Journal
JOURNAL OF CLINICAL INVESTIGATION
Volume 122, Issue 11, Pages 3990-4002Publisher
AMER SOC CLINICAL INVESTIGATION INC
DOI: 10.1172/JCI65508
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Funding
- Deutsche Forschungsgemeinschaft (DFG) [BA1773/5-1, MA5028/1-2, RU1508/1-1]
- Max-Delbruck-Center
- DFG scholarship
- Wellcome Trust
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Translocations are chromosomal rearrangements that are frequently associated with a variety of disease states and developmental disorders. We identified 2 families with brachydactyly type E (BDE) resulting from different translocations affecting chromosome 12p. Both translocations caused downregulation of the parathyroid hormone-like hormone (PTHLH) gene by disrupting the cis-regulatory landscape. Using chromosome conformation capturing, we identified a regulator on chromosome 12q that interacts in cis with PTHLH over a 24.4-megabase distance and in trans with the sex-determining region Y-box 9 (SOX9) gene on chromosome 17q. The element also harbored a long noncoding RNA (IncRNA). Silencing of the IncRNA, PTHLH, or SOX9 revealed a feedback mechanism involving an expression-dependent network in humans. In the BDE patients, the human IncRNA was upregulated by the disrupted chromosomal association. Moreover, the IncRNA occupancy at the PTHLH locus was reduced. Our results document what we believe to be a novel in cis- and in trans-acting DNA and IncRNA regulatory feedback element that is reciprocally regulated by coding genes. Furthermore, our findings provide a systematic and combinatorial view of how enhancers encoding IncRNAs may affect gene expression in normal development.
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