198 related articles for article (PubMed ID: 1531633)
21. Ribozyme, antisense RNA, and antisense DNA inhibition of U7 small nuclear ribonucleoprotein-mediated histone pre-mRNA processing in vitro.
Cotten M; Schaffner G; Birnstiel ML
Mol Cell Biol; 1989 Oct; 9(10):4479-87. PubMed ID: 2479828
[TBL] [Abstract][Full Text] [Related]
22. Cloning and characterization of the Drosophila U7 small nuclear RNA.
Dominski Z; Yang XC; Purdy M; Marzluff WF
Proc Natl Acad Sci U S A; 2003 Aug; 100(16):9422-7. PubMed ID: 12872004
[TBL] [Abstract][Full Text] [Related]
23. In vivo assembly of functional U7 snRNP requires RNA backbone flexibility within the Sm-binding site.
Kolev NG; Steitz JA
Nat Struct Mol Biol; 2006 Apr; 13(4):347-53. PubMed ID: 16547514
[TBL] [Abstract][Full Text] [Related]
24. The Sm binding site targets U7 snRNA to coiled bodies (spheres) of amphibian oocytes.
Wu CH; Murphy C; Gall JG
RNA; 1996 Aug; 2(8):811-23. PubMed ID: 8752090
[TBL] [Abstract][Full Text] [Related]
25. Conserved terminal hairpin sequences of histone mRNA precursors are not involved in duplex formation with the U7 RNA but act as a target site for a distinct processing factor.
Vasserot AP; Schaufele FJ; Birnstiel ML
Proc Natl Acad Sci U S A; 1989 Jun; 86(12):4345-9. PubMed ID: 2734288
[TBL] [Abstract][Full Text] [Related]
26. Length suppression in histone messenger RNA 3'-end maturation: processing defects of insertion mutant premessenger RNAs can be compensated by insertions into the U7 small nuclear RNA.
Scharl EC; Steitz JA
Proc Natl Acad Sci U S A; 1996 Dec; 93(25):14659-64. PubMed ID: 8962110
[TBL] [Abstract][Full Text] [Related]
27. A 5'-3' exonuclease activity involved in forming the 3' products of histone pre-mRNA processing in vitro.
Walther TN; Wittop Koning TH; Schümperli D; Müller B
RNA; 1998 Sep; 4(9):1034-46. PubMed ID: 9740123
[TBL] [Abstract][Full Text] [Related]
28. U7 small nuclear ribonucleoprotein represses histone gene transcription in cell cycle-arrested cells.
Ideue T; Adachi S; Naganuma T; Tanigawa A; Natsume T; Hirose T
Proc Natl Acad Sci U S A; 2012 Apr; 109(15):5693-8. PubMed ID: 22451911
[TBL] [Abstract][Full Text] [Related]
29. Composition and processing activity of a semi-recombinant holo U7 snRNP.
Bucholc K; Aik WS; Yang XC; Wang K; Zhou ZH; Dadlez M; Marzluff WF; Tong L; Dominski Z
Nucleic Acids Res; 2020 Feb; 48(3):1508-1530. PubMed ID: 31819999
[TBL] [Abstract][Full Text] [Related]
30. Protein composition of catalytically active U7-dependent processing complexes assembled on histone pre-mRNA containing biotin and a photo-cleavable linker.
Skrajna A; Yang XC; Dadlez M; Marzluff WF; Dominski Z
Nucleic Acids Res; 2018 May; 46(9):4752-4770. PubMed ID: 29529248
[TBL] [Abstract][Full Text] [Related]
31. Assembly, nuclear import and function of U7 snRNPs studied by microinjection of synthetic U7 RNA into Xenopus oocytes.
Stefanovic B; Hackl W; Lührmann R; Schümperli D
Nucleic Acids Res; 1995 Aug; 23(16):3141-51. PubMed ID: 7667090
[TBL] [Abstract][Full Text] [Related]
32. The steady state levels and structure of the U7 snRNP are constant during the human cell cycle: lack of cell cycle regulation of histone mRNA 3' end formation.
Bond U; Yario TA
Cell Mol Biol Res; 1994; 40(1):27-34. PubMed ID: 7804324
[TBL] [Abstract][Full Text] [Related]
33. Multiple processing-defective mutations in a mammalian histone pre-mRNA are suppressed by compensatory changes in U7 RNA both in vivo and in vitro.
Bond UM; Yario TA; Steitz JA
Genes Dev; 1991 Sep; 5(9):1709-22. PubMed ID: 1885007
[TBL] [Abstract][Full Text] [Related]
34. Formation of the 3' end of histone mRNA.
Dominski Z; Marzluff WF
Gene; 1999 Oct; 239(1):1-14. PubMed ID: 10571029
[TBL] [Abstract][Full Text] [Related]
35. The cDNA sequences of the sea urchin U7 small nuclear RNA suggest specific contacts between histone mRNA precursor and U7 RNA during RNA processing.
Strub K; Galli G; Busslinger M; Birnstiel ML
EMBO J; 1984 Dec; 3(12):2801-7. PubMed ID: 6084590
[TBL] [Abstract][Full Text] [Related]
36. Genetic complementation in the Xenopus oocyte: co-expression of sea urchin histone and U7 RNAs restores 3' processing of H3 pre-mRNA in the oocyte.
Strub K; Birnstiel ML
EMBO J; 1986 Jul; 5(7):1675-82. PubMed ID: 2943587
[TBL] [Abstract][Full Text] [Related]
37. The site of 3' end formation of histone messenger RNA is a fixed distance from the downstream element recognized by the U7 snRNP.
Scharl EC; Steitz JA
EMBO J; 1994 May; 13(10):2432-40. PubMed ID: 8194533
[TBL] [Abstract][Full Text] [Related]
38. Domains of yeast U4 spliceosomal RNA required for PRP4 protein binding, snRNP-snRNP interactions, and pre-mRNA splicing in vivo.
Bordonné R; Banroques J; Abelson J; Guthrie C
Genes Dev; 1990 Jul; 4(7):1185-96. PubMed ID: 2145195
[TBL] [Abstract][Full Text] [Related]
39. Variable effects of the conserved RNA hairpin element upon 3' end processing of histone pre-mRNA in vitro.
Streit A; Koning TW; Soldati D; Melin L; Schümperli D
Nucleic Acids Res; 1993 Apr; 21(7):1569-75. PubMed ID: 8479907
[TBL] [Abstract][Full Text] [Related]
40. A novel zinc finger protein is associated with U7 snRNP and interacts with the stem-loop binding protein in the histone pre-mRNP to stimulate 3'-end processing.
Dominski Z; Erkmann JA; Yang X; Sànchez R; Marzluff WF
Genes Dev; 2002 Jan; 16(1):58-71. PubMed ID: 11782445
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
