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EMBO J. 1990 Nov;9(11):3743-51
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RNA 3' processing regulates histone mRNA levels in a mammalian cell cycle mutant. A processing factor becomes limiting in G1-arrested cells.
EMBO J. 1987 Jun;6(6):1721-6
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Iron regulation of transferrin receptor mRNA levels requires iron-responsive elements and a rapid turnover determinant in the 3' untranslated region of the mRNA.
EMBO J. 1989 Dec 1;8(12):3693-9
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H2A.X. a histone isoprotein with a conserved C-terminal sequence, is encoded by a novel mRNA with both DNA replication type and polyA 3' processing signals.
Nucleic Acids Res. 1989 Nov 25;17(22):9113-26
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Poly(A), poly(A) binding protein and the regulation of mRNA stability.
Trends Biochem Sci. 1989 Sep;14(9):373-7
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The efficiency of 3'-end formation contributes to the relative levels of different histone mRNAs.
Mol Cell Biol. 1989 Aug;9(8):3499-508
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Regulated expression of a chimeric histone gene introduced into mouse fibroblasts.
Mol Cell Biol. 1985 Sep;5(9):2316-24
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Cell. 1986 Sep 12;46(6):905-11
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Differential expression of two clusters of mouse histone genes.
J Mol Biol. 1985 May 25;183(2):179-94
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3' end formation of U1 snRNA precursors is coupled to transcription from snRNA promoters.
Cell. 1986 Oct 24;47(2):259-66
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Multiple regulatory steps control histone mRNA concentrations.
Trends Biochem Sci. 1988 Feb;13(2):49-52
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A stem-loop in the 3' untranslated region mediates iron-dependent regulation of transferrin receptor mRNA stability in the cytoplasm.
Cell. 1988 Jun 3;53(5):815-25
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The stem-loop structure at the 3' end of histone mRNA is necessary and sufficient for regulation of histone mRNA stability.
Mol Cell Biol. 1987 Dec;7(12):4557-9
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A conserved AU sequence from the 3' untranslated region of GM-CSF mRNA mediates selective mRNA degradation.
Cell. 1986 Aug 29;46(5):659-67
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A mouse Ulb-2 gene with extensive sequence similarity to a rat Ula gene for 670 nucleotides 5' to the gene.
Nucleic Acids Res. 1987 Apr 24;15(8):3622
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Formation of the 3' end of U1 snRNA requires compatible snRNA promoter elements.
Cell. 1986 Oct 24;47(2):249-58
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Intracellular site of U1 small nuclear RNA processing and ribonucleoprotein assembly.
J Cell Biol. 1984 Jan;98(1):188-92
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Histone mRNA concentrations are regulated at the level of transcription and mRNA degradation.
Proc Natl Acad Sci U S A. 1983 Apr;80(7):1849-53
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The cap and poly(A) tail function synergistically to regulate mRNA translational efficiency.
Genes Dev. 1991 Nov;5(11):2108-16
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Mature mRNA 3' end formation stimulates RNA export from the nucleus.
EMBO J. 1991 Nov;10(11):3513-22
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Do the poly(A) tail and 3' untranslated region control mRNA translation?
Cell. 1990 Jul 13;62(1):15-24
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An intact histone 3'-processing site is required for transcription termination in a mouse histone H2a gene.
Mol Cell Biol. 1991 Jan;11(1):497-509
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Regulation of histone mRNA in the unperturbed cell cycle: evidence suggesting control at two posttranscriptional steps.
Mol Cell Biol. 1991 May;11(5):2416-24
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Maturation-specific polyadenylation and translational control: diversity of cytoplasmic polyadenylation elements, influence of poly(A) tail size, and formation of stable polyadenylation complexes.
Mol Cell Biol. 1990 Nov;10(11):5634-45
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Poly(A) tail shortening is the translation-dependent step in c-myc mRNA degradation.
Mol Cell Biol. 1990 Dec;10(12):6132-40
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Expression of histone-U1 snRNA chimeric genes: U1 promoters are compatible with histone 3' end formation.
Gene Expr. 1991 Apr;1(1):41-53
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The poly(A) binding protein is required for poly(A) shortening and 60S ribosomal subunit-dependent translation initiation.
Cell. 1989 Sep 8;58(5):857-67
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Each of the conserved sequence elements flanking the cleavage site of mammalian histone pre-mRNAs has a distinct role in the 3'-end processing reaction.
Mol Cell Biol. 1989 Jul;9(7):3105-8
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Different 3'-end processing produces two independently regulated mRNAs from a single H1 histone gene.
Proc Natl Acad Sci U S A. 1989 Sep;86(18):7002-6
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Accurate and efficient 3' processing of U2 small nuclear RNA precursor in a fractionated cytoplasmic extract.
Mol Cell Biol. 1987 Sep;7(9):3131-7
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Isolation and characterization of two linked mouse U1b small nuclear RNA genes.
Nucleic Acids Res. 1983 Sep 24;11(18):6255-70
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Structure of a cluster of mouse histone genes.
Nucleic Acids Res. 1983 Oct 11;11(19):6679-97
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Regulation of human histone gene expression: kinetics of accumulation and changes in the rate of synthesis and in the half-lives of individual histone mRNAs during the HeLa cell cycle.
Mol Cell Biol. 1983 Apr;3(4):539-50
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Rapid reversible changes in the rate of histone gene transcription and histone mRNA levels in mouse myeloma cells.
Mol Cell Biol. 1984 Feb;4(2):351-7
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Different complexes are formed on the 3' end of histone mRNA with nuclear and polyribosomal proteins.
Nucleic Acids Res. 1991 Oct 25;19(20):5653-9
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mRNA poly(A) tail, a 3' enhancer of translational initiation.
Mol Cell Biol. 1990 Jul;10(7):3441-55
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Poly(A) removal during oocyte maturation: a default reaction selectively prevented by specific sequences in the 3' UTR of certain maternal mRNAs.
Genes Dev. 1990 Dec;4(12B):2287-98
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Changes in the stability of a human H3 histone mRNA during the HeLa cell cycle.
Mol Cell Biol. 1991 Jan;11(1):544-53
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The trimethylguanosine cap structure of U1 snRNA is a component of a bipartite nuclear targeting signal.
Cell. 1990 Aug 10;62(3):569-77
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An essential signaling role for the m3G cap in the transport of U1 snRNP to the nucleus.
Science. 1990 Aug 17;249(4970):786-90
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Monomethylated cap structures facilitate RNA export from the nucleus.
Cell. 1990 Oct 5;63(1):109-18
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Yeast mutation thought to arrest mRNA transport markedly increases the length of the 3' poly(A) on polyadenylated RNA.
J Mol Biol. 1989 Aug 20;208(4):697-700
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The poly(A)-poly(A)-binding protein complex is a major determinant of mRNA stability in vitro.
Mol Cell Biol. 1989 Feb;9(2):659-70
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The mouse histone H2a.2 gene from chromosome 3.
Nucleic Acids Res. 1989 Nov 11;17(21):8876
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Ribonucleoprotein particles in cellular processes.
J Cell Biol. 1988 May;106(5):1419-25
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Expression of mouse histone genes: transcription into 3' intergenic DNA and cryptic processing sites downstream from the 3' end of the H3 gene.
Mol Cell Biol. 1987 Mar;7(3):1039-47
PMID: 2882414
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Coupling of replication type histone mRNA levels to DNA synthesis requires the stem-loop sequence at the 3' end of the mRNA.
Proc Natl Acad Sci U S A. 1987 Sep;84(17):6189-93
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Localization and expression of U1 RNA in early mouse embryo development.
Dev Biol. 1988 Jun;127(2):349-61
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Generation of histone mRNA 3' ends by endonucleolytic cleavage of the pre-mRNA in a snRNP-dependent in vitro reaction.
EMBO J. 1986 Jun;5(6):1319-26
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Sequences of four mouse histone H3 genes: implications for evolution of mouse histone genes.
J Mol Evol. 1986;23(3):242-9
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Translation is required for regulation of histone mRNA degradation.
Cell. 1987 Feb 27;48(4):615-26
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3' processing of pre-mRNA plays a major role in proliferation-dependent regulation of histone gene expression.
Nucleic Acids Res. 1988 Oct 25;16(20):9399-414
PMID: 3141900
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Structural and functional characterization of mouse U7 small nuclear RNA active in 3' processing of histone pre-mRNA.
Mol Cell Biol. 1988 Apr;8(4):1518-24
PMID: 3380087
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Differential expression of individual members of the histone multigene family due to sequences in the 5' and 3' regions of the genes.
Mol Cell Biol. 1988 May;8(5):1887-95
PMID: 3386629
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High-frequency transfection of CHO cells using polybrene.
Somat Cell Mol Genet. 1986 May;12(3):237-44
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H4 histone messenger RNA decay in cell-free extracts initiates at or near the 3' terminus and proceeds 3' to 5'.
J Mol Biol. 1986 Apr 20;188(4):579-93
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Nucleocytoplasmic transport and processing of small nuclear RNA precursors.
Mol Cell Biol. 1990 Jul;10(7):3365-75
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