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ReklamaPutting the brakes on centromere drive in Mimulus
Authors: Ching-Ho Chang aff001; Harmit S. Malik aff001
Authors place of work: Division of Basic Sciences, Fred Hutchinson Cancer Research Center, Seattle, Washington, United States of America aff001; Howard Hughes Medical Institute, Fred Hutchinson Cancer Research Center, Seattle, Washington, United States of America aff002
Published in the journal: Putting the brakes on centromere drive in Mimulus. PLoS Genet 17(4): e1009494. doi:10.1371/journal.pgen.1009494
Category: Perspective
doi: https://doi.org/10.1371/journal.pgen.1009494Asymmetric female meiosis in plants and animals is a battleground. Homologous chromosomes compete with each other for transmission through meiosis based on their centromeric DNA that recruits the chromosome segregation apparatus. Larger centromeres may recruit more centromeric proteins (centromere strength) and segregate into eggs more often than expected by mendelian inheritance (“centromere drive”) [1]. This subversion of female meiosis by “selfish centromeres” can be harmful and lower host fitness. Therefore, suppressors of centromere drive are predicted to arise, especially in centromeric proteins like CenH3/CENP-A. There is ample support for the first step of centromere drive [2–4], with one of the best demonstrations coming from studies in Mimulus monkeyflowers, in which a centromeric variant locus (D) undergoes centromere drive in interspecies and intraspecies crosses [2,5]. However, evidence of the second step of the model, i.e., suppression of centromere drive by centromeric proteins, remains elusive. A new study by Finseth and colleagues [6] dates the evolutionary origin of the D centromere to within the past 1,500 years of Mimulus guttatus evolution. It also reveals genetic variation in susceptibility to drive within M. guttatus, including a modifier of drive that maps to a CenH3 paralog, which adaptively evolved after the driving D centromere.
A previous study had associated expanded centromere-specific repeats within D with its drive ability [2]. In the new study, Finseth and colleagues showed that half of Chromosome 11 (>12 Mb) is genetically linked to the selfish centromere on D (MDL11). Only 9 unique SNPs have accumulated in approximately 256,000 nucleotides of coding sequences across 13 distinct D lines. Based on this high similarity, the authors conclude that D arose within the last 1,000 to 1,500 years in M. guttatus after experiencing a recent selective sweep. In addition to an expanded array of repetitive satellite DNA, the MDL11 locus spans >387 protein-coding genes, including 45 genes unique to D chromosomes. It is likely that both centromeric repeats and linked genes contribute to drive (Fig 1).
Fig. 1. Three inferred stages of centromere drive and suppression in Mimulus guttatus. In the first stage (“Centromere drive”), a chromosome with non-driving centromeres (D−) acquires structural mutations, such as an inversion, and expansion of a centromeric satellite, which confers a transmission advantage in asymmetric female meiosis. Subsequently, it accumulates additional genes that enhance the drive, resulting in D. Due to the ensuing costs to fertility, D chromosomes cannot fix in the population. In this scenario, suppressor alleles will arise in the second stage of this process (“Drive suppression”). One such suppressor allele may have arisen from a single amino acid variant of CenH3A. This allele underwent a selective sweep because it restored fitness in M. guttatus populations containing D chromosomes. Both driver and suppressor alleles are expected to coexist in populations due to frequency-dependent selection. Eventually, as suppressor alleles fix in populations, they negate the meiotic advantage of D chromosomes, which will then be lost and replaced by D− chromosomes in the third stage of the process (“Loss of drive”), resulting in fixed changes in CenH3A and potentially centromeric satellites. M. guttatus D drives strongly against its counterpart centromere (d) from the self-fertilizing sister species Mimulus nasutus (D:d = >98 : 2 [7]), and it drives weakly against intraspecies D− (D:D− = 58 : 42 [2]). A trade-off between its drive ability and its cost to fertility maintains D at a frequency of 30% to 45% in M. guttatus populations [2,5]. Finseth and colleagues explored whether other genetic loci could influence the strength of D drive. Genetic loci linked to the drive locus should accumulate enhancers of drive, whereas unlinked genomic loci should accumulate suppressors of drive to restore genome fitness [8–10].
To identify modifiers of drive, Finseth and colleagues adopted an ingenious genetic mapping strategy. They tested drive of M. guttatus D against M. nasutus d or M. guttatus D− in distinct genetic backgrounds comprised of different genomic combinations of both species. Consistent with expectations, D drive against M. nasutus d was stronger than against M. guttatus D−, with the strongest determinants of drive strength mapping to a closely linked region of MDL11. However, other genetic loci in the “mixed” genetic background also affected the strength of D drive. For example, in hybrid backgrounds, D/d drive was slightly weakened from 98 : 2 to 93 : 7, whereas D/D− drive was enhanced from 58 : 42 to 73 : 27. This meant that other genetic loci mapping outside of MDL11 in some M. guttatus genomes but absent in M. nasutus could suppress drive strength.
Further quantitative trait loci (QTL) mapping revealed 2 unlinked regions on Chromosome 9 and 14 associated with drive strength. The Chromosome 14 QTL locus center encodes one paralog of CenH3 (named CenH3A), one of the leading candidates originally proposed as centromere drive suppressors [11]. Indeed, stratifying the data on CenH3A genotypes alone reveals a substantial contribution of this QTL on drive strength. Finseth and colleagues highlight a single segregating amino acid polymorphism in CenH3A that may contribute to its drive suppression properties. More precise genome editing will be required to directly test this prediction. Other analyses revealed that the CenH3A locus also experienced a recent selective sweep within the last 1,000 years after the selfish D centromere arose in M. guttatus populations [11]. For many drive systems, the ensuing cost is not necessarily caused by drive itself, but rather a result of linked deleterious mutations that accumulate due to suppression of recombination [10,12]. The finding that a CenH3A variant was positively selected in Mimulus populations exposed to centromere drive suggests that suppressing centromere drive is sufficient to restore fitness. These results provide strong support for a role of CenH3 proteins in affecting the strength of centromere drive.
The study also highlights the challenges in tracking drive amidst variable suppression in natural populations. Such suppressors could evolve contemporaneously with drive in situations like Mimulus, where the D centromere cannot become fixed in the population due to fitness costs. Alternatively, these suppressors could evolve subsequent to centromere drive going to fixation, as long as the costs of expanded centromeres remain manifest. In that respect, Mimulus is even more valuable as a model because it may have captured drive “in the act” where drive and suppressor alleles coexist and vie for supremacy in the same populations.
Cell biological studies of centromere drive in mice and Drosophila provide valuable clues to the molecular mechanism by which CenH3A alleles might suppress drive in the Mimulus system. For example, expansion of centromeric repeat satellites and increased recruitment of CenH3 proteins are directly associated with drive in mice [3]. By analogy, the driving D centromere might recruit more CenH3A relative to D− or d. Conversely, CenH3A proteins from M. guttatus might have been selected to disfavor binding to D, thereby suppressing centromere drive. Indeed, centromere-binding proteins with low centromeric affinity can weaken meiotic drive in mice [13]. The relative affinity of Mimulus CenH3A proteins for satellites between competing centromeres could explain why this new study found no straightforward hierarchy in CenH3A allele combinations and drive suppression in the new study. This difference could be the result of relative affinity differences between CenH3A variants for satellite DNA. Alternatively, this could be a result of protein–protein interactions. Indeed, Finseth and colleagues found that the CenH3 chaperone NASPSim3 [14] is closely linked to the driving D centromere. Allelic differences in NASPSim3 could directly affect chaperone:CenH3A binding affinity and ultimately CenH3A deposition, like they do in Drosophila [15]. Some of these predictions will be testable in future experiments via cytological localization and biochemical affinity tests of the various CenH3A variants. Such experiments will establish the Mimulus system both as a premier ecological as well as cell biological model of centromere drive.
Zdroje
1. Henikoff S, Ahmad K, Malik HS. The centromere paradox: stable inheritance with rapidly evolving DNA. Science. 2001;293(5532):1098–102. Epub 2001/08/11. doi: 10.1126/science.1062939 11498581.
2. Fishman L, Saunders A. Centromere-associated female meiotic drive entails male fitness costs in monkeyflowers. Science. 2008;322(5907):1559–62. Epub 2008/12/06. doi: 10.1126/science.1161406 19056989.
3. Iwata-Otsubo A, Dawicki-McKenna JM, Akera T, Falk SJ, Chmatal L, Yang K, et al. Expanded Satellite Repeats Amplify a Discrete CENP-A Nucleosome Assembly Site on Chromosomes that Drive in Female Meiosis. Curr Biol. 2017;27(15):2365–73 e8. Epub 2017/08/02. doi: 10.1016/j.cub.2017.06.069 28756949; PubMed Central PMCID: PMC5567862.
4. Chmatal L, Gabriel SI, Mitsainas GP, Martinez-Vargas J, Ventura J, Searle JB, et al. Centromere strength provides the cell biological basis for meiotic drive and karyotype evolution in mice. Curr Biol. 2014;24(19):2295–300. Epub 2014/09/23. doi: 10.1016/j.cub.2014.08.017 25242031; PubMed Central PMCID: PMC4189972.
5. Fishman L, Kelly JK. Centromere-associated meiotic drive and female fitness variation in Mimulus. Evolution. 2015;69(5):1208–18. Epub 2015/04/16. doi: 10.1111/evo.12661 25873401; PubMed Central PMCID: PMC5958614.
6. Finseth FR, Nelson TC, Fishman L. Selfish chromosomal drive shapes recent centromeric histone evolution in monkeyflowers. PLoS Genet. Forthcoming [2021].
7. Fishman L, Willis JH. A novel meiotic drive locus almost completely distorts segregation in mimulus (monkeyflower) hybrids. Genetics. 2005;169(1):347–53. Epub 2004/10/07. doi: 10.1534/genetics.104.032789 15466426; PubMed Central PMCID: PMC1448871.
8. Hartl DL. Modifier theory and meiotic drive. Theor Popul Biol. 1975;7(2):168–74. Epub 1975/04/01. doi: 10.1016/0040-5809(75)90012-x 1145501.
9. Courret C, Chang CH, Wei KH, Montchamp-Moreau C, Larracuente AM. Meiotic drive mechanisms: lessons from Drosophila. Proc Biol Sci. 2019;286(1913):20191430. Epub 2019/10/24. doi: 10.1098/rspb.2019.1430 31640520; PubMed Central PMCID: PMC6834043.
10. Larracuente AM, Presgraves DC. The selfish Segregation Distorter gene complex of Drosophila melanogaster. Genetics. 2012;192(1):33–53. Epub 2012/09/12. doi: 10.1534/genetics.112.141390 22964836; PubMed Central PMCID: PMC3430544.
11. Finseth FR, Dong Y, Saunders A, Fishman L. Duplication and Adaptive Evolution of a Key Centromeric Protein in Mimulus, a Genus with Female Meiotic Drive. Mol Biol Evol. 2015;32(10):2694–706. Epub 2015/06/25. doi: 10.1093/molbev/msv145 26104011.
12. Hartl DL. Complementation analysis of male fertility among the segregation distorter chromosomes of Drosophila melanogaster. Genetics. 1973;73(4):613–29. Epub 1973/04/01. 4197166; PubMed Central PMCID: PMC1212918.
13. Kumon T, Ma J, Stefanik D, Nordgren EC, Akins RB, Kim J, et al. Centromere drive and suppression by parallel pathways for recruiting microtubule destabilizers. biorXiv. 2020. doi: 10.1101/2020.11.26.400515
14. Le Goff S, Keceli BN, Jerabkova H, Heckmann S, Rutten T, Cotterell S, et al. The H3 histone chaperone NASP(SIM3) escorts CenH3 in Arabidopsis. Plant J. 2020;101(1):71–86. Epub 2019/08/30. doi: 10.1111/tpj.14518 31463991.
15. Rosin L, Mellone BG. Co-evolving CENP-A and CAL1 Domains Mediate Centromeric CENP-A Deposition across Drosophila Species. Dev Cell. 2016;37(2):136–47. Epub 2016/04/20. doi: 10.1016/j.devcel.2016.03.021 27093083; PubMed Central PMCID: PMC4861639.
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