Literature DB >> 29211876

Interplay between FMRP and lncRNA TUG1 regulates axonal development through mediating SnoN-Ccd1 pathway.

Ye Guo1,2, Xu Chen1,3, Ruxiao Xing1,3, Min Wang1, Xiaojuan Zhu2, Weixiang Guo1.   

Abstract

LncRNAs have recently emerged to influence the pathogenesis of fragile X syndrome (FXS), which is caused by the functional loss of fragile X mental retardation protein (FMRP). However, the interaction between FMRP and lncRNAs on regulating neuronal development remains elusive. Here, we reported that FMRP directly interacted with lncRNA TUG1, and decreased its stability. Furthermore, TUG1 bond to transcriptional regulator, SnoN, and negatively modulated SnoN-Ccd1 pathway to specifically control axonal development. These observations suggested interplay between FMRP and lncRNAs might contribute to the pathogenesis of FXS.
© The Author(s) 2017. Published by Oxford University Press. All rights reserved. For Permissions, please email: journals.permissions@oup.com.

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Year:  2018        PMID: 29211876     DOI: 10.1093/hmg/ddx417

Source DB:  PubMed          Journal:  Hum Mol Genet        ISSN: 0964-6906            Impact factor:   6.150


  9 in total

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Review 5.  Long Noncoding RNA Can Be a Probable Mechanism and a Novel Target for Diagnosis and Therapy in Fragile X Syndrome.

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Review 8.  On the functional relevance of spatiotemporally-specific patterns of experience-dependent long noncoding RNA expression in the brain.

Authors:  Wei-Siang Liau; Sarbani Samaddar; Sourav Banerjee; Timothy W Bredy
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Journal:  Development       Date:  2020-03-16       Impact factor: 6.862

  9 in total

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