Suppr超能文献

编码γ/γ'型叶酸受体的多态性基因的结构与调控

Structure and regulation of a polymorphic gene encoding folate receptor type gamma/gamma'.

作者信息

Wang H, Ross J F, Ratnam M

机构信息

Department of Biochemistry and Molecular Biology, Medical College of Ohio, Toledo, OH 43699-0008, USA.

出版信息

Nucleic Acids Res. 1998 May 1;26(9):2132-42. doi: 10.1093/nar/26.9.2132.

Abstract

The human folate receptor (hFR) type gamma and gamma' are constitutively secreted proteins that are expressed primarily in hematopoietic tissues and are potential serum markers for certain hematopoietic malignancies. hFR-gamma' is a variant of hFR-gamma with a two base deletion in its cDNA resulting in a truncated polypeptide. The gene encoding hFR-gamma' was isolated from a placental genomic library. The gene has five exons, four introns and a 5' flanking sequence which contains multiple putative regulatory elements. From RNase protection assay and RACE analysis, the major site of transcriptional initiation was identified at -56 nt. Systematically deleted fragments in the 5' region of the genomic DNA of FR-gamma' were ligated into the PGL3Basic plasmid and the reporter luciferase activity was assayed in cell lysates from transiently transfected NIH3T3 cells. From those results, putative positive and negative regulatory regions in the 5' flanking sequences were noted, and a TATA-less proximal promoter was located between -206 and -22 nt. Gel mobility shift and supershift analyses as well as mutagenesis experiments revealed that Sp1 and ets binding elements in the proximal promoter region confer transcriptional activity. From partial sequencing of genomic DNA, genomic Southern blots, RACE analysis and RNase protection assays, it appears that hFR-gamma shares the gene organization of hFR-gamma'. The results of the analysis of genomic DNA in spleen tissues from several individuals, were consistent with the interpretation that hFR-gamma and hFR-gamma' are encoded by a polymorphic gene.

摘要

人γ型和γ'型叶酸受体是组成型分泌蛋白,主要在造血组织中表达,是某些造血系统恶性肿瘤的潜在血清标志物。hFR-γ'是hFR-γ的一种变体,其cDNA中有两个碱基缺失,导致多肽截短。编码hFR-γ'的基因是从胎盘基因组文库中分离出来的。该基因有5个外显子、4个内含子和一个5'侧翼序列,其中包含多个推定的调控元件。通过核糖核酸酶保护分析和RACE分析,确定转录起始的主要位点在-56 nt处。将FR-γ'基因组DNA 5'区域的系统缺失片段连接到PGL3Basic质粒中,并在瞬时转染的NIH3T3细胞的细胞裂解物中检测报告荧光素酶活性。根据这些结果,注意到5'侧翼序列中推定的正负调控区域,并且在-206至-22 nt之间定位了一个无TATA的近端启动子。凝胶迁移率变动和超迁移分析以及诱变实验表明,近端启动子区域中的Sp1和ets结合元件赋予转录活性。从基因组DNA的部分测序、基因组Southern印迹、RACE分析和核糖核酸酶保护分析来看,hFR-γ似乎与hFR-γ'具有相同的基因结构。对几个个体脾脏组织中的基因组DNA分析结果与hFR-γ和hFR-γ'由一个多态性基因编码的解释一致。

相似文献

本文引用的文献

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验