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RUNX1T1/MTG8/ETO基因在人t(8;21)(q22;q22)阳性急性髓系白血病细胞中的表达状态。

RUNX1T1/MTG8/ETO gene expression status in human t(8;21)(q22;q22)-positive acute myeloid leukemia cells.

作者信息

Migas Alexandr A, Mishkova Olga A, Ramanouskaya Tatiana V, Ilyushonak Ilya M, Aleinikova Olga V, Grinev Vasily V

机构信息

Laboratory of the Genetic Biotechnology, Department of Research, Belarusian Research Center for Pediatric Oncology, Hematology and Immunology, Minsk, Belarus.

Department of Genetics, Faculty of Biology, Belarusian State University, Minsk, Belarus.

出版信息

Leuk Res. 2014 Sep;38(9):1102-10. doi: 10.1016/j.leukres.2014.06.002. Epub 2014 Jun 13.

Abstract

The RUNX1-RUNX1T1 fusion gene, a product of the nonhomologous balanced translocation t(8;21)(q22;q22), is a complex genetic locus. We performed extensive bioinformatic analysis of transcription initiation as well as transcription termination sites in this locus and predicted a number of different RUNX1T1 transcripts. To confirm and quantify the RUNX1T1 gene expression, we analyzed samples from seven acute myeloid leukemia (AML) patients and from the Kasumi-1 cell line. We found variable activity of the four predicted RUNX1T1 promoters located downstream of the chromosome breakpoint. Nineteen alternative RUNX1T1 transcripts were identified by sequencing at least seventeen of which predictably can be translated into functional proteins. While the RUNX1T1 gene is not expressed in normal hematopoietic cells, it may participate in t(8;21)(q22;q22)-dependent leukemic transformation due to its multiple interactions in cell regulatory network particularly through synergistic or antagonistic effects in relation to activity of RUNX1-RUNX1T1 fusion gene.

摘要

RUNX1-RUNX1T1融合基因是8号和21号染色体非同源平衡易位t(8;21)(q22;q22)的产物,是一个复杂的基因位点。我们对该位点的转录起始和转录终止位点进行了广泛的生物信息学分析,并预测了许多不同的RUNX1T1转录本。为了确认并量化RUNX1T1基因的表达,我们分析了7例急性髓系白血病(AML)患者以及Kasumi-1细胞系的样本。我们发现位于染色体断点下游的4个预测的RUNX1T1启动子具有可变活性。通过测序鉴定出19种RUNX1T1可变转录本,其中至少17种可预测地能翻译成功能蛋白。虽然RUNX1T1基因在正常造血细胞中不表达,但由于其在细胞调控网络中的多种相互作用,特别是通过与RUNX1-RUNX1T1融合基因活性的协同或拮抗作用,它可能参与t(8;21)(q22;q22)依赖的白血病转化。

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