Literature DB >> 7799958

Lack of an effect of the efficiency of RNA 3'-end formation on the efficiency of removal of either the final or the penultimate intron in intact cells.

D Nesic1, J Zhang, L E Maquat.   

Abstract

Evidence exists from studies using intact cells that intron removal can be influenced by the reactivity of upstream and downstream splice sites and that cleavage and polyadenylation can be influenced by the reactivity of upstream splice sites. These results indicate that sequences within 3'-terminal introns can function in the removal of upstream introns as well as the formation of RNA 3' ends. Evidence from studies using intact cells for an influence of RNA 3'-end formation on intron removal is lacking. We report here that mutations within polyadenylation sequences that either decrease or increase the efficiency of RNA 3'-end formation have no effect on the efficiencies with which either the 3'-terminal or the penultimate intron is removed by splicing. Northern (RNA) blot hybridization, RNase mapping, and an assay that couples reverse transcription and PCR were used to analyze the effects of deletions and a substitution of the polyadenylation sequences within the human gene for triosephosphate isomerase (TPI). TPI pre-mRNA harbors six introns that are constitutively removed by splicing. Relative to normal levels, each of the deletions was found to reduce the nuclear and cytoplasmic levels of TPI mRNA, increase the nuclear level of unprocessed RNA 3' ends, and decrease the nuclear level of processed RNA 3' ends. The simplest interpretation of these data indicates that (i) the rate of 3'-end formation normally limits the amount of mRNA produced and (ii) the deletions decrease and the substitution increases the efficiency of RNA 3'-end formation. While each of the deletions and the substitution altered the absolute levels of intron 6-containing, intron 5-containing, intron 6-free, and intron 5-free RNAs, in no case was there an abnormal ratio of intron-containing to intron-free RNA for either intron. Therefore, at least for TPI RNA, while the efficiency of removal of the 3'-terminal intron influences the efficiency of removal of either the 3'-end formation, the efficiency of RNA 3'-end formation does not influence the efficiency of removal of either the 3'-terminal or penultimate intron. The dependence of TPI RNA 3'-end formation on splicing may reflect the suboptimal strengths of the corresponding regulatory sequences and may function to ensure that TPI pre-mRNA is not released from the chromatin template until it has formed a complex with spliceosomes. If so, then the independence of TPI RNA splicing on 3'-end formation may be rationalized by the lack of a comparable function.

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Year:  1995        PMID: 7799958      PMCID: PMC231997          DOI: 10.1128/MCB.15.1.488

Source DB:  PubMed          Journal:  Mol Cell Biol        ISSN: 0270-7306            Impact factor:   4.272


  43 in total

Review 1.  The biochemistry of 3'-end cleavage and polyadenylation of messenger RNA precursors.

Authors:  E Wahle; W Keller
Journal:  Annu Rev Biochem       Date:  1992       Impact factor: 23.643

2.  Are vertebrate exons scanned during splice-site selection?

Authors:  M Niwa; C C MacDonald; S M Berget
Journal:  Nature       Date:  1992-11-19       Impact factor: 49.962

3.  3' RNA processing efficiency plays a primary role in generating termination-competent RNA polymerase II elongation complexes.

Authors:  G Edwalds-Gilbert; J Prescott; E Falck-Pedersen
Journal:  Mol Cell Biol       Date:  1993-06       Impact factor: 4.272

4.  Simian virus 40 late mRNA leader sequences involved in augmenting mRNA accumulation via multiple mechanisms, including increased polyadenylation efficiency.

Authors:  H C Chiou; C Dabrowski; J C Alwine
Journal:  J Virol       Date:  1991-12       Impact factor: 5.103

5.  Polyadenylation site selection cannot occur in vivo after excision of the 3'-terminal intron.

Authors:  X Liu; J E Mertz
Journal:  Nucleic Acids Res       Date:  1993-11-11       Impact factor: 16.971

6.  Association with terminal exons in pre-mRNAs: a new role for the U1 snRNP?

Authors:  K M Wassarman; J A Steitz
Journal:  Genes Dev       Date:  1993-04       Impact factor: 11.361

7.  Sequences within the last intron function in RNA 3'-end formation in cultured cells.

Authors:  D Nesic; J Cheng; L E Maquat
Journal:  Mol Cell Biol       Date:  1993-06       Impact factor: 4.272

8.  Specific commitment of different pre-mRNAs to splicing by single SR proteins.

Authors:  X D Fu
Journal:  Nature       Date:  1993-09-02       Impact factor: 49.962

9.  Order of intron removal during splicing of endogenous adenine phosphoribosyltransferase and dihydrofolate reductase pre-mRNA.

Authors:  O Kessler; Y Jiang; L A Chasin
Journal:  Mol Cell Biol       Date:  1993-10       Impact factor: 4.272

10.  Nonsense codons can reduce the abundance of nuclear mRNA without affecting the abundance of pre-mRNA or the half-life of cytoplasmic mRNA.

Authors:  J Cheng; L E Maquat
Journal:  Mol Cell Biol       Date:  1993-03       Impact factor: 4.272

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  10 in total

Review 1.  Formation of mRNA 3' ends in eukaryotes: mechanism, regulation, and interrelationships with other steps in mRNA synthesis.

Authors:  J Zhao; L Hyman; C Moore
Journal:  Microbiol Mol Biol Rev       Date:  1999-06       Impact factor: 11.056

2.  Identification of two cis-acting elements that independently regulate the length of poly(A) on Xenopus albumin pre-mRNA.

Authors:  J Das Gupta; H Gu; E Chernokalskaya; X Gao; D R Schoenberg
Journal:  RNA       Date:  1998-07       Impact factor: 4.942

3.  Regulated nuclear polyadenylation of Xenopus albumin pre-mRNA.

Authors:  M N Rao; E Chernokalskaya; D R Schoenberg
Journal:  Nucleic Acids Res       Date:  1996-10-15       Impact factor: 16.971

4.  3' Processing and termination of mouse histone transcripts synthesized in vitro by RNA polymerase II.

Authors:  X Gu; W F Marzluff
Journal:  Nucleic Acids Res       Date:  1996-10-01       Impact factor: 16.971

5.  An interaction between U2AF 65 and CF I(m) links the splicing and 3' end processing machineries.

Authors:  Stefania Millevoi; Clarisse Loulergue; Sabine Dettwiler; Sarah Zeïneb Karaa; Walter Keller; Michael Antoniou; Stéphan Vagner
Journal:  EMBO J       Date:  2006-10-05       Impact factor: 11.598

6.  The 3'-end-processing factor CPSF is required for the splicing of single-intron pre-mRNAs in vivo.

Authors:  Y Li; Z Y Chen; W Wang; C C Baker; R M Krug
Journal:  RNA       Date:  2001-06       Impact factor: 4.942

7.  Efficient 3'-end formation of human beta-globin mRNA in vivo requires sequences within the last intron but occurs independently of the splicing reaction.

Authors:  M Antoniou; F Geraghty; J Hurst; F Grosveld
Journal:  Nucleic Acids Res       Date:  1998-02-01       Impact factor: 16.971

8.  Mammalian heat shock p70 and histone H4 transcripts, which derive from naturally intronless genes, are immune to nonsense-mediated decay.

Authors:  L E Maquat; X Li
Journal:  RNA       Date:  2001-03       Impact factor: 4.942

9.  The carboxyl terminus of vertebrate poly(A) polymerase interacts with U2AF 65 to couple 3'-end processing and splicing.

Authors:  S Vagner; C Vagner; I W Mattaj
Journal:  Genes Dev       Date:  2000-02-15       Impact factor: 11.361

10.  Evidence that the decay of nucleus-associated nonsense mRNA for human triosephosphate isomerase involves nonsense codon recognition after splicing.

Authors:  J Zhang; L E Maquat
Journal:  RNA       Date:  1996-03       Impact factor: 4.942

  10 in total

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