2018
DOI: 10.1186/s12864-018-4823-6
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Distinct sperm nucleus behaviors between genotypic and temperature-dependent sex determination males are associated with replication and expression-related pathways in a gynogenetic fish

Abstract: BackgroundCoexistence and transition of diverse sex determination strategies have been revealed in some ectothermic species, but the variation between males caused by different sex determination strategies and the underlying mechanism remain unclear. Here, we used the gynogenetic gibel carp (Carassius gibelio) with both genotypic sex determination (GSD) and temperature-dependent sex determination (TSD) strategies to illustrate this issue.ResultsWe found out that males of GSD and TSD in gibel carp had similar m… Show more

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Cited by 25 publications
(20 citation statements)
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“…Gibel carp clone F was raised and collected from the National Aquatic Biological Resource Center, NABRC. Artificial fertilization, larval hatching, and fry nursing were performed as previously described ( Zhu et al. 2018 ).…”
Section: Methodsmentioning
confidence: 99%
“…Gibel carp clone F was raised and collected from the National Aquatic Biological Resource Center, NABRC. Artificial fertilization, larval hatching, and fry nursing were performed as previously described ( Zhu et al. 2018 ).…”
Section: Methodsmentioning
confidence: 99%
“…Genetic mechanisms that determine sex in animals are highly diverse (Li & Gui, ) and vertebrates commonly have distinct sex determination systems with either male heterogamy (XX/XY), or female heterogamy (ZZ/ZW) (Devlin & Nagahama, ; Mei & Gui, ). Fish sex determination mechanism ranges from simple environmental to complex genetic mechanisms, even these two mechanisms can coexist in one species (Li et al, ; Mittwoch, ; Zhu et al, ). The study of sex determination in fish provides a new perspective for understanding genetic mechanism of sex determination and the origin and evolution of sex chromosomes (Ellegren, ; Mei & Gui, ).…”
Section: Introductionmentioning
confidence: 99%
“…Liver tissues were cut in sections and fixed in 4% paraformaldehyde (PFA) overnight at 4 °C, and subsequently embedded in paraffin. One part of sections was stained with hematoxylin & eosin (HE) (Beyotime, Suzhou) and performed as previously described [ 75 , 76 ]. The Carl-Zeiss microscopy (Analytical & Testing Center, IHB, CAS) was used for histological structure observation and photomicrographs.…”
Section: Methodsmentioning
confidence: 99%