东亚和南亚固有绵羊群体X-蛋白等位基因特有频率分布的研究

本研究利用单向水平板淀粉凝胶电泳以我国5个固有地方绵羊品种包括湖羊（Hu）、同羊（Tong）、滩羊（Tan）、小尾寒羊（Han）、洼地羊（WD）为研究对象对X-蛋白遗传多样性进行了检测,并引用我国周边国家、地区绵羊品种为分析背景。结果表明以喜马拉雅山脉为界的亚洲东部和南部的北部群体和南部群体在编码的X（＋）型的显性等位基因X频率上存在极显著差异（P〈0．01）。北部检测的群体中X等位基因频率范围为0～0．18,平均值为0．0878,包括属于藏羊和蒙古羊系统的小尾寒羊（Han）、不丹羊（Bhutan）、同羊（Tong）、湖羊（Hu）、滩羊（Tan）、洼地绵羊（WD）、Bhyanglung绵羊（Bhy）、Baruwal绵羊（Bar）、云南绵羊（Yunnan）、哈拉和林绵羊（Kh）和乌兰巴托绵羊（Ub）。南部检测的群体中X等位基因频率范围为0．2037～0．4655,平均值为0．3082,包括属于印度绵羊系统的孟加拉国绵羊（Ban）、Kagi绵羊（Kagi）、Lampuchhre绵羊（Lamp）、越南占部落绵羊（Cham）和缅甸绵羊（Mya）。本研究揭示X等位基因可作印度绵羊的标记,在绵羊群体尤其是亚洲东部和南部绵羊系统形成的研究中具有潜在的重要作用。     

藏山羊和藏绵羊小肠黏膜免疫相关细胞的比较研究

为了探讨藏山羊和藏绵羊在低氧环境中小肠黏膜免疫屏障结构的适应特征,本试验采用组织化学方法和图像分析法对4只成年藏山羊和4只成年藏绵羊小肠不同肠段的上皮内淋巴细胞、杯状细胞和肥大细胞的数量进行比较研究。结果显示:藏山羊小肠各段杯状细胞和肥大细胞的数量均高于藏绵羊(P<0.05),其中藏山羊十二指肠、空肠和回肠的上皮内杯状细胞数量分别比藏绵羊多37.87%(P<0.05)、21.43%(P>0.05)和31.68%(P<0.05),藏山羊十二指肠、空肠和回肠的肥大细胞数量分别比藏绵羊多85.20%(P<0.05)、50.73%(P<0.05)和22.52%(P>0.05);而藏山羊小肠各段上皮内淋巴细胞的数量(36.35±0.98)低于藏绵羊(48.84±2.12)(P<0.05)。结果提示,成年藏山羊的小肠黏膜免疫屏障功能强于藏绵羊;藏绵羊小肠中上皮内淋巴细胞起重要的黏膜防御功能,而在藏山羊小肠中杯状细胞和肥大细胞起重要的黏膜防御功能。     

添加烟酸条件下绵羊瘤胃发酵底物降解动力学变化特征

试验用瘤胃液来自3只安装永久性瘤胃瘘管的绵羊,饲喂玉米-豆粕型基础日粮.通过体外试验,添加450 mg/kg烟酸,测定在不同培养时间内培养液中NH3-N浓度、瘤胃细菌N产量、原虫数量、总VFA量及乙酸、丙酸、丁酸产量和乙酸/丙酸值的降解动力学特征.结果表明:添加烟酸可提高培养液NH3-N利用率;培养液中细菌N、原虫数、总VFA量及乙酸、丙酸、丁酸产量随采样时间变化而呈不同的动力学变化趋势;但乙酸/丙酸值则不受采样时间变化的影响,与对照组相比差异不显著(P>0.05).     

绵羊多羔主效基因BMPR1B的研究进展

骨形态发生蛋白受体1B(Bone morphogenetic protein receptor 1B,BMPR1B)是一种重要的跨膜受体蛋白,主要参与转化生长因子β(TGF-β)通路,其在调控成骨分化、细胞扩散以及卵巢卵泡发育等过程中起重要作用,并直接影响如绵羊等动物的繁殖性状。绵羊BMPR1B基因发生A746G突变(命名为FecB突变),导致第249位氨基酸由谷氨酰胺(Q)转变为精氨酸(R),进而使得绵羊排卵数和产羔数显著增加,因此BMPR1B成为目前最受关注的绵羊多羔主效基因。论文就绵羊BMPR1B基因定位、功能机制研究进展及其对高繁殖力绵羊的影响进行了综述,同时也对BMPR1B功能研究中一些亟待解决的问题展开了讨论。     

PMSG对甘肃高山细毛羊同期发情和繁殖率的影响

在甘肃省肃南县康乐乡对甘肃高山细毛羊应用阴道栓与孕马血清促性腺激素(PMSG) 结合处理,结果表明,不同注射剂量和处理方式对母羊的同期发情和繁殖率均有影响,在埋栓后12.5 d注射550 IU PMSG并在放栓后14 d撤除阴道栓后的0-48 h发情率显著高于其他试验组(P<0.05);在埋栓后13 d注射600 IU PMSG同时撤除阴道栓的试验组繁殖率最高(P<0.05)。但综合繁殖率和经济效益考虑,在埋栓后间隔12.5 d注射550 IU PMSG并在放栓后14 d撤除阴道栓0-48 h的试验组效果最好,平均每只母羊净收入可达773.7元。     

用酶法制备藏羊血食用蛋白粉的研究

采用四因素三水平正交试验,对藏羊血制备食用蛋白的工艺进行了分析。经分析食用蛋白粉水解最佳条件为：酶解用酶量4.5g,酶解温度为46℃,酶解时间为7.5h,酶解的pH值为10.5,活性炭作用于水解液时由室温升至80℃所需最佳时间为6～8min。     

湖羊肌肉营养成分组成及风味物质研究

选取5、10、18月龄及4岁湖羊各10只,屠宰后取背最长肌和肱三头肌分析常规营养成分;取10月龄湖羊背最长肌分析氨基酸;取肱三头肌测风味物质。结果表明:湖羊肌肉水分含量随年龄增长而降低(P<0.05),粗蛋白含量、粗脂肪、粗灰分的含量随年龄增长而增加(P<0.05)。湖羊肌肉蛋白质中8种必需氨基酸组成全面,与FAO模式比较,各种氨基酸评分均接近或大于1。湖羊肌肉脂肪中检测到的70种挥发性风味化合物,包括14种酸、7种酮、9种醛、5种醇、10种酯类、13种烃、12种其他化合物(包括呋喃、吡嗪、吡啶、吲哚等含氮硫氧等杂环化合物)。其中酯类含量最高,占肉中总风味物24.1%~28.3%,其次为烃和酸,分别占20.5%~21.2%和19.0%~20.0%。     

8个微卫星座位在海北金银滩藏羊群体中的多态性分析

研究旨在分析金银滩藏羊的微卫星DNA多态性,以期了解该品种的遗传多样性,为该品种的保种选育和品质的进一步提高提供有益资料。利用8对微卫星引物,以金银滩藏羊为研究对象,通过计算基因频率、多态性信息含量、有效等位基因数和杂合度,评估其品种内的遗传变异。结果表明：在8个微卫星座位中,共检测到83个等位基因,每个座位平均10.38个等位基因;平均杂合度0.893;平均有效等位基因数9.06;平均多态性信息含量0.871。结果提示,金银滩藏羊群体存在丰富的遗传多样性,所选微卫星标记可用于绵羊遗传多样性评估。     

Chemerin analog regulates energy metabolism in sheep

Accumulating data suggest a relationship between chemerin and energy metabolism. Our group previously described gene cloning, expression analysis and the regulatory mechanism of chemerin and its own receptor in mice and cattle. The objective of the present study was to investigate the physiological effect of chemerin on endocrine changes and energy metabolism in sheep using a biologically stable chemerin analog. The chemerin analog was intravenously administrated (100 or 500 µg/head) to sheep, and plasma insulin and metabolites (glucose, nonesterified fatty acids (NEFA), triglyceride, total cholesterol and high‐density lipoprotein (HDL) cholesterol) were analyzed. The chemerin analog dramatically increased the insulin levels, and glucose levels were decreased. NEFA levels were slightly decreased at 20 min but then increased gradually from 60 to 180 min after analog administration. In addition, injection of the chemerin analog immediately increased triglyceride and total cholesterol but not HDL levels. These results suggested that chemerin analog regulated insulin secretion related to glucose metabolism and the release of triglycerides in sheep in vivo. This study provides new information about endocrine and metabolic changes in response to chemerin in sheep.     

Bioinformatics Analysis of Bone Morphogenetic Protein 4 (BMP4) of Sheep

The assay was aimed to explore the biological characteristics of bone morphogenetic protein 4 (BMP4) of sheep,NCBI,DNAMAN DNAStar,TMHMM Server v.2.0,PsortⅡ,SignalP various bioinformatical softwares were used to speculate the physical and chemical properties,hydrophobic property,phosphorylation site,conservative structure domain,protein secondary structure of BMP4 protein.Also,the three-dimensional structure was forecasted with the SWISS-MODEL Workspace software.The results indicated that the BMP4 of sheep had high homologies with the BMP4 of various species.The encoded protein was a hydrophilic protein which was unstable.There was no transmembrane regions and it was likely to be located in the nucleus.What was more,there was signal peptide and eighteen phosphorylation sites.Through the forecast of functional domains,the protein had two functional domains,including the transforming growth factor-beta (TGF-beta) superfamily and TGF-beta propeptide superfamily.The result was consistent with the function of BMP4 gene family,it also demonstrated that BMP4 was a growth factor and it had the function of signal transduction.The amino acid homology between the predicted 3D structure of protein and template 3bmp.1.A was 88.29%.The bioinformatics analysis of BMP4 gene could provide reference for the further study in practice.