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Haploid selection within a single ejaculate increases offspring fitness

Alavioon, Ghazal (author)
Uppsala universitet,Evolutionsbiologi
Hotzy, Cosima (author)
Uppsala universitet,Evolutionsbiologi
Nakhro, Khriezhanuo (author)
Uppsala universitet,Evolutionsbiologi
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Rudolf, Sandra (author)
Uppsala universitet,Evolutionsbiologi
Scofield, Douglas, 1966- (author)
Uppsala universitet,Evolutionsbiologi
Zajitschek, Susanne (author)
Uppsala universitet,Evolutionsbiologi,Spanish Natl Res Council, Donana Biol Stn, Seville 41092, Spain
Maklakov, Alex A (author)
Uppsala universitet,Zooekologi,Univ East Anglia, Sch Biol Sci, Norwich NR4 7TJ, Norfolk, England
Immler, Simone (author)
Uppsala universitet,Evolutionsbiologi,Univ East Anglia, Sch Biol Sci, Norwich NR4 7TJ, Norfolk, England
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 (creator_code:org_t)
2017-07-11
2017
English.
In: Proceedings of the National Academy of Sciences of the United States of America. - : Proceedings of the National Academy of Sciences. - 0027-8424 .- 1091-6490. ; :30, s. 8053-8058
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • An inescapable consequence of sex in eukaryotes is the evolution of a biphasic life cycle with alternating diploid and haploid phases. The occurrence of selection during the haploid phase can have far-reaching consequences for fundamental evolutionary processes including the rate of adaptation, the extent of inbreeding depression, and the load of deleterious mutations, as well as for applied research into fertilization technology. Although haploid selection is well established in plants, current dogma assumes that in animals, intact fertile sperm within a single ejaculate are equivalent at siring viable offspring. Using the zebrafish Danio rerio, we show that selection on phenotypic variation among intact fertile sperm within an ejaculate affects offspring fitness. Longer-lived sperm sired embryos with increased survival and a reduced number of apoptotic cells, and adult male offspring exhibited higher fitness. The effect on embryo viability was carried over into the second generation without further selection and was equally strong in both sexes. Sperm pools selected by motile phenotypes differed genetically at numerous sites throughout the genome. Our findings clearly link within-ejaculate variation in sperm phenotype to offspring fitness and sperm genotype in a vertebrate and have major implications for adaptive evolution.

Subject headings

NATURVETENSKAP  -- Biologi -- Evolutionsbiologi (hsv//swe)
NATURAL SCIENCES  -- Biological Sciences -- Evolutionary Biology (hsv//eng)

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