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PMID: 13705509 Published · ppublish English Journal Article

Nucleuc acid synthesis in types 4 and 5 adenovirus-infected HeLa cells.

The Journal of experimental medicine ·Vol. 113 ·1961-02-01 ·Pages 283-99

GINSBERG HS, DIXON MK

Abstract

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.

Keywords
ADENOVIRUS/culture NUCLEIC ACIDS/metabolism
MeSH Terms
Adenoviridae/ethnology DNA HeLa Cells Humans Nucleic Acids/metabolism RNA
Chemicals
Nucleic Acids RNA DNA
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
GINSBERG H S
DIXON M K
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27 references, click to expand
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Article Info
Journal
The Journal of experimental medicine
Abbr.
J Exp Med
ISSN
0022-1007
Published
1961-02-01
Pages
283-99
Language
English
Region
United States
NLM ID
2985109R
PMCID
PMC2137360
Subset
OM
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