Differential Expression Characteristics of Two Isoforms nr5a2f and nr5a2m in Gonadal Differentiation of Chinese Giant Salamanders, Andrias davidianus.

IF 2.7 2区 农林科学 Q1 AGRICULTURE, DAIRY & ANIMAL SCIENCE
Animals Pub Date : 2025-06-05 DOI:10.3390/ani15111667
Dan Hu, Guanglve Li, Guohua Zou, Jiaqing Xu, Wenyin Luo, Qiaomu Hu
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Abstract

Nr5a2 (nuclear receptor subfamily 5, group a, member 2) is involved in gonad development and sex hormone synthesis. In this study, the full length of Nr5a2f and Nr5a2m were obtained by Nr5a2 variable splicing from Andrias davidianus, and the tissue distribution was detected. We identified Nr5a2f of 2455 bp and Nr5a2m of 2150 bp length, encoding 479 and 325 amino, respectively. We first characterized Nr5a2f and Nr5a2m gene expression in developing gonads. Results showed that Nr5a2f had significantly high expression in the ovary and little expression in other tissues, during the sex differentiation and sex reversal, Nr5a2f expression was gradually decreased in the ovary and the expression in the testis was significantly lower than in the ovary from 1 year to 6 year old. Significantly high expression was observed in the ovary and reversal ovary, while low expression was in the testis and reversal testis. While Nr5a2m expression exhibited the opposite profile, high expression was observed in the brain and testis. During sex differentiation and sex reversal, high expression was shown in the testis and low expression in the ovary from one year to six years old and significantly higher expression emerged in testis and reversal testis than in ovary and reversal ovary. In situ hybridization, results showed that Nr5a2f began to express in female undifferentiated gonads and the expression level increased from 48 dpf to 91, while Nr5a2m was expressed in male undifferentiated gonads. Three RNA interference sites were designed and we detected that site 293 exhibited a significant inhibitory effect in ovary cells. After Nr5a2f expression was inhibited by site 293, we observed that female-based gene Nr5a2f, foxl2 and cyp19 expression were decreased, while the male-based gene dmrt1 and cyp17 expression was increased. These results suggested that Nr5a2f and Nr5a2m exhibited different expression patterns in the process of sex differentiation, which provided a foundation for further functional characterizations.

nr5a2f和nr5a2m亚型在大鲵性腺分化中的差异表达特征
Nr5a2(核受体亚家族5,a族,成员2)参与性腺发育和性激素合成。本研究从大鲵中通过Nr5a2可变剪接获得Nr5a2f和Nr5a2m的全长,并检测其组织分布。Nr5a2f全长2455 bp, Nr5a2m全长2150 bp,分别编码479个和325个氨基酸。我们首先表征了Nr5a2f和Nr5a2m基因在发育性腺中的表达。结果表明,Nr5a2f在卵巢中表达量显著高,在其他组织中表达量很少,在性别分化和性别逆转过程中,Nr5a2f在卵巢中的表达量逐渐降低,1 ~ 6岁时睾丸中的表达量显著低于卵巢。在卵巢和逆行卵巢中表达显著高,而在睾丸和逆行睾丸中表达低。而Nr5a2m的表达表现出相反的特征,在大脑和睾丸中观察到高表达。在性别分化和性别反转过程中,1 ~ 6岁睾丸表达量高,卵巢表达量低,且睾丸和反转睾丸的表达量明显高于卵巢和反转卵巢。原位杂交结果显示,Nr5a2f在雌性未分化性腺中开始表达,表达量从48dpf增加到91,而Nr5a2m在雄性未分化性腺中表达。我们设计了3个RNA干扰位点,检测到293位点对卵巢细胞有明显的抑制作用。在293位点抑制Nr5a2f表达后,我们观察到雌性基因Nr5a2f、foxl2和cyp19的表达减少,而雄性基因dmrt1和cyp17的表达增加。这些结果表明Nr5a2f和Nr5a2m在性别分化过程中表现出不同的表达模式,为进一步的功能鉴定提供了基础。
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来源期刊
Animals
Animals Agricultural and Biological Sciences-Animal Science and Zoology
CiteScore
4.90
自引率
16.70%
发文量
3015
审稿时长
20.52 days
期刊介绍: Animals (ISSN 2076-2615) is an international and interdisciplinary scholarly open access journal. It publishes original research articles, reviews, communications, and short notes that are relevant to any field of study that involves animals, including zoology, ethnozoology, animal science, animal ethics and animal welfare. However, preference will be given to those articles that provide an understanding of animals within a larger context (i.e., the animals'' interactions with the outside world, including humans). There is no restriction on the length of the papers. Our aim is to encourage scientists to publish their experimental and theoretical research in as much detail as possible. Full experimental details and/or method of study, must be provided for research articles. Articles submitted that involve subjecting animals to unnecessary pain or suffering will not be accepted, and all articles must be submitted with the necessary ethical approval (please refer to the Ethical Guidelines for more information).
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