Conservation of Sex-Linked Markers among Conspecific Populations of a Viviparous Skink, Niveoscincus ocellatus, Exhibiting Genetic and Temperature-Dependent Sex Determination

被引:41
作者
Hill, Peta L. [1 ]
Burridge, Christopher P. [1 ]
Ezaz, Tariq [2 ]
Wapstra, Erik [1 ]
机构
[1] Univ Tasmania, Sch Biol Sci, Sandy Bay, Tas, Australia
[2] Univ Canberra, Inst Appl Ecol, Bruce, ACT, Australia
基金
澳大利亚研究理事会;
关键词
GSD; TSD; heterogamety; population divergence; sex chromosomes; reptiles; CHROMOSOME EVOLUTION; DETERMINING SYSTEMS; OFFSPRING SEX; LIZARD; REPTILES; TRANSITIONS; REVERSAL; RATIOS; ORIGIN; ZW;
D O I
10.1093/gbe/evy042
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Sex determination systems are exceptionally diverse and have undergone multiple and independent evolutionary transitions among species, particularly reptiles. However, the mechanisms underlying these transitions have not been established. Here, we tested for differences in sex-linked markers in the only known reptile that is polymorphic for sex determination system, the spotted snow skink, Niveoscincus ocellatus, to quantify the genomic differences that have accompanied this transition. In a highland population, sex is determined genetically, whereas in a lowland population, offspring sex ratio is influenced by temperature. We found a similar number of sex-linked loci in each population, including shared loci, with genotypes consistent with male heterogamety (XY). However, population-specific linkage disequilibrium suggests greater differentiation of sex chromosomes in the highland population. Our results suggest that transitions between sex determination systems can be facilitated by subtle genetic differences.
引用
收藏
页码:1079 / 1087
页数:9
相关论文
共 73 条
[1]   Sexual Dimorphism in Body Size and the Origin of Sex-Determination Systems [J].
Adkins-Regan, Elizabeth ;
Reeve, Hudson K. .
AMERICAN NATURALIST, 2014, 183 (04) :519-536
[2]   Sex reversal and primary sex ratios in the common frog (Rana temporaria) [J].
Alho, Jussi S. ;
Matsuba, Chikako ;
Merila, Juha .
MOLECULAR ECOLOGY, 2010, 19 (09) :1763-1773
[3]  
[Anonymous], 2006, INT J COMPLEX SYST
[4]  
[Anonymous], 2017, R LANG ENV STAT COMP
[5]   Sex Determination: Why So Many Ways of Doing It? [J].
Bachtrog, Doris ;
Mank, Judith E. ;
Peichel, Catherine L. ;
Kirkpatrick, Mark ;
Otto, Sarah P. ;
Ashman, Tia-Lynn ;
Hahn, Matthew W. ;
Kitano, Jun ;
Mayrose, Itay ;
Ming, Ray ;
Perrin, Nicolas ;
Ross, Laura ;
Valenzuela, Nicole ;
Vamosi, Jana C. .
PLOS BIOLOGY, 2014, 12 (07) :1-13
[6]  
Benjamini Y, 2001, ANN STAT, V29, P1165
[7]   Extreme heterochiasmy and nascent sex chromosomes in European tree frogs [J].
Berset-Braendli, Laura ;
Jaquiery, Julie ;
Broquet, Thomas ;
Ulrich, Yuko ;
Perrin, Nicolas .
PROCEEDINGS OF THE ROYAL SOCIETY B-BIOLOGICAL SCIENCES, 2008, 275 (1642) :1577-1585
[8]   Under what conditions do climate-driven sex ratios enhance versus diminish population persistence? [J].
Boyle, Maria ;
Hone, Jim ;
Schwanz, Lisa E. ;
Georges, Arthur .
ECOLOGY AND EVOLUTION, 2014, 4 (23) :4522-4533
[9]   SEX DETERMINATION IN REPTILES [J].
BULL, JJ .
QUARTERLY REVIEW OF BIOLOGY, 1980, 55 (01) :3-21
[10]   EFFECTS OF INCUBATION-TEMPERATURE ON SEX-RATIOS IN PINE SNAKES - DIFFERENTIAL VULNERABILITY OF MALES AND FEMALES [J].
BURGER, J ;
ZAPPALORTI, RT .
AMERICAN NATURALIST, 1988, 132 (04) :492-505