MLLT1 YEATS domain mutations in clinically distinctive Favourable Histology Wilms tumours
AuthorsPerlman, Elizabeth J
Arold, Stefan T.
Gerhard, Daniela S.
Guidry Auvil, Jaime M.
Davidsen, Tanja M.
Dome, Jeffrey S.
Hsu, Chih Hao
Mungall, Andrew J
Moore, Richard A.
Marra, Marco A.
Mullighan, Charles G
Wheeler, David A.
Hampton, Oliver A.
Gastier-Foster, Julie M.
Smith, Malcolm A
KAUST DepartmentBiological and Environmental Sciences and Engineering (BESE) Division
Computational Bioscience Research Center (CBRC)
Computer, Electrical and Mathematical Sciences and Engineering (CEMSE) Division
Department of Biochemistry and Molecular Biology
Online Publication Date2015-12-04
Print Publication Date2015-12
Permanent link to this recordhttp://hdl.handle.net/10754/584245
MetadataShow full item record
AbstractWilms tumour is an embryonal tumour of childhood that closely resembles the developing kidney. Genomic changes responsible for the development of the majority of Wilms tumours remain largely unknown. Here we identify recurrent mutations within Wilms tumours that involve the highly conserved YEATS domain of MLLT1 (ENL), a gene known to be involved in transcriptional elongation during early development. The mutant MLLT1 protein shows altered binding to acetylated histone tails. Moreover, MLLT1-mutant tumours show an increase in MYC gene expression and HOX dysregulation. Patients with MLLT1-mutant tumours present at a younger age and have a high prevalence of precursor intralobar nephrogenic rests. These data support a model whereby activating MLLT1 mutations early in renal development result in the development of Wilms tumour.
CitationMLLT1 YEATS domain mutations in clinically distinctive Favourable Histology Wilms tumours 2015, 6:10013 Nature Communications
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