The conserved CAAGAAAGA spacer sequence is an essential element for the formation of 3' termini of the sea urchin H3 histone mRNA by RNA processing.
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Genetic complementation in the Xenopus oocyte: co-expression of sea urchin histone and U7 RNAs restores 3' processing of H3 pre-mRNA in the oocyteStem-loop binding protein facilitates 3'-end formation by stabilizing U7 snRNP binding to histone pre-mRNASpecific contacts between mammalian U7 snRNA and histone precursor RNA are indispensable for the in vitro 3' RNA processing reactionThe site of 3' end formation of histone messenger RNA is a fixed distance from the downstream element recognized by the U7 snRNP3' end processing of mouse histone pre-mRNA: evidence for additional base-pairing between U7 snRNA and pre-mRNANucleotide sequence of transforming human c-sis cDNA clones with homology to platelet-derived growth factorAnalysis of a sea urchin gene cluster coding for the small nuclear U7 RNA, a rare RNA species implicated in the 3' editing of histone precursor mRNAsStructural and functional characterization of mouse U7 small nuclear RNA active in 3' processing of histone pre-mRNALength 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 RNAA 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 processingFormation of the 3' end of histone mRNA: getting closer to the endEach of the conserved sequence elements flanking the cleavage site of mammalian histone pre-mRNAs has a distinct role in the 3'-end processing reactionFungal small nuclear ribonucleoproteins share properties with plant and vertebrate U-snRNPs.Generation of histone mRNA 3' ends by endonucleolytic cleavage of the pre-mRNA in a snRNP-dependent in vitro reaction.A signal regulating mouse histone H4 mRNA levels in a mammalian cell cycle mutant and sequences controlling RNA 3' processing are both contained within the same 80-bp fragment.RNA 3' processing regulates histone mRNA levels in a mammalian cell cycle mutant. A processing factor becomes limiting in G1-arrested cellsCleavage and polyadenylation of messenger RNA precursors in vitro occurs within large and specific 3' processing complexes.Formation of the 3' end of U1 snRNA is directed by a conserved sequence located downstream of the coding region.Deletion of a yeast small nuclear RNA gene impairs growth.Compilation of DNA sequences of Escherichia coli (update 1990)3' end processing of Drosophila melanogaster histone pre-mRNAs: requirement for phosphorylated Drosophila stem-loop binding protein and coevolution of the histone pre-mRNA processing system.Functional importance of conserved nucleotides at the histone RNA 3' processing siteThe inability of the Psammechinus miliaris H3 RNA to be processed in the Xenopus oocyte is associated with sequences distinct from those highly conserved amongst sea urchin histone RNAs.An alternative pathway of histone mRNA 3' end formation in mouse round spermatidsSynthesis of U1 RNA in a DNA-dependent system from sea urchin embryos.Histone genes of Volvox carteri: DNA sequence and organization of two H3-H4 gene lociBoth conserved signals on mammalian histone pre-mRNAs associate with small nuclear ribonucleoproteins during 3' end formation in vitro.The highly conserved U small nuclear RNA 3'-end formation signal is quite tolerant to mutation.RNA processing and expression of an intron-encoded protein in yeast mitochondria: role of a conserved dodecamer sequencePromoter sequences required for transcription of Xenopus laevis histone genes in injected frog oocyte nuclei.Regulation of amyloid A gene expression in cultured cells.Identification of a cis-regulatory element involved in accumulation of human T-cell leukemia virus type II genomic mRNA.Stimulation of sea urchin H2B histone gene transcription by a chromatin-associated protein fraction depends on gene sequences downstream of the transcription start siteATTAAA as well as downstream sequences are required for RNA 3'-end formation in the E3 complex transcription unit of adenovirus.An AU-rich element in the 3' untranslated region of the spinach chloroplast petD gene participates in sequence-specific RNA-protein complex formation.Evolutionary conserved multiprotein complexes interact with the 3' untranslated region of histone transcripts.Poly(A) polymerase purified from HeLa cell nuclear extract is required for both cleavage and polyadenylation of pre-mRNA in vitro.Mature mRNA 3' end formation stimulates RNA export from the nucleus.Two spliceosomes can form simultaneously and independently on synthetic double-intron messenger RNA precursors.Maturation of Escherichia coli tryptophan operon mRNA: evidence for 3' exonucleolytic processing after rho-dependent termination.
P2860
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P2860
The conserved CAAGAAAGA spacer sequence is an essential element for the formation of 3' termini of the sea urchin H3 histone mRNA by RNA processing.
description
1985 nî lūn-bûn
@nan
1985 թուականի Փետրուարին հրատարակուած գիտական յօդուած
@hyw
1985 թվականի փետրվարին հրատարակված գիտական հոդված
@hy
1985年の論文
@ja
1985年論文
@yue
1985年論文
@zh-hant
1985年論文
@zh-hk
1985年論文
@zh-mo
1985年論文
@zh-tw
1985年论文
@wuu
name
The conserved CAAGAAAGA spacer ...... istone mRNA by RNA processing.
@ast
The conserved CAAGAAAGA spacer ...... istone mRNA by RNA processing.
@en
type
label
The conserved CAAGAAAGA spacer ...... istone mRNA by RNA processing.
@ast
The conserved CAAGAAAGA spacer ...... istone mRNA by RNA processing.
@en
prefLabel
The conserved CAAGAAAGA spacer ...... istone mRNA by RNA processing.
@ast
The conserved CAAGAAAGA spacer ...... istone mRNA by RNA processing.
@en
P2860
P1433
P1476
The conserved CAAGAAAGA spacer ...... istone mRNA by RNA processing.
@en
P2093
Birnstiel ML
Georgiev O
P2860
P304
P407
P577
1985-02-01T00:00:00Z