Literature DB >> 8098272

Operons in C. elegans: polycistronic mRNA precursors are processed by trans-splicing of SL2 to downstream coding regions.

J Spieth1, G Brooke, S Kuersten, K Lea, T Blumenthal.   

Abstract

The mRNAs of six C. elegans genes are known to be trans-spliced to SL2. We report here that a similarly oriented gene is located 100-300 bp upstream of each. We present evidence that the genes in these clusters are cotranscribed and downstream mRNAs are formed by cleavage at the polyadenylation site and trans-splicing. From one three-gene cluster we isolated cDNA clones representing both polycistronic RNAs and mRNAs polyadenylated at the free 3' end created by trans-splicing, suggesting that polycistronic RNAs can be processed by trans-splicing. Several experiments indicate that SL2 trans-splicing is a consequence of a gene's downstream location in an operon. In particular, when an SL1-accepting gene was moved to a downstream location, its mRNA was trans-spliced largely to SL2. The possible regulatory significance of cotranscription of C. elegans genes is discussed.

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Year:  1993        PMID: 8098272     DOI: 10.1016/0092-8674(93)90139-h

Source DB:  PubMed          Journal:  Cell        ISSN: 0092-8674            Impact factor:   41.582


  112 in total

1.  Intercistronic region required for polycistronic pre-mRNA processing in Caenorhabditis elegans.

Authors:  T Huang; S Kuersten; A M Deshpande; J Spieth; M MacMorris; T Blumenthal
Journal:  Mol Cell Biol       Date:  2001-02       Impact factor: 4.272

2.  trans splicing of polycistronic Caenorhabditis elegans pre-mRNAs: analysis of the SL2 RNA.

Authors:  D Evans; T Blumenthal
Journal:  Mol Cell Biol       Date:  2000-09       Impact factor: 4.272

3.  Operons and SL2 trans-splicing exist in nematodes outside the genus Caenorhabditis.

Authors:  D Evans; D Zorio; M MacMorris; C E Winter; K Lea; T Blumenthal
Journal:  Proc Natl Acad Sci U S A       Date:  1997-09-02       Impact factor: 11.205

4.  An uncapped RNA suggests a model for Caenorhabditis elegans polycistronic pre-mRNA processing.

Authors:  Yingmiao Liu; Scott Kuersten; Tao Huang; Alison Larsen; Margaret MacMorris; Thomas Blumenthal
Journal:  RNA       Date:  2003-06       Impact factor: 4.942

5.  Nematode m7GpppG and m3(2,2,7)GpppG decapping: activities in Ascaris embryos and characterization of C. elegans scavenger DcpS.

Authors:  Leah S Cohen; Claudette Mikhli; Cassandra Friedman; Marzena Jankowska-Anyszka; Janusz Stepinski; Edward Darzynkiewicz; Richard E Davis
Journal:  RNA       Date:  2004-10       Impact factor: 4.942

6.  RNA polymerase II C-terminal domain phosphorylation patterns in Caenorhabditis elegans operons, polycistronic gene clusters with only one promoter.

Authors:  Alfonso Garrido-Lecca; Thomas Blumenthal
Journal:  Mol Cell Biol       Date:  2010-05-24       Impact factor: 4.272

7.  A global analysis of C. elegans trans-splicing.

Authors:  Mary Ann Allen; LaDeana W Hillier; Robert H Waterston; Thomas Blumenthal
Journal:  Genome Res       Date:  2010-12-22       Impact factor: 9.043

8.  Identification and analysis of internal promoters in Caenorhabditis elegans operons.

Authors:  Peiming Huang; Erin D Pleasance; Jason S Maydan; Rebecca Hunt-Newbury; Nigel J O'Neil; Allan Mah; David L Baillie; Marco A Marra; Donald G Moerman; Steven J M Jones
Journal:  Genome Res       Date:  2007-08-21       Impact factor: 9.043

9.  Characterization of the let-653 gene in Caenorhabditis elegans.

Authors:  S J Jones; D L Baillie
Journal:  Mol Gen Genet       Date:  1995-10-25

10.  mRNA processing in Antonospora locustae spores.

Authors:  Nicolas Corradi; Lena Burri; Patrick J Keeling
Journal:  Mol Genet Genomics       Date:  2008-09-26       Impact factor: 3.291

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