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Updated: Mar 19, 2026

Dissecting Cell-Autonomous Function of Fragile X Mental Retardation Protein in an Auditory Circuit by In Ovo Electroporation
Published on: July 6, 2022
BMP signaling turns up in fragile X syndrome: FMRP represses BMPR2
1Department of Neurosciences, Case Western Reserve University School of Medicine, Cleveland, OH 44106, USA. heather.broihier@case.edu.
Abstract:
Fragile X syndrome is the most common inherited form of intellectual disability and results from a loss of function of the translational repressor FMRP. In this issue of Science Signaling, Kashima et al find that FMRP binds to and represses a specific isoform of BMPR2, a type II bone morphogenetic protein (BMP) receptor. Reducing signaling through this BMP pathway reverses neuroanatomical defects observed in fragile X models.
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