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EDITORIAL article

Front. Genet., 23 January 2023
Sec. Livestock Genomics
This article is part of the Research Topic Reproduction in Aquatic Animals View all 8 articles

Editorial: Reproduction in aquatic animals

Shubo Jin,Shubo Jin1,2Lingbo Ma
Lingbo Ma3*Hongtuo Fu,
Hongtuo Fu1,2*
  • 1Wuxi Fisheries College, Nanjing Agricultural University, Wuxi, China
  • 2Key Laboratory of Freshwater Fisheries and Germplasm Resources Utilization, Ministry of Agriculture and Rural Affairs, Freshwater Fisheries Research Center, Chinese Academy of Fishery Sciences, Wuxi, China
  • 3Key Laboratory of Marine and Estuarine Fisheries, Ministry of Agriculture and Rural Affairs, East China Sea Fisheries Research Institute, Chinese Academy of Fishery Sciences, Shanghai, China

Editorial on the Research Topic
Reproduction in aquatic animals

Reproduction exhibits great diversity in aquatic animals. The maturation of gonads takes a long time in some aquatic animals (ie., Amur sturgeon, Acipenser schrenckii) (Qu et al., 2010), while some aquatic animals take only 1–2 months to reach gonad maturation (ie., Oriental river prawn, Macrobrachium nipponense) (Jin et al., 2016). Slow gonad development can prolong the reproductive cycle, while rapid gonad development leads to mixing multigenerational populations in a pond. There is also great variation among aquatic animals in egg-laying ability and hatchability. Reproduction is a complicated process consisting of gonad maturation, molting (crustaceans), mating, embryonic development, larval rearing, and so on. At the same time, reproduction is vulnerable to external factors such as diet (Hu et al., 2009), temperature and light (Om et al., 2015; Wedekind, 2017). Therefore, comprehensive research on the genetic basis and underlying mechanisms of aquatic animal reproduction are essential for successful aquaculture seedling production. In recent decades, significant progress has been made in understanding aquatic animal reproduction. Genes, regulatory mechanisms, and externalities associated with reproduction continue to be deciphered. A better understanding of reproduction is very valuable for the development of techniques to control the reproductive process of aquatic animals. The article contents of this Research Topic are shown in Figure 1.

FIGURE 1
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FIGURE 1. The main article contents of this Research Topic

1 Identification of the effects of steroid hormone on gonad development

Steroid hormones can regulate the process of sex determination, gonadal development, and growth in aquatic species via interactions with endocrine factors (Couch et al., 1987). The effects of luteinizing hormone releasing hormone A2 (LH-A2) on gonad development in juvenile A. schrenckii were determined through performing the transcriptome profiling analysis, treated at a dose of 3 μg/kg. The treatment of LH-A2 resulted in the gradual increase of 17β-estradiol levels, while inhibited the secretion of testosterone. Transcriptome profiling analysis revealed that signal transduction, global and overview maps, immune system, endocrine system and lipid metabolism were the main enriched metabolic pathways of differentially expressed genes (DEGs) in both the pituitary and gonads, predicting these metabolic pathways and the DEGs enriched in these metabolic pathways play essential roles in the regulation of gonad development in A. schrenckii (Lv et al.).

This article analysed the possibilities of 17α-methyltestosterone (17-MT) and 17β-estradiol (E2) to replace the pituitary extract (PE) in European silver eels (AnguillaAnguilla L.) industry. 17-MT was used as potent androgen to activate the androgen receptor, while E2 can be considered as an inducer of vitellogenesis to shorten the duration of PE treatment. This article identified that 17-MT + E2 group has more significantly regulatory effects on eye index and gonadosomatic index than the other treated groups (17-MT group, E2 group, control group), and the expression of follicle-stimulating hormone receptor in 17 MT + E2 group was 44-folder higher than that of control group, indicating the combination can improve oocyte quality, leading to the production of more vital larvae in A. anguilla aquaculture (Palstra et al.).

2 Identification of the abnormalities in the spermatozoa of 3nDTCC

The cytological structural differences of spermatozoa ultrastructure between diploid red crucian carp and triploid gynogenetic crucian carp (Carassius auratus) (3nDTCC) were analysed. Furthermore, the molecular expression characteristics of the spermatozoa packaging process in 3nDTCC were also determined through measuring the mRNA expression of centriole-related genes, including cep57, cetn1, rootletin, and nek2. This article identified the abnormal head structure of spermatozoa, and abnormal expression of centriole-related genes in 3nDTCC, affecting the motility of spermatozoa, and the normally genetic composition of the gynogenesis offspring (He et al.).

3 Identification of reproduction-related genes

Identification of reproduction-related genes plays essential roles in the establishment of artificial technique to regulate the reproductive process in aquatic animals. Seven Dmrt (Doublesex and Mab-3 related transcription factor) genes were identified from the genome of the channel catfish (Ictalurus punctatus). These Dmrt genes included Dmrt1, Dmrt2a, Dmrt2b, Dmrt3, Dmrt4, Dmrt5 and Dmrt6, and distributed unevenly across five chromosomes. qPCR analysis in different tissues and treatment with 17β-estradiol revealed that Dmrt1 and Dmrt6 has potential functions in the regulation of testis differentiation/development, while Dmrt2b and Dmrt5 are involved in the relation of ovary development in this species (Xu et al.).

In invertebrates, the ovaries and hepatopancreas were sampling from the Chinese mitten crab (Eriocheir sinensis) during ovarian stages I -Ⅲ, and performed the transcriptome profiling analysis, in order to select the candidate genes and metabolic pathways, involved in the ovarian development. Twenty-five genes and several pathways were mainly predicted to regulate the process of oogenesis in E. sinensis. The candidate pathways included the ubiquitin-proteasome pathway, cyclic AMP-protein kinase A signalling pathway, and mitogen-activated protein kinase signalling pathway, playing essential roles in the regulation of ovarian development in E. sinensis (Feng et al.).

The differences between the first vitellogenesis period (FVP) and second vitellogenesis period (SVP) in the ovary, hepatopancreas and muscle of mud crab (Scylla paramamosain) were determined. This article indicated that the ovary can re-mature after spawning in S. paramamosain and can maintain the status of the first ovarian maturation. However, the hepatopancreas gradually degenerate during the SVP (Ren et al.).

The potential functions of Cyclin A (CycA) in male reproduction were investigated in M. nipponense. This article revealed that the ablations of the eyestalk of male M. nipponense significantly stimulated the mRNA expressions of CycA, and the CycA expressions in the testis and androgenic gland taken from the reproductive season were significantly higher than those during the non-reproductive season. Furthermore, knockdown the expressions of CycA in male M. nipponense by RNAi resulted in the decrease of insulin-like androgenic gland hormone expressions, and the delay of testis development, indicating CycA was involved in the regulation of male reproduction in M. nipponense (Zhang et al.).

Author contributions

SJ wrote the editorial. LM and HF supervised the editorial.

Funding

This research was supported by grants from the Natural Science Foundation of Jiangsu Province (BK20221207), Central Public-Interest Scientific Institution Basal Research Fund, CAFS (2021JBFM02 and 2020TD36), National Key R&D Program of China (2018YFD0900201, 2020YFD0900802), Jiangsu Agricultural Industry Technology System (JATS[2020]461), China Agriculture Research System-48 (CARS-48), and New Cultivar Breeding Major Project of Jiangsu Province (PZCZ201745).

Conflict of interest

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Publisher’s note

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.

References

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Keywords: aquatic animals, steroid hormone, triploid, reproduction-related genes, reproduction

Citation: Jin S, Ma L and Fu H (2023) Editorial: Reproduction in aquatic animals. Front. Genet. 14:1127764. doi: 10.3389/fgene.2023.1127764

Received: 20 December 2022; Accepted: 17 January 2023;
Published: 23 January 2023.

Edited and reviewed by:

Prapansak Srisapoome, Kasetsart University, Thailand

Copyright © 2023 Jin, Ma and Fu. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

*Correspondence: Lingbo Ma, malingbo@vip.sina.com; Hongtuo Fu, fuht@ffrc.cn

Disclaimer: All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.