Grady L J, Campbell W P, North A B
Nucleic Acids Res. 1979 Sep 11;7(1):259-69. doi: 10.1093/nar/7.1.259.
Initial RNA excess hybridization experiments employing total cell RNA and the complete complement of nonrepetitive DNA sequences showed no differences between normal and regenerating rat liver. However, when the DNA from the RNA-DNA hybrids was isolated and then reacted with homologous and heterologous RNAs the sensitivity of the assay was sufficiently improved to reveal that some of the nonrepetitive DNA transcrips present in normal liver are missing at 24 h and 48 h after a 70% partial hepatectomy. Additional experiments showed that while some of the missing sequences were common to both stages of regeneration, some were also different. The data thus suggest both quantitative and qualitative changes during liver regeneration in the population of RNA molecules transcribed from nonrepetitive DNA.
最初使用全细胞RNA和非重复DNA序列的完全互补序列进行的RNA过量杂交实验表明,正常大鼠肝脏和再生大鼠肝脏之间没有差异。然而,当从RNA-DNA杂交体中分离出DNA,然后与同源和异源RNA反应时,该检测方法的灵敏度得到了充分提高,从而揭示出在70%部分肝切除术后24小时和48小时,正常肝脏中存在的一些非重复DNA转录本缺失了。进一步的实验表明,虽然一些缺失的序列在再生的两个阶段都存在,但也有一些是不同的。因此,这些数据表明,在肝脏再生过程中,从非重复DNA转录的RNA分子群体发生了数量和质量上的变化。