Germline mutation rates and fine-scale recombination parameters in zebra finch

被引:0
作者
Prentout, Djivan [1 ]
Bykova, Daria [1 ]
Hoge, Carla [1 ,6 ]
Hooper, Daniel M. [2 ,3 ]
Mcdiarmid, Callum S. [4 ]
Wu, Felix [5 ,7 ]
Griffith, Simon C. [4 ]
de Manuel, Marc [1 ,8 ]
Przeworski, Molly [1 ,5 ]
机构
[1] Columbia Univ, Dept Biol Sci, New York, NY 10027 USA
[2] Amer Museum Nat Hist, Inst Comparat Genom, New York, NY USA
[3] Amer Museum Nat Hist, Richard Gilder Grad Sch, New York, NY USA
[4] Macquarie Univ, Sch Nat Sci, Sydney, NSW, Australia
[5] Columbia Univ, Dept Syst Biol, New York, NY 10027 USA
[6] Univ Chicago, Dept Human Genet, Chicago, IL USA
[7] Harvard Univ, Dept Organismal & Evolutionary Biol, Cambridge, MA USA
[8] Univ Barcelona, Dept Genet, Barcelona, Spain
基金
美国国家卫生研究院; 澳大利亚研究理事会;
关键词
DE-NOVO MUTATIONS; LINKAGE DISEQUILIBRIUM; MEIOTIC RECOMBINATION; GENOME ANALYSIS; POPULATIONS; DROSOPHILA; SIGNATURES; EVOLUTION; PATTERNS; PRDM9;
D O I
10.1371/journal.pgen.1011661
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Most of our understanding of the fundamental processes of mutation and recombination stems from a handful of disparate model organisms and pedigree studies of mammals, with little known about other vertebrates. To gain a broader comparative perspective, we focused on the zebra finch (Taeniopygia castanotis), which, like other birds, differs from mammals in its karyotype (which includes many micro-chromosomes), in the mechanism by which recombination is directed to the genome, and in aspects of ontogenesis. We collected genome sequences from three generation pedigrees that provide information about 80 meioses, inferring 202 single-point de novo mutations, 1,088 crossovers, and 275 non-crossovers. On that basis, we estimated a sex-averaged mutation rate of 5.0 x 10(-9) per base pair per generation, on par with mammals that have a similar generation time (similar to 2-3 years). Also as in mammals, we found a paternal germline mutation bias at later stages of gametogenesis (of 1.7:1) but no discernible difference between sexes in early development. Examining recombination patterns, we found that the sex-averaged crossover rate on macro-chromosomes is 0.93 cM/Mb, with a pronounced enrichment of crossovers near telomeres. In contrast, non-crossover rates are more uniformly distributed. On micro-chromosomes, sex-averaged crossover rates are substantially higher (3.96 cM/Mb), in accordance with crossover homeostasis, and both crossover and non-crossover events are more uniformly distributed. At a finer scale, recombination events overlap CpG islands more often than expected by chance, as expected in the absence of PRDM9. Estimates of the degree of GC-biased gene conversion (59%), the mean non-crossover conversion tract length (similar to 32 bp), and the non-crossover-to-crossover ratio (5.4:1) are all comparable to those reported in primates and mice. Therefore, properties of germline mutation and recombination resolutions remain similar over large phylogenetic distances.
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