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Cooperativity of imprinted genes inactivated by acquired chromosome 20q deletions

Aziz, A; Baxter, EJ; Edwards, C; Cheong, CY; Ito, M; Bench, A; Kelley, R; Silber, Y; Beer, PA; Chng, K; Renfree, MB; McEwen, K; Gray, D; Nangalia, J; Mufti, GJ; Hellstrom-Lindberg, E; Kiladjian, JJ; McMullin, MF; Campbell, PJ; Ferguson-Smith, AC; Green, AR

Authors

EJ Baxter

C Edwards

CY Cheong

M Ito

A Bench

R Kelley

Y Silber

PA Beer

K Chng

MB Renfree

K McEwen

D Gray

J Nangalia

GJ Mufti

E Hellstrom-Lindberg

JJ Kiladjian

MF McMullin

PJ Campbell

AC Ferguson-Smith

AR Green



Abstract

Large regions of recurrent genomic loss are common in cancers; however, with a few well-characterized exceptions, how they contribute to tumor pathogenesis remains largely obscure. Here we identified primate-restricted imprinting of a gene cluster on chromosome 20 in the region commonly deleted in chronic myeloid malignancies. We showed that a single heterozygous 20q deletion consistently resulted in the complete loss of expression of the imprinted genes L3MBTL1 and SGK2, indicative of a pathogenetic role for loss of the active paternally inherited locus. Concomitant loss of both L3MBTL1 and SGK2 dysregulated erythropoiesis and megakaryopoiesis, 2 lineages commonly affected in chronic myeloid malignancies, with distinct consequences in each lineage. We demonstrated that L3MBTL1 and SGK2 collaborated in the transcriptional regulation of MYC by influencing different aspects of chromatin structure. L3MBTL1 is known to regulate nucleosomal compaction, and we here showed that SGK2 inactivated BRG1, a key ATP-dependent helicase within the SWI/SNF complex that regulates nucleosomal positioning. These results demonstrate a link between an imprinted gene cluster and malignancy, reveal a new pathogenetic mechanism associated with acquired regions of genomic loss, and underline the complex molecular and cellular consequences of “simple” cancer-associated chromosome deletions.

Citation

Aziz, A., Baxter, E., Edwards, C., Cheong, C., Ito, M., Bench, A., …Green, A. (2013). Cooperativity of imprinted genes inactivated by acquired chromosome 20q deletions. Journal of Clinical Investigation, 123(5), 2169-2182. https://doi.org/10.1172/JCI66113

Journal Article Type Article
Publication Date Jan 1, 2013
Deposit Date Jun 27, 2014
Publicly Available Date Jun 27, 2014
Journal Journal of Clinical Investigation
Print ISSN 0021-9738
Publisher American Society for Clinical Investigation
Peer Reviewed Peer Reviewed
Volume 123
Issue 5
Pages 2169-2182
DOI https://doi.org/10.1172/JCI66113
Publisher URL http://dx.doi.org/10.1172/JCI66113
Related Public URLs http://www.jci.org/

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