家蝇抗菌肽的研究进展马红霞

从家蝇抗菌肽的分类、结构特点、作用机理、诱变、活性检验以及分子生物学研究等方面介绍了家蝇抗菌肽的研究进展。家蝇抗菌肽独特的作用机理、成熟的诱导、分离纯化技术及其相关基因的克隆、表达等研究成果均为对家蝇抗菌肽进行更深入的研究奠定了基础。采用分子生物学技术有望筛选并制备大量的高效家蝇抗菌肽。     

Construction of Brucella ClpS Gene Mutant Strain and Its Effect on Virulence

The present study aimed to determine the role of ClpS gene,and to analyse the impact of ClpS mutation on the virulence of Brucella.A ClpS gene mutant strain,named ΔClpS was constructed by homologous recombination technology.The bacterial growth kinetics,the LPS synthesis ability and the survival ability of bacterial within macrophages as well as the virulence in mouse model were measured.In addition,the difference between parent strain 2308 and the mutant strain ΔClpS were compared.The results showed that under the same culture conditions,no difference in bacterial concentration was observed between 2308 and ΔClpS strains.The silver staining examination showed that the expression level of LPS extracted from two strains were similar,indicating ClpS gene mutation did not alter the growth rate and LPS synthesis ability of Brucella. In the cell infection assay,the survival ability of ΔClpS strain in cells was extremely significantly lower than that of 2308 strain at 72 h after infection (P<0.01).The results of mouse infection experiment showed that in the first week after infection,no significant difference in spleen weight and bacterial concentration between 2308 and ΔClpS strains infected mice was observed.However,at 4 weeks after infection,the bacterial concentration in spleen of ΔClpS infected mice was 10^3.93 CFU/g spleen,which was significantly lower than that of 2308 strain (10^6.68 CFU/g spleen,P<0.01).The spleen weight of ΔClpS infected mice was also remarkably lower than that of 2308 strain (P<0.01).In summary,the results suggested that the ClpS gene of Brucella did not play a role in Brucella growth rate and ability of LPS synthesis,whereas ClpS gene mutation decreased the ability of Brucella colonization in mouse spleen.     

苹果新品种‘天汪1号’

 ‘天汪1号’是从‘红星’的芽变中选育出的苹果短枝型新品种, 在天水地区9月中旬成熟,果实生育期148 d。果实圆锥形, 五棱突起, 果形指数0.90～0.98, 平均单果质量210 g, 果实全面浓红,色相片红; 果肉细而致密, 汁多, 味香甜, 可溶性固形物含量11.9%～14.1%。树势强健, 丰产, 稳产。     

无子沙糖橘(十月橘)的选育

采用芽变选种的方法,在四会市石狗镇选出了无子柑橘新品种—无子沙糖橘(十月橘)。果略小,单果重平均40g左右,单果平均种子数0.5粒以内,达到柑橘无子的标准。果实扁平,皮橘红色,薄而脆;果肉橙黄色,味清甜,可溶性固形物13%以上,肉质爽脆化渣,品质上等。早结丰产性好,发梢能力强,3月上中旬开花,12月上旬果实开始成熟。     

狗牙根品种及辐射诱变M1代变异植株的过氧化物同工酶分析

采用聚丙烯酰胺凝胶电泳法对辐射诱变M1代变异植株及其对照、‘Tifway’和‘Tifgreen’共18个狗牙根材料的过氧化物同工酶进行了分析。结果表明：供试材料共出现了97条酶带，单个材料最多为8条，最少只有2条；材料HN009和HN010、HN012和HN013的POD酶带特征完全相同；HN015和HN016的P013酶带在P8位点上有强弱不同，HN004和HN018的POD酶带在P5和P6位点上有强弱不同，它们的酶带数和位点均相同；其它各材料之间酶带总数不同，在各个区域分布的位点及酶谱特征明显不同。除HN010和其对照HN009的酶谱特征相同外，其它形态变异植株和其对照之间的酶谱特征均存在明显差异。     

苹果新品种‘红锦富’

 ‘红锦富’是‘长富2号’富士苹果的早熟芽变新品系，与‘长富2号’相比果实成熟期提前约45 d，早果，丰产，稳产，适应性强，果形端正，萼洼处果锈少，耐贮性好。     

Novel p53 tumour suppressor mutations in cases of spindle cell sarcoma,pleomorphic sarcoma and fibrosarcoma in cats

Twenty feline neoplasms were sequenced in the region from exons 5 to 8 for the presence of tumour suppressor gene p53 mutations. In a spindle cell sarcoma of the bladder, a missense mutation (codon 164 AAGGAG, lysineglutamic acid) in exon 5 was detected. In a pleomorphic sarcoma, a 23 bp deletion involving the splicing junction between intron 5 and exon 6 was observed. In a fibrosarcoma, a 6 bp deletion of p53 covering 2 bp of exon 7 and 4 bp of intron 7, including the splicing junction, was found. The study demonstrates three new p53 mutations in different types of sarcomas in cats.     

新色型突变棕色貉毛色遗传初探

2006年首次发现新色型突变棕色貉，近3年内累计扩繁89只。依据孟德尔遗传定律，对不同选配组合后代毛色分离数据的统计分析和x^2适合性检验证明，其突变棕色毛色基因为显性，基因型为杂合体。建议其基因符号用“G”表示，基因型为“Gg”。     

早熟葡萄新品种选育(Ⅰ)

“90 - 1”是从乍娜的芽变中选出的葡萄新品种。多年的研究试验表明 :该品种除保持母本的优质、丰产、适合保护地栽培等优良性状外 ,最突出的特点是极早熟 ,果实 6月下旬成熟 ,果实发育期 35d。果实不易感病 ,不宜用膨大剂处理。     

绵羊FecB突变检测方法的建立及高繁滩羊核心群的构建

旨在建立快速、高效、精准检测FecB突变的荧光qPCR技术,为滩羊多羔性能研究、群体改良及肉用多羔滩羊新品系培育提供技术支撑。基于荧光qPCR技术基本原理,设计特异性引物对,开发基于荧光qPCR检测绵羊FecB突变的方法;对85只已知FecB基因型的健康、适繁雌性滩羊血液基因组DNA样品分别采用PCR-Sanger测序法、TaqMan探针法和荧光qPCR法进行FecB基因分型,统计3种方法的准确率;采用开发的荧光qPCR方法对939只健康、适繁滩羊进行FecB基因分型,统计不同FecB基因型经产母羊的产羔率。结果表明,使用TaqMan探针法、PCR-Sanger测序法和开发的荧光qPCR法对已知FecB基因型样品检测的比较中,荧光qPCR法对各基因型鉴定的准确度均达100%,高于前两者。939只滩羊FecB基因分型结果显示,6只滩羊为FecB突变纯合型（BB）、57只为杂合型（B+）、876只为野生型（++）,BB型、B+型和++型滩羊的基因型频率分别为0.64%、6.07%和93.29%,其中B等位基因频率为0.04,+等位基因频率为0.96;监测母羊群体的产羔数发现,FecB突变纯合型滩羊产羔率为166.67%,突变杂合型滩羊产羔率为153.12%,野生型滩羊产羔率为105.78%,纯合突变型和杂合突变型母羊群体的产羔率极显著高于野生型群体（P<0.01）。综上所述,与TaqMan探针法及PCR-Sanger测序法相比,本研究建立的绵羊FecB突变荧光qPCR分型方法具有简便易行、廉价高效的优点,在绵羊的分子选育中具有较高应用价值;同时本研究证实了滩羊FecB突变可显著提高母羊产羔率,为多羔滩羊的分子选育提供了坚实的技术支撑。