Yamage Mat, Joshi Manju B, Dwyer Dennis M
Cell Biology Section, Laboratory of Parasitic Diseases, Division of Intramural Research, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD 20892-0425, USA.
J Mol Biol. 2007 Oct 19;373(2):296-307. doi: 10.1016/j.jmb.2007.08.014. Epub 2007 Aug 21.
Here, we show that Crithidia luciliae, a primitive trypanosomatid, purine auxotroph, up-expressed its unique, bi-functional, surface membrane 3'-nucleotidase/nuclease (Cl 3'NT/NU) activity by approximately 1000-fold in response to purine starvation. A second surface membrane phospho-monoesterase, i.e. a tartrate-resistant acid phosphatase (Cl MAcP) was also found to be up-expressed in such purine-starved cells. Here, we used homologous episomal-expression of an antisense construct of the Cl3'NT/NU to dissect the functional expression of these two surface membrane enzymes. In antisense transfected cells, a large excess of the antisense transcript was produced and no trace of any endogenous Cl3'NT/NU sense message was detected. Further, the purine-starvation hyper-induced levels of 3'NT/NU enzyme activity were completely abrogated in these transfected cells versus controls. Moreover, such antisense transcription completely abolished the ability of these transfectants to grow in poly(A)-containing medium demonstrating the essential nature of the 3'NT/NU for the growth/survival of this parasite. In contrast, antisense transcription had no apparent deleterious effects on either endogenous or purine-starvation-induced levels of MAcP enzyme activity, its steady-state mRNA levels, or the constitutive expression of house-keeping genes (e.g. Cl alpha-tubulin) in these transfectants. Cumulatively, results of our antisense experiments demonstrated that the functional nuclease activity of the surface membrane Cl 3'NT/NU was, in fact, critical/essential for the growth and development of these primitive parasites.
在此,我们发现利什曼原虫,一种原始的锥虫,嘌呤营养缺陷型,在嘌呤饥饿时其独特的双功能表面膜3'-核苷酸酶/核酸酶(Cl 3'NT/NU)活性上调约1000倍。还发现另一种表面膜磷酸单酯酶,即抗酒石酸酸性磷酸酶(Cl MAcP)在这种嘌呤饥饿的细胞中也上调表达。在此,我们使用Cl3'NT/NU反义构建体的同源附加型表达来剖析这两种表面膜酶的功能表达。在反义转染细胞中,产生了大量过量的反义转录本,未检测到任何内源性Cl3'NT/NU正义信息的痕迹。此外,与对照相比,这些转染细胞中嘌呤饥饿超诱导的3'NT/NU酶活性水平完全被消除。而且,这种反义转录完全消除了这些转染体在含聚(A)培养基中生长的能力,证明了3'NT/NU对该寄生虫生长/存活的本质重要性。相反,反义转录对这些转染体中MAcP酶活性的内源性或嘌呤饥饿诱导水平、其稳态mRNA水平或管家基因(如Clα-微管蛋白)的组成型表达均无明显有害影响。总的来说,我们的反义实验结果表明,表面膜Cl 3'NT/NU的功能性核酸酶活性实际上对这些原始寄生虫的生长和发育至关重要。