Getz M J, Birnie G D, Young B D, MacPhail E, Paul J
Cell. 1975 Feb;4(2):121-9. doi: 10.1016/0092-8674(75)90118-x.
Complementary DNA (cDNA) has been transcribed by viral reverse transcriptase from poly(A)-containing nuclear RNA prepared from growing mouse Friend cells (clone M2). Annealing experiments with this cDNA have demonstrated that a large proportion of the poly(A) tracts in M2 cell nuclear RNA are adjacent to RNA sequences which are transcribed from nonrepetitive DNA in the mouse genome. The kinetics of hybridization of cDNA to template RNA indicate that nuclear poly(A)-containing RNA consists of at least two abundance classes, the more complex of which is transcribed from approximately 3 percent of the genome. Thus there are at least 5 times more unique DNA sequences represented in nuclear polyadenylated RNA than in polysomal polyadenylated RNA. Moreover, there is evidence for posttranscriptional mechanisms which alter the relative concentrations of some (at least) gene transcripts between nucleus and cytoplasm.
互补DNA(cDNA)由病毒逆转录酶从生长中的小鼠Friend细胞(克隆M2)制备的含多聚腺苷酸(poly(A))的核RNA转录而来。用这种cDNA进行的退火实验表明,M2细胞核RNA中很大一部分多聚腺苷酸序列与从小鼠基因组中非重复DNA转录而来的RNA序列相邻。cDNA与模板RNA杂交的动力学表明,核内含有多聚腺苷酸的RNA至少由两个丰度类别组成,其中较复杂的一类是从约3%的基因组转录而来。因此,核内多聚腺苷酸化RNA中所代表的独特DNA序列比多核糖体多聚腺苷酸化RNA中至少多5倍。此外,有证据表明存在转录后机制,可改变某些(至少)基因转录本在细胞核和细胞质之间的相对浓度。