Novel BRD4-NUT fusion isoforms increase the pathogenic complexity in NUT midline carcinoma

被引:36
|
作者
Thompson-Wicking, K. [1 ]
Francis, R. W. [2 ]
Stirnweiss, A. [1 ]
Ferrari, E. [1 ]
Welch, M. D. [1 ]
Baker, E. [3 ]
Murch, A. R. [3 ,4 ]
Gout, A. M. [1 ]
Carter, K. W. [2 ]
Charles, A. K. [4 ,5 ]
Phillips, M. B. [6 ]
Kees, U. R. [1 ]
Beesley, A. H. [1 ]
机构
[1] Univ Western Australia, Div Childrens Leukaemia & Canc Res, Telethon Inst Child Hlth Res, Ctr Child Hlth Res, Perth, WA 6009, Australia
[2] Univ Western Australia, Div Bioinformat, Telethon Inst Child Hlth Res, Ctr Child Hlth Res, Perth, WA 6009, Australia
[3] King Edward Mem Hosp Women, PathWest Lab Med, Dept Cytogenet, Perth, WA, Australia
[4] Univ Western Australia, Sch Pathol & Lab Med, Perth, WA 6009, Australia
[5] PathWest Lab Med, Dept Pathol, Perth, WA, Australia
[6] Princess Margaret Hosp Children, Dept Haematol & Oncol, Perth, WA, Australia
关键词
BRD4; NUT; carcinoma; NMC; RNA-Seq; transcriptome; T(15-19)(Q15-P13) CHROMOSOME ABNORMALITY; BET BROMODOMAIN INHIBITION; THYMIC CARCINOMA; AGGRESSIVE CARCINOMA; YOUNG-PATIENTS; C-MYC; DIFFERENTIATION; REARRANGEMENT; LEUKEMIA; CHROMATIN;
D O I
10.1038/onc.2012.487
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Nuclear protein in testis (NUT)-midline carcinoma (NMC) is a rare, aggressive disease typically presenting with a single t(15; 19) translocation that results in the generation of a bromodomain-containing protein 4 (BRD4)-NUT fusion. PER-624 is a cell line generated from an NMC patient with an unusually complex karyotype that gave no initial indication of the involvement of the NUT locus. Analysis of PER-624 next-generation transcriptome sequencing (RNA-Seq) using the algorithm FusionFinder identified a novel transcript in which Exon 15 of BRD4 was fused to Exon 2 of NUT, therefore differing from all published NMC fusion transcripts. The three additional exons contained in the PER-624 fusion encode a series of polyproline repeats, with one predicted to form a helix. In the NMC cell line PER-403, we identified the 'standard' NMC fusion and two novel isoforms. Knockdown by small interfering RNA in either cell line resulted in decreased proliferation, increased cell size and expression of cytokeratins consistent with epithelial differentiation. These data demonstrate that the novel BRD4-NUT fusion in PER-624 encodes a functional protein that is central to the oncogenic mechanism in these cells. Genomic PCR indicated that in both PER-624 and PER-403, the translocation fuses an intron of BRD4 to a region upstream of the NUT coding sequence. Thus, the generation of BRD4-NUT fusion transcripts through post-translocation RNA-splicing appears to be a common feature of these carcinomas that has not previously been appreciated, with the mechanism facilitating the expression of alternative isoforms of the fusion. Finally, ectopic expression of wild-type NUT, a protein normally restricted to the testis, could be demonstrated in PER-403, indicating additional pathways for aberrant cell signaling in NMC. This study contributes to our understanding of the genetic diversity of NMC, an important step towards finding therapeutic targets for a disease that is refractory to current treatments.
引用
收藏
页码:4664 / 4674
页数:11
相关论文
共 50 条
  • [1] Novel BRD4–NUT fusion isoforms increase the pathogenic complexity in NUT midline carcinoma
    K Thompson-Wicking
    R W Francis
    A Stirnweiss
    E Ferrari
    M D Welch
    E Baker
    A R Murch
    A M Gout
    K W Carter
    A K Charles
    M B Phillips
    U R Kees
    A H Beesley
    Oncogene, 2013, 32 : 4664 - 4674
  • [2] BRD4-NUT fusion oncogene:: A novel mechanism in aggressive carcinoma
    French, CA
    Miyoshi, I
    Kubonishi, I
    Grier, HE
    Perez-Atayde, AR
    Fletcher, JA
    CANCER RESEARCH, 2003, 63 (02) : 304 - 307
  • [3] The BRD4-NUT Fusion Alone Drives Malignant Transformation of NUT Carcinoma
    Durall, R. Taylor
    Huang, Julianna
    Wojenski, Luke
    Huang, Yeying
    Gokhale, Prafulla C.
    Leeper, Brittaney A.
    Nash, Joshua O.
    Ballester, Pedro L.
    Davidson, Scott
    Shlien, Adam
    Sotirakis, Emmanuel
    Bertaux, Fabien
    Dubus, Vincent
    Luo, Jia
    Wu, Catherine J.
    Keskin, Derin B.
    Eagen, Kyle P.
    Shapiro, Geoffrey I.
    French, Christopher A.
    CANCER RESEARCH, 2023, 83 (23) : 3846 - 3860
  • [4] A novel BRD4-NUT fusion in an undifferentiated sinonasal tumor highlights alternative splicing as a contributing oncogenic factor in NUT midline carcinoma
    A Stirnweiss
    K McCarthy
    J Oommen
    M L Crook
    K Hardy
    U R Kees
    S D Wilton
    A Anazodo
    A H Beesley
    Oncogenesis, 2015, 4 : e174 - e174
  • [5] A novel BRD4-NUT fusion in an undifferentiated sinonasal tumor highlights alternative splicing as a contributing oncogenic factor in NUT midline carcinoma
    Stirnweiss, A.
    McCarthy, K.
    Oommen, J.
    Crook, M. L.
    Hardy, K.
    Kees, U. R.
    Wilton, S. D.
    Anazodo, A.
    Beesley, A. H.
    ONCOGENESIS, 2015, 4 : e174 - e174
  • [6] Perturbation of BRD4 Protein Function by BRD4-NUT Protein Abrogates Cellular Differentiation in NUT Midline Carcinoma
    Yan, Junpeng
    Diaz, Jason
    Jiao, Jing
    Wang, Ranran
    You, Jianxin
    JOURNAL OF BIOLOGICAL CHEMISTRY, 2011, 286 (31) : 27663 - 27675
  • [7] Activation of SOX2 Expression by BRD4-NUT Oncogenic Fusion Drives Neoplastic Transformation in NUT Midline Carcinoma
    Wang, Ranran
    Liu, Wei
    Helfer, Christine M.
    Bradner, James E.
    Hornick, Jason L.
    Janicki, Susan M.
    French, Christopher A.
    You, Jianxin
    CANCER RESEARCH, 2014, 74 (12) : 3332 - 3343
  • [8] The BRD4-NUT Fusion Protein from Nut-Midline Carcinoma modulates DNA Damage Signaling and Ionizing Radiation Response
    Balkanska-Sinclair, E.
    Edwards, D. S.
    Floyd, S. R.
    Maffa, A. D.
    Lam, F. C.
    ENVIRONMENTAL AND MOLECULAR MUTAGENESIS, 2017, 58 : S85 - S86
  • [9] Genetic modifiers of the BRD4-NUT dependency of NUT midline carcinoma uncovers a synergism between BETis and CDK4/6is
    Liao, Sida
    Maertens, Ophelia
    Cichowski, Karen
    Elledge, Stephen J.
    GENES & DEVELOPMENT, 2018, 32 (17-18) : 1188 - 1200
  • [10] A novel NUT translocation partner binds to BRD4 and is necessary for the blockade of differentiation in NUT midline carcinoma
    French, Christopher
    Walsh, Erica
    Kuhnle, Simone
    Rahman, Shaila
    Grayson, Adlai
    Lemieux, Madeleine
    Howley, Peter
    FASEB JOURNAL, 2014, 28 (01):