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The genetic determinants of symptoms in a rare chromosomal deletion disorder

03.17.16 | JCI Journals

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Individuals with 2p15p16.1 microdeletion syndrome present with intellectual disability, microcephaly, delayed growth, dysmorphic craniofacial features, and digital abnormalities. The precise genetic region responsible for this syndrome has been challenging to identify. However, recent reports indicate that 4 genes ( XPO1 , USP34 , BCL11A , and REL ) are commonly deleted in this syndrome. A study in the current issue of JCI Insight describes 8 new subjects with microdeletions in chromosomal region 2p15p16.1 and provides evidence that loss of XPO1 , REL , and BCL11A underlie this syndrome. Mark O'Driscoll, Cheryl Gregory-Evans, Evica Rajcan-Separovic, and colleagues at University of Sussex and the University of British Columbia reviewed all published cases of 2p15p16.1 microdeletion syndrome and characterized the microdeletions present in 8 newly identified patients. Cells from patients had reduced expression of XPO1 , USP34 , BCL11A , and REL . Moreover, knock down of 3 of these homologous genes in zebrafish resulted in abnormalities consistent with patient phenotypes. Together, the results of this study provide strong evidence that the combined loss of XPO1 , BCL11A , and REL is responsible for 2p15p16.1 microdeletion syndrome.

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TITLE:

Identifying candidate genes for 2p15-16.1 microdeletion syndrome using clinical, genomic and functional analysis

AUTHOR CONTACT:

Mark O'Driscoll
University of Sussex
E-mail: m.o-driscoll@sussex.ac.uk

Cheryl Y. Gregory-Evans
University of British Columbia
E-mail: cge30@mail.ubc.ca

Evica Rajcan-Separovic
University of British Columbia
E-mail: eseparovic@cw.bc.ca

View this article at: http://insight.jci.org/articles/view/85461?key=30e3e67ae21267897c78

JCI Insight is the newest publication from the American Society of Clinical Investigation, a nonprofit honor organization of physician-scientists. JCI Insight is dedicated to publishing a range of translational biomedical research with an emphasis on rigorous experimental methods and data reporting. All articles published in JCI Insight are freely available at the time of publication. For more information about JCI Insight and all of the latest articles go to http://www.insight.jci.org .

JCI Insight

10.1172/jci.insight.85461

Keywords

Article Information

Contact Information

Corinne Williams
JCI Journals
press_releases@the-jci.org

How to Cite This Article

APA:
JCI Journals. (2016, March 17). The genetic determinants of symptoms in a rare chromosomal deletion disorder. Brightsurf News. https://www.brightsurf.com/news/14G3909L/the-genetic-determinants-of-symptoms-in-a-rare-chromosomal-deletion-disorder.html
MLA:
"The genetic determinants of symptoms in a rare chromosomal deletion disorder." Brightsurf News, Mar. 17 2016, https://www.brightsurf.com/news/14G3909L/the-genetic-determinants-of-symptoms-in-a-rare-chromosomal-deletion-disorder.html.