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Constitutional haploinsufficiency of tumor suppressor genes in mentally retarded patients with microdeletions in 17p13.1

Constitutional haploinsufficiency of tumor suppressor genes in mentally retarded patients with microdeletions in 17p13.1
Constitutional haploinsufficiency of tumor suppressor genes in mentally retarded patients with microdeletions in 17p13.1
Chromosome microdeletions or duplications are detected in 10-20% of patients with mental impairment and normal karyotypes. A few cases have been reported of mental impairment with microdeletions comprising tumor suppressor genes. By array-CGH we detected 4 mentally impaired individuals carrying de novo microdeletions sharing an overlapping segment of ~180 kb in 17p13.1. This segment encompasses 18 genes, including 3 involved in cancer, namely KCTD11/REN, DLG4/PSD95, and GPS2. Furthermore, in 2 of the patients, the deletions also included TP53, the most frequently inactivated gene in human cancers. The 3 tumor suppressor genes KCTD11, DLG4, and GPS2, in addition to the GABARAP gene, have a known or suspected function in neuronal development and are candidates for causing mental impairment in our patients. Among our 4 patients with deletions in 17p13.1, 3 were part of a Brazilian cohort of 300 mentally retarded individuals, suggesting that this segment may be particularly prone to rearrangements and appears to be an important cause (~1%) of mental retardation. Further, the constitutive deletion of tumor suppressor genes in these patients, particularly TP53, probably confers a significantly increased lifetime risk for cancer and warrants careful oncological surveillance of these patients. Constitutional chromosome deletions containing tumor suppressor genes in patients with mental impairment or congenital abnormalities may represent an important mechanism linking abnormal phenotypes with increased risks of cancer.
1424-8581
1-7
Krepischi-Santos, A.C.V.
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Rajan, D.
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Temple, I.K.
d63e7c66-9fb0-46c8-855d-ee2607e6c226
Shrubb, V.
5345525d-6ed6-4c1f-b565-9abeaf7dd37c
Crolla, J.A.
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Huang, S.
a8beb2a3-8e04-4d81-b6b8-453af8791721
Beal, S.
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Otto, P.A.
fd24e467-c121-4714-a59e-8ed0c821a448
Carter, N.P.
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Vianna-Morgante, A.M.
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Rosenberg, C.
ff3e6ad3-508c-4364-9289-cc83aadf950e
Krepischi-Santos, A.C.V.
0d1d33d7-70e7-487c-863f-7e363cd77a89
Rajan, D.
b0e25bae-775e-41e7-b88e-3ad250b110d8
Temple, I.K.
d63e7c66-9fb0-46c8-855d-ee2607e6c226
Shrubb, V.
5345525d-6ed6-4c1f-b565-9abeaf7dd37c
Crolla, J.A.
c5f23751-8de9-4a55-9cc5-ca2fb635769c
Huang, S.
a8beb2a3-8e04-4d81-b6b8-453af8791721
Beal, S.
8482d461-d637-4a0d-b2db-6775979b13ad
Otto, P.A.
fd24e467-c121-4714-a59e-8ed0c821a448
Carter, N.P.
d9377125-5da4-45eb-bfbf-4e797d1c048a
Vianna-Morgante, A.M.
f460cdf6-9b5e-4be2-aaa4-34e0594304ae
Rosenberg, C.
ff3e6ad3-508c-4364-9289-cc83aadf950e

Krepischi-Santos, A.C.V., Rajan, D., Temple, I.K., Shrubb, V., Crolla, J.A., Huang, S., Beal, S., Otto, P.A., Carter, N.P., Vianna-Morgante, A.M. and Rosenberg, C. (2009) Constitutional haploinsufficiency of tumor suppressor genes in mentally retarded patients with microdeletions in 17p13.1. Cytogenetic and Genome Research, 125 (1), 1-7. (doi:10.1159/000218743).

Record type: Article

Abstract

Chromosome microdeletions or duplications are detected in 10-20% of patients with mental impairment and normal karyotypes. A few cases have been reported of mental impairment with microdeletions comprising tumor suppressor genes. By array-CGH we detected 4 mentally impaired individuals carrying de novo microdeletions sharing an overlapping segment of ~180 kb in 17p13.1. This segment encompasses 18 genes, including 3 involved in cancer, namely KCTD11/REN, DLG4/PSD95, and GPS2. Furthermore, in 2 of the patients, the deletions also included TP53, the most frequently inactivated gene in human cancers. The 3 tumor suppressor genes KCTD11, DLG4, and GPS2, in addition to the GABARAP gene, have a known or suspected function in neuronal development and are candidates for causing mental impairment in our patients. Among our 4 patients with deletions in 17p13.1, 3 were part of a Brazilian cohort of 300 mentally retarded individuals, suggesting that this segment may be particularly prone to rearrangements and appears to be an important cause (~1%) of mental retardation. Further, the constitutive deletion of tumor suppressor genes in these patients, particularly TP53, probably confers a significantly increased lifetime risk for cancer and warrants careful oncological surveillance of these patients. Constitutional chromosome deletions containing tumor suppressor genes in patients with mental impairment or congenital abnormalities may represent an important mechanism linking abnormal phenotypes with increased risks of cancer.

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Published date: 2009

Identifiers

Local EPrints ID: 69702
URI: http://eprints.soton.ac.uk/id/eprint/69702
ISSN: 1424-8581
PURE UUID: 78028156-35dc-467e-9f22-505bbeaafdd8
ORCID for I.K. Temple: ORCID iD orcid.org/0000-0002-6045-1781

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Date deposited: 30 Nov 2009
Last modified: 14 Mar 2024 02:42

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Contributors

Author: A.C.V. Krepischi-Santos
Author: D. Rajan
Author: I.K. Temple ORCID iD
Author: V. Shrubb
Author: J.A. Crolla
Author: S. Huang
Author: S. Beal
Author: P.A. Otto
Author: N.P. Carter
Author: A.M. Vianna-Morgante
Author: C. Rosenberg

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