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

被引:20
作者
Adra, CN
Iyengar, AR
Syed, FA
Kanaan, IN
Rilo, HLR
Yu, WJ
Kheraj, R
Lin, SR
Horiuchi, T
Khan, S
Weremowicz, S
Lim, B
Morton, CC
Higgs, DR
机构
[1] Harvard Univ, Sch Med, Brigham & Womens Hosp, Harvard Inst Med, Boston, MA 02215 USA
[2] Harvard Univ, Sch Med, Brigham & Womens Hosp, Beth Israel Deaconess Med Ctr, Boston, MA 02215 USA
[3] Harvard Univ, Sch Med, Brigham & Womens Hosp, Dept Pathol, Boston, MA 02215 USA
[4] Harvard Univ, Sch Med, Brigham & Womens Hosp, Dept Obstet Gynecol & Reprod Biol, Boston, MA 02215 USA
[5] John Radcliffe Hosp, Inst Mol Med, MRC, Mol Haematol Unit, Oxford OX3 9DU, England
[6] Univ Chicago, Dept Surg, Sect Transplantat, Chicago, IL 60637 USA
关键词
D O I
10.1006/geno.1998.5482
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 [微生物学]; 0836 [生物工程]; 090102 [作物遗传育种]; 100705 [微生物与生化药学];
摘要
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 RhoGDI gamma. 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 live 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 RhoGDI gamma suggest its importance and underscore the need for further investigation into its biology. (C) 1998 Academic Press.
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收藏
页码:104 / 109
页数:6
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