Ambrose H E, Keely S P, Aliouat E M, Dei-Cas E, Wakefield A E, Miller R F, Stringer J R
Molecular Infectious Diseases Group, Weatherall Institute of Molecular Medicine, University of Oxford, Oxford OX3 9DU, UK.
Department of Molecular Genetics, Biochemistry & Microbiology, University of Cincinnati, Cincinnati, OH 45267-0524, USA.
Microbiology (Reading). 2004 Feb;150(Pt 2):293-300. doi: 10.1099/mic.0.26539-0.
Pneumocystis carinii has a multigene family, PRT1, that encodes proteins with homology to KEX2-like proteases. PRT1 genes cluster with MSG genes near the telomeres and, like MSG, PRT1 proteins seem to be surface-expressed. The clustering of PRT1 and MSG genes suggested that expression of the two multigene families might be coordinated. Studying gene expression in P. carinii has been hampered by the lack of a culture system, and by lack of clonality in P. carinii populations in naturally infected rats, the host of this fungus. Heterogeneity can be reduced, however, by low-dose intratracheal inoculation, which can produce P. carinii populations dominated by organisms derived from a single progenitor. To study PRT1 expression, nude rats were inoculated with approximately 10 P. carinii each. The clonality of the P. carinii populations from inoculated rats was assessed by analysis of the UCS locus, a site in the genome that is known to be very heterogeneous in naturally infected rats, but nearly homogeneous in rats infected by low-dose intratracheal inoculation. Each of the populations had the same MSG gene at the UCS locus in at least 80 % of the organisms. To investigate PRT1 gene expression, RNA was amplified using primers that amplify numerous PRT1 genes. Seventy-four cloned cDNAs were sequenced, including at least 12 clones from each population of P. carinii. Many differently expressed PRT1 sequences were identified in each population, and a total of 45 different sequences were detected. However, the same PRT1 sequence was present in 15 of 74 plasmids and was found in 3 of the 5 P. carinii populations, suggesting that some PRT1 genes may be either more commonly expressed or expressed at a higher level. These data show that many members of the PRT1 gene family can be expressed in populations of P. carinii derived from few progenitors and suggest that the regulation of this family is different from that governing expression of the MSG gene family.
卡氏肺孢子菌有一个多基因家族PRT1,它编码的蛋白质与KEX2样蛋白酶具有同源性。PRT1基因与端粒附近的MSG基因聚集在一起,并且和MSG一样,PRT1蛋白似乎在表面表达。PRT1和MSG基因的聚集表明这两个多基因家族的表达可能是协调的。由于缺乏培养系统,以及作为这种真菌宿主的自然感染大鼠体内卡氏肺孢子菌群体缺乏克隆性,对卡氏肺孢子菌基因表达的研究受到了阻碍。然而,通过低剂量气管内接种可以降低异质性,这种接种方式可以产生以源自单个祖细胞的生物体为主的卡氏肺孢子菌群体。为了研究PRT1的表达,给裸鼠每只接种约10个卡氏肺孢子菌。通过分析UCS位点来评估接种大鼠体内卡氏肺孢子菌群体的克隆性,UCS位点是基因组中的一个位点,已知在自然感染的大鼠中非常异质,但在低剂量气管内接种感染的大鼠中几乎是同质的。每个群体中至少80%的生物体在UCS位点具有相同的MSG基因。为了研究PRT1基因的表达,使用能扩增众多PRT1基因的引物对RNA进行扩增。对74个克隆的cDNA进行了测序,其中包括来自每个卡氏肺孢子菌群体的至少12个克隆。在每个群体中鉴定出了许多表达不同的PRT1序列,总共检测到45个不同的序列。然而,74个质粒中有15个存在相同的PRT1序列,并且在5个卡氏肺孢子菌群体中的3个群体中发现了该序列,这表明一些PRT1基因可能更常表达或表达水平更高。这些数据表明,PRT1基因家族的许多成员可以在源自少数祖细胞的卡氏肺孢子菌群体中表达,并表明该家族的调控与控制MSG基因家族表达的调控不同。