A theory of age-dependent mutation and senescence.

نویسندگان

  • Jacob A Moorad
  • Daniel E L Promislow
چکیده

Laboratory experiments show us that the deleterious character of accumulated novel age-specific mutations is reduced and made less variable with increased age. While theories of aging predict that the frequency of deleterious mutations at mutation-selection equilibrium will increase with the mutation's age of effect, they do not account for these age-related changes in the distribution of de novo mutational effects. Furthermore, no model predicts why this dependence of mutational effects upon age exists. Because the nature of mutational distributions plays a critical role in shaping patterns of senescence, we need to develop aging theory that explains and incorporates these effects. Here we propose a model that explains the age dependency of mutational effects by extending Fisher's geometrical model of adaptation to include a temporal dimension. Using a combination of simple analytical arguments and simulations, we show that our model predicts age-specific mutational distributions that are consistent with observations from mutation-accumulation experiments. Simulations show us that these age-specific mutational effects may generate patterns of senescence at mutation-selection equilibrium that are consistent with observed demographic patterns that are otherwise difficult to explain.

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

تجربه آغاز حس سالمندی: یک مطالعه کیفی

Background and purpose: Different sources have provided various descriptions on the onset of senescence and its associated factors. Any person may become senile at a different age. The objective of the present study was to explore the feelings related to the onset of aging and factors influencing it based on old women’s experience. Materials and methods: This study used a qualitative approach ...

متن کامل

Age-dependent mutational effects curtail the evolution of senescence by antagonistic pleiotropy.

One of the two main hypotheses to account for ageing is antagonistic pleiotropy (AP). This model requires alleles that increase vital rates (reproduction or survival) at early age at the expense of vital rates at late age. An important focus of evolutionary studies has been to assess the relative abundance of AP-type aging alleles that arise through mutation. Here, we develop theory that predic...

متن کامل

Senescence in Animals: Why Evolutionary Theories Matter

This is a clearly deleterious process, which seems difficult to conciliate with natural selection, which predicts evolution towards increasing fitness. Historically, the first evolutionary explanation able to conciliate these two processes is known as the mutation accumulation theory (Medawar, 1952). According to this theory, in age-structured populations the force of selection decreases with i...

متن کامل

Outbreeding Alleviates Senescence in Hermaphroditic Snails as Expected from the Mutation-Accumulation Theory

Senescence, the decline in fitness components of an organism with age [1], is a nearly universal characteristic of living beings [2-6]. This ubiquity is challenging because natural selection does not favor the evolution of traits decreasing fitness [1, 7, 8]. Senescence may result from two nonexclusive mechanisms: the accumulation of deleterious mutations acting late in life, when the strength ...

متن کامل

The evolution of senescence through decelerating selection for system reliability.

Senescence is a universal phenomenon in organisms, characterized by increasing mortality and decreasing fecundity with advancing chronological age. Most proximate agents of senescence, such as reactive oxygen species and UV radiation, are thought to operate by causing a gradual build-up of bodily damage. Yet most current evolutionary theories of senescence emphasize the deleterious effects of f...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

عنوان ژورنال:
  • Genetics

دوره 179 4  شماره 

صفحات  -

تاریخ انتشار 2008