Hu Xinyue, Ouyang Qingyuan, Tang Bincheng, Zhang Xin, Hu Jiwei, Hu Bo, Hu Shenqiang, Li Liang, He Hua, Liu Hehe, Wang Jiwen
Farm Animal Genetic Resources Exploration and Innovation Key Laboratory of Sichuan Province, Sichuan Agricultural University, Chengdu 611130, China.
Animals (Basel). 2022 Nov 3;12(21):3023. doi: 10.3390/ani12213023.
Semen volume is an important factor in artificial insemination (AI) of ducks. In drakes, seminal plasma that is produced by the epididymis determines the semen volume. However, the mechanism of epididymis regulating semen volume of drakes remains unclear. Therefore, the aim of the present study was to preliminarily reveal the mechanism regulating the semen volume through comparing the epididymal histomorphology and mRNA expression profiles between drakes with high-volume semen (HVS) and low-volume semen (LVS). Phenotypically, drakes in the HVS group produced more sperm than drakes in the LVS group. In addition, compared with the HVS group, the ductal square of ductuli conjugentes (DC) and dutus epididymidis (DE) in epididymis was significantly smaller in the LVS group, and the lumenal diameter and epithelial thickness of DC/DE were significantly shorter in the LVS group. In transcriptional regulation, 72 different expression genes (DEGs) were identified from the epididymis between HVS and LVS groups. Gene Ontology (GO) analysis indicated that the DEGs were mainly related to hormone secretion, neurotransmitter synthesis/transport, transmembrane signal transduction, transmembrane transporter activity, and nervous system development (p < 0.05). Kyoto Encyclopedia of Genes and Genomes (KEGG) functional enrichment analysis showed that the DEGs were significantly enriched in pathways associated with hormone and neurotransmitter transmission (p < 0.05). In addition, further analysis of the top five pathways enriched by KEGG, nine key candidate genes (including SLC18A2, SNAP25, CACNA1B, GABRG2, DRD3, CAMK2A, NR5A1, and STAR) were identified, which could play a crucial role in the formation of semen. These data provide new insights into the molecular mechanism regulating semen volume of drakes and make feasible the breeding of drakes by semen volume.
精液体积是鸭人工授精中的一个重要因素。在公鸭中,附睾产生的精浆决定了精液体积。然而,附睾调节公鸭精液体积的机制仍不清楚。因此,本研究的目的是通过比较高精液体积(HVS)和低精液体积(LVS)公鸭的附睾组织形态学和mRNA表达谱,初步揭示调节精液体积的机制。从表型上看,HVS组公鸭产生的精子比LVS组公鸭多。此外,与HVS组相比,LVS组附睾中联合小管(DC)和附睾管(DE)的管腔面积显著更小,LVS组DC/DE的管腔直径和上皮厚度显著更短。在转录调控方面,从HVS和LVS组的附睾中鉴定出72个差异表达基因(DEG)。基因本体论(GO)分析表明,这些DEG主要与激素分泌、神经递质合成/运输、跨膜信号转导、跨膜转运体活性和神经系统发育有关(p<0.05)。京都基因与基因组百科全书(KEGG)功能富集分析表明,这些DEG在与激素和神经递质传递相关的通路中显著富集(p<0.05)。此外,对KEGG富集的前五条通路进行进一步分析,鉴定出九个关键候选基因(包括SLC18A2、SNAP25、CACNA1B、GABRG2、DRD3、CAMK2A、NR5A1和STAR),它们可能在精液形成中起关键作用。这些数据为调节公鸭精液体积的分子机制提供了新的见解,并使通过精液体积对公鸭进行育种成为可能。