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在伴有t(12;13)(p13;q14)的急性淋巴细胞白血病中鉴定出一种与ETV6融合的新型融合基因TTL及其在白血病发生中的意义。

Identification of a novel fusion gene, TTL, fused to ETV6 in acute lymphoblastic leukemia with t(12;13)(p13;q14), and its implication in leukemogenesis.

作者信息

Qiao Y, Ogawa S, Hangaishi A, Yuji K, Izutsu K, Kunisato A, Imai Y, Wang L, Hosoya N, Nannya Y, Sato Y, Maki K, Mitani K, Hirai H

机构信息

Department of Hematology and Oncology, Graduate School of Medicine, University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo 113-8655, Japan.

出版信息

Leukemia. 2003 Jun;17(6):1112-20. doi: 10.1038/sj.leu.2402919.

Abstract

ETS variant gene 6 (ETV6)/translocation, ETS, leukemia (TEL)-involving chromosomal translocations are frequently observed in various hematologic neoplasms. We describe here a novel ETV6-involving translocation, t(12;13)(p13;q14), found in the case of acute lymphoblastic leukemia, in which ETV6 fused with a previously unknown gene, named Twelve-thirteen Translocation Leukemia gene (TTL), at 13q14. TTL was weakly but ubiquitously expressed in normal human tissues as detected by reverse transcribed-PCR. Three TTL splicing forms were identified, TTL-T from a human testis cDNA library, with an open-reading frame of 402 bp encoding 133 amino acids (aa), and TTL-B1 and -B2 from a human brain cDNA library. These proteins have no homology to known proteins. In leukemic cells from the patient, both reciprocal fusion transcripts, ETV6/TTL and TTL/ETV6, were expressed. The predominant fusion transcript, TTL/ETV6-1, encodes a predicted 530 aa fusion protein containing 89 aa of the N-terminal TTL fusing to the helix-loop-helix domain and ETS-binding domain of ETV6. Although the function of TTL is yet to be elucidated, our findings will provide another insight into the molecular pathogenesis of leukemia having ETV6-involving translocations.

摘要

ETS变异基因6(ETV6)/易位、ETS、白血病(TEL)相关的染色体易位在各种血液系统肿瘤中经常被观察到。我们在此描述了一种新的涉及ETV6的易位,t(12;13)(p13;q14),在一例急性淋巴细胞白血病中发现,其中ETV6在13q14处与一个先前未知的基因融合,该基因命名为十二 - 十三易位白血病基因(TTL)。通过逆转录 - PCR检测发现,TTL在正常人体组织中弱表达但广泛存在。鉴定出三种TTL剪接形式,来自人睾丸cDNA文库的TTL - T,其开放阅读框为402 bp,编码133个氨基酸(aa),以及来自人脑cDNA文库的TTL - B1和 - B2。这些蛋白质与已知蛋白质无同源性。在该患者的白血病细胞中,两种相互的融合转录本ETV6/TTL和TTL/ETV6均有表达。主要的融合转录本TTL/ETV6 - 1编码一种预测的530 aa融合蛋白,该蛋白包含N端TTL的89 aa与ETV6的螺旋 - 环 - 螺旋结构域和ETS结合结构域融合。尽管TTL的功能尚待阐明,但我们的发现将为具有涉及ETV6易位的白血病分子发病机制提供另一种见解。

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