Details

Autor(en) / Beteiligte

• Sripathy, Smitha
• Leko, Vid
• Adrianse, Robin L
• Loe, Taylor
• Foss, Eric J
• Dalrymple, Emily
• Lao, Uyen
• Gatbonton-Schwager, Tonibelle
• Carter, Kelly T
• Payer, Bernhard
• Paddison, Patrick J
• Grady, William M
• Lee, Jeannie T
• Bartolomei, Marisa S
• Bedalov, Antonio

Titel

Screen for reactivation of MeCP2 on the inactive X chromosome identifies the BMP/TGF-[Beta] superfamily as a regulator of XIST expression

Ist Teil von

• Proceedings of the National Academy of Sciences - PNAS, 2017-02, Vol.114 (7), p.1619

Ort / Verlag

Washington: National Academy of Sciences

Erscheinungsjahr

2017

Quelle

EZB Electronic Journals Library

Beschreibungen/Notizen

• Rett syndrome (RS) is a debilitating neurological disorder affecting mostly girls with heterozygous mutations in the gene encoding the methyl-CpG-binding protein MeCP2 on the X chromosome. Because restoration of MeCP2 expression in a mouse model reverses neurologic deficits in adult animals, reactivation of the wild-type copy of MeCP2 on the inactive X chromosome (Xi) presents a therapeutic opportunity in RS. To identify genes involved in MeCP2 silencing, we screened a library of 60,000 shRNAs using a cell line with a MeCP2 reporter on the Xi and found 30 genes clustered in seven functional groups. More than half encoded proteins with known enzymatic activity, and six were members of the bone morphogenetic protein (BMP)/TGF-β pathway. shRNAs directed against each of these six genes down-regulated X-inactive specific transcript (XIST), a key player in X-chromosome inactivation that encodes an RNA that coats the silent X chromosome, and modulation of regulators of this pathway both in cell culture and in mice demonstrated robust regulation of XIST. Moreover, we show that Rnf12, an X-encoded ubiquitin ligase important for initiation of X-chromosome inactivation and XIST transcription in ES cells, also plays a role in maintenance of the inactive state through regulation of BMP/TGF-β signaling. Our results identify pharmacologically suitable targets for reactivation of MeCP2 on the Xi and a genetic circuitry that maintains XIST expression and X-chromosome inactivation in differentiated cells.