An RNA polymerase III subunit determines sites of retrotransposon integration

Author:

Bridier-Nahmias Antoine12,Tchalikian-Cosson Aurélie1,Baller Joshua A.34,Menouni Rachid1,Fayol Hélène1,Flores Amando5,Saïb Ali12,Werner Michel5,Voytas Daniel F.3,Lesage Pascale1

Affiliation:

1. Université Paris Diderot, Sorbonne Paris Cité, INSERM U944, CNRS UMR 7212, Institut Universitaire d'Hématologie, Hôpital St. Louis, 75010 Paris, France.

2. Department CASER Conservatoire National des Arts et Métiers (Cnam), 75003 Paris, France.

3. Department of Genetics, Cell Biology and Development and Center for Genome Engineering, University of Minnesota, Minneapolis, MN 55455, USA.

4. Minnesota Supercomputing Institute, University of Minnesota, Minneapolis, MN 55455, USA.

5. IBiTec-S, Institut de Biologie Intégrative de la Cellule (I2BC), Commissariat à l'Energie Atomique et aux Energies Alternatives (CEA), CNRS, Université Paris-Sud, CP 22, CEA-Saclay, 91191 Gif-sur-Yvette, France.

Abstract

Keeping jumping genes out of harm's way The genomes of most eukaryotes, including our own, are jam-packed with parasitic mobile DNA elements. Most are nonfunctional remnants, but a few are still active, capable of jumping about in our DNA, potentially causing serious damage to our genes. Nevertheless, they avoid landing in and disrupting coding regions. For example, in yeast, the retrotransposon Ty1 is targeted away from protein genes to positions upstream of yeast RNA polymerase III genes. Bridier-Nahmias et al. show that Ty1 is targeted to these “safe havens” through an interaction between a Ty1-encoded protein that controls its genome jumping activity and a subunit of the yeast RNA polymerase III complex. Science , this issue p. 585

Funder

CNRS

INSERM

Universite Paris Diderot Sorbonne Paris Cite

Agence nationale de recherches sur le sida et les hepatites virales

Agence Nationale de la Recherche

FP7 project HIVINNOV

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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