HMGA2 is expressed in an allele-specific manner in human lipomas

被引:18
作者
Ashar, HR [1 ]
Tkachenko, A [1 ]
Shah, P [1 ]
Chada, K [1 ]
机构
[1] Univ Med & Dent New Jersey, Robert Wood Johnson Med Sch, Dept Biochem, Piscataway, NJ 08854 USA
关键词
D O I
10.1016/S0165-4608(03)00037-2
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The architectural transcription factor HMGA2 is almost exclusively expressed in undifferentiated mesenchymal cells. Interestingly, it has been mapped to the translocation site in a variety of human mesenchymal tumors that reveal a terminally differentiated phenotype. The expression of chimeric HMGA2 transcripts encoding three DNA-binding domains fused to novel transcriptional regulatory domains was previously described in lipomas. In this study with lipoma ST91-198, we report the expression of truncated HMGA2 transcripts that gained no functional domains. The highly polymorphic region in the 5' untranslated region (UTR) of HMGA2 was used to determine the allele-specific expression of HMGA2 in lipomas. Microsatellite PCR revealed a monoallelic expression pattern, and only the translocated allele was expressed when the DNA-binding domains of the rearranged allele were fused with transcription activation domains. Surprisingly, a diallelic expression pattern of HMGA2 was observed in lipoma ST91-198, and the wild-type allele was also expressed. In conjunction with studies involving rearrangements of HMGA genes in other benign mesenchymal tumors, our results support a model in which the expression of the wild-type HMGA allele is critical for the pathogenesis of mesenchymal tumors and in which rearrangements of HMGA do not lead to a gain of function in the chimeric HMGA protein. (C) 2003 Elsevier Inc. All rights reserved.
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页码:160 / 168
页数:9
相关论文
共 51 条
[1]   MYC ONCOGENE ACTIVATION IN B-LYMPHOID AND T-LYMPHOID TUMORS [J].
ADAMS, JM ;
CORY, S .
PROCEEDINGS OF THE ROYAL SOCIETY SERIES B-BIOLOGICAL SCIENCES, 1985, 226 (1242) :59-72
[2]   Transgenic mice expressing a truncated form of the high mobility group I-C protein develop adiposity and an abnormally high prevalence of lipomas [J].
Arlotta, P ;
Tai, AKF ;
Manfioletti, G ;
Clifford, C ;
Jay, G ;
Ono, SJ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (19) :14394-14400
[3]   IFG, GLI, MDM1, MDM2, AND MDM3 - CANDIDATE GENES FOR THE MOUSE PG LOCUS [J].
ASHAR, HR ;
BENSON, KF ;
JENKINS, NA ;
GILBERT, DJ ;
COPELAND, NG ;
CHADA, KK .
MAMMALIAN GENOME, 1994, 5 (10) :608-611
[4]  
ASHAR HR, 1995, CELL, V82, P57
[5]   Genomic characterization of human HMGIC, a member of the accessory transcription factor family found at translocation breakpoints in lipomas [J].
Ashar, HR ;
Cherath, L ;
Przybysz, KM ;
Chada, K .
GENOMICS, 1996, 31 (02) :207-214
[6]  
Battista S, 1999, CANCER RES, V59, P4793
[7]  
BERLINGIERI MT, 1995, MOL CELL BIOL, V15, P1545
[8]   HMGIC, the gene for an architectural transcription factor, is amplified and rearranged in a subset of human sarcomas [J].
Berner, JM ;
MezaZepeda, LA ;
Kools, PFJ ;
Forus, A ;
Schoenmakers, EFPM ;
VandeVen, WJM ;
Fodstad, O ;
Myklebost, O .
ONCOGENE, 1997, 14 (24) :2935-2941
[9]   THE GENE FOR THE HUMAN ARCHITECTURAL TRANSCRIPTION FACTOR HMGI-C CONSISTS OF 5 EXONS EACH CODING FOR A DISTINCT FUNCTIONAL ELEMENT [J].
CHAU, KY ;
PATEL, UA ;
LEE, KLD ;
LAM, HYP ;
CRANEROBINSON, C .
NUCLEIC ACIDS RESEARCH, 1995, 23 (21) :4262-4266
[10]  
CHIAPPETTA G, 1995, ONCOGENE, V10, P1307