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 26 条
  • [21] Mechanistic Analysis of the Role of Bromodomain-containing Protein 4 (BRD4) in BRD4-NUT Oncoprotein-induced Transcriptional Activation
    Wang, Ranran
    You, Jianxin
    JOURNAL OF BIOLOGICAL CHEMISTRY, 2015, 290 (05) : 2744 - 2758
  • [22] Clinical Response of Carcinomas Harboring the BRD4-NUT Oncoprotein to the Targeted Bromodomain Inhibitor OTX015/MK-8628
    Stathis, Anastasios
    Zucca, Emanuele
    Bekradda, Mohamed
    Gomez-Roca, Carlos
    Delord, Jean-Pierre
    Rouge, Thibault de La Motte
    Uro-Coste, Emmanuelle
    de Braud, Filippo
    Pelosi, Giuseppe
    French, Christopher A.
    CANCER DISCOVERY, 2016, 6 (05) : 492 - 500
  • [23] First evidence of treatment efficacy in metastatic carcinoma of the parotid gland with BRD4/NUT translocation
    Vulsteke, Christof
    Lurquin, Eveline
    Debiec-Rychter, Maria
    Gheysens, Olivier
    Nuyts, Sandra
    Schoenaers, Joseph
    Politis, Constantinus
    Mebis, Jeroen
    Hauben, Esther
    Clement, Paul M.
    JOURNAL OF CHEMOTHERAPY, 2016, 28 (03) : 242 - 246
  • [24] Nuclear protein in testis (NUT) midline carcinoma with a novel three-way translocation (4;15;19)(q13;q14;p13.1)
    Shatavi, Seerin
    Fawole, Adewale
    Haberichter, Kristle
    Jaiyesimi, Ishmael
    French, Christopher
    PATHOLOGY, 2016, 48 (06) : 620 - 623
  • [25] "Z4" Complex Member Fusions in NUT Carcinoma: Implications for a Novel Oncogenic Mechanism
    Shiota, Hitoshi
    Elya, Janine E.
    Alekseyenko, Artyom A.
    Chou, Pauline M.
    Gorman, Shelby A.
    Barbash, Olena
    Becht, Kelly
    Danga, Kristina
    Kuroda, Mitzi I.
    Nardi, Valentina
    French, Christopher A.
    MOLECULAR CANCER RESEARCH, 2018, 16 (12) : 1826 - 1833
  • [26] Exceptional Response to Bromodomain and Extraterminal Domain Inhibitor Therapy With BMS-986158 in BRD4-NUTM1 NUT Carcinoma Harboring a BRD4 Splice Site Mutation
    Cheng, Michael L.
    Huang, Yeying
    Luong, Nhi
    LoPiccolo, Jaclyn
    Nishino, Mizuki
    Sholl, Lynette M.
    Chirieac, Lucian R.
    Santucci, Alison D.
    Rabin, Michael S.
    Jaenne, Pasi A.
    Coker, Shodeinde
    Diamond, Jennifer R.
    Hilton, John
    Shapiro, Geoffrey I.
    French, Christopher A.
    JCO PRECISION ONCOLOGY, 2023, 7