ライフサイエンスコーパス: nuclear export factor

1 XF1, a ubiquitously expressed essential mRNA nuclear export factor.

2 ev NES and of NESs found in other retroviral nuclear export factors.

3 expand on mechanisms known to be mediated by nuclear export factor 1 (NXF1) by describing SR proteins

4 Nuclear export factor 1 (NXF1) exports mRNA to the cytop

5 s, the nuclear export of mRNA is mediated by nuclear export factor 1 (NXF1) receptors.

6 mportant for general mRNA export mediated by nuclear export factor 1 (Nxf1).

7 by interacting with the export receptor TAP/nuclear export factor 1 (NXF1).

8 etween SR-rich splicing factor 1 (SRSF1) and nuclear export factor 1 (NXF1).

9 Here we show that Nuclear Export Factor 2 (Nxf2) and its co-factor, Nxt1,

10 enome-wide shRNA-based screen, we identified nuclear export factor 3 (NXF3) as a transporter that alt

11 h a subset of nucleoporins and with the Crm1 nuclear export factor and can functionally replace the e

12 independently able to interact with the Crm1 nuclear export factor and substitute for the HIV-1 Rev N

13 han import, and involves the Crm1 (exportin) nuclear export factor and the dcd1+/pim1+ gene that enco

14 Like HIV-1 Rev, K-Rev binds to both the Crm1 nuclear export factor and to a cis-acting viral RNA targ

15 A precursors, competition for the Exportin 5 nuclear export factor, and inhibition of Dicer function

16 t sequences essential for binding to the CAS nuclear export factor are located near the Imp alpha COO

17 ic shuttling proteins that interact with the nuclear export factor CRM1 (chromosomal region maintenan

18 Downregulating the nuclear export factor CRM1 also leads to temperature-dep

19 tomycin B (LMB), a specific inhibitor of the nuclear export factor CRM1 potently inhibits the stabili

20 NS2 protein of minute virus of mice and the nuclear export factor Crm1 results in a block to egress

21 ITA, impair its ability to interact with the nuclear export factor CRM1, and enhance CIITA-induced ge

22 tion induces the association of p53 with the nuclear export factor CRM1, leading to p53 nuclear expor

23 In contrast, direct binding of Gag to the nuclear export factor CRM1, via the CRM1-RanGTP heterodi

24 g molecules, contains a binding site for the nuclear export factor Crm1.

25 ation by increasing the interaction with the nuclear export factor CRM1.

26 nteraction of Gcn4 with the highly conserved nuclear export factor Crm1/Xpo1.

27 ITA, and impaired its ability to bind to the nuclear export factor, CRM1.

28 when phosphorylated, prevents binding of the nuclear export factor, CRM1.

29 anBP2 associate with high specificity to the nuclear export factor, exportin-1 (CRM1).

30 quires CG13741/Bootlegger and the Drosophila nuclear export factor family protein Nxf3.

31 NXF1-like members of the NXF (nuclear export factor) family orchestrate bulk nuclear e

32 c reticulum, has been found to function as a nuclear export factor for a large family of nuclear rece

33 he Mex67:Mtr2 complex is the principal yeast nuclear export factor for bulk mRNA and also contributes

34 at the Ran-binding protein RanBP3L acts as a nuclear export factor for Smad1/5/8.

35 ly inserted into the Drosophila melanogaster nuclear export factor gene nxf2.

36 recent work demonstrated the involvement of nuclear export factors in this process, suggesting that

37 Nuclear export factors mediate mRNA transit through nucl

38 d by a GTPase that blocks recruitment of the nuclear export factor Nmd3 until remodeling of the pre-r

39 mplementation cloning identifies Mvb1 as the nuclear export factor Nxf1, providing an unexpected link

40 specifically interacts with a distinct mRNA nuclear export factor NXF2 but not with its close relati

41 ulted in cytoplasmic accumulation of the 60S nuclear export factor PA2G4, aberrant ribosome profiles,

42 ex (also known as TAP:p15) is a general mRNA nuclear export factor that is conserved from yeast to hu

43 ast in part, by recruiting the cellular Crm1 nuclear export factor to HIV-1 transcripts bearing the R

44 y, we show that direct tethering of the Crm1 nuclear export factor to target mRNAs, by fusion to a he

45 gnificant role in the recruitment of the Tap nuclear export factor to target RNA molecules in vivo.

46 small bristles (sbr), which encodes an mRNA nuclear export factor, to disrupt the normal cytoplasmic

47 The splicing and nuclear export factor U2AF65 has the opposite effect, de

48 However, depletion of the nuclear export factors XPO1 or MEX67 recapitulates the e

49 nt is mutated, these mRNPs still contain the nuclear export factor Yra1p.