Expression of a G-protein {beta} subunit-related gene during lymphocyte activation |
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Authors: | Shan, Xiaochuan Luo, Hongyu Houle, Benoit Wu, Jiangping |
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Affiliation: | 1 Laboratory of Nephrology and Transplantation immunology, Notre-Dame Hospital Research Center and Nephrology Service, Department of Medicine, Faculty of Medicine, University of Montreal Montreal, Quebec H2L 4M1, Canada 2 Montreal Cancer institute Montreal, Quebec H2L 4M1, Canada |
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Abstract: | Using a subtractlve strategy, we have cloned an activation-relatedgene from a human B cell cDNA library. Sequence analysis revealedthat this gene was identical to H12.3, a gene belonging to anexpanding family of guanlne nucleotlde-blndlng protein ßsubunlts. The expression of H12.3 was induclble in the latephase of mltogen-stlmulated T and B cells. In T cells, IL-2and IL-4 by themselves had no direct effect on the expressionof H12.3, but they could augment the level of steady-state H12.3mRNA stimulated by phytohemagglutlnln. On the other hand, IFN-and IL-6 had no obvious effect on the expression in B cellswith or without Staphytococcus aureus Cowan l-stlmulatlon. CyclosporinA, a strong immunosuppressant, Inhibited the mltogen-stlmulatedexpression of H12.3, but rapamycin, another such agent, didnot. In synchronized Jurkat cells, the expression of H12.3 hadno cell cycle-dependent decrease in S and G2/M phase, whilecyclin E, which controls the progression of the cell cycle unlate G1 phase, did show a periodic expression pattern. The resultssuggest that H12.3 might be involved in regulation of lymphocyteactivation. |
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Keywords: | cyclin E H12 3 rapamycin |
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