His decision came as an investigation into sexual harassment allegations against him was ongoing.
Researchers uncover the central role of a protein linked to Fragile X Syndrome in mice, one of the leading causes of autism and intellectual disability.
November 7, 2017|
ROCKEFELLER UNIVERSITYFragile X syndrome is a leading cause of autism and intellectual disability, and is characterized by a loss of function of a particular protein, fragile X mental retardation protein (FMRP). In mice, this results in changes in chromatin regulation and abnormal gene expression. Scientists have previously discovered that FMRP plays an important role in regulating the synthesis of various proteins that control the activity of genes expressed in the mouse brain. One of these proteins is Brd4, which in the absence of FMRP begins to tinker unhindered with the expression of other genes.
In a new study, scientists found that inhibiting Brd4 with a drug could alleviate many of the changes linked to Fragile X Syndrome. The researchers believe that targeting proteins like Brd4 could lead the way to new treatments for the disorder.
See E. Korb et al., “Excess translation of epigenetic regulators contributes to fragile X syndrome and is alleviated by Brd4 inhibition,” Cell, doi:10.1016/07.033, 2017.