## Abstract Osteoclast inhibitory lectin (OCIL) is a novel regulator of bone remodeling, however, little is known concerning how OCIL is regulated to date. In this study, approximately 4.4 kb of the 5′‐flanking sequence of rat OCIL gene was cloned into the promoter‐less reporter vector pGL3‐basic a
Genomic cloning and promoter analysis of the GAHSP40 gene
✍ Scribed by Fumiyasu Hamajima; Tadao Hasegawa; Izumi Nakashima; Ken-ichi Isobe
- Publisher
- John Wiley and Sons
- Year
- 2002
- Tongue
- English
- Weight
- 246 KB
- Volume
- 84
- Category
- Article
- ISSN
- 0730-2312
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
The new heat shock protein (GAHSP40), which binds to Gadd34, is a member of the Hsp40 family gene and has a J domain, which is similar to bacterial DNAJ. We have isolated and sequenced the mouse GAHSP40 gene including 1.6 kb of the 5′‐flanking region. Primer extension analysis revealed that the transcription initiation site was located 36‐bp upstream of the ATG translation initiation codon. In order to identify the heat‐responsive regions in the GAHSP40, NIH3T3 cells were transiently transfected with a series of 5′ terminus‐truncated mutants of the GAHSP40 promoter linked to the luciferase reporter gene. We found that the region of −284 to −184 bp from initiation start site responded to heat shock treatment. By the gel shift analysis, we found the heat shock elements (HSEs) located in this region from −257 to −225. This HSEs has five 5 bp motifs. The transfection studies using HSEs mutant vectors revealed that those 3′ two 5 bp motifs are essential for heat responsive transcription. J. Cell. Biochem. 84: 401–407, 2002. © 2001 Wiley‐Liss, Inc.
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