Current evidence has suggested the possible involvement of ROS as signaling messengers in IL-1-or LPS-induced gene expression. We previously reported that both IL-1 and LPS induce uPA in RC-K8 human lymphoma cells. Here, we provide evidence that ROS-generating anthracycline antibiotics, including
Genomic organization and expression of the rearranged REL proto-oncogene in the human B-cell lymphoma cell line RC-K8
✍ Scribed by Demetrios Kalaitzidis; Thomas D. Gilmore
- Publisher
- John Wiley and Sons
- Year
- 2002
- Tongue
- English
- Weight
- 258 KB
- Volume
- 34
- Category
- Article
- ISSN
- 1045-2257
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
The human large B‐cell lymphoma cell line RC‐K8 has a rearranged REL locus that is transcribed into a chimeric mRNA, termed REL‐NRG (__N__on‐__R__el __G__ene). By analyzing the recently completed human genome sequence, we have found that the normal REL and NRG loci are separated by approximately 28 megabase pairs on chromosome 2, suggesting that a deletion created the REL‐NRG locus in RC‐K8 cells. Using computer‐based and molecular approaches, we have determined the structure of the altered REL locus in RC‐K8 cells. The REL‐NRG transcript is encoded by 7 REL exons and 6 NRG‐derived exons. Direct DNA sequencing has identified the site of the REL‐NRG fusion in RC‐K8 cells. We also show that both wild‐type c‐Rel and c‐Rel‐Nrg proteins are expressed and in a complex in RC‐K8 cells. Furthermore, like c‐Rel, c‐Rel‐Nrg is a cytoplasmic protein when overexpressed in fibroblasts in culture and can bind to a κB DNA site in vitro. © 2002 Wiley‐Liss, Inc.
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