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
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ZFP100, a component of the active U7 snRNP limiting for histone pre-mRNA processing, is required for entry into S phaseKnockdown of SLBP results in nuclear retention of histone mRNAUnique Sm core structure of U7 snRNPs: assembly by a specialized SMN complex and the role of a new component, Lsm11, in histone RNA processingConserved zinc fingers mediate multiple functions of ZFP100, a U7snRNP associated proteinU7 snRNP-specific Lsm11 protein: dual binding contacts with the 100 kDa zinc finger processing factor (ZFP100) and a ZFP100-independent function in histone RNA 3' end processingSymplekin and multiple other polyadenylation factors participate in 3'-end maturation of histone mRNAsEvolutionary conservation of the U7 small nuclear ribonucleoprotein in Drosophila melanogaster.U7 snRNA mutations in Drosophila block histone pre-mRNA processing and disrupt oogenesisA CPSF-73 homologue is required for cell cycle progression but not cell growth and interacts with a protein having features of CPSF-100The 68 kDa subunit of mammalian cleavage factor I interacts with the U7 small nuclear ribonucleoprotein and participates in 3'-end processing of animal histone mRNAsThe Drosophila U7 snRNP proteins Lsm10 and Lsm11 are required for histone pre-mRNA processing and play an essential role in developmentBinding of human SLBP on the 3'-UTR of histone precursor H4-12 mRNA induces structural rearrangements that enable U7 snRNA anchoringCloning and characterization of the Drosophila U7 small nuclear RNAEarly evolution of histone mRNA 3' end processingInteraction of the Histone mRNA Hairpin with Stem–Loop Binding Protein (SLBP) and Regulation of the SLBP–RNA Complex by Phosphorylation and Proline IsomerizationStem-loop binding protein accumulates during oocyte maturation and is not cell-cycle-regulated in the early mouse embryoFormation of the 3' end of histone mRNA: getting closer to the endTranscription termination by nuclear RNA polymerasesCoupling of DNA synthesis and histone synthesis in S phase independent of cyclin/cdk2 activity.Developmental control of histone mRNA and dSLBP synthesis during Drosophila embryogenesis and the role of dSLBP in histone mRNA 3' end processing in vivo.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.Nuclear export of metazoan replication-dependent histone mRNAs is dependent on RNA length and is mediated by TAP.Nucleases of the metallo-beta-lactamase family and their role in DNA and RNA metabolism.Results and prospects of the yeast three-hybrid system.FUS/TLS contributes to replication-dependent histone gene expression by interaction with U7 snRNPs and histone-specific transcription factorsU7 small nuclear ribonucleoprotein represses histone gene transcription in cell cycle-arrested cells.Splicing-independent recruitment of spliceosomal small nuclear RNPs to nascent RNA polymerase II transcripts.Deletion of the nuclear exosome component RRP6 leads to continued accumulation of the histone mRNA HTB1 in S-phase of the cell cycle in Saccharomyces cerevisiaeDrosophila stem-loop binding protein intracellular localization is mediated by phosphorylation and is required for cell cycle-regulated histone mRNA expression.Recent Selection Changes in Human Genes under Long-Term Balancing Selection.Replication stress-induced alternative mRNA splicing alters properties of the histone RNA-binding protein HBP/SLBP: a key factor in the control of histone gene expression.Darwinian and demographic forces affecting human protein coding genesThe stem-loop binding protein regulates translation of histone mRNA during mammalian oogenesis.Regulation of mRNA transport, localization and translation in the nervous system of mammals (Review).The control of histone gene expression.Making ends meet: coordination between RNA 3'-end processing and transcription initiation.Differences and similarities between Drosophila and mammalian 3' end processing of histone pre-mRNAs.The B-subdomain of the Xenopus laevis XFIN KRAB-AB domain is responsible for its weaker transcriptional repressor activity compared to human ZNF10/Kox1.Genome-wide survey of putative RNA-binding proteins encoded in the human proteome.FLASH is required for the endonucleolytic cleavage of histone pre-mRNAs but is dispensable for the 5' exonucleolytic degradation of the downstream cleavage product.
P2860
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P2860
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
description
2002 nî lūn-bûn
@nan
2002 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
2002 թվականի հունվարին հրատարակված գիտական հոդված
@hy
2002年の論文
@ja
2002年論文
@yue
2002年論文
@zh-hant
2002年論文
@zh-hk
2002年論文
@zh-mo
2002年論文
@zh-tw
2002年论文
@wuu
name
A novel zinc finger protein is ...... to stimulate 3'-end processing
@ast
A novel zinc finger protein is ...... to stimulate 3'-end processing
@en
A novel zinc finger protein is ...... to stimulate 3'-end processing
@nl
type
label
A novel zinc finger protein is ...... to stimulate 3'-end processing
@ast
A novel zinc finger protein is ...... to stimulate 3'-end processing
@en
A novel zinc finger protein is ...... to stimulate 3'-end processing
@nl
prefLabel
A novel zinc finger protein is ...... to stimulate 3'-end processing
@ast
A novel zinc finger protein is ...... to stimulate 3'-end processing
@en
A novel zinc finger protein is ...... to stimulate 3'-end processing
@nl
P2093
P2860
P356
P1433
P1476
A novel zinc finger protein is ...... to stimulate 3'-end processing
@en
P2093
Judith A Erkmann
Ricardo Sànchez
William F Marzluff
Xiaocui Yang
Zbigniew Dominski
P2860
P356
10.1101/GAD.932302
P407
P577
2002-01-01T00:00:00Z