Tate Jennifer J, Cooper Terrance G
Department of Molecular Sciences, University of Tennessee, Memphis, Tennessee 38163, USA.
J Biol Chem. 2003 Sep 19;278(38):36924-33. doi: 10.1074/jbc.M301829200. Epub 2003 Jul 7.
Retrograde genes of Saccharomyces cerevisiae encode the enzymes needed to synthesize alpha-ketoglutarate, required for ammonia assimilation, when mitochondria are damaged or non-functional because of glucose fermentation. Therefore, it is not surprising that a close association exists between control of the retrograde regulon and expression of nitrogen catabolic genes. Expression of these latter genes is nitrogen catabolite repression (NCR)-sensitive, i.e. expression is low with good nitrogen sources (e.g. glutamine) and high when only poor (e.g. proline) or limiting nitrogen sources are available. It has been reported recently that both NCR-sensitive and retrograde gene expression is negatively regulated by glutamine and induced by treating cells with the Tor1/2 inhibitor, rapamycin. These conclusions predict that NCR-sensitive and retrograde gene expression should respond in parallel to nitrogen sources, ranging from those that highly repress NCR-sensitive transcription to those that elicit minimal NCR. Because this prediction did not accommodate earlier observations that CIT2 (a retrograde gene) expression is higher in glutamine than proline containing medium, we investigated retrograde regulation further. We show that (i) retrograde gene expression correlates with intracellular ammonia and alpha-ketoglutarate generated by a nitrogen source rather than the severity of NCR it elicits, and (ii) in addition to its known regulation by NCR, NAD-glutamate dehydrogenase (GDH2) gene expression is down-regulated by ammonia under conditions where NCR is minimal. Therefore, intracellular ammonia plays a pivotal dual role, regulating the interface of nitrogen and carbon metabolism at the level of ammonia assimilation and production. Our results also indicate the effects of rapamycin treatment on CIT2 transcription, and hence Tor1/2 regulation of retrograde gene expression occur indirectly as a consequence of alterations in ammonia and glutamate metabolism.
酿酒酵母的逆向调控基因编码在因葡萄糖发酵导致线粒体受损或无功能时,氨同化所需的合成α-酮戊二酸的酶。因此,逆向调控子的控制与氮分解代谢基因的表达之间存在密切关联也就不足为奇了。后一类基因的表达对氮分解代谢物阻遏(NCR)敏感,即使用优质氮源(如谷氨酰胺)时表达水平低,而仅使用劣质(如脯氨酸)或有限氮源时表达水平高。最近有报道称,NCR敏感基因和逆向调控基因的表达均受到谷氨酰胺的负调控,并可通过用Tor1/2抑制剂雷帕霉素处理细胞来诱导表达。这些结论预测,NCR敏感基因和逆向调控基因的表达应与氮源平行响应,范围从高度抑制NCR敏感转录的氮源到引起最小NCR的氮源。由于这一预测与早期观察结果不符,即CIT2(一个逆向调控基因)在含谷氨酰胺的培养基中的表达高于含脯氨酸的培养基,因此我们进一步研究了逆向调控。我们发现:(i)逆向调控基因的表达与氮源产生的细胞内氨和α-酮戊二酸相关,而非其引发的NCR的严重程度相关;(ii)除了已知的受NCR调控外,NAD-谷氨酸脱氢酶(GDH2)基因的表达在NCR最小的条件下会受到氨的下调。因此,细胞内氨起着关键的双重作用,在氨同化和产生水平上调节氮和碳代谢的界面。我们的结果还表明,雷帕霉素处理对CIT2转录的影响,进而Tor1/2对逆向调控基因表达的调控是氨和谷氨酸代谢改变的间接结果。