Coupling of replication type histone mRNA levels to DNA synthesis requires the stem-loop sequence at the 3' end of the mRNA.
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Human La protein: a stabilizer of histone mRNAThe stem-loop structure at the 3' end of histone mRNA is necessary and sufficient for regulation of histone mRNA stabilityThe prolyl isomerase Pin1 targets stem-loop binding protein (SLBP) to dissociate the SLBP-histone mRNA complex linking histone mRNA decay with SLBP ubiquitinationLoss of the histone pre-mRNA processing factor stem-loop binding protein in Drosophila causes genomic instability and impaired cellular proliferationEach of the conserved sequence elements flanking the cleavage site of mammalian histone pre-mRNAs has a distinct role in the 3'-end processing reactionThe efficiency of 3'-end formation contributes to the relative levels of different histone mRNAsGammaH2AX and cancermRNA stability in mammalian cellsThe Integrator complex controls the termination of transcription at diverse classes of gene targets.The histone 3'-terminal stem-loop is necessary for translation in Chinese hamster ovary cellsA genomic clone encoding a novel proliferation-dependent histone H2A.1 mRNA enriched in the poly(A)+ fraction.Polyadenylated and 3' processed mRNAs are transcribed from the mouse histone H2A.X geneA region in the coding sequence is required for high-level expression of murine histone H3 gene.Intronless mRNA transport elements may affect multiple steps of pre-mRNA processing.Human beta-globin mRNAs that harbor a nonsense codon are degraded in murine erythroid tissues to intermediates lacking regions of exon I or exons I and II that have a cap-like structure at the 5' termini.Different 3'-end processing produces two independently regulated mRNAs from a single H1 histone gene.The histone 3'-terminal stem-loop-binding protein enhances translation through a functional and physical interaction with eukaryotic initiation factor 4G (eIF4G) and eIF3Histone mRNAs do not accumulate during S phase of either mitotic or endoreduplicative cycles in the chordate Oikopleura dioica.Accelerated poly(A) loss and mRNA stabilization are independent effects of protein synthesis inhibition on alpha-tubulin mRNA in ChlamydomonasAn alternative pathway of histone mRNA 3' end formation in mouse round spermatidsDrosophila stem loop binding protein coordinates accumulation of mature histone mRNA with cell cycle progressionAn estrogen-dependent polysomal protein binds to the 5' untranslated region of the chicken vitellogenin mRNA.Down modulation of HIV-1 gene expression using a procaryotic RNA-binding protein.The histone mRNA 3' end is required for localization of histone mRNA to polyribosomes.3' processing of pre-mRNA plays a major role in proliferation-dependent regulation of histone gene expression.The mouse histone H2a gene contains a small element that facilitates cytoplasmic accumulation of intronless gene transcripts and of unspliced HIV-1-related mRNAsDNA-activated protein kinase functions in a newly observed S phase checkpoint that links histone mRNA abundance with DNA replication.Multiple instability-regulating sites in the 3' untranslated region of the urokinase-type plasminogen activator mRNA.Histone H2A.X gene transcription is regulated differently than transcription of other replication-linked histone genesNonsense but not missense mutations can decrease the abundance of nuclear mRNA for the mouse major urinary protein, while both types of mutations can facilitate exon skipping.Nonsense codons can reduce the abundance of nuclear mRNA without affecting the abundance of pre-mRNA or the half-life of cytoplasmic mRNA.Selective destabilization of short-lived mRNAs with the granulocyte-macrophage colony-stimulating factor AU-rich 3' noncoding region is mediated by a cotranslational mechanismAn intact histone 3'-processing site is required for transcription termination in a mouse histone H2a gene.Changes in the stability of a human H3 histone mRNA during the HeLa cell cycleRegulation of histone mRNA in the unperturbed cell cycle: evidence suggesting control at two posttranscriptional stepsNuclease activity associated with mammalian mRNA in its native state: possible basis for selectivity in mRNA decay.Coding and noncoding sequences at the 3' end of yeast histone H2B mRNA confer cell cycle regulationExpression of replication-dependent histone genes in avian spermatids involves an alternate pathway of mRNA 3'-end formation.Differential expression of individual members of the histone multigene family due to sequences in the 5' and 3' regions of the genes.Stabilization of tubulin mRNA by inhibition of protein synthesis in sea urchin embryos.
P2860
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P2860
Coupling of replication type histone mRNA levels to DNA synthesis requires the stem-loop sequence at the 3' end of the mRNA.
description
1987 nî lūn-bûn
@nan
1987 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
1987 թվականի սեպտեմբերին հրատարակված գիտական հոդված
@hy
1987年の論文
@ja
1987年論文
@yue
1987年論文
@zh-hant
1987年論文
@zh-hk
1987年論文
@zh-mo
1987年論文
@zh-tw
1987年论文
@wuu
name
Coupling of replication type h ...... nce at the 3' end of the mRNA.
@ast
Coupling of replication type h ...... nce at the 3' end of the mRNA.
@en
Coupling of replication type h ...... nce at the 3' end of the mRNA.
@nl
type
label
Coupling of replication type h ...... nce at the 3' end of the mRNA.
@ast
Coupling of replication type h ...... nce at the 3' end of the mRNA.
@en
Coupling of replication type h ...... nce at the 3' end of the mRNA.
@nl
prefLabel
Coupling of replication type h ...... nce at the 3' end of the mRNA.
@ast
Coupling of replication type h ...... nce at the 3' end of the mRNA.
@en
Coupling of replication type h ...... nce at the 3' end of the mRNA.
@nl
P2093
P2860
P356
P1476
Coupling of replication type h ...... nce at the 3' end of the mRNA.
@en
P2093
A I Skoultchi
B J Levine
N Chodchoy
W F Marzluff
P2860
P304
P356
10.1073/PNAS.84.17.6189
P407
P577
1987-09-01T00:00:00Z