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人ARHGDIG,一种Rho蛋白的GDP解离抑制剂:基因组结构、序列、表达分析及定位于染色体16p13.3。

Human ARHGDIG, a GDP-dissociation inhibitor for Rho proteins: genomic structure, sequence, expression analysis, and mapping to chromosome 16p13.3.

作者信息

Adra C N, Iyengar A R, Syed F A, Kanaan I N, Rilo H L, Yu W, Kheraj R, Lin S R, Horiuchi T, Khan S, Weremowicz S, Lim B, Morton C C, Higgs D R

机构信息

Harvard Medical School, Beth Israel Deaconess Medical Center, Boston, Massachusetts, 02215, USA.

出版信息

Genomics. 1998 Oct 1;53(1):104-9. doi: 10.1006/geno.1998.5482.

DOI:10.1006/geno.1998.5482
PMID:9787082
Abstract

GDP-dissociation inhibitors (GDIs) play a primary role in modulating the activity of GTPases. We recently reported the identification of a new GDI for the Rho-related GTPases named RhoGDIgamma. This gene is now designated ARHGDIG by HUGO. Here, in a detailed analysis of tissue expression of ARHGDIG, we observe high levels in the entire brain, with regional variations. The mRNA is also present at high levels in kidney and pancreas and at moderate levels in spinal cord, stomach, and pituitary gland. In other tissues examined, the mRNA levels are very low (lung, trachea, small intestine, colon, placenta) or undetectable. RT-PCR analysis of total RNA isolated from exocrine pancreas and islets shows that the gene is expressed in both tissues. We also report the genomic structure of ARHGDIG. The gene spans over 4 kb and is organized into six exons and five introns. The upstream region lacks a canonical TATA box and contains several putative binding sites for ubiquitous and tissue-specific factors active in central nervous system development. Using FISH, we have mapped the gene to chromosome band 16p13.3. This band is rich in deletion mutants of genes involved in several human diseases, notably polycystic kidney disease, alpha-thalassemia, tuberous sclerosis, mental retardation, and cancer. The promoter structure and the chromosomal location of RhoGDIgamma suggest its importance and underscore the need for further investigation into its biology.

摘要

GDP解离抑制剂(GDIs)在调节GTP酶的活性中起主要作用。我们最近报告了一种名为RhoGDIγ的Rho相关GTP酶新GDI的鉴定。该基因现在被HUGO命名为ARHGDIG。在此,在对ARHGDIG组织表达的详细分析中,我们观察到其在整个大脑中表达水平较高,且存在区域差异。该mRNA在肾脏和胰腺中也高水平存在,在脊髓、胃和垂体中中等水平存在。在其他检测的组织中,mRNA水平非常低(肺、气管、小肠、结肠、胎盘)或无法检测到。对外分泌胰腺和胰岛分离的总RNA进行RT-PCR分析表明该基因在这两种组织中均有表达。我们还报告了ARHGDIG的基因组结构。该基因跨度超过4kb,由六个外显子和五个内含子组成。上游区域缺乏典型的TATA盒,并含有几个在中枢神经系统发育中活跃的普遍存在和组织特异性因子的假定结合位点。使用荧光原位杂交技术,我们已将该基因定位到染色体带16p13.3。该染色体带富含与几种人类疾病相关的基因缺失突变体,特别是多囊肾病、α地中海贫血、结节性硬化症、智力迟钝和癌症。RhoGDIγ的启动子结构和染色体定位表明了其重要性,并强调了对其生物学特性进行进一步研究的必要性。

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