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A Strategy for Probing the Function of Noncoding RNAs Finds a Repressor of NFAT
A. T. Willingham,1A. P. Orth,2S. Batalov,2E. C. Peters,2B. G. Wen,2P. Aza-Blanc,2J. B. Hogenesch,2*P. G. Schultz1,2
Noncoding RNA molecules (ncRNAs) have been implicated in numerousbiological processes including transcriptional regulation andthe modulation of protein function. Yet, in spite of the apparentabundance of ncRNA, little is known about the biological roleof the projected thousands of ncRNA genes present in the humangenome. To facilitate functional analysis of these RNAs, wehave created an arrayed library of short hairpin RNAs (shRNAs)directed against 512 evolutionarily conserved putative ncRNAsand, via cell-based assays, we have begun to determine theirroles in cellular pathways. Using this system, we have identifiedan ncRNA repressor of the nuclear factor of activated T cells(NFAT), which interacts with multiple proteins including membersof the importin-beta superfamily and likely functions as a specificregulator of NFAT nuclear trafficking.
1 Department of Chemistry, Scripps Research Institute, 10550 North Torrey Pines Road, La Jolla, CA 92037, USA. 2 Genomics Institute of the Novartis Research Foundation, 10675 John Jay Hopkins Drive, San Diego, CA 92121, USA.
NRED: a database of long noncoding RNA expression.
M. E. Dinger, K. C. Pang, T. R. Mercer, M. L. Crowe, S. M. Grimmond, and J. S. Mattick (2008)
Nucleic Acids Res.
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Long noncoding RNAs in mouse embryonic stem cell pluripotency and differentiation.
M. E. Dinger, P. P. Amaral, T. R. Mercer, K. C. Pang, S. J. Bruce, B. B. Gardiner, M. E. Askarian-Amiri, K. Ru, G. Solda, C. Simons, et al. (2008)
Genome Res.
18, 1433-1445
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Organization and transcriptional output of a novel mRNA-like piRNA gene (mpiR) located on mouse chromosome 10.
M. Kim, B. Patel, K. E. Schroeder, A. Raza, and J. Dejong (2008)
RNA
14, 1005-1011
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RNAs as extracellular signaling molecules.
M. E Dinger, T. R Mercer, and J. S Mattick (2008)
J. Mol. Endocrinol.
40, 151-159
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Development of Hepatocellular Carcinoma in Iqgap2-Deficient Mice Is IQGAP1 Dependent.
V. A. Schmidt, C. S. Chiariello, E. Capilla, F. Miller, and W. F. Bahou (2008)
Mol. Cell. Biol.
28, 1489-1502
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Specific expression of long noncoding RNAs in the mouse brain.
T. R. Mercer, M. E. Dinger, S. M. Sunkin, M. F. Mehler, and J. S. Mattick (2008)
PNAS
105, 716-721
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Raising the estimate of functional human sequences.
EGO, a novel, noncoding RNA gene, regulates eosinophil granule protein transcript expression.
L. A. Wagner, C. J. Christensen, D. M. Dunn, G. J. Spangrude, A. Georgelas, L. Kelley, M. S. Esplin, R. B. Weiss, and G. J. Gleich (2007)
Blood
109, 5191-5198
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RNAdb 2.0--an expanded database of mammalian non-coding RNAs.
K. C. Pang, S. Stephen, M. E. Dinger, P. G. Engstrom, B. Lenhard, and J. S. Mattick (2007)
Nucleic Acids Res.
35, D178-D182
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Eukaryotic regulatory RNAs: an answer to the 'genome complexity' conundrum.
Exportin-5 orthologues are functionally divergent among species.
S. Shibata, M. Sasaki, T. Miki, A. Shimamoto, Y. Furuichi, J. Katahira, and Y. Yoneda (2006)
Nucleic Acids Res.
34, 4711-4721
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A noncoding RNA is a potential marker of cell fate during mammary gland development.
M. R. Ginger, A. N. Shore, A. Contreras, M. Rijnkels, J. Miller, M. F. Gonzalez-Rimbau, and J. M. Rosen (2006)
PNAS
103, 5781-5786
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Experimental approaches to identify non-coding RNAs.
Transcriptional Landscape of the Human and Fly Genomes: Nonlinear and Multifunctional Modular Model of Transcriptomes.
A.T. WILLINGHAM, S. DIKE, J. CHENG, J.R. MANAK, I. BELL, E. CHEUNG, J. DRENKOW, E. DUMAIS, R. DUTTAGUPTA, M. GANESH, et al. (2006)
Cold Spring Harb Symp Quant Biol
71, 101-110
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RNA as a Flexible Scaffold for Proteins: Yeast Telomerase and Beyond.
D.C. ZAPPULLA and T.R. CECH (2006)
Cold Spring Harb Symp Quant Biol
71, 217-224
|Abstract »|PDF »