Brown J W, Reeve J N
J Bacteriol. 1985 Jun;162(3):909-17. doi: 10.1128/jb.162.3.909-917.1985.
Polyadenylated [poly(A)+] RNA molecules have been isolated from Methanococcus vannielii by oligodeoxythymidylate-cellulose affinity chromatography at 4 degrees C. Approximately 16% of the label in RNA isolated from cultures allowed to incorporate [3H]uridine for 3 min at 37 degrees C was poly(A)+ RNA. In contrast, less than 1% of the radioactivity in RNA labeled over a period of several generations was contained in poly(A)+ RNA molecules. Electrophoretic separation of poly(A)+ RNA molecules showed a heterogeneous population with mobilities indicative of sizes ranging from 900 to 3,000 bases in length. The population of poly(A)+ RNA molecules was found to have a half-life in vivo of approximately 12 min. Polyadenylate [poly(A)] tracts were isolated by digestion with RNase A and RNase T1 after 3' end labeling of the poly(A)+ RNA with RNA ligase. These radioactively labeled poly(A) oligonucleotides were shown by electrophoresis through DNA sequencing gels to average 10 bases in length, with major components of 5, 9, 10, 11, and 12 bases. The lengths of these poly(A) sequences are in agreement with estimates obtained from RNase A and RNase T1 digestions of [3H]adenine-labeled poly(A)+ RNA molecules. Poly(A)+ RNA molecules from M. vannielii were labeled at their 5' termini with T4 polynucleotide kinase after dephosphorylation with calf intestine alkaline phosphatase. Pretreatment of the RNA molecules with tobacco acid pyrophosphatase did not increase the amount of phosphate incorporated into poly(A)+ RNA molecules by polynucleotide kinase, indicating that the poly(A)+ RNA molecules did not have modified bases (caps) at their 5' termini. The relatively short poly(A) tracts, the lack of 5' cap structures, and the instability of the poly(A)+ RNA molecules isolated from M. vannielii indicate that these archaebacterial poly(A)+ RNAs more closely resemble eubacterial mRNAs than eucaryotic mRNAs.
在4℃下,通过寡聚脱氧胸苷酸 - 纤维素亲和层析从万氏甲烷球菌中分离出聚腺苷酸化[poly(A)+]RNA分子。从在37℃下掺入[3H]尿苷3分钟的培养物中分离出的RNA中,约16%的标记物是poly(A)+RNA。相比之下,在几代时间内标记的RNA中,poly(A)+RNA分子所含的放射性不到1%。poly(A)+RNA分子的电泳分离显示出一个异质群体,其迁移率表明长度范围为900至3000个碱基。发现poly(A)+RNA分子群体在体内的半衰期约为12分钟。在用RNA连接酶对poly(A)+RNA进行3'末端标记后,通过用核糖核酸酶A和核糖核酸酶T1消化来分离聚腺苷酸[poly(A)]片段。通过DNA测序凝胶电泳显示,这些放射性标记的聚(A)寡核苷酸平均长度为10个碱基,主要成分是5、9、10、11和12个碱基。这些聚(A)序列的长度与从[3H]腺嘌呤标记的poly(A)+RNA分子的核糖核酸酶A和核糖核酸酶T1消化中获得的估计值一致。在用小牛肠碱性磷酸酶去磷酸化后,用T4多核苷酸激酶对来自万氏甲烷球菌的poly(A)+RNA分子的5'末端进行标记。用烟草酸焦磷酸酶对RNA分子进行预处理并没有增加多核苷酸激酶掺入poly(A)+RNA分子中的磷酸盐量,这表明poly(A)+RNA分子在其5'末端没有修饰碱基(帽)。从万氏甲烷球菌中分离出的相对较短的聚(A)片段、缺乏5'帽结构以及poly(A)+RNA分子的不稳定性表明,这些古细菌的poly(A)+RNA与真细菌mRNA的相似性比与真核mRNA的相似性更高。