Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2004 Mar;166(3):1571-9.
doi: 10.1534/genetics.166.3.1571.

Stochastic tunnels in evolutionary dynamics

Affiliations

Stochastic tunnels in evolutionary dynamics

Yoh Iwasa et al. Genetics. 2004 Mar.

Abstract

We study a situation that arises in the somatic evolution of cancer. Consider a finite population of replicating cells and a sequence of mutations: type 0 can mutate to type 1, which can mutate to type 2. There is no back mutation. We start with a homogeneous population of type 0. Mutants of type 1 emerge and either become extinct or reach fixation. In both cases, they can generate type 2, which also can become extinct or reach fixation. If mutation rates are small compared to the inverse of the population size, then the stochastic dynamics can be described by transitions between homogeneous populations. A "stochastic tunnel" arises, when the population moves from all 0 to all 2 without ever being all 1. We calculate the exact rate of stochastic tunneling for the case when type 1 is as fit as type 0 or less fit. Type 2 has the highest fitness. We discuss implications for the elimination of tumor suppressor genes and the activation of genetic instability. Although our theory is developed for cancer genetics, stochastic tunnels are general phenomena that could arise in many circumstances.

PubMed Disclaimer

Similar articles

Cited by

References

    1. Genetics. 2001 Jan;157(1):399-411 - PubMed
    1. Mutat Res. 2000 Jan 17;447(1):73-116 - PubMed
    1. Proc Natl Acad Sci U S A. 1971 Apr;68(4):820-3 - PubMed
    1. Br J Cancer. 1957 Jun;11(2):161-9 - PubMed
    1. Cell Tissue Kinet. 1973 Mar;6(2):125-34 - PubMed

Publication types