Transcriptome profiling of UPF3B/NMD-deficient lymphoblastoid cells from patients with various forms of intellectual disability-Reference-Cited by-同舟云学术

Transcriptome profiling of UPF3B/NMD-deficient lymphoblastoid cells from patients with various forms of intellectual disability

Published:2011-12-20 Issue:11 Volume:17 Page:1103-1115
ISSN:1359-4184
Container-title:Molecular Psychiatry
language:en
Short-container-title:Mol Psychiatry

Author:

Nguyen L S,Jolly L,Shoubridge C,Chan W K,Huang L,Laumonnier F,Raynaud M,Hackett A,Field M,Rodriguez J,Srivastava A K,Lee Y,Long R,Addington A M,Rapoport J L,Suren S,Hahn C N,Gamble J,Wilkinson M F,Corbett M A,Gecz J

Publisher

Springer Science and Business Media LLC

Subject

Cellular and Molecular Neuroscience,Psychiatry and Mental health,Molecular Biology

Link

http://www.nature.com/articles/mp2011163.pdf

Reference62 articles.

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2. Gehring NH, Neu-Yilik G, Schell T, Hentze MW, Kulozik AE . Y14 and hUpf3b form an NMD-activating complex. Mol Cell 2003; 11: 939–949.

3. Kim VN, Kataoka N, Dreyfuss G . Role of the nonsense-mediated decay factor hUpf3 in the splicing-dependent exon-exon junction complex. Science 2001; 293: 1832–1836.

4. Chamieh H, Ballut L, Bonneau F, Le Hir H . NMD factors UPF2 and UPF3 bridge UPF1 to the exon junction complex and stimulate its RNA helicase activity. Nat Struct Mol Biol 2008; 15: 85–93.

5. Kashima I, Yamashita A, Izumi N, Kataoka N, Morishita R, Hoshino S et al. Binding of a novel SMG-1-Upf1-eRF1-eRF3 complex (SURF) to the exon junction complex triggers Upf1 phosphorylation and nonsense-mediated mRNA decay. Genes Dev 2006; 20: 355–367.

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