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急性髓系白血病(M5)中的t(10;11)易位始终将AF10的亮氨酸拉链基序融合到HRX基因上。

The t(10;11) translocation in acute myeloid leukemia (M5) consistently fuses the leucine zipper motif of AF10 onto the HRX gene.

作者信息

Chaplin T, Bernard O, Beverloo H B, Saha V, Hagemeijer A, Berger R, Young B D

机构信息

Imperial Cancer Research Fund, Department of Medical Oncology, St Bartholomew's Hospital Medical College, London, UK.

出版信息

Blood. 1995 Sep 15;86(6):2073-6.

PMID:7662954
Abstract

The gene on chromosome 10 at band p12 (AF10), involved in the t(10;11) translocation in acute myeloid leukemia, has been identified and shown to contain conserved zinc finger and leucine zipper domains. These regions are highly homologous to the equivalent regions on AF17, the gene involved in the t(11;17) translocations. A series of adult, childhood, and infant leukemias with either simple or complex versions of the t(10;11) has been examined by Southern analysis and shown to involve rearrangement to the HRX locus. Reverse transcriptase-polymerase chain reaction from either bone marrow or peripheral blood cells showed that HRX sequence was fused to AF10 sequence in all 8 cases and subsequent sequence analysis showed an in-frame fusion between the HRX and AF10 sequence. A consistent feature of these fusions was the juxtaposition of the leucine dimerization motif of AF10 onto the NH2-terminal region of HRX. The published data suggest that a similar conclusion can be drawn about the t(11;17) translocation, implying a critical role for this motif in the chimaeric HRX protein.

摘要

位于10号染色体p12带的基因(AF10),参与急性髓系白血病中的t(10;11)易位,已被鉴定并显示含有保守的锌指和亮氨酸拉链结构域。这些区域与AF17上的等效区域高度同源,AF17是参与t(11;17)易位的基因。通过Southern分析检测了一系列伴有简单或复杂t(10;11)的成人、儿童和婴儿白血病,结果显示其与HRX基因座发生了重排。对骨髓或外周血细胞进行逆转录聚合酶链反应表明,在所有8例病例中HRX序列均与AF10序列融合,随后的序列分析显示HRX与AF10序列发生了读码框内融合。这些融合的一个一致特征是AF10的亮氨酸二聚化基序并列于HRX的NH2末端区域。已发表的数据表明,对于t(11;17)易位可得出类似结论,这意味着该基序在嵌合HRX蛋白中起关键作用。

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