Stanfield S W, Lengyel J A
Biochemistry. 1980 Aug 5;19(16):3873-7. doi: 10.1021/bi00557a036.
We have recently characterized small circular DNA of Drosophila cultured cells in terms of its average size, sequence complexity, and homology to intermediate repetitive DNA. We show here that transcripts homologous to small circular DNA are present in various RNA fractions. Nuclear poly(A+), nuclear poly(A-), and polysomal poly(A+) RNA drive 10, 7, and 20%, respectively, of in vitro labeled small circular DNA tracer into hybrid. Sequences complementary to small circular DNA are at least 10-fold more concentrated in nuclear poly(A+) RNA than in nuclear poly(A-) or polysomal poly(A+) RNA. We do not detect significant homology between poly(A-) cytoplasmic RNA and small circular DNA. Assuming that only the least complex component of small circular DNA is driven into hybrid and that transcription is asymmetric, we use the results obtained here and previously published data to calculate the sequence complexity and relative concentration of nuclear poly(A+), nuclear poly(A-), and polysomal poly(A+) RNA homologous to small circular DNA.
我们最近根据果蝇培养细胞中小环状DNA的平均大小、序列复杂性以及与中度重复DNA的同源性对其进行了表征。我们在此表明,与小环状DNA同源的转录本存在于各种RNA组分中。核聚腺苷酸加尾(poly(A+))RNA、核聚腺苷酸未加尾(poly(A-))RNA和多核糖体聚腺苷酸加尾(polysomal poly(A+))RNA分别将体外标记的小环状DNA示踪剂的10%、7%和20%驱动形成杂交体。与小环状DNA互补的序列在核聚腺苷酸加尾RNA中的浓度至少比在核聚腺苷酸未加尾RNA或多核糖体聚腺苷酸加尾RNA中高10倍。我们未检测到聚腺苷酸未加尾细胞质RNA与小环状DNA之间存在显著同源性。假设只有小环状DNA中最不复杂的组分被驱动形成杂交体,并且转录是不对称的,我们利用此处获得的结果和先前发表的数据来计算与小环状DNA同源的核聚腺苷酸加尾RNA、核聚腺苷酸未加尾RNA和多核糖体聚腺苷酸加尾RNA的序列复杂性和相对浓度。