Rosen A, Daniel V
Department of Biochemistry, Weizmann Institute of Science, Rehovot, Israel.
Gene. 1988 Sep 30;69(2):275-85. doi: 10.1016/0378-1119(88)90438-6.
A bacteriophage gamma Ch4A clone containing a 22-kb rat DNA insert was isolated and found to contain a solitary tRNA(Phe)GAA gene and, 436 bp downstream of it, an Alu-like element. The nucleotide sequence of a 1141-bp DNA fragment containing these genes was determined. The rat tRNA(Phe)GAA gene, with the exception of an additional A in the extra arm, has a sequence identical to that of a rabbit liver tRNA(Phe). The Alu-like element belongs to the rodent B2 family of short interspersed repetitive nucleotide sequences. This repetitive element, B2Phe, is flanked by 12-bp direct repeats, contains an internal split promoter (block A and block B) for RNA polymerase III and is devoid of an A-rich segment at the 3' end. Like other members of the B2 family, the B2Phe element presents 64% sequence homology with rat serine tRNA and contains a serine (GCT) anticodon. Both tRNA(Phe)GAA gene and B2Phe element were found to be transcriptionally active in HeLa cell and Xenopus oocyte nuclear extracts. The tRNA(Phe) gene transcripts were processed during the course of transcription to form mature-size tRNA(Phe). The transcription efficiency of the B2Phe element was found to be an order of magnitude higher than that of the tRNA(Phe) gene. Competition experiments demonstrate that the B2Phe DNA can form a more stable transcription complex than the tRNA(Phe) gene and compete with it for binding of transcription factors.
分离出一个含有22kb大鼠DNA插入片段的噬菌体γCh4A克隆,发现它含有一个单独的tRNA(Phe)GAA基因,并且在其下游436bp处有一个类似Alu的元件。测定了包含这些基因的1141bp DNA片段的核苷酸序列。大鼠tRNA(Phe)GAA基因除了在额外臂中有一个额外的A外,其序列与兔肝tRNA(Phe)的序列相同。类似Alu的元件属于短散在重复核苷酸序列的啮齿动物B2家族。这个重复元件B2Phe两侧是12bp的直接重复序列,包含一个用于RNA聚合酶III的内部分裂启动子(A区和B区),并且在3'端没有富含A的片段。与B2家族的其他成员一样,B2Phe元件与大鼠丝氨酸tRNA具有64%的序列同源性,并含有一个丝氨酸(GCT)反密码子。发现tRNA(Phe)GAA基因和B2Phe元件在HeLa细胞和非洲爪蟾卵母细胞核提取物中均具有转录活性。tRNA(Phe)基因转录本在转录过程中被加工形成成熟大小的tRNA(Phe)。发现B2Phe元件的转录效率比tRNA(Phe)基因高一个数量级。竞争实验表明,B2Phe DNA能形成比tRNA(Phe)基因更稳定的转录复合物,并与它竞争转录因子的结合。