GINSBERG H S, DIXON M K
J Exp Med. 1961 Feb 1;113(2):283-99. doi: 10.1084/jem.113.2.283.
Type 4 adenovirus infection of HeLa cells effected a marked increase in synthesis of the saline-soluble DNA fraction, but not the host-cell DNA (the water-soluble fraction). This was demonstrated by the marked increase in specific activity of saline-soluble DNA but not water-soluble DNA when P(32)-inorganic phosphate or sodium formate-C(14) was employed. When these isotopes were used to label cells before viral infection rather than during the process of viral propagation, the saline-soluble DNA from infected cells had a specific activity of 10 to 20 per cent less than that of uninfected cells, indicating that the saline-soluble DNA was synthesized both from prelabeled precursors of the cell pools and unlabeled materials from the medium. Saline-soluble DNA began to increase between 10 to 12 hours after viral infection and 3 to 4 hours before appearance of newly propagated infectious virus. The specific activity of the acid-soluble pool of infected cells also increased between 10 to 12 hours after viral inoculation when sodium formate-C(14) was used as a radioisotope. When P(32)-inorganic phosphate was utilized, the specific activity of infected-cell RNA was increased approximately the same relative amount as when total RNA was determined chemically; i.e., 30 to 40 per cent. With type 5 adenovirus, not only did a 3- to 5-fold increase in saline-soluble DNA occur, but also an increase was measured in specific activity of RNA when P(32)-inorganic phosphate was used.
4型腺病毒感染HeLa细胞后,可使盐溶性DNA组分的合成显著增加,但宿主细胞DNA(水溶性组分)的合成不受影响。当使用P(32)-无机磷酸盐或甲酸钠-C(14)时,盐溶性DNA的比活性显著增加,而水溶性DNA则不然,这证明了上述情况。当在病毒感染前而非病毒增殖过程中使用这些同位素标记细胞时,感染细胞的盐溶性DNA的比活性比未感染细胞低10%至20%,这表明盐溶性DNA是由细胞池预先标记的前体和培养基中的未标记物质合成的。盐溶性DNA在病毒感染后10至12小时开始增加,在新繁殖的感染性病毒出现前3至4小时达到高峰。当使用甲酸钠-C(14)作为放射性同位素时,感染细胞的酸溶性池的比活性在病毒接种后10至12小时也会增加。当使用P(32)-无机磷酸盐时,感染细胞RNA的比活性增加的相对量与化学测定总RNA时大致相同,即增加30%至40%。对于5型腺病毒,不仅盐溶性DNA增加了3至5倍,而且当使用P(32)-无机磷酸盐时,RNA的比活性也有所增加。