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骨髓增殖性疾病中因t(3;12)(q26;p13)导致的ETV6与MDS1/EVI1融合

Fusion of ETV6 to MDS1/EVI1 as a result of t(3;12)(q26;p13) in myeloproliferative disorders.

作者信息

Peeters P, Wlodarska I, Baens M, Criel A, Selleslag D, Hagemeijer A, Van den Berghe H, Marynen P

机构信息

Center for Human Genetics, Flanders Interuniversity Institute for Biotechnology, University of Leuven, Belgium.

出版信息

Cancer Res. 1997 Feb 15;57(4):564-9.

PMID:9044825
Abstract

We identified a fusion between ETV6 on 12p13 and MDS1/EVI1 on 3q26 in a t(3;12)(q26;p13) found in two cases of myeloproliferative disorder. The resulting chimeric transcript consists of the first two exons of ETV6 fused to MDS1 sequences, which in turn is fused to the second exon of the EVI1 gene. It has recently been reported that MDS1 can be expressed in normal tissues both as a single gene and fused to EVI1. ETV6 does not contribute any known functional domain to the predicted fusion protein. Association with blast crisis and myelodysplastic syndrome-derived leukemia, bad prognosis, and relative complex karyotype are in agreement with observations made in other cases of t(3;12)(q26;p13). Furthermore, a comparison can be made with the formation of an AML1/MDS1/EVI1 fusion gene in translocations (3;21)(q26;q22).

摘要

我们在两例骨髓增殖性疾病中发现的t(3;12)(q26;p13)中,鉴定出12p13上的ETV6与3q26上的MDS1/EVI1之间的融合。产生的嵌合转录本由ETV6的前两个外显子与MDS1序列融合而成,MDS1序列又与EVI1基因的第二个外显子融合。最近有报道称,MDS1在正常组织中既可以作为单个基因表达,也可以与EVI1融合表达。ETV6对预测的融合蛋白没有贡献任何已知的功能结构域。与急变期和骨髓增生异常综合征衍生的白血病相关、预后不良以及相对复杂的核型,与其他t(3;12)(q26;p13)病例中的观察结果一致。此外,可与易位(3;21)(q26;q22)中AML1/MDS1/EVI1融合基因的形成进行比较。

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