Literature DB >> 12941705

The 3' ends of human pre-snRNAs are produced by RNA polymerase II CTD-dependent RNA processing.

Patricia Uguen1, Shona Murphy.   

Abstract

Proper 3' end formation of the human pre-snRNAs synthesized by pol II requires the cis-acting 3' box, although the precise function of this element has proved difficult to determine. In vivo, 3' end formation is tightly linked to transcription. However, we have now been able to obtain transcription-independent 3' box-dependent processing in vitro. This finally demonstrates that the 3' end of pre-snRNAs is produced by RNA processing rather than by termination of transcription. The phosphorylated form of the C-terminal domain (CTD) of pol II activates the processing event in vitro, consistent with our previous demonstration of the role of the CTD in pre-snRNA 3' end formation in vivo. In addition, we show that sequences upstream from the 3' box of the U2 snRNA gene influence 3' end formation both in vivo and in vitro.

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Year:  2003        PMID: 12941705      PMCID: PMC202372          DOI: 10.1093/emboj/cdg430

Source DB:  PubMed          Journal:  EMBO J        ISSN: 0261-4189            Impact factor:   11.598


  46 in total

1.  The human U1 snRNA promoter correctly initiates transcription in vitro and is activated by PSE1.

Authors:  S I Gunderson; M W Knuth; R R Burgess
Journal:  Genes Dev       Date:  1990-12       Impact factor: 11.361

2.  5'-Capping enzymes are targeted to pre-mRNA by binding to the phosphorylated carboxy-terminal domain of RNA polymerase II.

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Journal:  Genes Dev       Date:  1997-12-15       Impact factor: 11.361

3.  3' processing of human pre-U2 small nuclear RNA: a base-pairing interaction between the 3' extension of the precursor and an internal region.

Authors:  Q Huang; M R Jacobson; T Pederson
Journal:  Mol Cell Biol       Date:  1997-12       Impact factor: 4.272

4.  Increasing the distance between the snRNA promoter and the 3' box decreases the efficiency of snRNA 3'-end formation.

Authors:  L Ramamurthy; T C Ingledue; D R Pilch; B K Kay; W F Marzluff
Journal:  Nucleic Acids Res       Date:  1996-11-15       Impact factor: 16.971

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Journal:  DNA       Date:  1988 Jan-Feb

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Authors:  C Allmang; J Kufel; G Chanfreau; P Mitchell; E Petfalski; D Tollervey
Journal:  EMBO J       Date:  1999-10-01       Impact factor: 11.598

7.  RNA polymerase II C-terminal domain required for enhancer-driven transcription.

Authors:  H P Gerber; M Hagmann; K Seipel; O Georgiev; M A West; Y Litingtung; W Schaffner; J L Corden
Journal:  Nature       Date:  1995-04-13       Impact factor: 49.962

8.  Purification and characterization of the Pac1 ribonuclease of Schizosaccharomyces pombe.

Authors:  G Rotondo; D Frendewey
Journal:  Nucleic Acids Res       Date:  1996-06-15       Impact factor: 16.971

9.  The polyribosomal protein bound to the 3' end of histone mRNA can function in histone pre-mRNA processing.

Authors:  Z Dominski; J Sumerel; R J Hanson; W F Marzluff
Journal:  RNA       Date:  1995-11       Impact factor: 4.942

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Authors:  S Bienroth; W Keller; E Wahle
Journal:  EMBO J       Date:  1993-02       Impact factor: 11.598

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  29 in total

1.  3'-box-dependent processing of human pre-U1 snRNA requires a combination of RNA and protein co-factors.

Authors:  Patricia Uguen; Shona Murphy
Journal:  Nucleic Acids Res       Date:  2004-06-01       Impact factor: 16.971

Review 2.  The Cajal body: a meeting place for spliceosomal snRNPs in the nuclear maze.

Authors:  David Stanek; Karla M Neugebauer
Journal:  Chromosoma       Date:  2006-03-31       Impact factor: 4.316

3.  DSP1 and DSP4 Act Synergistically in Small Nuclear RNA 3' End Maturation and Pollen Growth.

Authors:  Xuepiao Pu; Chunmei Meng; Weili Wang; Siyu Yang; Yuan Chen; Qingjun Xie; Bin Yu; Yunfeng Liu
Journal:  Plant Physiol       Date:  2019-06-21       Impact factor: 8.340

Review 4.  Formation of the 3' end of histone mRNA: getting closer to the end.

Authors:  Zbigniew Dominski; William F Marzluff
Journal:  Gene       Date:  2007-05-04       Impact factor: 3.688

5.  Transcription termination by nuclear RNA polymerases.

Authors:  Patricia Richard; James L Manley
Journal:  Genes Dev       Date:  2009-06-01       Impact factor: 11.361

6.  P-TEFb is not an essential elongation factor for the intronless human U2 snRNA and histone H2b genes.

Authors:  Joanne Medlin; Andrew Scurry; Alice Taylor; Fan Zhang; B Matija Peterlin; Shona Murphy
Journal:  EMBO J       Date:  2005-11-24       Impact factor: 11.598

7.  Tho1, a novel hnRNP, and Sub2 provide alternative pathways for mRNP biogenesis in yeast THO mutants.

Authors:  Sonia Jimeno; Rosa Luna; María García-Rubio; Andrés Aguilera
Journal:  Mol Cell Biol       Date:  2006-06       Impact factor: 4.272

8.  Alternative splicing of DSP1 enhances snRNA accumulation by promoting transcription termination and recycle of the processing complex.

Authors:  Weili Wang; Xuepiao Pu; Siyu Yang; Yujie Feng; Chan Lin; Mu Li; Xi Li; Huali Li; Chunmei Meng; Qingjun Xie; Bin Yu; Yunfeng Liu
Journal:  Proc Natl Acad Sci U S A       Date:  2020-08-03       Impact factor: 11.205

9.  HSSB1 and hSSB2 form similar multiprotein complexes that participate in DNA damage response.

Authors:  Yongjiang Li; Emma Bolderson; Rakesh Kumar; Parameswary A Muniandy; Yutong Xue; Derek J Richard; Michael Seidman; Tej K Pandita; Kum Kum Khanna; Weidong Wang
Journal:  J Biol Chem       Date:  2009-07-14       Impact factor: 5.157

10.  The scaRNA2 is produced by an independent transcription unit and its processing is directed by the encoding region.

Authors:  Marie-Aline Gérard; Evelyne Myslinski; Natassia Chylak; Stéphanie Baudrey; Alain Krol; Philippe Carbon
Journal:  Nucleic Acids Res       Date:  2009-11-11       Impact factor: 16.971

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