Evtushenko V I, Khanson K P
Tsitologiia. 1984 Jun;26(6):719-23.
The sequence complexity of the total cellular RNA was measured by RNA-driven hybridization to 125I-single copy DNA (sc-DNA). In the high density subfraction of thymocytes 4.5% of sc-DNA was saturated with cellular RNA. The sc-DNA probe was recovered from the DNA--RNA hybrids and rehybridized with homologous RNA and heterologous RNA from the cells with low density and middle density. Heterologous hybridization reactions with recycling sc-DNA probes revealed that 5.5% RNA sequences were specific of the cells from the high density subfraction and absent in both low and middle density subfractions. This is equivalent to expression of approximately 1100 additional structural genes in the high density subfraction of thymocytes.
通过RNA驱动与125I标记的单拷贝DNA(sc-DNA)杂交来测量总细胞RNA的序列复杂性。在胸腺细胞的高密度亚组分中,4.5%的sc-DNA被细胞RNA饱和。从DNA-RNA杂交体中回收sc-DNA探针,并与来自低密度和中密度细胞的同源RNA和异源RNA重新杂交。用循环sc-DNA探针进行的异源杂交反应表明,5.5%的RNA序列是高密度亚组分细胞特有的,在低密度和中密度亚组分中均不存在。这相当于在胸腺细胞的高密度亚组分中额外表达了约1100个结构基因。