Skip to main content

Advertisement

Log in

Preferential amplification and phenotypic selection in a population of deleted and wild-type mitochondrial DNA in cultured cells

  • ORIGINAL PAPER
  • Published:
Current Genetics Aims and scope Submit manuscript

Abstract

In order to study the still poorly understood dynamics of mitochondrial gene segregation, we attempted to alter the percentage of deleted mtDNA (del-mtDNA) over wild-type mtDNA in cell-culture by manipulating respiratory chain capacity. For this purpose, we used a cell-line harbouring a 6-kb mtDNA-deletion which normally was present in 70% of the molecules. The results show that in the presence of low concentrations of doxycycline (DC), an inhibitor of mitochondrial protein synthesis, the average percentage of del-mtDNA in culture steadily declined. After short-term DC treatment most cells still contained del-mtDNA and removal of DC led to a rapid increase in the proportion of del-mtDNA. In contrast, long-term DC treatment rendered del-mtDNA undetectable by Southern analysis, reflecting the complete absence of del-mtDNA in most cells. In this case, del-mtDNA in culture remained at a constant low level after removal of the drug. The results clearly show the importance of phenotypic selection in the segregation of a deleterious mtDNA mutation.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

Author information

Authors and Affiliations

Authors

Additional information

Received: 24 March / 12 May 1997

Rights and permissions

Reprints and permissions

About this article

Cite this article

Spelbrink, J., Zwart, R., Van Galen, M. et al. Preferential amplification and phenotypic selection in a population of deleted and wild-type mitochondrial DNA in cultured cells. Curr Genet 32, 115–124 (1997). https://doi.org/10.1007/s002940050255

Download citation

  • Issue Date:

  • DOI: https://doi.org/10.1007/s002940050255

Navigation