Frequent Paternal Mitochondrial Inheritance and Rapid Haplotype

Frequent Paternal Mitochondrial Inheritance and Rapid Haplotype

bioRxiv preprint doi: https://doi.org/10.1101/2021.05.10.443310; this version posted May 11, 2021. The copyright holder for this preprint (which was not certified by peer review) is the author/funder. All rights reserved. No reuse allowed without permission. 1 Title: Frequent paternal mitochondrial inheritance and rapid haplotype frequency shifts in 2 copepod hybrids 3 Running title: Uncommon paternal mtDNA haplotypes frequently found in copepod hybrids 4 Authors: Jeeyun Lee ([email protected]), Christopher S. Willett ([email protected]) 5 Current affiliation for both authors and institution at which the research was conducted: 6 University of North Carolina at Chapel Hill, Chapel Hill, NC 27599 7 1 bioRxiv preprint doi: https://doi.org/10.1101/2021.05.10.443310; this version posted May 11, 2021. The copyright holder for this preprint (which was not certified by peer review) is the author/funder. All rights reserved. No reuse allowed without permission. 8 ABSTRACT 9 Mitochondria are assumed to be maternally inherited in most animal species, and this 10 foundational concept has fostered advances in phylogenetics, conservation, and population 11 genetics. Like other animals, mitochondria were thought to be solely maternally inherited in the 12 marine copepod Tigriopus californicus, which has served as a useful model for studying 13 mitonuclear interactions, hybrid breakdown, and environmental tolerance. However, we present 14 PCR, Sanger sequencing, and Illumina Nextera sequencing evidence that extensive paternal 15 mitochondrial DNA (mtDNA) transmission is occurring in inter-population hybrids of T. 16 californicus. PCR on four types of crosses between three populations (total sample size of 376 17 F1 individuals) with 20% genome-wide mitochondrial divergence showed 2% to 59% of F1 18 hybrids with both paternal and maternal mtDNA, where low and high paternal leakage values 19 were found in different cross directions of the same population pairs. Sequencing methods 20 further verified nucleotide similarities between F1 mtDNA and paternal mtDNA sequences. 21 Interestingly, the paternal mtDNA in F1s from some crosses inherited haplotypes that were 22 uncommon in the paternal population. Compared to some previous research on paternal leakage, 23 we employed more rigorous methods to rule out contamination and false detection of paternal 24 mtDNA due to non-functional nuclear mitochondrial DNA fragments. Our results raise the 25 potential that other animal systems thought to only inherit maternal mitochondria may also have 26 paternal leakage, which would then affect the interpretation of past and future population 27 genetics or phylogenetic studies that rely on mitochondria as uniparental markers. 28 29 30 Key words: 31 mitochondria, paternal leakage, marine invertebrate, nuclear mitochondrial DNA fragment 32 (NUMT), mitonuclear incompatibility 33 2 bioRxiv preprint doi: https://doi.org/10.1101/2021.05.10.443310; this version posted May 11, 2021. The copyright holder for this preprint (which was not certified by peer review) is the author/funder. All rights reserved. No reuse allowed without permission. 34 INTRODUCTION 35 In most animal taxa, maternal mitochondrial inheritance is widely accepted as the norm, 36 as deviations from this mode of inheritance could have significant evolutionary consequences. If 37 paternal mitochondrial DNA (mtDNA) were also transmitted, there could be lethal genomic 38 conflict due to mitochondrial competition (Hurst and Hamilton 1992; Hastings 1992), zygotes 39 may receive sperm mtDNA that is damaged from deleterious effects associated with heavy 40 respiration (Allen 1996), or there could be an increased propagation of deleterious mitochondrial 41 mutations (Xu 2005). To prevent these potential deleterious effects of paternal mtDNA, animals 42 have evolved various mechanisms to exclude paternal mitochondria, such as ubiquitination or 43 degradation of sperm mitochondria in primates (Sutovsky et al. 1999; Sutovsky et al. 2000; 44 Thompson et al. 2003) and fruit flies (Reilly and Thomas Jr. 1980; DeLuca and O'Farrell 2012). 45 Despite mechanisms to ensure maternal inheritance of mtDNA, reports of paternal 46 mtDNA in the offspring - termed paternal leakage - have been accumulating in hybrids of 47 various animal species. A subset of examples includes paternal leakage in heterospecific or 48 conspecific hybrids of fruit flies (Kondo et al. 1990; Matsuura et al. 1991; Sherengul et al. 2006; 49 Dokianakis and Ladoukakis 2014), mice (Gyllensten et al. 1991; Shitara et al. 1998), periodical 50 cicadas (Fontaine et al. 2007), ticks (Mastrantonio et al. 2019), and nematodes (Hoolahan et al. 51 2011; Ross et al. 2016). There are several bivalve species in which mitochondria are doubly 52 inherited from both parents as a norm (Zouros et al. 1994; Gusman et al. 2016). While possible 53 artifacts have not been completely ruled out in all of these latter cases, evidence was consistent 54 with at least some paternal leakage in experimental or natural (Matsuura et al. 1991; 55 Mastrantonio et al. 2019) hybrid populations, along with continued maternal transmission of 56 mtDNA. Some of these studies additionally tested and showed that leaked paternal mtDNA 57 could proliferate to later developmental stages (Sherengul et al. 2006; Fontaine et al. 2007) and 58 persist for multiple generations (Gyllensten et al. 1991). This phenomenon likely has significant 59 consequences for how we understand mitochondria and its applications, because the assumption 60 that mitochondria are only inherited maternally in animals has been the basis for using mtDNA 61 as important molecular markers in phylogenetic inference (Avise et al. 1987), population 62 genetics (Wilson et al. 1985), and conservation (Moritz 1994). Additionally, the presence of 63 paternal mtDNA would impact estimates of genetic diversity and gene flow (Takahata and 64 Maruyama 1981; Chapman et al. 1982; Hoolahan et al. 2011). 3 bioRxiv preprint doi: https://doi.org/10.1101/2021.05.10.443310; this version posted May 11, 2021. The copyright holder for this preprint (which was not certified by peer review) is the author/funder. All rights reserved. No reuse allowed without permission. 65 The mechanism of frequent paternal leakage and the effects of the phenomena on hybrid 66 fitness are presently unknown. It is speculated that paternal leakage is more commonly found in 67 hybrids compared to pure populations because hybridization may disrupt mechanisms that 68 eliminate paternal mtDNA (White et al. 2008), or because it is easier to experimentally detect 69 paternal mtDNA that is genetically different from the maternal mtDNA (Kaneda et al. 1995; 70 Shitara et al. 1998; Sutovsky et al. 2000). Literature on mitochondrial heteroplasmy, where 71 multiple mitochondrial haplotypes are present in a cell, suggest that certain haplotypes are able 72 to increase in abundance rapidly (Yoneda et al. 1992; Blok et al. 1997; White et al. 1999; 73 Brandstätter et al. 2004), but whether this contributes to increased detection of paternal leakage 74 in hybrids has not been explored. Whether specific paternal mtDNA haplotypes and frequent 75 paternal leakage affect hybrid fitness is also unknown. In several species ranging from seed 76 beetles to centrarchid fishes with highly coadapted mitochondrial and nuclear genomes (Burton 77 et al. 2013), hybrids exhibit decreased fitness due to a breakdown in mito-nuclear coadaptation 78 (Burton and Barreto 2012; Wolff et al. 2014). Paternal leakage may have complicated effects on 79 hybrid fitness in such systems with mitonuclear coadaptation: inherited paternal mtDNA may be 80 beneficial if they interact with the paternal nuclear DNA to restore coadpated functions, or 81 alternatively be harmful if they compete with maternal mtDNA and cause genomic conflict 82 (Hastings 1992; Hurst and Hamilton 1992). 83 Here we report substantial paternal mtDNA inheritance in inter-population hybrids of the 84 marine copepod Tigriopus californicus. T. californicus is a rocky intertidal copepod with many 85 genetically distinct populations along the western coast of North America (Burton 1997; 86 Edmands 2001; Willett and Ladner 2009). This species has previously been thought to solely 87 inherit maternal mitochondria (Burton and Lee 1994), and has been an important model to study 88 the role of mtDNA in inter-population hybrid breakdown (Burton 1990; Edmands 1999; Ellison 89 and Burton 2008; Burton and Barreto 2012; Healy and Burton 2020). MtDNA sequences have 90 diverged in allopatry among populations of T. californicus, and several lines of evidence suggest 91 that the mitochondrial and nuclear genomes within each population have coevolved (Rawson and 92 Burton 2002; Barreto and Burton 2013; Barreto et al. 2018). When different populations mate, 93 the hybrids may no longer have a complete set of co-adapted mitochondrial and nuclear products 94 from each parent population. This results in suboptimal cellular functions or lowered fitness, 95 called "mitonuclear incompatibility" (Ellison and Burton 2008; Barreto et al. 2015). Since 4 bioRxiv preprint doi: https://doi.org/10.1101/2021.05.10.443310; this version posted May 11, 2021. The copyright holder for this preprint (which was not certified by peer review) is the author/funder. All rights reserved. No reuse allowed without permission. 96 mitochondrial genes greatly influence the fitness of T. californicus hybrids, the presence of 97 paternal mtDNA presents novel evolutionary repercussions to consider,

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