Kleiman L, Heron T, Essagian C, Nicoghosian K, Cedergren R J
Nucleic Acids Res. 1983 May 11;11(9):2585-98. doi: 10.1093/nar/11.9.2585.
A pBR322 plasmid containing the initiator tRNAmet gene of Xenopus (pt145 - donated by Stuart Clarkson) will specifically bind to mouse initiator tRNAmet (tRNAmeti) when total mouse tRNA, extracted from uninduced Friend erythroleukemia cells, is hybridized to the gene probe. One dimensional electrophoresis of the hybridizing tRNA in 20% polyacrylamide reveals one major band (95%) and a minor band. The hybridizing tRNA has been identified as initiator tRNAmet by RNA sequencing. Hybridization of tRNAtotal to another plasmid containing the Xenopus gene for tRNAasn results in two bound species with different electrophoretic mobilities than the tRNA bound to the initiator tRNAmet gene. pt145 has been used to measure the steady state concentration of initiator tRNAmet in the uninduced and erythroid Friend cell, and in the unfertilized egg and 21 h blastula of the sea urchin. Initiator tRNAmet represents 0.91% and 0.52% of the tRNA populations extracted from uninduced and erythroid Friend cells, respectively. Based upon the total tRNA content per cell, there is a 3.8 fold decrease in initiator tRNAmet per cell during erythroid differentiation. tRNA extracted from unfertilized eggs and 21 h blastula of the sea urchin both have 0.5% of total tRNA as initiator tRNAmet (approximately 1.5 pg).
一种含有非洲爪蟾起始tRNAmet基因的pBR322质粒(pt145 - 由斯图尔特·克拉克森提供),当从未诱导的Friend红白血病细胞中提取的总小鼠tRNA与该基因探针杂交时,它将特异性结合小鼠起始tRNAmet(tRNAmeti)。在20%聚丙烯酰胺中对杂交tRNA进行一维电泳,显示出一条主要条带(95%)和一条次要条带。通过RNA测序已将杂交tRNA鉴定为起始tRNAmet。总tRNA与另一种含有非洲爪蟾tRNAasn基因的质粒杂交,产生两种结合产物,其电泳迁移率与结合到起始tRNAmet基因上的tRNA不同。pt145已被用于测量未诱导的和红系Friend细胞、海胆未受精卵和21小时囊胚中起始tRNAmet的稳态浓度。起始tRNAmet分别占从未诱导的和红系Friend细胞中提取的tRNA群体的0.91%和0.52%。根据每个细胞的总tRNA含量,在红系分化过程中每个细胞的起始tRNAmet减少了3.8倍。从海胆未受精卵和21小时囊胚中提取的tRNA,作为起始tRNAmet均占总tRNA的0.5%(约1.5皮克)。