335 related articles for article (PubMed ID: 9477940)
1. The histone binding protein nucleoplasmin does not facilitate binding of transcription factor IIIA to nucleosomal Xenopus laevis 5S rRNA genes.
Howe L; Itoh T; Katagiri C; Ausio J
Biochemistry; 1998 Feb; 37(5):1174-7. PubMed ID: 9477940
[TBL] [Abstract][Full Text] [Related]
2. Differential nucleosome positioning on Xenopus oocyte and somatic 5 S RNA genes determines both TFIIIA and H1 binding: a mechanism for selective H1 repression.
Panetta G; Buttinelli M; Flaus A; Richmond TJ; Rhodes D
J Mol Biol; 1998 Sep; 282(3):683-97. PubMed ID: 9737930
[TBL] [Abstract][Full Text] [Related]
3. Xenopus transcription factor IIIA and the 5S nucleosome: development of a useful in vitro system.
Yang Z; Hayes JJ
Biochem Cell Biol; 2003 Jun; 81(3):177-84. PubMed ID: 12897852
[TBL] [Abstract][Full Text] [Related]
4. Stable co-occupancy of transcription factors and histones at the HIV-1 enhancer.
Steger DJ; Workman JL
EMBO J; 1997 May; 16(9):2463-72. PubMed ID: 9171359
[TBL] [Abstract][Full Text] [Related]
5. Purification and properties of the first specific 5S rRNA binding protein from plants which shows transcription factor IIIA activity.
Wyszko E; Barciszewski J; Barciszewska M
Nucleic Acids Symp Ser; 1995; (33):53-5. PubMed ID: 8643397
[TBL] [Abstract][Full Text] [Related]
6. Histone H1 binding does not inhibit transcription of nucleosomal Xenopus laevis somatic 5S rRNA templates.
Howe L; Itoh T; Katagiri C; Ausió J
Biochemistry; 1998 May; 37(20):7077-82. PubMed ID: 9585517
[TBL] [Abstract][Full Text] [Related]
7. Nucleosome translational position, not histone acetylation, determines TFIIIA binding to nucleosomal Xenopus laevis 5S rRNA genes.
Howe L; Ausió J
Mol Cell Biol; 1998 Mar; 18(3):1156-62. PubMed ID: 9488430
[TBL] [Abstract][Full Text] [Related]
8. Nucleoplasmin-mediated unfolding of chromatin involves the displacement of linker-associated chromatin proteins.
Ramos I; Prado A; Finn RM; Muga A; Ausió J
Biochemistry; 2005 Jun; 44(23):8274-81. PubMed ID: 15938617
[TBL] [Abstract][Full Text] [Related]
9. A mechanism for histone chaperoning activity of nucleoplasmin: thermodynamic and structural models.
Taneva SG; Bañuelos S; Falces J; Arregi I; Muga A; Konarev PV; Svergun DI; Velázquez-Campoy A; Urbaneja MA
J Mol Biol; 2009 Oct; 393(2):448-63. PubMed ID: 19683001
[TBL] [Abstract][Full Text] [Related]
10. Remodeling somatic nuclei in Xenopus laevis egg extracts: molecular mechanisms for the selective release of histones H1 and H1(0) from chromatin and the acquisition of transcriptional competence.
Dimitrov S; Wolffe AP
EMBO J; 1996 Nov; 15(21):5897-906. PubMed ID: 8918467
[TBL] [Abstract][Full Text] [Related]
11. Differential binding of oocyte-type and somatic-type 5S rRNA to TFIIIA and ribosomal protein L5 in Xenopus oocytes: specialization for storage versus mobilization.
Allison LA; North MT; Neville LA
Dev Biol; 1995 Apr; 168(2):284-95. PubMed ID: 7729570
[TBL] [Abstract][Full Text] [Related]
12. Studies on interaction of different zinc-finger domains of Xenopus laevis TFIIIA with eukaryotic 5S rRNAs.
Barciszewska MZ; Giel-Pietraszuk M; Thogersen HC; Barciszewski J
Nucleic Acids Symp Ser; 1995; (33):56-8. PubMed ID: 8643398
[TBL] [Abstract][Full Text] [Related]
13. The H3-H4 N-terminal tail domains are the primary mediators of transcription factor IIIA access to 5S DNA within a nucleosome.
Vitolo JM; Thiriet C; Hayes JJ
Mol Cell Biol; 2000 Mar; 20(6):2167-75. PubMed ID: 10688663
[TBL] [Abstract][Full Text] [Related]
14. Two DNA-binding sites on the globular domain of histone H5 are required for binding to both bulk and 5 S reconstituted nucleosomes.
Duggan MM; Thomas JO
J Mol Biol; 2000 Nov; 304(1):21-33. PubMed ID: 11071807
[TBL] [Abstract][Full Text] [Related]
15. Genetic analysis of Xenopus transcription factor IIIA.
Bumbulis MJ; Wroblewski G; McKean D; Setzer DR
J Mol Biol; 1998 Dec; 284(5):1307-22. PubMed ID: 9878352
[TBL] [Abstract][Full Text] [Related]
16. A histone-binding protein, nucleoplasmin, stimulates transcription factor binding to nucleosomes and factor-induced nucleosome disassembly.
Chen H; Li B; Workman JL
EMBO J; 1994 Jan; 13(2):380-90. PubMed ID: 8313883
[TBL] [Abstract][Full Text] [Related]
17. The methyl-CpG binding transcriptional repressor MeCP2 stably associates with nucleosomal DNA.
Chandler SP; Guschin D; Landsberger N; Wolffe AP
Biochemistry; 1999 Jun; 38(22):7008-18. PubMed ID: 10353812
[TBL] [Abstract][Full Text] [Related]
18. SWI/SNF remodeling and p300-dependent transcription of histone variant H2ABbd nucleosomal arrays.
Angelov D; Verdel A; An W; Bondarenko V; Hans F; Doyen CM; Studitsky VM; Hamiche A; Roeder RG; Bouvet P; Dimitrov S
EMBO J; 2004 Oct; 23(19):3815-24. PubMed ID: 15372075
[TBL] [Abstract][Full Text] [Related]
19. The interaction of transcription factors with nucleosomal DNA.
Hayes JJ; Wolffe AP
Bioessays; 1992 Sep; 14(9):597-603. PubMed ID: 1365915
[TBL] [Abstract][Full Text] [Related]
20. Human TFIIIA alone is sufficient to prevent nucleosomal repression of a homologous 5S gene.
Stünkel W; Kober I; Kauer M; Taimor G; Seifart KH
Nucleic Acids Res; 1995 Jan; 23(1):109-16. PubMed ID: 7870575
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]