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Strict adherence to Mendel’s First Law across a large sample of human sperm genomes

View ORCID ProfileSara A. Carioscia, View ORCID ProfileKathryn J. Weaver, View ORCID ProfileAndrew N. Bortvin, View ORCID ProfileDaniel Ariad, View ORCID ProfileAvery Davis Bell, View ORCID ProfileRajiv C. McCoy
doi: https://doi.org/10.1101/2021.11.19.469261
Sara A. Carioscia
1Department of Biology, Johns Hopkins University, Baltimore, MD, 21218, USA
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Kathryn J. Weaver
1Department of Biology, Johns Hopkins University, Baltimore, MD, 21218, USA
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Andrew N. Bortvin
1Department of Biology, Johns Hopkins University, Baltimore, MD, 21218, USA
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Daniel Ariad
1Department of Biology, Johns Hopkins University, Baltimore, MD, 21218, USA
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Avery Davis Bell
2School of Biological Sciences, Georgia Institute of Technology, Atlanta, GA, 30332, USA
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Rajiv C. McCoy
1Department of Biology, Johns Hopkins University, Baltimore, MD, 21218, USA
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  • For correspondence: rajiv.mccoy@jhu.edu
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Abstract

Mendel’s Law of Segregation states that the offspring of a diploid, heterozygous parent will inherit either allele with equal probability. While the vast majority of loci adhere to this rule, research in model and non-model organisms has uncovered numerous exceptions whereby “selfish” alleles are disproportionately transmitted to the next generation. Evidence of such “transmission distortion” (TD) in humans remains equivocal in part because scans of human pedigrees have been under-powered to detect small effects. Recently published single-cell sequencing data from individual human sperm (n = 41,189; 969-3,377 cells from each of 25 donors) offer an opportunity to revisit this question with unprecedented statistical power, but require new methods tailored to extremely low-coverage data (∼0.01 × per cell). To this end, we developed a method, named rhapsodi, that leverages sparse gamete genotype data to phase the diploid genomes of the donor individuals, impute missing gamete genotypes, and discover meiotic recombination breakpoints, benchmarking its performance across a wide range of study designs. After applying rhapsodi to the sperm sequencing data, we then scanned the gametes for evidence of TD. Our results exhibited close concordance with binomial expectations under balanced transmission, in contrast to tenuous signals of TD that were previously reported in pedigree-based studies. Together, our work excludes the existence of even weak TD in this sample, while offering a powerful quantitative framework for testing this and related hypotheses in other cohorts and study systems.

Competing Interest Statement

A.D.B. is an inventor on a US Patent Application (US20210230667A1, applicant: President and Fellows of Harvard College) relating to the Sperm-seq single-cell sequencing method. A.D.B. was an occasional consultant for Ohana Biosciences between October 2019 and March 2020.

Footnotes

  • Fig. 5 has been updated to include a larger number of simulations. The description of the methods accompanying Fig. S11 have been expanded. Fig. S13 (Power Analysis) has been updated to include multiple testing correction. Several minor typos corrected throughout.

  • https://github.com/mccoy-lab/rhapsodi

  • https://github.com/mccoy-lab/transmission-distortion

Copyright 
The copyright holder for this preprint is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under a CC-BY 4.0 International license.
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Posted January 09, 2022.
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Strict adherence to Mendel’s First Law across a large sample of human sperm genomes
Sara A. Carioscia, Kathryn J. Weaver, Andrew N. Bortvin, Daniel Ariad, Avery Davis Bell, Rajiv C. McCoy
bioRxiv 2021.11.19.469261; doi: https://doi.org/10.1101/2021.11.19.469261
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Strict adherence to Mendel’s First Law across a large sample of human sperm genomes
Sara A. Carioscia, Kathryn J. Weaver, Andrew N. Bortvin, Daniel Ariad, Avery Davis Bell, Rajiv C. McCoy
bioRxiv 2021.11.19.469261; doi: https://doi.org/10.1101/2021.11.19.469261

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