Molecular genetic structure and relationship of Chinese and Hungarian common carp (Cyprinus carpio L.) strains based on mitochondrial sequence

China and Hungary are major providers of the common carp (Cyprinus carpio L.) in East Asia and Europe respectively. However, the genetic variation and relationship of this species in the two countries have been poorly understood. In this study, mitochondrial COII‐tRNA^Lys and D‐loop sequences were analysed to investigate the genetic structure and relationships of the representative wild and domesticated common carps distributed in China and Hungary. The results indicated that the genetic diversities of the Chinese common carps are higher than those of Hungarian common carps, and the diversities of the wild common carps are higher than those of domesticated common carps in both the countries. Analysis of molecular variance and pairwise F_ST demonstrated a significant genetic divergence between the Chinese and the Hungarian common carps, and between the wild and the domesticated common carps. Bayesian phylogenetic analysis and statistical parsimony network showed an obvious genetic differentiation between the Chinese and the Hungarian common carps, between the wild and the domesticated common carps. However, a few specimens and haplotypes from the Chinese wild common carps appeared in the Hungarian common carps, demonstrating that there was no absolutely isolated and possible genetic linker between the Chinese and the Hungarian common carps.     

Establishing Cytoplasmic Male Sterility in Brassica napus by Mitochondrial Recombination with B. tournefortii

Fusion experiments between B. napus and X-ray-treated B. tournefortii protoplasts were carried out to develop cytoplasmic male sterility (ems) in B. napus. From the regenerants, six lines containing male sterile plants were selected; five lines segregated for male sterility, but one line (25–143) was completely male-sterile from the beginning. Molecular analyses of mitochondrial (mt) and chloroplast (cp) DNA of B. napus, B. tournefortii, B. juncea and cms juncea indicated that the original cytoplasmic donor of the cms juncea-system in B. napus was a B. tournefortii form, while the B. napus genotype used for the fusion experiments had a B. campestris cytoplasm. By analysis (it regenerated plants, line 25–143 was identified as possessing mt-DNA recombined between B. campestris and B. tournefortii. with the major part derived from B. campestris. No differences were detected between epDNAs from H. campestris and from line 25—143. The other five lines were similar to B. campestris with all the probes used. The low frequency of sterile lines from the fusion experiments and the inheritance of the cms in segregating progenies are both discussed.     

东亚4个黑山羊群体mtDNA D-环遗传多样性及其起源

为了研究地方山羊品种的起源与分化，了解其遗传背景，为山羊资源的合理利用提供基础资料，利用PCR产物直接测序法对3个中国黑山羊群体和1个韩国黑山羊群体共39个个体的mtDNA D-环部分序列进行了测定和分析。测定的序列经排列比对后选取441bp分析，发现了55个多态位点，单一多态位点11个，简约信息位点44个，确定了29种单倍型，单倍型多样度为0.984。构建系统发育树将29种单倍型分成了明显的3个分支，角猾羊聚入A分支。同时利用群体间的单倍型的错配分布和遗传距离分析了各群体的亲缘关系。结果表明：4个黑山羊群体遗传多样性丰富，至少拥有3个不同的母系起源，角猾羊是家山羊的一个母系祖先。     

Hatchery introgression blurs ancient hybridization between brown trout (Salmo trutta) lineages as indicated by complementary allozymes and mtDNA markers

Populations living on the periphery of a species range are subjected to intense habitat pressures that stress their vulnerability to threats. South Iberian brown trout (Salmo trutta) populations are located on the southwestern boundary of the species range in Europe. This region has been described as a contact zone between Atlantic and Mediterranean populations in other fish species, and allozyme data detected natural hybridization between native Atlantic and Mediterranean brown trout in this area. Nevertheless, native pattern of populations relationships are threatened by hybridization with exogenous hatchery fish. Allozyme data and complete mtDNA control region sequences were used to analyse the ongoing processes of human mediated hybridization between native and hatchery brown trout in this region. Estimates of the persistence of hatchery genes detected a high level of introgression in some of the sampled locations (hatchery ancestry more than 25% in GF-1, GF-2 and GF-3), but results differed from both kinds of markers. The low intrapopulation diversity (H_s = 0.051) indicated that genetic drift could explain discrepancies between markers. At individual level, the complementary use of both markers detected more hatchery origin fish than those detected by the use of a single technique. Based on these results, the importance of considering a large number of genetic markers to evaluate introgression accurately is emphasized. The ability of the current management policies to the protection and conservation of marginal populations that retain complex and special evolutionary histories such as those studied is also questioned.     

瓯江彩鲤线粒体DNA的限制性内切酶分析

用 13种限制性内切酶对瓯江彩鲤的线粒体DNA(mtDNA)进行RFLP分析 ,结果表明 :(1)共产生 18种限制性态型 ,其中 5种酶产生限制性片段长度多态性 (RFLPs) ,归结为 5种基因单倍型。 (2 )瓯江彩鲤mtDNA大小为 16 .6 0± 0 .15kb ,单倍型间的基因多样性指数和群体核苷酸多样性指数分别为 0 .75 17、0 .0 2 86 ,遗传多样性较丰富     

马铃薯亚细胞结构线粒体DNA的分离与提取

以马铃薯块茎为材料,通过差速离心分离出线粒体,过垫梯度离心进一步纯化。显微镜下观察所得的线粒体的纯度、形态;并用数码相机进行照相。线粒体样用SDS、蛋白酶K、核酸酶处理后用饱和酚、苯酚/氯仿及氯仿/异戊醇提取处理,乙醇沉淀,提取得线粒体DNA(mtDNA)。紫外分光光度计检测提取浓度、纯度,1%琼脂糖电泳获得清晰、整齐的条带。     

烟草雄性不育的分子机理研究进展

综述了烟草雄性不育分子机理研究的最新进展，包括：线粒体DNA与雄性不育；叶绿体DNA与雄性不育；核DNA与雄性不育等研究。     

Sequence Analysis of mtDNA COIGene and Molecular Phylogeny of Different Geographical Populations of Bemisia tabaci (Gennadius)

Bemisia tabaci(Gennadius) is a serious pest in many cropping systems worldwide and occurs in different biotypes. The mtDNA COI gene of the 12 Bemisia tabaci (Gennadius) populations from different regions and countries were analyzed.Based on mtDNA COI sequences, their biotypes were characterized and phylogenetic relationships among these populations were established with the method of UPGMA. The results indicated the genetic similarity between those populations from Beijing, Zhengzhou, Zaozhuang, Nanjing, Shanghai, Haikou, and the B-biotype populations from California, Texas, Arizona reached 99.8-100%, which meant the nation-wide infested populations of B. tabaci in China in recent years were B-biotypes. Another population collected from Kunming of Yunnan Province showed very high similarity with Q-biotype B. tabaci from Spain and Morocco, which meant the Kunming population was Q-biotype. This is the first report on the invasion of Q-biotype into China.     

线粒体DNA在动物分子系统学研究中的应用

mtDNA由于其自身的特点和优越性,已被广泛地应用于动植物分子系统学的研究。本文概述了mtDNA的基本特征、遗传特点和用于系统分类的优点,并对mtDNA在动物分子系统学中的部分研究成果做了概括。     

亚洲部分地区东方蜜蜂mtDNA多态性研究

 就云南省7个不同样点共7群东方蜜蜂蜂群开展mtDNA内切酶位点测试和分析研究,并与菲律宾的东方蜜蜂作对比分析。内切酶DraI分析7个蜂群,共发现4个内切酶位点;云南东方蜜蜂mtDNA的tRNAleu-COII基因的序列没有长度多态性,EcoRI内切酶位点共有4个,与菲律宾的吕宋岛的东方蜜蜂属于同一单倍型。另外,对来自尼泊尔、泰国、越南、老挝以及我国北京、云南等地的共13群蜜蜂mtDNA COII基因的420个碱基对进行测序分析,发现13群东方蜜蜂分析的420个碱基序列里,位点变异从0个到5个不等,变异率从0到1.19％. 用邻接法(neighbor-joining)构建的分子系统树可以看出分枝树主要分为两个类群:高纬度或高海拔的蜂群为一个类群,它们主要来自撒营盘（2）（China 4）、丽江(China 7)、北京(1)（China 1）、尼泊尔（Nepal）、北京（2）（China 2）、河口（1）（China 8）和越南（2）（Vietnam 2）。另一个类群的主要来自低纬度或低海拔的蜂群,它们主要来自撒营盘（1）（China 3）、景洪（China 5）、越南（1）（Vietnam 1）、泰国（Thailand）、河口(2) (China 6)和老挝(Laos)。该实验为我国东方蜜蜂资源的保护和开发研究提供了重要的信息和手段。