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葡萄糖对粟酒裂殖酵母ura4+基因表达的转录后调控

Post-transcriptional regulation of ura4+ gene expression by glucose in Schizosaccharomyces pombe.

作者信息

Kim Min Ji, Kim Minkyu, Park Sang Dai

机构信息

School of Biological Sciences, Seoul National University, Seoul 151-742, Korea.

出版信息

Mol Cells. 2002 Dec 31;14(3):437-43.

Abstract

Glucose-inducible gene expression is a fundamental cellular response for optimal cell growth, but identities of glucose-inducible genes and its regulatory mechanism remain largely elusive in Schizosaccharomyces pombe. Here we report that ura4+, encoding orotidine monophosphate decarboxylase (OMPdecase), shows glucose-inducible expression regulated at post-transcriptional level. The ura4+ mRNA level was rapidly decreased by approximately 50% within 20 min after glucose depletion and it was readily recovered upon glucose-readdition within 1 h. Glucose at above 2% similarly raised the transcript level of ura4+, while low concentration (0.1%) was not effective. Interestingly, control of mRNA turnover would be the main regulatory step of the glucose-dependent expression of ura4+. Moreover, stress-activated MAPK (SAPK) pathway was partially responsible for the glucose-regulated expression of ura4+ and rrg1+, another example of glucose-dependent mRNA stability control in S. pombe. These results suggest that the SAPK pathway might participate in the glucose-dependent regulation of ura4+ and rrg1+ mRNA stabilities.

摘要

葡萄糖诱导的基因表达是细胞实现最佳生长的一种基本反应,但在粟酒裂殖酵母中,葡萄糖诱导基因的身份及其调控机制仍基本不明。在此我们报告,编码乳清苷酸脱羧酶(OMP脱羧酶)的ura4+呈现出在转录后水平受到调控的葡萄糖诱导型表达。在葡萄糖耗尽后20分钟内,ura4+ mRNA水平迅速下降约50%,而在1小时内重新添加葡萄糖后,其水平又迅速恢复。2%以上的葡萄糖同样能提高ura4+的转录水平,而低浓度(0.1%)则无效。有趣的是,mRNA周转的控制可能是ura4+葡萄糖依赖性表达的主要调控步骤。此外,应激激活的丝裂原活化蛋白激酶(SAPK)途径部分参与了ura4+和rrg1+的葡萄糖调控表达,rrg1+是粟酒裂殖酵母中另一个葡萄糖依赖性mRNA稳定性控制的例子。这些结果表明,SAPK途径可能参与了ura4+和rrg1+ mRNA稳定性的葡萄糖依赖性调控。

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