Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/129857
Citations
Scopus Web of Science® Altmetric
?
?
Type: Journal article
Title: RLIM Is a candidate dosage-sensitive gene for individuals with varying duplications of Xq13, intellectual disability, and distinct facial features
Author: Palmer, E.E.
Carroll, R.
Shaw, M.
Kumar, R.
Minoche, A.E.
Leffler, M.
Murray, L.
Macintosh, R.
Wright, D.
Troedson, C.
McKenzie, F.
Townshend, S.
Ward, M.
Nawaz, U.
Ravine, A.
Runke, C.K.
Thorland, E.C.
Hummel, M.
Foulds, N.
Pichon, O.
et al.
Citation: American Journal of Human Genetics, 2020; 107(6):1157-1169
Publisher: Elsevier (Cell Press)
Issue Date: 2020
ISSN: 0002-9297
1537-6605
Statement of
Responsibility: 
Elizabeth E. Palmer, Renee Carroll, Marie Shaw, Raman Kumar, Andre E. Minoche, Melanie Leffler, Lucinda Murray, Rebecca Macintosh, Dale Wright, Chris Troedson, Fiona McKenzie, Sharron Townshend, Michelle Ward, Urwah Nawaz, Anja Ravine, Cassandra K. Runke, Erik C. Thorland, Marybeth Hummel, Nicola Foulds, Olivier Pichon, Bertrand Isidor, Cédric Le Caignec, Bénédicte Demeer, Joris Andrieux, Salam Hadah Albarazi, Ann Bye, Rani Sachdev, Edwin P. Kirk, Mark J. Cowley, Mike Field, and Jozef Gecz
Abstract: Interpretation of the significance of maternally inherited X chromosome variants in males with neurocognitive phenotypes continues to present a challenge to clinical geneticists and diagnostic laboratories. Here we report 14 males from 9 families with duplications at the Xq13.2-q13.3 locus with a common facial phenotype, intellectual disability (ID), distinctive behavioral features, and a seizure disorder in two cases. All tested carrier mothers had normal intelligence. The duplication arose de novo in three mothers where grandparental testing was possible. In one family the duplication segregated with ID across three generations. RLIM is the only gene common to our duplications. However, flanking genes duplicated in some but not all the affected individuals included the brain-expressed genes NEXMIF, SLC16A2, and the long non-coding RNA gene FTX. The contribution of the RLIM-flanking genes to the phenotypes of individuals with different size duplications has not been fully resolved. Missense variants in RLIM have recently been identified to cause X-linked ID in males, with heterozygous females typically having normal intelligence and highly skewed X chromosome inactivation. We detected consistent and significant increase of RLIM mRNA and protein levels in cells derived from seven affected males from five families with the duplication. Subsequent analysis of MDM2, one of the targets of the RLIM E3 ligase activity, showed consistent downregulation in cells from the affected males. All the carrier mothers displayed normal RLIM mRNA levels and had highly skewed X chromosome inactivation. We propose that duplications at Xq13.2-13.3 including RLIM cause a recognizable but mild neurocognitive phenotype in hemizygous males.
Keywords: RLIM; NEXMIF; Xq13; dosage sensitive gene; Tonne-Kalscheuer syndrome; chromosomal duplication; chromosomal microarray; intellectual disability; autism; whole genome sequencing
Rights: © 2020 American Society of Human Genetics.
DOI: 10.1016/j.ajhg.2020.10.005
Grant ID: http://purl.org/au-research/grants/nhmrc/GNT11149630
http://purl.org/au-research/grants/nhmrc/1155224
http://purl.org/au-research/grants/nhmrc/1091593
Appears in Collections:Aurora harvest 8
Medicine publications

Files in This Item:
There are no files associated with this item.


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.