[PDF][PDF] Genetic heterogeneity in Rubinstein-Taybi syndrome: mutations in both the CBP and EP300 genes cause disease

JH Roelfsema, SJ White, Y Ariyürek, D Bartholdi… - The American Journal of …, 2005 - cell.com
JH Roelfsema, SJ White, Y Ariyürek, D Bartholdi, D Niedrist, F Papadia, CA Bacino…
The American Journal of Human Genetics, 2005cell.com
CREB-binding protein and p300 function as transcriptional coactivators in the regulation of
gene expression through various signal-transduction pathways. Both are potent histone
acetyl transferases. A certain level of CREB-binding protein is essential for normal
development, since inactivation of one allele causes Rubinstein-Taybi syndrome (RSTS).
There is a direct link between loss of acetyl transferase activity and RSTS, which indicates
that the disorder is caused by aberrant chromatin regulation. We screened the entire CREB …
CREB-binding protein and p300 function as transcriptional coactivators in the regulation of gene expression through various signal-transduction pathways. Both are potent histone acetyl transferases. A certain level of CREB-binding protein is essential for normal development, since inactivation of one allele causes Rubinstein-Taybi syndrome (RSTS). There is a direct link between loss of acetyl transferase activity and RSTS, which indicates that the disorder is caused by aberrant chromatin regulation. We screened the entire CREB-binding protein gene (CBP) for mutations in patients with RSTS by using methods that find point mutations and larger rearrangements. In 92 patients, we were able to identify a total of 36 mutations in CBP. By using multiple ligation-dependent probe amplification, we found not only several deletions but also the first reported intragenic duplication in a patient with RSTS. We extended the search for mutations to the EP300 gene and showed that mutations in EP300 also cause this disorder. These are the first mutations identified in EP300 for a congenital disorder.
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