Rabitts T H, Forster A, Smith M, Gillam S
Eur J Immunol. 1977 Jan;7(1):43-8. doi: 10.1002/eji.1830070111.
RNA-driven complementary DNA (cDNA) hybridization experiments have been carried out in order to detect complementary sequences in RNA prepared from a mouse T cell lymphoma line (EL4). In conditions where efficient hybridization of L-chain cDNA with homologous P3 myeloma mRNA was observed, poor hybridization was observed with EL4 mRNA unless a low criterion of hybrid formation was employed (i.e. hydroxyapatite fractionation). The hybrid formed between EL4 mRNA and L-chain cDNA was found to melt about 5 degrees C below the homologous hybrid indicating that the sequence detected in EL4 mRNA is similar but not identical with the P3 mRNA sequence. However, a similar sequence was detectable in a Clambda-producing myeloma cell line but in this line the concentration of the sequence was found to be an order of magnitude lower than in EL4 cells.
为了检测从小鼠T细胞淋巴瘤系(EL4)制备的RNA中的互补序列,进行了RNA驱动的互补DNA(cDNA)杂交实验。在观察到L链cDNA与同源P3骨髓瘤mRNA有效杂交的条件下,除非采用低杂交形成标准(即羟基磷灰石分级分离),否则与EL4 mRNA的杂交效果较差。发现EL4 mRNA与L链cDNA之间形成的杂交体在比同源杂交体低约5摄氏度的温度下解链,这表明在EL4 mRNA中检测到的序列与P3 mRNA序列相似但不相同。然而,在产生Clambda的骨髓瘤细胞系中也可检测到类似序列,但在该细胞系中,该序列的浓度比EL4细胞中的低一个数量级。