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C11orf95-MKL2 是软骨样脂肪瘤中 t(11;16)(q13;p13) 的融合致癌基因。

C11orf95-MKL2 is the resulting fusion oncogene of t(11;16)(q13;p13) in chondroid lipoma.

机构信息

Department of Pathology and Microbiology, University of Nebraska Medical Center, Omaha, NE 68198-3135, USA.

出版信息

Genes Chromosomes Cancer. 2010 Sep;49(9):810-8. doi: 10.1002/gcc.20788.

DOI:10.1002/gcc.20788
PMID:20607705
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2904421/
Abstract

Chondroid lipoma, a rare benign adipose tissue tumor, may histologically resemble myxoid liposarcoma or extraskeletal myxoid chondrosarcoma, but is genetically distinct. In this study, an identical reciprocal translocation, t(11;16)(q13;p13), was identified in three chondroid lipomas, a finding consistent with previously isolated reports. A fluorescence in situ hybridization (FISH)-based positional cloning strategy using a series of bacterial artificial chromosome (BAC) probe combinations designed to narrow the 16p13 breakpoint revealed MKL2 as the candidate gene. Subsequent 5' RACE studies demonstrated C11orf95 as the MKL2 fusion gene partner. MKL/myocardin-like 2 (MKL2) encodes myocardin-related transcription factor B in a megakaryoblastic leukemia gene family, and C11orf95 (chromosome 11 open reading frame 95) is a hypothetical protein. Sequencing analysis of reverse transcription-polymerse chain reaction (RT-PCR) generated transcripts from all three chondroid lipomas defined the fusion as occurring between exons 5 and 9 of C11orf95 and MKL2, respectively. Dual-color breakpoint spanning probe sets custom-designed for recognition of the translocation event in interphase cells confirmed the anticipated rearrangements of the C11orf95 and MKL2 loci in all cases. The FISH and RT-PCR assays developed in this study can serve as diagnostic adjuncts for the identification of this novel C11orf95-MKL2 fusion oncogene in chondroid lipoma.

摘要

软骨样脂肪瘤是一种罕见的良性脂肪组织肿瘤,在组织学上可能类似于黏液样脂肪肉瘤或 extraskeletal myxoid chondrosarcoma,但在遗传学上是不同的。在这项研究中,三个软骨样脂肪瘤中都发现了相同的相互易位,t(11;16)(q13;p13),这与之前的孤立报道一致。使用一系列设计用于缩小 16p13 断点的细菌人工染色体 (BAC) 探针组合的荧光原位杂交 (FISH) 基于位置的克隆策略揭示了 MKL2 是候选基因。随后的 5'RACE 研究表明 C11orf95 是 MKL2 融合基因的伙伴。MKL/myocardin-like 2 (MKL2) 在巨核细胞白血病基因家族中编码心肌相关转录因子 B,而 C11orf95(染色体 11 开放阅读框 95)是一种假设蛋白。对所有三个软骨样脂肪瘤的逆转录-聚合酶链反应 (RT-PCR) 生成的转录本进行测序分析,确定融合分别发生在 C11orf95 的外显子 5 和 9 与 MKL2 之间。为识别间期细胞中的易位事件而专门设计的双色断点跨越探针集在所有情况下均确认了 C11orf95 和 MKL2 基因座的预期重排。本研究中开发的 FISH 和 RT-PCR 检测可作为鉴定软骨样脂肪瘤中这种新型 C11orf95-MKL2 融合癌基因的诊断辅助手段。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f9fe/2904421/da76855aa1a0/nihms203810f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f9fe/2904421/eb7bc050871d/nihms203810f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f9fe/2904421/5082b487d7fc/nihms203810f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f9fe/2904421/70d7b17d2278/nihms203810f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f9fe/2904421/da76855aa1a0/nihms203810f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f9fe/2904421/eb7bc050871d/nihms203810f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f9fe/2904421/5082b487d7fc/nihms203810f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f9fe/2904421/70d7b17d2278/nihms203810f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f9fe/2904421/da76855aa1a0/nihms203810f4.jpg

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