Abstract
Nearly all human genetic disorders result from a limited repertoire of mutations in an associated gene or its regulatory elements. We recently described an individual with an inherited form of anemia (α-thalassemia) who has a deletion that results in a truncated, widely expressed gene (LUC7L) becoming juxtaposed to a structurally normal α-globin gene (HBA2). Although it retains all of its local and remote cis-regulatory elements, expression of HBA2 is silenced and its CpG island becomes completely methylated early during development. Here we show that in the affected individual, in a transgenic model and in differentiating embryonic stem cells, transcription of antisense RNA mediates silencing and methylation of the associated CpG island. These findings identify a new mechanism underlying human genetic disease.
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Acknowledgements
We are grateful to L. Rose for preparation of the manuscript, C. Porcher for help setting up the ES cell differentiation assay, E. Li and T. Chen for helpful advice and on-going collaboration and V. Samara and S. Butler for technical assistance. D.G. was supported by the Medical Research Council and the Staines Research Fellowship, Exeter College, Oxford. This work was supported by the Medical Research Council.
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Tufarelli, C., Stanley, J., Garrick, D. et al. Transcription of antisense RNA leading to gene silencing and methylation as a novel cause of human genetic disease. Nat Genet 34, 157–165 (2003). https://doi.org/10.1038/ng1157
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DOI: https://doi.org/10.1038/ng1157
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