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Frequent mutation of histone-modifying genes in non-Hodgkin lymphoma
Authors:Morin Ryan D  Mendez-Lago Maria  Mungall Andrew J  Goya Rodrigo  Mungall Karen L  Corbett Richard D  Johnson Nathalie A  Severson Tesa M  Chiu Readman  Field Matthew  Jackman Shaun  Krzywinski Martin  Scott David W  Trinh Diane L  Tamura-Wells Jessica  Li Sa  Firme Marlo R  Rogic Sanja  Griffith Malachi  Chan Susanna  Yakovenko Oleksandr  Meyer Irmtraud M  Zhao Eric Y  Smailus Duane  Moksa Michelle  Chittaranjan Suganthi  Rimsza Lisa  Brooks-Wilson Angela  Spinelli John J  Ben-Neriah Susana  Meissner Barbara  Woolcock Bruce  Boyle Merrill  McDonald Helen  Tam Angela  Zhao Yongjun  Delaney Allen  Zeng Thomas  Tse Kane
Affiliation:Canada's Michael Smith Genome Sciences Centre, BC Cancer Agency, Vancouver, British Columbia V5Z 1L3, Canada.
Abstract:
Follicular lymphoma (FL) and diffuse large B-cell lymphoma (DLBCL) are the two most common non-Hodgkin lymphomas (NHLs). Here we sequenced tumour and matched normal DNA from 13 DLBCL cases and one FL case to identify genes with mutations in B-cell NHL. We analysed RNA-seq data from these and another 113 NHLs to identify genes with candidate mutations, and then re-sequenced tumour and matched normal DNA from these cases to confirm 109 genes with multiple somatic mutations. Genes with roles in histone modification were frequent targets of somatic mutation. For example, 32% of DLBCL and 89% of FL cases had somatic mutations in MLL2, which encodes a histone methyltransferase, and 11.4% and 13.4% of DLBCL and FL cases, respectively, had mutations in MEF2B, a calcium-regulated gene that cooperates with CREBBP and EP300 in acetylating histones. Our analysis suggests a previously unappreciated disruption of chromatin biology in lymphomagenesis.
Keywords:
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