MUTATION LOAD AND THE SURVIVAL OF SMALL POPULATIONS

被引:191
作者
LYNCH, M [1 ]
GABRIEL, W [1 ]
机构
[1] MAX PLANCK INST LIMNOL, DEPT PHYSIOL ECOL, W-2320 PLON, GERMANY
关键词
D O I
10.1111/j.1558-5646.1990.tb05244.x
中图分类号
Q14 [生态学(生物生态学)];
学科分类号
071012 ; 0713 ;
摘要
Previous attempts to model the joint action of selection and mutation in finite populations have treated population size as being independent of the mutation load. However, the accumulation of deleterious mutations is expected to cause a gradual reduction in population size. Consequently, in small populations random genetic drift will progressively overpower selection making it easier to fix future mutations. This synergistic interaction, which we refer to as a mutational melt-down, ultimately leads to population extinction. For many conditions, the coefficient of variation of extinction time is less than 0.1, and for species that reproduce by binary fission, the expected extinction time is quite insensitive to population carrying capacity. These results are consistent with observations that many cultures of ciliated protozoans and vertebrate fibroblasts have characteristic extinction times. The model also predicts that clonal lineages are unlikely to survive more than 10(4) to 10(5) generations, which is consistent with existing data on parthenogenetic animals. Contrary to the usual view that Muller's ratchet does more damage when selection is weak, we show that the mean extinction time declines as mutations become more deleterious. Although very small sexual populations, such as self-fertilized lines, are subject to mutational melt-downs, recombination effectively eliminates the process when the effective population size exceeds a dozen or so. The concept of the effective mutation load is developed, and several procedures for estimating it are described. It is shown that this load can be reduced substantially when mutational effects are highly variable.
引用
收藏
页码:1725 / 1737
页数:13
相关论文
共 44 条
[1]   CLONAL ATTENUATION IN CHICK-EMBRYO FIBROBLASTS - EXPERIMENTAL-DATA, A MODEL AND COMPUTER-SIMULATIONS [J].
ANGELLO, JC ;
PROTHERO, JW .
CELL AND TISSUE KINETICS, 1985, 18 (01) :27-43
[2]   CLONAL AGING IN PARAMECIUM-TETRAURELIA - ABSENCE OF EVIDENCE FOR A CYTOPLASMIC FACTOR [J].
AUFDERHEIDE, KJ .
MECHANISMS OF AGEING AND DEVELOPMENT, 1984, 28 (01) :57-66
[3]   CLONAL AGING IN PARAMECIUM-TETRAURELIA .2. EVIDENCE OF FUNCTIONAL-CHANGES IN THE MACRONUCLEUS WITH AGE [J].
AUFDERHEIDE, KJ .
MECHANISMS OF AGEING AND DEVELOPMENT, 1987, 37 (03) :265-279
[4]   RECOMBINATION AND THE IMMORTALITY OF THE GERM LINE [J].
BELL, G .
JOURNAL OF EVOLUTIONARY BIOLOGY, 1988, 1 (01) :67-82
[5]  
Bell G., 1982, MASTERPIECE NATURE
[6]   EVOLUTION OF SEX IN RNA VIRUSES [J].
CHAO, L .
JOURNAL OF THEORETICAL BIOLOGY, 1988, 133 (01) :99-112
[7]   The variant call format and VCFtools [J].
Danecek, Petr ;
Auton, Adam ;
Abecasis, Goncalo ;
Albers, Cornelis A. ;
Banks, Eric ;
DePristo, Mark A. ;
Handsaker, Robert E. ;
Lunter, Gerton ;
Marth, Gabor T. ;
Sherry, Stephen T. ;
McVean, Gilean ;
Durbin, Richard .
BIOINFORMATICS, 2011, 27 (15) :2156-2158
[8]  
FELSENSTEIN J, 1974, GENETICS, V78, P737
[9]   PARTHENOGENETIC POPULATIONS CAN REMAIN STABLE IN SPITE OF HIGH MUTATION-RATE AND RANDOM DRIFT [J].
GABRIEL, W ;
WAGNER, GP .
NATURWISSENSCHAFTEN, 1988, 75 (04) :204-205
[10]   The effect of variation on fitness [J].
Haldane, JBS .
AMERICAN NATURALIST, 1937, 71 :337-349