Literature DB >> 16230528

Symplekin and multiple other polyadenylation factors participate in 3'-end maturation of histone mRNAs.

Nikolay G Kolev1, Joan A Steitz.   

Abstract

Most metazoan messenger RNAs encoding histones are cleaved, but not polyadenylated at their 3' ends. Processing in mammalian cell extracts requires the U7 small nuclear ribonucleoprotein (U7 snRNP) and an unidentified heat-labile factor (HLF). We describe the identification of a heat-sensitive protein complex whose integrity is required for histone pre-mRNA cleavage. It includes all five subunits of the cleavage and polyadenylation specificity factor (CPSF), two subunits of the cleavage stimulation factor (CstF), and symplekin. Reconstitution experiments reveal that symplekin, previously shown to be necessary for cytoplasmic poly(A) tail elongation and translational activation of mRNAs during Xenopus oocyte maturation, is the essential heat-labile component. Thus, a common molecular machinery contributes to the nuclear maturation of mRNAs both lacking and possessing poly(A), as well as to cytoplasmic poly(A) tail elongation.

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Year:  2005        PMID: 16230528      PMCID: PMC1276732          DOI: 10.1101/gad.1371105

Source DB:  PubMed          Journal:  Genes Dev        ISSN: 0890-9369            Impact factor:   11.361


  63 in total

1.  The RNA 3' cleavage factors CstF 64 kDa and CPSF 100 kDa are concentrated in nuclear domains closely associated with coiled bodies and newly synthesized RNA.

Authors:  W Schul; B Groenhout; K Koberna; Y Takagaki; A Jenny; E M Manders; I Raska; R van Driel; L de Jong
Journal:  EMBO J       Date:  1996-06-03       Impact factor: 11.598

2.  Compensatory mutations suggest that base-pairing with a small nuclear RNA is required to form the 3' end of H3 messenger RNA.

Authors:  F Schaufele; G M Gilmartin; W Bannwarth; M L Birnstiel
Journal:  Nature       Date:  1986 Oct 30-Nov 5       Impact factor: 49.962

3.  Fractionation of transcription factors for RNA polymerase II from Drosophila Kc cell nuclear extracts.

Authors:  D H Price; A E Sluder; A L Greenleaf
Journal:  J Biol Chem       Date:  1987-03-05       Impact factor: 5.157

4.  Crystal structure of a G-protein beta gamma dimer at 2.1A resolution.

Authors:  J Sondek; A Bohm; D G Lambright; H E Hamm; P B Sigler
Journal:  Nature       Date:  1996-01-25       Impact factor: 49.962

5.  Formation of the 3' end of histone mRNA by post-transcriptional processing.

Authors:  P A Krieg; D A Melton
Journal:  Nature       Date:  1984 Mar 8-14       Impact factor: 49.962

6.  3' editing of mRNAs: sequence requirements and involvement of a 60-nucleotide RNA in maturation of histone mRNA precursors.

Authors:  C Birchmeier; D Schümperli; G Sconzo; M L Birnstiel
Journal:  Proc Natl Acad Sci U S A       Date:  1984-02       Impact factor: 11.205

7.  Products of in vitro cleavage and polyadenylation of simian virus 40 late pre-mRNAs.

Authors:  M D Sheets; P Stephenson; M P Wickens
Journal:  Mol Cell Biol       Date:  1987-04       Impact factor: 4.272

8.  Generation of histone mRNA 3' ends by endonucleolytic cleavage of the pre-mRNA in a snRNP-dependent in vitro reaction.

Authors:  O Gick; A Krämer; W Keller; M L Birnstiel
Journal:  EMBO J       Date:  1986-06       Impact factor: 11.598

9.  The cDNA sequences of the sea urchin U7 small nuclear RNA suggest specific contacts between histone mRNA precursor and U7 RNA during RNA processing.

Authors:  K Strub; G Galli; M Busslinger; M L Birnstiel
Journal:  EMBO J       Date:  1984-12-01       Impact factor: 11.598

10.  RNA 3' processing regulates histone mRNA levels in a mammalian cell cycle mutant. A processing factor becomes limiting in G1-arrested cells.

Authors:  B Lüscher; D Schümperli
Journal:  EMBO J       Date:  1987-06       Impact factor: 11.598

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  102 in total

1.  snRNA 3' end formation requires heterodimeric association of integrator subunits.

Authors:  Todd R Albrecht; Eric J Wagner
Journal:  Mol Cell Biol       Date:  2012-01-17       Impact factor: 4.272

2.  Non-canonical Cajal bodies form in the nucleus of late stage avian oocytes lacking functional nucleolus.

Authors:  Tatiana Khodyuchenko; Elena Gaginskaya; Alla Krasikova
Journal:  Histochem Cell Biol       Date:  2012-03-02       Impact factor: 4.304

Review 3.  The Cajal body and histone locus body.

Authors:  Zehra Nizami; Svetlana Deryusheva; Joseph G Gall
Journal:  Cold Spring Harb Perspect Biol       Date:  2010-05-26       Impact factor: 10.005

Review 4.  Pre-mRNA 3'-end processing complex assembly and function.

Authors:  Serena Chan; Eun-A Choi; Yongsheng Shi
Journal:  Wiley Interdiscip Rev RNA       Date:  2010-10-18       Impact factor: 9.957

5.  A subset of Drosophila integrator proteins is essential for efficient U7 snRNA and spliceosomal snRNA 3'-end formation.

Authors:  Nader Ezzeddine; Jiandong Chen; Bernhard Waltenspiel; Brandon Burch; Todd Albrecht; Ming Zhuo; William D Warren; William F Marzluff; Eric J Wagner
Journal:  Mol Cell Biol       Date:  2010-11-15       Impact factor: 4.272

6.  Effects of Transcription Elongation Rate and Xrn2 Exonuclease Activity on RNA Polymerase II Termination Suggest Widespread Kinetic Competition.

Authors:  Nova Fong; Kristopher Brannan; Benjamin Erickson; Hyunmin Kim; Michael A Cortazar; Ryan M Sheridan; Tram Nguyen; Shai Karp; David L Bentley
Journal:  Mol Cell       Date:  2015-10-15       Impact factor: 17.970

Review 7.  Birth and Death of Histone mRNAs.

Authors:  William F Marzluff; Kaitlin P Koreski
Journal:  Trends Genet       Date:  2017-08-31       Impact factor: 11.639

8.  U1 snRNP-mediated poly(A) site suppression: beneficial and deleterious for mRNA fate.

Authors:  Jörg Langemeier; Maximilian Radtke; Jens Bohne
Journal:  RNA Biol       Date:  2013-01-16       Impact factor: 4.652

9.  Studies of the 5' exonuclease and endonuclease activities of CPSF-73 in histone pre-mRNA processing.

Authors:  Xiao-cui Yang; Kelly D Sullivan; William F Marzluff; Zbigniew Dominski
Journal:  Mol Cell Biol       Date:  2008-10-27       Impact factor: 4.272

10.  Maternally encoded stem-loop-binding protein is degraded in 2-cell mouse embryos by the co-ordinated activity of two separately regulated pathways.

Authors:  Wenling Zhang; Luc Poirier; Mario Martinez Diaz; Vilceu Bordignon; Hugh J Clarke
Journal:  Dev Biol       Date:  2009-01-23       Impact factor: 3.582

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