| Literature DB >> 27273096 |
Risa Kashima1, Sougata Roy1, Manuel Ascano2, Veronica Martinez-Cerdeno3, Jeanelle Ariza-Torres4, Sunghwan Kim1, Justin Louie1, Yao Lu1, Patricio Leyton5, Kenneth D Bloch5, Thomas B Kornberg1, Paul J Hagerman6, Randi Hagerman7, Giorgio Lagna1, Akiko Hata8.
Abstract
Epigenetic silencing of fragile X mental retardation 1 (FMR1) causes fragile X syndrome (FXS), a common inherited form of intellectual disability and autism. FXS correlates with abnormal synapse and dendritic spine development, but the molecular link between the absence of the FMR1 product FMRP, an RNA binding protein, and the neuropathology is unclear. We found that the messenger RNA encoding bone morphogenetic protein type II receptor (BMPR2) is a target of FMRP. Depletion of FMRP increased BMPR2 abundance, especially that of the full-length isoform that bound and activated LIM domain kinase 1 (LIMK1), a component of the noncanonical BMP signal transduction pathway that stimulates actin reorganization to promote neurite outgrowth and synapse formation. Heterozygosity for BMPR2 rescued the morphological abnormalities in neurons both in Drosophila and in mouse models of FXS, as did the postnatal pharmacological inhibition of LIMK1 activity. Compared with postmortem prefrontal cortex tissue from healthy subjects, the amount of full-length BMPR2 and of a marker of LIMK1 activity was increased in this brain region from FXS patients. These findings suggest that increased BMPR2 signal transduction is linked to FXS and that the BMPR2-LIMK1 pathway is a putative therapeutic target in patients with FXS and possibly other forms of autism.Entities:
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Year: 2016 PMID: 27273096 PMCID: PMC5274719 DOI: 10.1126/scisignal.aaf6060
Source DB: PubMed Journal: Sci Signal ISSN: 1945-0877 Impact factor: 8.192