scholarly journals Heterozygosity increases microsatellite mutation rate

2016 ◽  
Vol 12 (1) ◽  
pp. 20150929 ◽  
Author(s):  
William Amos

Whole genome sequencing of families of Arabidopsis has recently lent strong support to the heterozygote instability (HI) hypothesis that heterozygosity locally increases mutation rate. However, there is an important theoretical difference between the impact on base substitutions, where mutation rate increases in regions surrounding a heterozygous site, and the impact of HI on sequences such as microsatellites, where mutations are likely to occur at the heterozygous site itself. At microsatellite loci, HI should create a positive feedback loop, with heterozygosity and mutation rate mutually increasing each other. Direct support for HI acting on microsatellites is limited and contradictory. I therefore analysed AC microsatellites in 1163 genome sequences from the 1000 genomes project. I used the presence of rare alleles, which are likely to be very recent in origin, as a surrogate measure of mutation rate. I show that rare alleles are more likely to occur at locus-population combinations with higher heterozygosity even when all populations carry exactly the same number of alleles.

2012 ◽  
Vol 13 (12) ◽  
pp. 12533-12543 ◽  
Author(s):  
Jiangtao Luo ◽  
Ming Hao ◽  
Li Zhang ◽  
Jixiang Chen ◽  
Lianquan Zhang ◽  
...  

2017 ◽  
Vol 108 (6) ◽  
pp. 686-692 ◽  
Author(s):  
Hanna Panagiotopoulou ◽  
James D Austin ◽  
Katarzyna Zalewska ◽  
Magdalena Gonciarz ◽  
Kinga Czarnogórska ◽  
...  

2011 ◽  
Vol 52 (4) ◽  
pp. 391-401 ◽  
Author(s):  
Jaroslava Cieslarová ◽  
Pavel Hanáček ◽  
Eva Fialová ◽  
Miroslav Hýbl ◽  
Petr Smýkal

Genetics ◽  
2007 ◽  
Vol 177 (3) ◽  
pp. 1499-1507 ◽  
Author(s):  
Ryan McConnell ◽  
Sara Middlemist ◽  
Clea Scala ◽  
Joan E. Strassmann ◽  
David C. Queller

2013 ◽  
Vol 9 (1) ◽  
pp. 20120334 ◽  
Author(s):  
Chikako Matsuba ◽  
Dejerianne G. Ostrow ◽  
Matthew P. Salomon ◽  
Amit Tolani ◽  
Charles F. Baer

Mutation rate often increases with environmental temperature, but establishing causality is complicated. Asymmetry between physiological stress and deviation from the optimal temperature means that temperature and stress are often confounded. We allowed mutations to accumulate in two species of Caenorhabditis for approximately 100 generations at 18°C and for approximately 165 generations at 26°C; 26°C is stressful for Caenorhabditis elegans but not for Caenorhabditis briggsae . We report mutation rates at a set of microsatellite loci and estimates of the per-generation decay of fitness (Δ M w ), the genomic mutation rate for fitness ( U ) and the average effect of a new mutation ( E [ a ]), assayed at both temperatures. In C. elegans , the microsatellite mutation rate is significantly greater at 26°C than at 18°C whereas in C. briggsae there is only a slight, non-significant increase in mutation rate at 26°C, consistent with stress-dependent mutation in C. elegans . The fitness data from both species qualitatively reinforce the microsatellite results. The fitness results of C. elegans are potentially complicated by selection but also suggest temperature-dependent mutation; the difference between the two species suggests that physiological stress plays a significant role in the mutational process.


2001 ◽  
Vol 78 (1) ◽  
pp. 41-47 ◽  
Author(s):  
CARSTEN WIUF

In this paper the fitness of the ΔF508 heterozygote is assessed and the age of the ΔF508 mutation in the cystic fibrosis locus is estimated. Data from three microsatellite loci are applied. The analysis is performed conditional on the present-day frequency of the ΔF508 mutation and based on assumptions about the demographic history of the European population and the mutation rate in the three microsatellite loci. It is shown that the data gives evidence of positive selection (up to 2–3% per ΔF508 heterozygote), but also that data could be explained by negative selection of roughly the same order of magnitude. The age of the ΔF508 mutation is subsequently estimated; it is found that the mutation is at least 580 generations old, but could be much older depending on the microsatellite mutation rate and the exact number of substitutions experienced in the history of the three microsatellite loci.


Sign in / Sign up

Export Citation Format

Share Document