Resistance to paraquat in a mammalian cell Line

Jolene Starr, Shifra Sela, Christine M. Disteche, Peter S. Rabinovitch, Charles E. Ogburn, Annette C. Smith, George M. Martin

Research output: Contribution to journalArticlepeer-review

8 Scopus citations

Abstract

Paraquat-resistant variants were isolated in Chinese hamster ovary (CEO) cells by stepwise increases in paraquat concentrations. Three series of selective experiments gave variants which appeared to be using one or several different mechanisms of resistance. In all variants tested (PQ-1, PQ-2, PQ-3, PQ-2X and PQ-3X of series 1), radioactively labeled paraquat was taken up by the cells. These variants exhibited no unusual resistance to either oxygen or radiation, nor were increases found in the activities of free-radical scavenging enzymes. They had extra DNA (3-12%) and an unusual acrocentric marker chromosome which was common to all of the variants but never observed in the parental cells. Double minutes were observed in 29% of metaphases of the PQ-3 variant. One of the resistant lines exhibited evidence of an intrinsic chromosomal instability, a phenotype that could conceivably facilitate gene amplification. Selection series 2 and 3 were designed to further evaluate gene amplification as a mechanism of resistance. These variants exhibited high frequencies (40-100%) of tetraploidy or hypotetraploidy with loss of chromosomes and varying frequencies of double minutes (10-75% of metaphases). In two of the variants the same marker chromosome which was observed in the series 1 variants was seen. Two other lines exhibited a variant of this marker, incorporating it into a metacentric chromosome. It may be that gene amplification facilitates resistance to paraquat and that both stable and unstable methods of amplifying genes are used.

Original languageEnglish
Pages (from-to)141-152
Number of pages12
JournalSomatic Cell and Molecular Genetics
Volume12
Issue number2
DOIs
StatePublished - Mar 1986
Externally publishedYes

Funding

FundersFunder number
National Institute on AgingP01AG001751
National Institute of General Medical SciencesT32GM007735

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