Abstract
The transcriptional silencing of one of the female X-chromosomes is a finely regulated process that requires accumulation in cis of the long non-coding RNA X-inactive-specific transcript (Xist) followed by a series of epigenetic modifications. Little is known about the molecular machinery regulating initiation and maintenance of chromosomal silencing. Here, we introduce a new version of our algorithm catRAPID to investigate Xist associations with a number of proteins involved in epigenetic regulation, nuclear scaffolding, transcription and splicing processes. Our method correctly identifies binding regions and affinities of protein interactions, providing a powerful theoretical framework for the study of X-chromosome inactivation and other events mediated by ribonucleoprotein associations. © 2012 The Author(s). Published by Oxford University Press.
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CITATION STYLE
Agostini, F., Cirillo, D., Bolognesi, B., & Tartaglia, G. G. (2013). X-inactivation: Quantitative predictions of protein interactions in the Xist network. Nucleic Acids Research, 41(1). https://doi.org/10.1093/nar/gks968
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