AR regulates porcine immature Sertoli cell growth via binding to RNF4 and miR-124a

Sertoli cells are the only somatic cells in the seminiferous epithelium which directly contact with germ cells. Sertoli cells exhibit polarized alignment at the basal membrane of seminiferous tubules to maintain the microenvironment for growth and development of germ cells, and therefore play a crucial role in spermatogenesis. Androgens exert their action through androgen receptor (AR) and AR signalling in the testis is essential for maintenance of spermatogonial numbers, blood–testis barrier integrity, completion of meiosis, adhesion of spermatids and spermiation. In the present study, we demonstrated that AR gene could promote the proliferation of immature porcine Sertoli cells (ST cells) and the cell cycle procession, and accelerate the transition from G1 phase into S phase in ST cells. Meanwhile, miR-124a could affect the proliferation and cell cycle procession of ST cells by targeting 3′-UTR of AR gene. Furthermore, AR bound to the RNF4 via AR DNA-binding domain (DBD) and we verified that RNF4 was necessary for AR to regulate the growth of ST cells. Above all, this study suggests that AR regulates ST cell growth via binding to RNF4 and miR-124a, which may help us to further understand the function of AR in spermatogenesis.     

低血糖生成指数液态奶的开发及测试

为获得营养均衡的调制牛奶,满足人体的多种营养需求,添加多种维生素和矿物质,设计出一款适用于糖尿病人、亚健康人群、体重管理、皮肤管理等人群饮用的低血糖生成指数（Glycemic Index,GI）的牛奶。稳定性试验结果表明,静置12 天后,牛奶无显著脂肪上浮,体系稳定性良好;人体GI值试验结果表明,调制牛奶的餐后血糖值上升和下降均较葡萄糖餐后血糖值平稳,有较好稳定餐后血糖的效果,表明开发的调制牛奶为低GI食品（GI值=22.86）。人体饱腹感试验结果显示,和普通纯牛奶对比,调制牛奶具有显著提高饱腹感的效果。     

杂交构树叶多酚提取工艺优化及其抗氧化活性研究

为建立和优化杂交构树叶多酚的提取工艺,本试验采用超声波辅助提取的方法,以构树叶多酚得率为考察指标,通过单因素试验研究液料比、乙醇浓度、超声时间、超声温度4个因素对构树叶多酚得率的影响;在单因素试验的基础上,借助响应面法设计4因素3水平的试验方案,对构树叶多酚提取的工艺参数进行优化,建立回归模型并进行响应面分析,最终确定最佳的提取工艺参数,并进行3次平行验证;以维生素C为对照,通过测定构树叶多酚对DPPH和ABTS自由基的清除率,评价构树叶多酚的体外抗氧化活性。结果显示：4个因素对构树叶多酚得率的影响顺序依次为：乙醇浓度（B） > 液料比（A） > 超声温度（D） > 超声时间（C）,响应面分析结果显示：两两因素之间存在交互作用,但交互作用不显著（P>0.05）;在液料比为70：1、乙醇浓度为60%、超声时间为50 min、超声温度50 ℃的条件下,构树叶多酚的得率最大,为13.62 mg/g,与响应面法的预测值接近;体外抗氧化试验结果表明,构树叶多酚可以清除DPPH和ABTS自由基,并且在高浓度情况下可以达到与维生素C相当的水平。综上,试验建立的构树叶多酚提取工艺准确、可行,同时证明构树叶多酚具有良好的抗氧化活性;该结果可为构树叶多酚的生物活性研究以及构树叶的药用价值开发提供参考。     

猪场生物安全体系中十个通道的设计应用

2018年8月开始,非洲猪瘟在我国快速多点发生,该病是高度接触性传染性疾病,目前无有效的疫苗和药物控制,各大公司和养殖户开始了猪场生物安全体系的升级改造。两年后我国大部分猪场的成功复产,全国生猪出栏量的大幅提升,证明了生物安全措施巨大效力;同时在严格的生物安全措施下创新了精准剔除、快速复产等操作,进一步证明了生物安全措施的有效作用。文章主要介绍猪场生物安全体系中入口(大门)和出口(后门)最为关键防线处的通道设计,方便所有的生物安全操作能够高效落实,切断病原轻易进出猪场的途径。     

内蒙古贺兰山马鹿的种群数量及种群结构

为了掌握内蒙古贺兰山国家级自然保护区内马鹿(Cervus elaphus)的种群数量和种群结构,维护内蒙古贺兰山的生态平衡。于2017年11—12月,2018年4—6月、11—12月,2019年4—6月,在内蒙古贺兰山国家级自然保护区内,利用样线法对保护区内的马鹿进行调查,采用Distance R进行数据分析,估测种群数量和种群密度,并对种群结构进行探讨。研究发现,马鹿在2018年冬季种群数量最高约为2452(1678—3578)只,种群密度为3.705(2.539—5.048)只/km²,遇见率为1.943只/km。遇见率年际间变化不明显(F=0.12,P=0.986);混合群出现的次数最高,雄性群出现的次数最低,不同集群类型在不同季节的差异极显著(P<0.001);群大小在不同季节的差异不显著(P=0.132);雌雄比在不同季节中没有太大变化。     

地温空调井抽回灌效果影响关键因子识别

为了探析引起地温空调井抽回灌效果的主要制约因素,通过单相关系数分析、主成分绝对得分的源解析模型、拟合度检验和多元线性回归的方法分析影响单井回灌效率的影响因素。结果表明:井径、滤水管孔隙率及抽回灌井数比与单井回灌效率的相关性和拟合度较好,故将井径、滤水管孔隙率及抽回灌井数比作为影响单井回灌效率的关键因子,同时分析了单井回灌效率与关键因子的之间的拟合方程及多元线性回归方程,得到了单井回灌效率与关键因子之间的定量关系。     

垄作与保护性耕作联合技术研究

介绍了垄作技术与保护性耕作技术各自的发展现状,对垄作技术的特点和耕作模式进行了分析,并对保护性耕作技术的发展模式、特点及实施条件等进行了探讨。通过分析比较两种耕作方式的优缺点,对垄作技术与保护性耕作技术联合应用的技术模式进行了较为深入的探讨。     

不同灌溉方式下冬小麦穗部性状与产量关系的试验研究

采用田间试验,以豫麦69为试验材料,研究了不同水分处理下常规灌溉和一体化垄作沟灌的冬小麦产量与穗部性状的相互关系。结果表明,同常规灌溉方式相比,一体化垄作沟灌方式下,冬小麦的穗粒数、籽粒质量及产量分别增加了5.5356%、7.5489%、7.7454%,但穗数减少了0.4302%。常规灌溉和一体化垄作沟灌方式下,产量与穗数、穗粒数以及籽粒质量均正相关,但一体化垄作沟灌方式下的相关系数较常规灌溉方式大。一体化垄作灌溉有利于改善农田小气候、发挥作物的边行优势和提高小麦产量。     

Study on Expression Difference of IGFBP-5 Gene in Different Tissues of Kazakh and Yanqi Horses

The study aimed to explore the mRNA expression pattern of insulin-like growth factor binding protein-5 (IGFBP-5) gene in different tissues of Kazakh and Yanqi horses.The expression of IGFBP-5 gene in different tissues of heart,liver,spleen,lung,kidney,small intestine,large intestine,cecum,intercostal muscles,longissimus dorsi muscles,brachialis muscle and gluteus in two horses were detected by Real-time quantitative PCR and compared the mRNA expression in the same tissues of two breeds.The results showed that the expression of IGFBP-5 in longissimus dorsi muscle and brachialis muscle of two breeds were significantly higher than other tissues including heart,liver,spleen,lung,kidney,small intestine,large intestine and cecum (P<0.05),and was the lowest in large intestine.The expression of IGFBP-5 in kidney,small intestine,large intestine,cecum,longissimus dorsi muscle and brachialis muscles of Yanqi horse were higher than in the same part of Kazakh horse,and among those in longissimus dorsi muscle and large intestine of Yanqi horse were extremely significantly higher than in the same part of Kazakh horse (P<0.01),and in small intestine and cecum of Yanqi horse were significantly higher than in the same part of Kazakh horse (P<0.05).The test was for further researching the biological function of IGFBP-5 gene,and it could provide a theoretical basis for genetic improvement of production performance of horse in our country.     

Production and Identification of Clone Sheep Using Bone Marrow Mesenchymal Stem Cells as Donor Cell

In order to obtain the cloned sheep using bone marrow mesenchymal stem cells（BMSCs）as the donor cells,the BMSCs of sheep were chosen and reconstructed embryos were built to transfer.10 published microsatellite markers were chosen,and the DNA samples from clone sheep,donor cells and surrogate ewes were amplified,and the relationship of father-son（RCP）was analyzed using the Quantity One for genotyping.The results showed that the reconstructed embryos were successfully built for electric fusion using sheep BMSCs as nuclear donor,and making nuclear transplantation into enucleated mature oocytes of which the fusion rate was 80.62%.20 surrogate ewe were chosen to be implanted with the reconstructed embryos at morula stage by implant surgery,and 5 lambs were born and only 3 were survived.The genotype of cloned sheep was in line with the dornor cell and the RCP were more than 99.999%.In conclusion,the first clone sheep were obtained successfully by using BMSCs as a nuclear donor in this experiment.