ライフサイエンスコーパス: hnRNP D

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1 The two subunits of LR1, nucleolin and hnRNP D, bind with high affinity to G4 DNA (KD = 0.4 and

2 NA gel shift analyses established that AUF1 (hnRNP D) binds to the PCK-7, PCK-6, and PCK-2 segments w

3 AUF1/hnRNP-D could, therefore, be a general mRNA turnover fac

4 We refer to these proteins as AUF1/hnRNP-D.

5 The interaction of AUF1/hnRNP-D is more efficient with alphaCP1 relative to alph

6 differentially and selectively regulated by hnRNP D isoforms in mammalian cells.

7 to be the key feature recognized in vivo by hnRNP D for its negative effect on ARE-mediated mRNA dec

8 s heterogeneous nuclear ribonucleoprotein D [hnRNP D]) binds to numerous mRNAs and influences their p

9 ow show to be a specific isoform of hnRNP D. hnRNP D and nucleolin both contain canonical RNA binding

10 onstrate a specific cytoplasmic function for hnRNP D as an RNA-destabilizing protein in ARE-mediated

11 onservation suggests a critical function for hnRNP D.

12 The four hnRNP D isoforms, while differing in their ability to bl

13 These experiments identified hnRNP D, a heterogeneous nuclear ribonucleoprotein (hnRN

14 binds several regulatory proteins, including hnRNP D/AUF1, which comprises four isoforms of 37, 40, 4

15 Knockdown of MSH2, hnRNP D and GRHL2 resulted in a notable reduction of the

16 mechanisms underlie the inhibitory effect of hnRNP D on the two distinct mRNA decay pathways.

17 n hemin-treated cells, ectopic expression of hnRNP D restores the rapid decay directed by the ARE.

18 that we now show to be a specific isoform of hnRNP D. hnRNP D and nucleolin both contain canonical RN

19 ing effect varies among the four isoforms of hnRNP D, with p37 and p42 displaying the most profound e

20 A single gene encodes multiple isoforms of hnRNP D.

21 A sequestration of hnRNP D into a hemin-induced protein complex, termed hem

22 itous and highly conserved mammalian protein hnRNP D interacts specifically with the G-rich strand of

23 t from those of another ARE-binding protein, hnRNP D (also termed AUF1), which in vivo recognizes AUU

24 rs from that of another ARE-binding protein, hnRNP D, which has been implicated as an effector of mRN

25 poly(A) binding protein interacting protein; hnRNP D, an AU-rich element binding protein; and NSAP1,

26 vo interaction with the ARE-binding proteins hnRNP D and HuR in HVS-transformed T cells using a new c

27 estabilizes intrastrand G-G pairing and that hnRNP D interacts specifically with telomerase in human

28 We found that hnRNP D discriminates among the three classes of AU-rich

29 Our results support the notion that hnRNP D serves as a key factor broadly involved in gener

30 We show that hnRNP D binding to the G-rich strand destabilizes intras

31 Here, we show that hnRNP D plays a versatile role in cytoplasmic mRNA turno

32 This biochemical analysis suggest that hnRNP D could function in vivo to destabilize structures

33 The hnRNP D protein interacts with nucleic acids both in viv

34 f the human and murine genes that encode the hnRNP D protein.

35 Comparison of the predicted sequences of the hnRNP D proteins in human and mouse shows that they are

36 natively spliced isoforms D01 and D02 of the hnRNP D proteins, the E0 isoform of the hnRNP E proteins

37 geneous nuclear ribonucleoprotein (hnRNP)-U, hnRNP-D, CArG binding factor (CBF), P300/CBP associated

38 These procedures confirmed that hnRNP-U, hnRNP-D, PCAF, and P-300 bind to the KLF2 promoter.

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