scholarly journals Impact of deleterious mutations, sexually antagonistic selection, and mode of recombination suppression on transitions between male and female heterogamety

Heredity ◽  
2019 ◽  
Vol 123 (3) ◽  
pp. 419-428 ◽  
Author(s):  
Paul A. Saunders ◽  
Samuel Neuenschwander ◽  
Nicolas Perrin
2018 ◽  
Author(s):  
Paul A. Saunders ◽  
Samuel Neuenschwander ◽  
Nicolas Perrin

AbstractDeleterious mutations accumulating on non-recombining Y chromosomes can drive XY to XY turnovers, but are thought to prevent XY to ZW turnovers, because the latter require fixation of the ancestral Y. Using individual-based simulations, we explored whether and how a dominant W allele can spread in a young XY system that gradually accumulates deleterious mutations. We also investigated how sexually antagonistic (SA) polymorphism on the ancestral sex chromosomes, and the mechanism controlling X-Y recombination suppression affect these transitions. In contrast with XY to XY turnovers, XY to ZW turnovers cannot be favored by Y chromosome mutation load. If the arrest of X-Y recombination depends on genotypic sex, transitions are strongly hindered by deleterious mutations, and totally suppressed by very small SA cost, because deleterious mutations and female-detrimental SA alleles would have to fix with the Y. If, however, the arrest of X-Y recombination depends on phenotypic sex, X and Y recombine in XY ZW females, allowing for the purge of Y-linked deleterious mutations and loss of the SA polymorphism, causing XY to ZW turnovers to occur at a neutral rate. We generalize our results to other types of turnovers (e.g., triggered by non-dominant sex-determining mutations) and discuss their empirical relevance.


2016 ◽  
Vol 16 (1) ◽  
Author(s):  
David Berger ◽  
Tao You ◽  
Maravillas R. Minano ◽  
Karl Grieshop ◽  
Martin I. Lind ◽  
...  

Genetics ◽  
2010 ◽  
Vol 186 (2) ◽  
pp. 629-645 ◽  
Author(s):  
G. Sander van Doorn ◽  
Mark Kirkpatrick

Genetics ◽  
2017 ◽  
pp. genetics.300151.2017 ◽  
Author(s):  
Carl Veller ◽  
Pavitra Muralidhar ◽  
George W. A. Constable ◽  
Martin A. Nowak

Evolution ◽  
2006 ◽  
Vol 60 (10) ◽  
pp. 2168-2181 ◽  
Author(s):  
Matthew R. Robinson ◽  
Jill G. Pilkington ◽  
Tim H. Clutton-Brock ◽  
Josephine M. Pemberton ◽  
Loeske E.B. Kruuk

2021 ◽  
Vol 376 (1833) ◽  
pp. 20200102 ◽  
Author(s):  
Michail Rovatsos ◽  
Tony Gamble ◽  
Stuart V. Nielsen ◽  
Arthur Georges ◽  
Tariq Ezaz ◽  
...  

Differentiation of sex chromosomes is thought to have evolved with cessation of recombination and subsequent loss of genes from the degenerated partner (Y and W) of sex chromosomes, which in turn leads to imbalance of gene dosage between sexes. Based on work with traditional model species, theory suggests that unequal gene copy numbers lead to the evolution of mechanisms to counter this imbalance. Dosage compensation, or at least achieving dosage balance in expression of sex-linked genes between sexes, has largely been documented in lineages with male heterogamety (XX/XY sex determination), while ZZ/ZW systems are assumed to be usually associated with the lack of chromosome-wide gene dose regulatory mechanisms. Here, we document that although the pygopodid geckos evolved male heterogamety with a degenerated Y chromosome 32–72 Ma, one species in particular, Burton's legless lizard ( Lialis burtonis ), does not possess dosage balance in the expression of genes in its X-specific region. We summarize studies on gene dose regulatory mechanisms in animals and conclude that there is in them no significant dichotomy between male and female heterogamety. We speculate that gene dose regulatory mechanisms are likely to be related to the general mechanisms of sex determination instead of type of heterogamety. This article is part of the theme issue ‘Challenging the paradigm in sex chromosome evolution: empirical and theoretical insights with a focus on vertebrates (Part II)’.


2018 ◽  
Vol 32 (12) ◽  
pp. 2678-2688 ◽  
Author(s):  
Zbyszek Boratyński ◽  
Esa Koskela ◽  
Tapio Mappes ◽  
Suzanne C. Mills ◽  
Mikael Mokkonen

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