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编码人类白血病相关转录因子RUNX1/AML1的基因组位点的结构与解剖

Architecture and anatomy of the genomic locus encoding the human leukemia-associated transcription factor RUNX1/AML1.

作者信息

Levanon D, Glusman G, Bangsow T, Ben-Asher E, Male D A, Avidan N, Bangsow C, Hattori M, Taylor T D, Taudien S, Blechschmidt K, Shimizu N, Rosenthal A, Sakaki Y, Lancet D, Groner Y

机构信息

Dept of Molecular Genetics and Human Genome Center, The Weizmann Institute of Science, 76100, Rehovot, Israel

出版信息

Gene. 2001 Jan 10;262(1-2):23-33. doi: 10.1016/s0378-1119(00)00532-1.

Abstract

The RUNX1 gene on human chromosome 21q22.12 belongs to the 'runt domain' gene family of transcription factors (also known as AML/CBFA/PEBP2alpha). RUNX1 is a key regulator of hematopoiesis and a frequent target of leukemia associated chromosomal translocations. Here we present a detailed analysis of the RUNX1 locus based on its complete genomic sequence. RUNX1 spans 260 kb and its expression is regulated through two distinct promoter regions, that are 160 kb apart. A very large CpG island complex marks the proximal promoter (promoter-2), and an additional CpG island is located at the 3' end of the gene. Hitherto, 12 different alternatively spliced RUNX1 cDNAs have been identified. Genomic sequence analysis of intron/exon boundaries of these cDNAs has shown that all consist of properly spliced authentic coding regions. This indicates that the large repertoire of RUNX1 proteins, ranging in size between 20-52 kDa, are generated through usage of alternatively spliced exons some of which contain in frame stop codons. The gene's introns are largely depleted of repetitive sequences, especially of the LINE1 family. The RUNX1 locus marks the transition from a ~1 Mb of gene-poor region containing only pseudogenes, to a gene-rich region containing several functional genes. A search for RUNX1 sequences that may be involved in the high frequency of chromosomal translocations revealed that a 555 bp long segment originating in chromosome 11 FLI1 gene was transposed into RUNX1 intron 4.1. This intron harbors the t(8;21) and t(3;21) chromosomal breakpoints involved in acute myeloid leukemia. Interestingly, the FLI1 homologous sequence contains a breakpoint of the t(11;22) translocation associated with Ewing's tumors, and may have a similar function in RUNX1.

摘要

人类21号染色体21q22.12上的RUNX1基因属于转录因子的“ runt结构域”基因家族(也称为AML/CBFA/PEBP2alpha)。RUNX1是造血作用的关键调节因子,也是白血病相关染色体易位的常见靶点。在此,我们基于其完整的基因组序列对RUNX1基因座进行了详细分析。RUNX1跨度为260 kb,其表达通过两个相距160 kb的不同启动子区域进行调控。一个非常大的CpG岛复合体标记近端启动子(启动子-2),另一个CpG岛位于该基因的3'端。迄今为止,已鉴定出12种不同的可变剪接RUNX1 cDNA。对这些cDNA的内含子/外显子边界进行的基因组序列分析表明,所有序列均由正确剪接的真实编码区域组成。这表明,大小在20-52 kDa之间的大量RUNX1蛋白是通过使用可变剪接外显子产生的,其中一些外显子包含框内终止密码子。该基因的内含子在很大程度上缺乏重复序列,尤其是LINE1家族的重复序列。RUNX1基因座标志着从仅包含假基因的约1 Mb基因贫乏区域到包含几个功能基因的基因丰富区域的转变。对可能参与高频染色体易位的RUNX1序列进行的搜索显示,一个起源于11号染色体FLI1基因的555 bp长片段被转座到RUNX1内含子4.1中。该内含子包含与急性髓性白血病相关的t(8;21)和t(3;21)染色体断点。有趣的是,FLI1同源序列包含与尤因肉瘤相关的t(11;22)易位的断点,并且可能在RUNX1中具有类似功能。

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