Note to users. If you're seeing this message, it means that your browser cannot find this page's style/presentation instructions -- or possibly that you are using a browser that does not support current Web standards. Find out more about why this message is appearing, and what you can do to make your experience of our site the best it can be.


Published Online October 4, 2007
Science DOI: 10.1126/science.1147182

Research Articles

Submitted on June 28, 2007
Accepted on September 17, 2007

Telomeric Repeat–Containing RNA and RNA Surveillance Factors at Mammalian Chromosome Ends

Claus M. Azzalin 1, Patrick Reichenback 1, Lela Khoriauli 2, Elena Giulotto 2, Joachim Lingner 1*

1 Swiss Institute for Experimental Cancer Research (ISREC), CH-1066 Epalinges, Switzerland.; School of Life Sciences, Ecole Polytechnique Fédérale de Lausanne (EPFL), CH-1015 Lausanne, Switzerland.; "Frontiers in Genetics" National Centre for Competence in Research (NCCR), CH-1211 Geneva, Switzerland.
2 University of Pavia, Department of Genetics and Microbiology, 27100 Pavia, Italy.

* To whom correspondence should be addressed.
Joachim Lingner , E-mail: joachim.lingner{at}isrec.ch

Telomeres, the DNA-protein complexes located at the end of linear eukaryotic chromosomes, are essential for chromosome stability. Until now, telomeres have been considered to be transcriptionally silent. We demonstrate here that mammalian telomeres are transcribed into telomeric repeat containing RNA (TERRA). TERRA molecules are heterogeneous in length, are transcribed from several subtelomeric loci towards chromosome ends and localize to telomeres. We also show that Suppressors with Morphogenetic Defects in Genitalia (SMG) proteins, which are effectors of nonsense mediated RNA decay, are enriched at telomeres in vivo, negatively regulate TERRA association with chromatin and protect chromosome ends from telomere loss. Thus, telomeres are actively transcribed into TERRA, and SMG factors represent a molecular link between TERRA regulation and maintenance of telomere integrity.


THIS ARTICLE HAS BEEN CITED BY OTHER ARTICLES:
Telomeric armor: the layers of end protection.
L. Oganesian and J. Karlseder (2009)
J. Cell Sci. 122, 4013-4025
   Abstract »    Full Text »    PDF »
A global view of the nonprotein-coding transcriptome in Plasmodium falciparum.
C. A. Raabe, C. P. Sanchez, G. Randau, T. Robeck, B. V. Skryabin, S. V. Chinni, M. Kube, R. Reinhardt, G. H. Ng, R. Manickam, et al. (2009)
Nucleic Acids Res.
   Abstract »    Full Text »    PDF »
Stabilization of quadruplex DNA perturbs telomere replication leading to the activation of an ATR-dependent ATM signaling pathway.
A. Rizzo, E. Salvati, M. Porru, C. D'Angelo, M. F. Stevens, M. D'Incalci, C. Leonetti, E. Gilson, G. Zupi, and A. Biroccio (2009)
Nucleic Acids Res. 37, 5353-5364
   Abstract »    Full Text »    PDF »
Sequence, biogenesis, and function of diverse small RNA classes bound to the Piwi family proteins of Tetrahymena thermophila.
M. T. Couvillion, S. R. Lee, B. Hogstad, C. D. Malone, L. A. Tonkin, R. Sachidanandam, G. J. Hannon, and K. Collins (2009)
Genes & Dev. 23, 2016-2032
   Abstract »    Full Text »    PDF »
MLL Associates with Telomeres and Regulates Telomeric Repeat-Containing RNA Transcription.
C. Caslini, J. A. Connelly, A. Serna, D. Broccoli, and J. L. Hess (2009)
Mol. Cell. Biol. 29, 4519-4526
   Abstract »    Full Text »    PDF »
Non-coding murine centromeric transcripts associate with and potentiate Aurora B kinase.
F. Ferri, H. Bouzinba-Segard, G. Velasco, F. Hube, and C. Francastel (2009)
Nucleic Acids Res. 37, 5071-5080
   Abstract »    Full Text »    PDF »
Dicer independent small RNAs associate with telomeric heterochromatin.
F. Cao, X. Li, S. Hiew, H. Brady, Y. Liu, and Y. Dou (2009)
RNA 15, 1274-1281
   Abstract »    Full Text »    PDF »
Telomeric RNAs Mark Sex Chromosomes in Stem Cells.
L.-F. Zhang, Y. Ogawa, J. Y. Ahn, S. H. Namekawa, S. S. Silva, and J. T. Lee (2009)
Genetics 182, 685-698
   Abstract »    Full Text »    PDF »
Structure of Long Telomeric RNA Transcripts: THE G-RICH RNA FORMS A COMPACT REPEATING STRUCTURE CONTAINING G-QUARTETS.
A. Randall and J. D. Griffith (2009)
J. Biol. Chem. 284, 13980-13986
   Abstract »    Full Text »    PDF »
SMG-8 and SMG-9, two novel subunits of the SMG-1 complex, regulate remodeling of the mRNA surveillance complex during nonsense-mediated mRNA decay.
A. Yamashita, N. Izumi, I. Kashima, T. Ohnishi, B. Saari, Y. Katsuhata, R. Muramatsu, T. Morita, A. Iwamatsu, T. Hachiya, et al. (2009)
Genes & Dev. 23, 1091-1105
   Abstract »    Full Text »    PDF »
Telomere elongation involves intra-molecular DNA replication in cells utilizing alternative lengthening of telomeres.
A. Muntoni, A. A. Neumann, M. Hills, and R. R. Reddel (2009)
Hum. Mol. Genet. 18, 1017-1027
   Abstract »    Full Text »    PDF »
TRF1 Controls Telomere Length and Mitotic Fidelity in Epithelial Homeostasis.
P. Munoz, R. Blanco, G. de Carcer, S. Schoeftner, R. Benetti, J. M. Flores, M. Malumbres, and M. A. Blasco (2009)
Mol. Cell. Biol. 29, 1608-1625
   Abstract »    Full Text »    PDF »
Telomerase activity is associated with an increase in DNA methylation at the proximal subtelomere and a reduction in telomeric transcription.
L. J. Ng, J. E. Cropley, H. A. Pickett, R. R. Reddel, and C. M. Suter (2009)
Nucleic Acids Res. 37, 1152-1159
   Abstract »    Full Text »    PDF »
Genetic dissection of the mechanisms underlying telomere-associated diseases: impact of the TRF2 telomeric protein on mouse epidermal stem cells.
G. J. Stout and M. A. Blasco (2009)
Dis. Model. Mech. 2, 139-156
   Abstract »    Full Text »    PDF »
Fission yeast Ccq1 is telomerase recruiter and local checkpoint controller.
K. Tomita and J. P. Cooper (2008)
Genes & Dev. 22, 3461-3474
   Abstract »    Full Text »    PDF »
Hypomethylation of subtelomeric regions in ICF syndrome is associated with abnormally short telomeres and enhanced transcription from telomeric regions.
S. Yehezkel, Y. Segev, E. Viegas-Pequignot, K. Skorecki, and S. Selig (2008)
Hum. Mol. Genet. 17, 2776-2789
   Abstract »    Full Text »    PDF »
NMD is essential for hematopoietic stem and progenitor cells and for eliminating by-products of programmed DNA rearrangements.
J. Weischenfeldt, I. Damgaard, D. Bryder, K. Theilgaard-Monch, L. A. Thoren, F. C. Nielsen, S. E. W. Jacobsen, C. Nerlov, and B. T. Porse (2008)
Genes & Dev. 22, 1381-1396
   Abstract »    Full Text »    PDF »
The Eukaryotic Genome as an RNA Machine.
P. P. Amaral, M. E. Dinger, T. R. Mercer, and J. S. Mattick (2008)
Science 319, 1787-1789
   Abstract »    Full Text »    PDF »
The Cech Symposium: A celebration of 25 years of ribozymes, 10 years of TERT, and 60 years of Tom.
Q. Vicens, M. A. Allen, S. D. Gilbert, B. Reznik, A. R. Gooding, and R. T. Batey (2008)
RNA 14, 397-403
   Abstract »    Full Text »    PDF »



To Advertise     Find Products


Science. ISSN 0036-8075 (print), 1095-9203 (online)