Identification and Characterization of the Human Testes-Specific Protease 50 Gene Promoter

2008 ◽  
Vol 27 (6) ◽  
pp. 307-314 ◽  
Author(s):  
Miao Wang ◽  
Yong Li Bao ◽  
Yin Wu ◽  
Chun Lei Yu ◽  
XiangYing Meng ◽  
...  
Keyword(s):  
Gene Promoter ◽  
Specific Protease ◽  
Identification And Characterization

256 Identification and Characterization of a Human Ano1 Gene Promoter

2013 ◽  
Vol 144 (5) ◽  
pp. S-56 ◽  
Author(s):  
Amelia Mazzone ◽  
Cheryl E. Bernard ◽  
Simon J. Gibbons ◽  
Martin E. Fernandez-Zapico ◽  
Gianrico Farrugia
Keyword(s):  
Gene Promoter ◽  
Identification And Characterization

scholarly journals Identification and characterization of cis-acting elements conferring insulin responsiveness on hamster cholesterol 7α-hydroxylase gene promoter

2000 ◽  
Vol 347 (1) ◽  
pp. 147 ◽  
Author(s):  
Emma DE FABIANI ◽  
Maurizio CRESTANI ◽  
Maria MARRAPODI ◽  
Alessandra PINELLI ◽  
Viviana GOLFIERI ◽  
...  
Keyword(s):  
Gene Promoter ◽  
Cis Acting ◽  
Hydroxylase Gene ◽  
Insulin Responsiveness ◽  
Identification And Characterization

scholarly journals Identification and characterization of the human NOL7 gene promoter

Gene ◽  
2010 ◽  
Vol 456 (1-2) ◽  
pp. 36-44 ◽  
Author(s):  
Tanmayi P. Mankame ◽  
Guolin Zhou ◽  
Mark W. Lingen
Keyword(s):  
Gene Promoter ◽  
Identification And Characterization

Identification and characterization of the retinoic acid response elements in the human RIG1 gene promoter

2005 ◽  
Vol 331 (2) ◽  
pp. 630-639 ◽  
Author(s):  
Shun-Yuan Jiang ◽  
Meng-Shiun Wu ◽  
Liang-Ming Chen ◽  
Mei-Whey Hung ◽  
Huai-En Lin ◽  
...  
Keyword(s):  
Retinoic Acid ◽  
Gene Promoter ◽  
Response Elements ◽  
Identification And Characterization

Identification and Characterization of the Human Serotonin-4 Receptor Gene Promoter

2001 ◽  
Vol 289 (2) ◽  
pp. 337-344 ◽  
Author(s):  
Tomoko Hiroi ◽  
Naho Hayashi-Kobayashi ◽  
Satoko Nagumo ◽  
Miyuki Ino ◽  
Yoshinori Okawa ◽  
...  
Keyword(s):  
Receptor Gene ◽  
Gene Promoter ◽  
Identification And Characterization

Identification and characterization of human PCDH10 gene promoter

Gene ◽  
2011 ◽  
Vol 475 (1) ◽  
pp. 49-56 ◽  
Author(s):  
Zesong Li ◽  
Jun Xie ◽  
Wenjie Li ◽  
Aifa Tang ◽  
Xianxin Li ◽  
...  
Keyword(s):  
Gene Promoter ◽  
Identification And Characterization

scholarly journals Identification and characterization of a cDNA and the gene encoding the mouse ubiquitously expressed glucose-6-phosphatase catalytic subunit-related protein

2004 ◽  
Vol 32 (1) ◽  
pp. 33-53 ◽  
Author(s):  
JN Boustead ◽  
CC Martin ◽  
JK Oeser ◽  
CA Svitek ◽  
SI Hunter ◽  
...  
Keyword(s):  
Fusion Gene ◽  
Gene Promoter ◽  
Catalytic Subunit ◽  
Mouse Tissue ◽  
Related Protein ◽  
Subunit Gene ◽  
Chromosome 11 ◽  
Gene Encoding ◽  
Identification And Characterization

Glucose-6-phosphatase (G6Pase) catalyzes the final step in the gluconeogenic and glycogenolytic pathways, the hydrolysis of glucose-6-phosphate (G6P) to glucose and phosphate. This paper describes the identification and characterization of a cDNA and the gene encoding the mouse ubiquitously expressed G6Pase catalytic subunit-related protein (UGRP). The open reading frame of this UGRP cDNA encodes a protein (346 amino acids (aa); Mr 38,755) that shares 36% overall identity (56% similarity) with the mouse G6Pase catalytic subunit (357 aa; Mr 40,454). UGRP exhibits a similar predicted transmembrane topology and conservation of many of the catalytically important residues with the G6Pase catalytic subunit; however, unlike the G6Pase catalytic subunit, UGRP does not catalyze G6P hydrolysis and does not contain a carboxy-terminal di-lysine endoplasmic reticulum retention signal. UGRP mRNA was detected by RNA blot analysis in every mouse tissue examined with the highest expression in heart, brain, testis and kidney. Database analysis showed that the mouse UGRP gene is composed of six exons, spans approximately 4.2 kbp of genomic DNA and is located on chromosome 11 along with the G6Pase catalytic subunit gene. The UGRP gene transcription start sites were mapped by primer extension analysis, and the activity of the mouse UGRP gene promoter was analyzed using luciferase fusion gene constructs. In contrast to the G6Pase catalytic subunit gene promoter, the UGRP promoter was highly active in all cell lines examined.

Sign in / Sign up

Export Citation Format

Share Document