Guevara-Olvera L, Hung C Y, Yu J J, Cole G T
Department of Microbiology and Immunology, Medical College of Ohio, Toledo 43614-5806, USA.
Gene. 2000 Jan 25;242(1-2):437-48. doi: 10.1016/s0378-1119(99)00496-5.
The ornithine decarboxylase (ODC) gene of the human respiratory fungal pathogen, Coccidioides immitis (Ci) was cloned, sequenced, chromosome-mapped, and expressed in Escherichia coli (Ec). The genomic, cDNA and translated sequences are presented. Transformation of an ODC null mutant strain of Ec (EWH 319) with the Ci ODC gene was conducted to confirm function of the protein encoded by the fungal gene. Activity of the enzyme by the bacterial transformant was inhibited by 1, 4-diamino-2-butanone (DAB), a known inhibitor of eukaryotic ODC. Temporal expression of the Ci ODC gene during the parasitic cell cycle is constitutive, based on results of RT PCR. However, results of enzyme activity assays of cell homogenates obtained at different stages of parasitic cell development in vitro showed that the functional protein is present only during periods of isotropic growth and segmentation, and these morphogenetic events can be arrested by the addition of DAB. The observed absence of a difference in steady-state mRNA transcript amounts, and the developmentally correlated variation in levels of enzyme activity, suggest a translational or post-translational mechanism of ODC regulation. Since no PEST sequence was detected in the Ci ODC, enzyme regulation by programmed protein degradation as reported for many other eukaryotic ODCs may not occur in this case. ODC activity appears to play a key role in the morphogenesis of Ci, and the enzyme could be a rational target for therapy of disseminated coccidioidomycosis.
人类呼吸道真菌病原体粗球孢子菌(Ci)的鸟氨酸脱羧酶(ODC)基因被克隆、测序、进行染色体定位并在大肠杆菌(Ec)中表达。文中呈现了基因组、cDNA及翻译后的序列。用Ci ODC基因转化Ec的ODC缺失突变株(EWH 319),以确认该真菌基因编码蛋白的功能。细菌转化体中该酶的活性受到1,4 - 二氨基 - 2 - 丁酮(DAB)的抑制,DAB是一种已知的真核ODC抑制剂。基于逆转录聚合酶链反应(RT PCR)的结果,Ci ODC基因在寄生细胞周期中的表达是组成型的。然而,体外寄生细胞发育不同阶段获得的细胞匀浆的酶活性测定结果表明,功能性蛋白仅在各向同性生长和分裂阶段存在,并且添加DAB可阻止这些形态发生事件。观察到的稳态mRNA转录本量无差异以及酶活性水平与发育相关的变化,提示存在ODC调节的翻译或翻译后机制。由于在Ci ODC中未检测到PEST序列,因此在这种情况下可能不会像许多其他真核ODC那样通过程序性蛋白质降解进行酶调节。ODC活性似乎在Ci的形态发生中起关键作用,该酶可能是播散性球孢子菌病治疗的合理靶点。