Literature DB >> 19721006

Posttranslational interference of Ty1 retrotransposition by antisense RNAs.

Emiko Matsuda1, David J Garfinkel.   

Abstract

Transposable elements impact genome function by altering gene expression and causing chromosome rearrangements. As a result, organisms have evolved mechanisms, such as RNA-interference, to minimize the level of transposition. However, organisms without the conserved RNAi pathways, like Saccharomyces cerevisiae, must use other mechanisms to prevent transposon movement. Here, we provide evidence that antisense (AS) RNAs from the retrovirus-like element Ty1 inhibit retrotransposition posttranslationally in Saccharomyces. Multiple Ty1AS transcripts overlap Ty1 sequences necessary for copy number control (CNC) and inhibit transposition in trans. Altering Ty1 copy number or deleting sequences in the CNC region that are required for reverse transcription affect Ty1AS RNA level and Ty1 movement. Ty1AS RNAs are enriched in virus-like particles, and are associated with a dramatic decrease in the level of integrase, less reverse transcriptase, and an inability to synthesize Ty1 cDNA. Thus, Ty1AS RNAs are part of an intrinsic mechanism that limits retrotransposition by reducing the level of proteins required for replication and integration.

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Year:  2009        PMID: 19721006      PMCID: PMC2735561          DOI: 10.1073/pnas.0908305106

Source DB:  PubMed          Journal:  Proc Natl Acad Sci U S A        ISSN: 0027-8424            Impact factor:   11.205


  32 in total

1.  A nucleocapsid functionality contained within the amino terminus of the Ty1 protease that is distinct and separable from proteolytic activity.

Authors:  Joseph F Lawler; Gennady V Merkulov; Jef D Boeke
Journal:  J Virol       Date:  2002-01       Impact factor: 5.103

2.  Post-transcriptional cosuppression of Ty1 retrotransposition.

Authors:  David J Garfinkel; Katherine Nyswaner; Jun Wang; Jae-Yong Cho
Journal:  Genetics       Date:  2003-09       Impact factor: 4.562

3.  Ty1 mobilizes subtelomeric Y' elements in telomerase-negative Saccharomyces cerevisiae survivors.

Authors:  Patrick H Maxwell; Candice Coombes; Alison E Kenny; Joseph F Lawler; Jef D Boeke; M Joan Curcio
Journal:  Mol Cell Biol       Date:  2004-11       Impact factor: 4.272

4.  Differential effects of chromatin and Gcn4 on the 50-fold range of expression among individual yeast Ty1 retrotransposons.

Authors:  Antonin Morillon; Lionel Bénard; Mathias Springer; Pascale Lesage
Journal:  Mol Cell Biol       Date:  2002-04       Impact factor: 4.272

5.  Expression of an active form of recombinant Ty1 reverse transcriptase in Escherichia coli: a fusion protein containing the C-terminal region of the Ty1 integrase linked to the reverse transcriptase-RNase H domain exhibits polymerase and RNase H activities.

Authors:  M Wilhelm; M Boutabout; F X Wilhelm
Journal:  Biochem J       Date:  2000-06-01       Impact factor: 3.857

6.  A 5'-3' long-range interaction in Ty1 RNA controls its reverse transcription and retrotransposition.

Authors:  Gaël Cristofari; Carole Bampi; Marcelle Wilhelm; François-Xavier Wilhelm; Jean-Luc Darlix
Journal:  EMBO J       Date:  2002-08-15       Impact factor: 11.598

7.  Chromatin-associated genes protect the yeast genome from Ty1 insertional mutagenesis.

Authors:  Katherine M Nyswaner; Mary Ann Checkley; Ming Yi; Robert M Stephens; David J Garfinkel
Journal:  Genetics       Date:  2008-01       Impact factor: 4.562

8.  Analysis of a Ty1-less variant of Saccharomyces paradoxus: the gain and loss of Ty1 elements.

Authors:  Sharon P Moore; Gianni Liti; Karen M Stefanisko; Katherine M Nyswaner; Caroline Chang; Edward J Louis; David J Garfinkel
Journal:  Yeast       Date:  2004-06       Impact factor: 3.239

9.  Intergenic transcription is required to repress the Saccharomyces cerevisiae SER3 gene.

Authors:  Joseph A Martens; Lisa Laprade; Fred Winston
Journal:  Nature       Date:  2004-06-03       Impact factor: 49.962

10.  RNA from the yeast transposable element Ty1 has both ends in the direct repeats, a structure similar to retrovirus RNA.

Authors:  R T Elder; E Y Loh; R W Davis
Journal:  Proc Natl Acad Sci U S A       Date:  1983-05       Impact factor: 11.205

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  37 in total

Review 1.  Small RNAs, big impact: small RNA pathways in transposon control and their effect on the host stress response.

Authors:  Bayly S Wheeler
Journal:  Chromosome Res       Date:  2013-12       Impact factor: 5.239

Review 2.  Gene regulation by antisense transcription.

Authors:  Vicent Pelechano; Lars M Steinmetz
Journal:  Nat Rev Genet       Date:  2013-11-12       Impact factor: 53.242

3.  T-body formation precedes virus-like particle maturation in S. cerevisiae.

Authors:  Francisco Malagon; Torben Heick Jensen
Journal:  RNA Biol       Date:  2011-03-01       Impact factor: 4.652

Review 4.  Repetitive DNA loci and their modulation by the non-canonical nucleic acid structures R-loops and G-quadruplexes.

Authors:  Amanda C Hall; Lauren A Ostrowski; Violena Pietrobon; Karim Mekhail
Journal:  Nucleus       Date:  2017-03-04       Impact factor: 4.197

Review 5.  MicroRNAs and HIV-1: complex interactions.

Authors:  Zachary Klase; Laurent Houzet; Kuan-Teh Jeang
Journal:  J Biol Chem       Date:  2012-10-05       Impact factor: 5.157

6.  Ty1 escapes restriction by the self-encoded factor p22 through mutations in capsid.

Authors:  Jessica M Tucker; David J Garfinkel
Journal:  Mob Genet Elements       Date:  2016-03-07

7.  Multiple Transcriptional and Post-transcriptional Pathways Collaborate to Control Sense and Antisense RNAs of Tf2 Retroelements in Fission Yeast.

Authors:  Pierre-Luc Mallet; Marc Larochelle; François Bachand
Journal:  Genetics       Date:  2016-12-22       Impact factor: 4.562

8.  P-body components are required for Ty1 retrotransposition during assembly of retrotransposition-competent virus-like particles.

Authors:  Mary Ann Checkley; Kunio Nagashima; Stephen J Lockett; Katherine M Nyswaner; David J Garfinkel
Journal:  Mol Cell Biol       Date:  2009-11-09       Impact factor: 4.272

Review 9.  A self-encoded capsid derivative restricts Ty1 retrotransposition in Saccharomyces.

Authors:  David J Garfinkel; Jessica M Tucker; Agniva Saha; Yuri Nishida; Katarzyna Pachulska-Wieczorek; Leszek Błaszczyk; Katarzyna J Purzycka
Journal:  Curr Genet       Date:  2015-12-09       Impact factor: 3.886

10.  Sequence requirements for localization and packaging of Ty3 retroelement RNA.

Authors:  Kristina Clemens; Virginia Bilanchone; Nadejda Beliakova-Bethell; Liza S Z Larsen; Kim Nguyen; Suzanne Sandmeyer
Journal:  Virus Res       Date:  2012-10-13       Impact factor: 3.303

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