DNA damage re

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

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

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

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

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

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

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

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

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

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

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

124 CAPRIN1, an RNA-binding protein involved in RNA transport, translation, and stability.

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

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

127 In higher plants, long-distance RNA transport via the phloem is crucial for communicatio

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

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

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

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

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