Geranytgeraniol promotes entry of UT-2 cells into the cell cycle in the absence of mevalonate

Dean C. Crick, Douglas A. Andres, Charles J. Waechter

Research output: Contribution to journalArticlepeer-review

16 Scopus citations

Abstract

Although UT-2 cells, a mutant clone of Chinese hamster ovary cells, have been shown to require mevalonate for growth due to a deficiency in 3- hydroxy-3-methylglutaryl-CoA reductase, the precise mevalonate-derived product(s) essential for proliferation has not been identified. These studies show that UT-2 cells proliferate in the presence of free geranylgeraniol (GG-OH), as well as mevalonate. Cell growth was optimal when the culture medium was supplemented with 5-10 μM GG-OH. Under these growth conditions [3H]GG-OH is actively incorporated into UT-2 proteins. Prominent [3H]geranylgeranylated polypeptides in the size range (19-27 kDa) of the small GTP-binding proteins are observed by SDS-PAGE. Analysis of the butanol-soluble products released from the metabolically labeled proteins by digestion with Pronase E reveals that the proteins contain [3H]geranylgeranylated cysteine residues. Even though [3H]farnesol is also incorporated into cysteinyl residues of a different set of UT-2 proteins, farnesol added at 10 μM did not satisfy the mevalonate requirement for cell growth. These results show that UT-2 cells divide in the presence of exogenously supplied GG-OH, providing evidence that one or more geranylgeranylated proteins are essential for entry of UT-2 cells, and probably other mammalian cells, into the cell cycle.

Original languageEnglish
Pages (from-to)302-307
Number of pages6
JournalExperimental Cell Research
Volume231
Issue number2
DOIs
StatePublished - Mar 15 1997

Bibliographical note

Funding Information:
1This work was supported by NIH Grants GM36065 (C.J.W.) and EY11231 (D.A.A.).

Funding

1This work was supported by NIH Grants GM36065 (C.J.W.) and EY11231 (D.A.A.).

FundersFunder number
National Institutes of Health (NIH)GM36065
National Eye Institute (NEI)R29EY011231

    ASJC Scopus subject areas

    • Cell Biology

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