太平洋南美白对虾(Litopenaeus vannamei)性发育过程中一种新型睾丸特异性锌指蛋白的特征。

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC ACS Applied Electronic Materials Pub Date : 2024-10-17 DOI:10.1093/biolre/ioae151
Chi-Sheng Wang, Hao-Sheng Cheng, Wan-Ting Chang, Cheng-Chieh Hsiao, Peng-Wei Tseng, Hau-Wen Li, Amir Sagi, Ching-Fong Chang, Guan-Chung Wu
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引用次数: 0

摘要

由于雌性对虾生长速度较快,因此提出了全雌性养殖的建议。太平洋南美白对虾的环境条件并未影响遗传性别决定(ZZ/ZW 系统)。分泌胰岛素样雄性激素(IAG)的雄性激素腺(AG)是甲壳类雄性分化的关键控制因素。然而,操纵 IAG 的性转换尚未实现青虾的功能性逆转(新雄性)。因此,了解性腺分化的分子机制可能有助于建立适当的工具来产生全雌性育种的新雄性(ZW)。本研究描述了太平洋南美白对虾性腺中新型对雌虾特异性睾丸锌指蛋白(pTZFP)的潜在作用。首先,pTZFP转录本在未分化性腺中呈现雄性偏向表达模式,然后只在睾丸中表达,而在卵巢和其他组织中不表达或轻微表达。此外,在未分化的雄性中敲除 pTZFP 会导致睾丸变小,但不会出现性别逆转。增殖细胞核抗原(PCNA)的免疫组化染色进一步证实,pTZFP缺陷的雄性睾丸变小是由于精原细胞的增殖活性降低所致。这些数据表明,pTZFP可能参与了睾丸的发育,但对性腺分化的影响较小。此外,睾丸 pTZFP 的转录水平并不会因为雌二醇-17β(E2)的施用或 AG 的切除而降低。因此,我们的数据表明 pTZFP 可能通过调节精原细胞增殖的下游基因来调控睾丸的发育。此外,我们的数据还为鉴定未分化性腺的性别提供了一个合适的分子标记。
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Characterization of a novel and testis-specific zinc finger protein during sexual development of Pacific white shrimp Litopenaeus vannamei.

Since females grow faster in penaeid shrimp, all-female aquaculture was proposed. Environmental conditions in the Pacific white shrimp did not found to affect genetic sex determination (ZZ/ZW system). The androgenic gland (AG)-secreting insulin-like androgenic gland hormone (IAG) is a key controlling factor in crustacean male differentiation. However, functional sex reversal (neo-male) in penaeid shrimp has not yet been achieved by manipulating the IAG-sexual switch. Therefore, understanding the molecular mechanisms of gonadal differentiation may help build appropriate tools to generate neo-male (ZW) for all-female breeding. This study describes the potential role of the novel penaeid-specific testicular zinc finger protein (pTZFP) in the gonads of Pacific white shrimp. First, pTZFP transcripts show a male-bias expression pattern in undifferentiated gonads, which is then exclusively expressed in the testis and absent or slightly expressed in the ovary and other tissues. Besides, the knockdown of pTZFP in undifferentiated males results in smaller testes but no sex reversal. Immunohistochemical (IHC) staining of proliferating cell nuclear antigen (PCNA) further confirmed that the smaller testes in pTZFP-deficient males are due to the lower proliferating activity of spermatogonia. These data reveal that pTZFP may be involved in testicular development but have fewer effects on gonadal differentiation. Moreover, testicular pTZFP transcription levels were not reduced with estradiol-17β (E2) administration or AG excision. Therefore, our data suggest that pTZFP may regulate testicular development through downstream genes regulating spermatogonia proliferation. Moreover, our data provide an appropriate molecular marker for identifying the sex of undifferentiated gonads.

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