| scholarly article | Q13442814 |
| P50 | author | William F Marzluff | Q89582047 |
| P2093 | author name string | Kelly D Sullivan | |
| Mindy Steiniger | |||
| P2860 | cites work | The 160-kD subunit of human cleavage-polyadenylation specificity factor coordinates pre-mRNA 3'-end formation | Q24314710 |
| Symplekin, a novel type of tight junction plaque protein | Q24317634 | ||
| Knockdown of SLBP results in nuclear retention of histone mRNA | Q24318762 | ||
| Conserved motifs in both CPSF73 and CPSF100 are required to assemble the active endonuclease for histone mRNA 3'-end maturation | Q24321829 | ||
| Unique Sm core structure of U7 snRNPs: assembly by a specialized SMN complex and the role of a new component, Lsm11, in histone RNA processing | Q24323271 | ||
| Yhh1p/Cft1p directly links poly(A) site recognition and RNA polymerase II transcription termination | Q24534246 | ||
| Symplekin and multiple other polyadenylation factors participate in 3'-end maturation of histone mRNAs | Q24537115 | ||
| The stem-loop binding protein is required for efficient translation of histone mRNA in vivo and in vitro | Q24540149 | ||
| U7 snRNA mutations in Drosophila block histone pre-mRNA processing and disrupt oogenesis | Q24541402 | ||
| Complex protein interactions within the human polyadenylation machinery identify a novel component | Q24554306 | ||
| Cleavage and polyadenylation factor CPF specifically interacts with the pre-mRNA 3' processing signal AAUAAA | Q24564625 | ||
| RNA recognition by the human polyadenylation factor CstF | Q24646013 | ||
| Studies of the 5' exonuclease and endonuclease activities of CPSF-73 in histone pre-mRNA processing | Q24655247 | ||
| U2 snRNP binds intronless histone pre-mRNAs to facilitate U7-snRNP-dependent 3' end formation | Q24685896 | ||
| Pta1, a component of yeast CF II, is required for both cleavage and poly(A) addition of mRNA precursor | Q27930178 | ||
| PTA1, an essential gene of Saccharomyces cerevisiae affecting pre-tRNA processing | Q27932158 | ||
| A multisubunit 3' end processing factor from yeast containing poly(A) polymerase and homologues of the subunits of mammalian cleavage and polyadenylation specificity factor | Q27935985 | ||
| Different phosphorylated forms of RNA polymerase II and associated mRNA processing factors during transcription | Q28131686 | ||
| Polyadenylation factor CPSF-73 is the pre-mRNA 3'-end-processing endonuclease | Q28275724 | ||
| Metabolism and regulation of canonical histone mRNAs: life without a poly(A) tail | Q28297786 | ||
| The C-terminal domain of RNA polymerase II couples mRNA processing to transcription | Q28301744 | ||
| RNA polymerase II is an essential mRNA polyadenylation factor | Q29614773 | ||
| RNA polymerase II pauses and associates with pre-mRNA processing factors at both ends of genes. | Q34009055 | ||
| On the importance of being co-transcriptional | Q34150533 | ||
| Developmental control of histone mRNA and dSLBP synthesis during Drosophila embryogenesis and the role of dSLBP in histone mRNA 3' end processing in vivo | Q34276458 | ||
| Heat-labile regulatory factor is required for 3' processing of histone precursor mRNAs | Q34377328 | ||
| Rules of engagement: co-transcriptional recruitment of pre-mRNA processing factors | Q34419716 | ||
| Drosophila stem loop binding protein coordinates accumulation of mature histone mRNA with cell cycle progression | Q35076429 | ||
| The role of the yeast cleavage and polyadenylation factor subunit Ydh1p/Cft2p in pre-mRNA 3'-end formation | Q35186139 | ||
| New perspectives on connecting messenger RNA 3' end formation to transcription | Q35774183 | ||
| Developmental and cell cycle regulation of the Drosophila histone locus body | Q35901909 | ||
| The Drosophila melanogaster Cajal body | Q36117263 | ||
| Connections between mRNA 3' end processing and transcription termination | Q36131487 | ||
| NELF-mediated stalling of Pol II can enhance gene expression by blocking promoter-proximal nucleosome assembly | Q36802956 | ||
| Protein factors in pre-mRNA 3'-end processing. | Q37044967 | ||
| The Drosophila homologue of the 64 kDa subunit of cleavage stimulation factor interacts with the 77 kDa subunit encoded by the suppressor of forked gene | Q38317290 | ||
| Differences and similarities between Drosophila and mammalian 3' end processing of histone pre-mRNAs | Q38319470 | ||
| Cotranscriptional processing of Drosophila histone mRNAs. | Q39756702 | ||
| Globin gene transcripts can utilize histone gene 3' end processing signals | Q40418474 | ||
| P-TEFb is critical for the maturation of RNA polymerase II into productive elongation in vivo | Q41911078 | ||
| Sumoylation modulates the assembly and activity of the pre-mRNA 3' processing complex | Q42823824 | ||
| Functional interaction of yeast pre-mRNA 3' end processing factors with RNA polymerase II. | Q44017745 | ||
| Distribution of different phosphorylated forms of RNA polymerase II in relation to Cajal and PML bodies in human cells: an ultrastructural study | Q46723039 | ||
| A genome-wide RNA interference screen reveals that variant histones are necessary for replication-dependent histone pre-mRNA processing. | Q47070600 | ||
| NELF interacts with CBC and participates in 3' end processing of replication-dependent histone mRNAs | Q50336087 | ||
| A multisubunit factor, CstF, is required for polyadenylation of mammalian pre-mRNAs | Q68164668 | ||
| Formation of the 3' end of U1 snRNA requires compatible snRNA promoter elements | Q69638046 | ||
| Identifying phosphoCTD-associating proteins | Q75447267 | ||
| The polyadenylation factor CPSF-73 is involved in histone-pre-mRNA processing | Q81327465 | ||
| P433 | issue | 3 | |
| P921 | main subject | Cleavage and polyadenylation specificity factor 100 Dmel_CG1957 | Q29809646 |
| Cleavage stimulation factor 64 kD subunit Dmel_CG7697 | Q29809728 | ||
| Suppressor of forked Dmel_CG17170 | Q29809849 | ||
| Stem-loop binding protein Dmel_CG11886 | Q29810272 | ||
| Symplekin Dmel_CG2097 | Q29812732 | ||
| Cleavage and polyadenylation specificity factor 73 Dmel_CG7698 | Q29812973 | ||
| Lsm11 Dmel_CG12924 | Q29812989 | ||
| Cleavage stimulation factor 50 kD subunit Dmel_CG2261 | Q29819852 | ||
| P304 | page(s) | 322-332 | |
| P577 | publication date | 2009-05-01 | |
| P1433 | published in | Molecular Cell | Q3319468 |
| P1476 | title | A core complex of CPSF73, CPSF100, and Symplekin may form two different cleavage factors for processing of poly(A) and histone mRNAs | |
| P478 | volume | 34 |
| Q37448767 | 3'-End processing of histone pre-mRNAs in Drosophila: U7 snRNP is associated with FLASH and polyadenylation factors |
| Q35751961 | A Potential New Mechanism of Arsenic Carcinogenesis: Depletion of Stem-Loop Binding Protein and Increase in Polyadenylated Canonical Histone H3.1 mRNA. |
| Q34485087 | A Subset of Drosophila Integrator Proteins Is Essential for Efficient U7 snRNA and Spliceosomal snRNA 3′-End Formation |
| Q35161971 | An RNA-protein complex links enhanced nuclear 3' processing with cytoplasmic mRNA stabilization |
| Q39253684 | An RNAi screen identifies additional members of the Drosophila Integrator complex and a requirement for cyclin C/Cdk8 in snRNA 3'-end formation. |
| Q36429776 | Antisense Transcription of Retrotransposons in Drosophila: An Origin of Endogenous Small Interfering RNA Precursors |
| Q28397679 | Arsenic induces polyadenylation of canonical histone mRNA by down-regulating stem-loop-binding protein gene expression |
| Q60481248 | Biosynthesis of histone messenger RNA employs a specific 3' end endonuclease |
| Q94522114 | CDK11 is required for transcription of replication-dependent histone genes |
| Q34430715 | CPSF30 and Wdr33 directly bind to AAUAAA in mammalian mRNA 3' processing |
| Q39269835 | Cleavage and polyadenylation: Ending the message expands gene regulation |
| Q36976457 | Concentrating pre-mRNA processing factors in the histone locus body facilitates efficient histone mRNA biogenesis. |
| Q36406376 | Context-dependent modulation of Pol II CTD phosphatase SSUP-72 regulates alternative polyadenylation in neuronal development |
| Q27646447 | Crystal Structure of the HEAT Domain from the Pre-mRNA Processing Factor Symplekin |
| Q35058505 | CstF-64 is necessary for endoderm differentiation resulting in cardiomyocyte defects |
| Q33983624 | CstF-64 supports pluripotency and regulates cell cycle progression in embryonic stem cells through histone 3' end processing. |
| Q34592882 | CstF64: cell cycle regulation and functional role in 3' end processing of replication-dependent histone mRNAs |
| Q52718270 | Cstf2t Regulates expression of histones and histone-like proteins in male germ cells. |
| Q53038876 | DSIF and NELF interact with Integrator to specify the correct post-transcriptional fate of snRNA genes. |
| Q38201414 | Degradation of oligouridylated histone mRNAs: see UUUUU and goodbye |
| Q33602636 | Delineating the structural blueprint of the pre-mRNA 3'-end processing machinery |
| Q50112983 | Dicer-2 promotes mRNA activation through cytoplasmic polyadenylation. |
| Q36189905 | Drosophila Symplekin localizes dynamically to the histone locus body and tricellular junctions |
| Q35196079 | Drosophila histone locus bodies form by hierarchical recruitment of components |
| Q33568513 | Drosophila melanogaster retrotransposon and inverted repeat-derived endogenous siRNAs are differentially processed in distinct cellular locations. |
| Q34213955 | Ending the message: poly(A) signals then and now |
| Q36791576 | From polyadenylation to splicing: Dual role for mRNA 3' end formation factors |
| Q36620799 | Functional analysis of the integrator subunit 12 identifies a microdomain that mediates activation of the Drosophila integrator complex |
| Q35690588 | Global Promotion of Alternative Internal Exon Usage by mRNA 3' End Formation Factors |
| Q58876653 | Histone supply: Multitiered regulation ensures chromatin dynamics throughout the cell cycle |
| Q35981897 | INT6 interacts with MIF4GD/SLIP1 and is necessary for efficient histone mRNA translation |
| Q33684999 | Identification and analysis of candidate fungal tRNA 3'-end processing endonucleases tRNase Zs, homologs of the putative prostate cancer susceptibility protein ELAC2 |
| Q35875832 | In vivo characterization of the Drosophila mRNA 3' end processing core cleavage complex |
| Q52374660 | Integrator subunit 4 is a 'Symplekin-like' scaffold that associates with INTS9/11 to form the Integrator cleavage module. |
| Q41976272 | Interaction between FLASH and Lsm11 is essential for histone pre-mRNA processing in vivo in Drosophila |
| Q89944477 | Loss of Histone Locus Bodies in the Mature Hemocytes of Larval Lymph Gland Result in Hyperplasia of the Tissue in mxc Mutants of Drosophila |
| Q46335657 | Molecular basis for the recognition of the human AAUAAA polyadenylation signal. |
| Q33871092 | Molecular mechanisms of eukaryotic pre-mRNA 3' end processing regulation |
| Q44882225 | Non-canonical Cajal bodies form in the nucleus of late stage avian oocytes lacking functional nucleolus. |
| Q37693565 | Pre-mRNA 3'-end processing complex assembly and function |
| Q52359095 | Protein composition of catalytically active U7-dependent processing complexes assembled on histone pre-mRNA containing biotin and a photo-cleavable linker. |
| Q34305741 | RNA polymerase II pausing downstream of core histone genes is different from genes producing polyadenylated transcripts |
| Q34960186 | RNA polymerase II transcription elongation control |
| Q34430722 | Reconstitution of CPSF active in polyadenylation: recognition of the polyadenylation signal by WDR33. |
| Q28245082 | Structural biology of poly(A) site definition |
| Q38195095 | Structure and function of pre-mRNA 5'-end capping quality control and 3'-end processing |
| Q89582051 | Structure of an active human histone pre-mRNA 3'-end processing machinery |
| Q55092205 | Targeting the Polyadenylation Signal of Pre-mRNA: A New Gene Silencing Approach for Facioscapulohumeral Dystrophy. |
| Q24630829 | The Cajal body and histone locus body |
| Q26775167 | The Chemical Biology of Human Metallo-β-Lactamase Fold Proteins |
| Q30416929 | The Integrator complex controls the termination of transcription at diverse classes of gene targets |
| Q28082339 | The end of the message: multiple protein-RNA interactions define the mRNA polyadenylation site |
| Q50529317 | The fission yeast Schizosaccharomyces pombe has two distinct tRNase Z(L)s encoded by two different genes and differentially targeted to the nucleus and mitochondria. |
| Q33995521 | The multifunctional SNM1 gene family: not just nucleases |
| Q33637722 | Tissue-specific mechanisms of alternative polyadenylation: testis, brain, and beyond. |
| Q87887544 | Transcription elongation rate affects nascent histone pre-mRNA folding and 3' end processing |
| Q34247752 | snRNA 3' end formation requires heterodimeric association of integrator subunits |
| Q37672314 | snRNA 3' end formation: the dawn of the Integrator complex |
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