Gray M W
Department of Biochemistry, Dalhousie University, Halifax, Nova Scotia, Canada.
Mol Cell Biol. 1981 Apr;1(4):347-57. doi: 10.1128/mcb.1.4.347-357.1981.
In a previous study from this laboratory, presumptive ribosomal ribonucleic acid (RNA) species were identified in the total cellular RNA directly extracted from intact cells of the trypanosomatid protozoan Crithidia fasciculata (M. W. Gray, Can. J. Biochem. 57:914-926, 1979). The results suggested that the C. fasciculata ribosome might be unusual in containing three novel, low-molecular-weight ribosomal RNA components, designated e, f, and g (apparent chain lengths 240, 195, and 135 nucleotides, respectively), in addition to analogs of eucaryotic 5S (species h) and 5.8S (species i) ribosomal RNAs. In the present study, all of the presumptive ribosomal RNAs were indeed found to be associated with purified C. fasciculata ribosomes, and their localization was investigated in subunits produced under different conditions of ribosome dissociation. When ribosomes were dissociated in a high-potassium (880 mM K+, 12.5 mM Mg2+) medium, species e to i were all found in the large ribosomal subunit, which also contained an additional, transfer RNA-sized component (species j). However, when subunits were prepared in a low-magnesium (60 mM K+, 0.1 mM Mg2+) medium, two of the novel species (e and g) did not remain with the large subunit, but were released, apparently as free RNAs. Control experiments have eliminated the possibility that the small RNAs are generated by quantitative and highly specific (albeit artifactual) ribonuclease cleavage of large ribosomal RNAs during isolation. In terms of RNA composition and dissociation properties, therefore, the ribosome of C. fasciculata is the most "atypical" eucaryotic ribosome yet described. These observations raise interesting questions about the function and evolutionary origin of C. fasciculata ribosomes and about the organization and expression of ribosomal RNA genes in this organism.
在本实验室之前的一项研究中,从锥虫原生动物纤细短膜虫(M. W. Gray,《加拿大生物化学杂志》57:914 - 926,1979)完整细胞中直接提取的总细胞RNA里,鉴定出了假定的核糖体核糖核酸(RNA)种类。结果表明,纤细短膜虫核糖体可能不同寻常,除了真核生物5S(h种类)和5.8S(i种类)核糖体RNA的类似物外,还含有三种新的低分子量核糖体RNA组分,分别命名为e、f和g(表观链长分别为240、195和135个核苷酸)。在本研究中,所有假定的核糖体RNA确实都与纯化的纤细短膜虫核糖体相关联,并在核糖体解离的不同条件下产生的亚基中研究了它们的定位。当核糖体在高钾(880 mM K⁺,12.5 mM Mg²⁺)培养基中解离时,e到i种类都存在于大核糖体亚基中,该亚基还含有一个额外的、转运RNA大小的组分(j种类)。然而,当在低镁(60 mM K⁺,0.1 mM Mg²⁺)培养基中制备亚基时, 两种新种类(e和g)没有与大核糖体亚基保留在一起,而是明显以游离RNA的形式被释放出来。对照实验排除了在分离过程中,小RNA是由大核糖体RNA经定量且高度特异性(尽管是人为的)核糖核酸酶切割产生的可能性。因此,就RNA组成和解离特性而言,纤细短膜虫核糖体是迄今所描述的最“非典型”的真核生物核糖体。这些观察结果引发了关于纤细短膜虫核糖体的功能和进化起源以及该生物体中核糖体RNA基因的组织和表达的有趣问题。