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编码具有SET结构域的ERG相关组蛋白甲基转移酶的小鼠ESET基因的基因组结构与表达

Genomic structure and expression of the mouse ESET gene encoding an ERG-associated histone methyltransferase with a SET domain.

作者信息

Blackburn Michael L, Chansky Howard A, Zielinska-Kwiatkowska Anna, Matsui Yoshito, Yang Liu

机构信息

Department of Orthopedics and Sports Medicine, University of Washington School of Medicine, Seattle, WA 98195, USA.

出版信息

Biochim Biophys Acta. 2003 Oct 1;1629(1-3):8-14. doi: 10.1016/s0167-4781(03)00155-6.

Abstract

ESET (ERG-associated protein with a SET domain, also called SETDB1) is a novel histone methyltransferase that catalyzes methylation of histone H3-lysine 9 (H3-K9). Here we describe the genomic structure and expression of the mouse ESET gene that gives rise to ESET protein and its alternative splicing product. ESET is a 36-kb single copy gene and full-length ESET transcript consisting of 22 exons. The splicing variant retains only the first 12 exons and thus lacks sequences encoding the methyl CpG-binding domain and the catalytic SET domain. The U2 type conserved GT/AG consensus sequence is present at all of the splicing junctions within the ESET gene. The transcription initiation site of the ESET gene was determined by 5'-RACE experiment and by primer extension. The 5'-flanking sequence of the ESET gene does not contain the consensus TATA box. Instead, this ESET promoter region has features such as SP1-binding sites that are typical of housekeeping genes. The ESET promoter was functionally active when tested in transfection and luciferase assay. Full-length ESET transcript appears to be ubiquitously expressed. While the SET domain-deficient splicing variant is present in immortalized cell lines, it is undetectable by RT-PCR in the majority of normal mouse tissues.

摘要

ESET(具有SET结构域的ERG相关蛋白,也称为SETDB1)是一种新型组蛋白甲基转移酶,可催化组蛋白H3赖氨酸9(H3-K9)的甲基化。在此,我们描述了产生ESET蛋白及其可变剪接产物的小鼠ESET基因的基因组结构和表达情况。ESET是一个36kb的单拷贝基因,全长ESET转录本由22个外显子组成。剪接变体仅保留前12个外显子,因此缺少编码甲基CpG结合结构域和催化SET结构域的序列。ESET基因内所有剪接连接处均存在U2型保守的GT/AG共有序列。通过5'-RACE实验和引物延伸确定了ESET基因的转录起始位点。ESET基因的5'侧翼序列不包含共有TATA框。相反,该ESET启动子区域具有诸如管家基因典型的SP1结合位点等特征。在转染和荧光素酶测定中测试时,ESET启动子具有功能活性。全长ESET转录本似乎在各处均有表达。虽然SET结构域缺陷型剪接变体存在于永生化细胞系中,但在大多数正常小鼠组织中通过RT-PCR检测不到。

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