Gray M W
Can J Biochem. 1979 Jun;57(6):914-26. doi: 10.1139/o79-111.
When extracted and analyzed under conditions which maintain noncovalently associated RNA-RNA complexes, the bulk cellular RNA of Crithidia fasciculata contains species of apparent molecular weights 1.3, 0.825, 0.08, 0.065, and 0.045 x 10(6) in addition to 5S rRNA and tRNA. Heat denaturation results in the disappearance of the 1.3 x 10(6) dalton RNA and the appearance of three new species having molecular weights of 0.67, 0.575, and 0.059 x 10(6). In addition, the apparent molecular weight of the 0.825 x 10(6) dalton component is reproducibly lowered to 0.81 x 10(6) after heat treatment. With the exception of tRNA, all of the RNA species are present in close to equimolar amounts in either undenatured or heat-denatured C. fasciculata bulk cellular RNA. On the basis of previous observations on the ribosomal RNA of the closely related organism, Crithidia oncopelti (Spencer, R. & Cross, G.A.M. (1976) J. Gen. Microbiol. 93, 82-88), the 1.3 and 0.825 x 10(6) dalton RNA's are considered to be components of the large and small subunits, respectively, of C. fasciculata ribosomes, but the subunit localization of the other RNA's described here has not yet been determined. O2'-Methylnucleosides account for about 1.4 mol% of the total nucleoside constituents of unfractionated C. fasciculata rRNA. Quantitative analysis suggests that the rRNA molecules in a C. fasciculata ribosome contain a total of 95-100 O2'-methyl groups, distributed in 80-85 Nm-Np sequences (including four 'hypermodified' Nm-Np, each containing a modification of a base or base-sugar linkage in addition to sugar methylation), six different Nm-Nm-Np sequences, and one Nm-Nm-Nm-Np sequence. While the specific pattern of O2'-methylation in the rRNA of C. fasciculata is distinct, both qualitatively and quantitatively, from the pattern observed in other organisms, Crithidia rRNA does contain certain 'universal' O2'-methylated sequences which appear to have been extensively conserved in evolution. The base-methylated nucleoside, N6,N6-dimethyladenosine (m26A), has been isolated from both C. fasciculata and wheat embryo rRNA in the form of the alkali-resistant dinucleotide, m26A-m26Ap. This dinucleotide and its enzymatic degradation products have been characterized by examination of their ultraviolet absorption spectra and electrophoretic and chromatographic properties.
当在维持非共价结合的RNA - RNA复合物的条件下提取和分析时,除了5S rRNA和tRNA外,纤细短膜虫的大量细胞RNA还含有表观分子量分别为1.3、0.825、0.08、0.065和0.045×10⁶的RNA种类。热变性导致1.3×10⁶道尔顿的RNA消失,并出现三种新的RNA种类,其分子量分别为0.67、0.575和0.059×10⁶。此外,热处理后,0.825×10⁶道尔顿组分的表观分子量可重复降低至0.81×10⁶。除了tRNA外,所有RNA种类在未变性或热变性的纤细短膜虫大量细胞RNA中均以接近等摩尔的量存在。根据对密切相关生物——昆虫短膜虫核糖体RNA的先前观察(Spencer, R. & Cross, G.A.M. (1976) J. Gen. Microbiol. 93, 82 - 88),1.3×10⁶和0.825×10⁶道尔顿的RNA分别被认为是纤细短膜虫核糖体大亚基和小亚基的组分,但此处描述的其他RNA的亚基定位尚未确定。O2'-甲基核苷约占未分级的纤细短膜虫rRNA总核苷成分的1.4摩尔%。定量分析表明,纤细短膜虫核糖体中的rRNA分子总共含有95 - 100个O2'-甲基基团,分布在80 - 至85个Nm - Np序列中(包括四个“超修饰”的Nm - Np,每个除了糖甲基化外还含有碱基或碱基 - 糖连接的修饰)、六个不同的Nm - Nm - Np序列和一个Nm - Nm - Nm - Np序列。虽然纤细短膜虫rRNA中O2'-甲基化的具体模式在质量和数量上与其他生物中观察到的模式不同,但纤细短膜虫rRNA确实含有某些“通用”的O2'-甲基化序列,这些序列在进化过程中似乎得到了广泛的保守。碱基甲基化核苷N6,N6 - 二甲基腺苷(m²⁶A)已从纤细短膜虫和小麦胚rRNA中以耐碱二核苷酸m²⁶A - m²⁶Ap的形式分离出来。通过检查其紫外吸收光谱以及电泳和色谱性质,对该二核苷酸及其酶促降解产物进行了表征。