行为遗传的双生子研究

本研究采用双生子法对人类几项行为 (简单的生理-心理动作、记忆、智能、个性) 进行了研究。以探讨上述行为中遗传与环境因素的不同影响。结果证明,上述行为均有不同程度的遗传倾向。但这种倾向随着行为的简单到复杂及与环境接触时间的增长有所不同。似乎有减弱的趋势。Abstract: In order to investigate genetic and inviromental factors influenceing human behavios. Authors studies some humen behaviors (Physical-psychological action, memory, intelligence, and personality) with twins method. The result shows that the above behaviors have different genetic prepotency. It seems to be decrease depending on times of contacting enviroment and from simple to complex behaviors.     

云南纵坑切梢小蠹四个地理种群同工酶比较研究

采用不连续聚丙烯酰胺凝胶电泳技术研究了纵坑切梢小蠹(Tomicus piniperda L.)4个自然种群的9个同工酶基因座。4个种群均在Es-1、Es-2、Es-4、Mdh-1、Mdh-2及AAT-1基因座上存在遗传多态现象。路南长湖、楚雄、蒙自3种群间的遗传距离为0.0036～0.0173, 平均值为0.0105, 表明其遗传结构基本相似。丽江种群与上述3种群之间的遗传距离为0.1421～0.2035, 平均值为0.1765,表明丽江种群与上述三种群已有了遗传分化。丽江种群近交系数较大,近亲繁殖程度较高。种群遗传结构的差异可能与不同蠹害程度之间存在一定的内在联系。 Abstract:　Using uncontinued polycrylamide gel electrophoresis, comparative studies of isozymes between the four geographical populations of Tomicus piniperda L. in Yunnan province were carried out in this paper. Among 9 loci, loci Es-1、Es-2 、Es-4、Mdh-1、Mdh-2 and AAT-1 exhibited the genetic polymorphs. The Nei's genetic distance (D) among Lunan's, Chuxiong's and Mengzi's populations was 0.0036 and 0.0173 with an average of 0.0105, indicating the similar genetic structure among them. The genetic distance between Lijiang population and other three populations was 0.1421～0.2035 with 0.1765 on average, which implied a certain degree of genetic differentiation between them. Investigation indicated the forest damages by the beetle were high in Lunan, Chuxiong and Mengzi, and was low in other population in Lijiang; whereas inbreeding coefficient was bigger and inbreeding degree was higher in Lijiang, but all low in other three districts. It is so proposed that the differentiation of population in genetic structure is related to the damage levels of Tomicus piniperda L.     

不同地区库蚊复组群体的同工酶遗传多样性研究

采用水平切片淀粉凝胶电泳的方法,对分布于我国5省的8个库蚊复组（Culex pipiens complex）野生群体的遗传多样性进行研究,分析了4个酶系统7个基因座(ME、MDH-1、MDH-2、MDH-3、GPD、EST-2、EST-3)的酶谱资料。结果显示：（1）群体内存在不同程度的遗传变异（He为0.098～0.41）;（2）较低的基因流水平（Nm=0.64）使遗传漂变起主要作用,造成群体之间的遗传分化（Gst=0.303）,而总群体的遗传多样性相对富集于群体之内(Hs/Dst=2)。（3）库蚊群体的遗传结构属于距离隔离模式。（4）群体间的遗传一致性(或遗传距离)反映出群体间的遗传分化程度,也表明与地理位置存在对应关系。Abstract: Eight field populations of Culex pipiens complex collected from five provinces (Guangdong, Henan, Shandong, Beijing and Yunnan) in 2001 were used to study genetic diversity by starch gel electrophoresis. Data from seven loci (ME、MDH-1、MDH-2、MDH-3、GPD、EST-2、EST-3) of four isozymes were analyzed by software Biosys2.0 and FSTAT(Version 2.9.3). The results were as follows: (1) The values of He (from 0.098 to 0.41) indicated genetic variabilities of different degree in populations.(2)The low level of gene flow (Nm=0.64) could not prevent genetic drift to cause the gene differentiation between populations. The genetic diversity between populations attributed to the genetic diversity of total populations is small (Gst =0.303), and the great part is accumulated within populations (Hs/Dst=2). (3) The genetic structure of Culex pipiens complex population was the isolation-by-distance model. (4) The genetic identity (or genetic distance) revealed the scale of genetic differentiation between populations which related to the collection sites.     

栓皮栎天然群体SSR遗传多样性研究

利用微卫星(SSR)标记对我国4个省内的5个栓皮栎（Quercus variabilis Bl.）天然群体的遗传多样性进行了研究。16对SSR标记揭示了栓皮栎丰富的遗传多样性：等位基因数（A）平均8.4375个,有效等位基因数(Ne)平均为5.9512个,平均期望杂合度(He)0.8059,Nei多样性指数(h)为0.8041。栓皮栎自然分布区中心地带的群体具有较高的遗传多样性,而人为对森林的破坏将降低林木群体的遗传多样性。栓皮栎群体的变异主要来源于群体内,群体间分化较小,遗传分化系数仅为0.0455。此外,栓皮栎群体间的遗传距离与地理距离之间存在显著的正相关。这些遗传信息为栓皮栎遗传多样性的保护和利用提供了一定依据。Abstract: Genetic diversity of five Quercus variabilis natural populations in four provinces of China was studied with microsatellite (SSR) markers. A relatively high level of genetic diversity was detected in Q. variabilis species with 16 polymorphic microsatellite loci. Average number of alleles (A) and effective number of alleles (Ne) were 8.4375 and 5.9512 respectively. The mean expected heterozygosity (He) was 0.8059 and Nei diversity index (h) was 0.8041. Higher diversity was found with the populations from the central range of the species in contrast to those from peripheral areas and human activities might decrease the genetic diversity of populations. The majority of genetic variation occurred within populations, which could be concluded from the low coefficient of genetic differentiation (Fst=0.0455). In addition, significant correlation was found between geographical distance and genetic distance. All these results present a basis to the conservation and utilization of genetic diversity of Quercus variabilis.     

数量性状发育遗传模型及其分析方法的研究进展

发育遗传模型是同时反映性状遗传和发育本质、提供影响遗传变异及调整发育进程的有关因素的信息的模型。建立在群体遗传学基础上的直接效应模型适用于单一基因控制的简单性状。渐成模型将遗传变异分解成直接分量和渐成分量(母体效应和互作效应),能更好地反映有机体遗传和发育的生物学机制。生长轨迹模型有效地综合了复杂性状各分量的发育动态,可获得连续的、综合的、详细的、动态的发育信息。条件遗传分析方法不仅可以估算特定时间段的净效应,且可将净效应分解为不同遗传分量,了解各效应分量的相对贡献。 Abstract：Developmental genetic models and analysis methods for quantitative traits are presented.Developmental genetic models should reflect the genetic and developmental essence,and provide the information of the factors influencing the genetic variation and the developmental process.Direct effect models,which based on the population genetics,may be suitable to analyze simple traits with single gene.Epigenetic models can decompose the whole genetic variation into direct and epigenetic components (maternal effects and epigenetic interaction effects),so that biological mechanism can be better understood.Growth trace models effectively synthesize the developmental dynamics of components of complex traits.With them,continuous,compositive,detailed,and dynamic information of development is available.Conditional analysis method can not only estimate the net effects in a specific time interval,but also depose them into genetic components and help to appreciate the contributions of different effects.     

寄生蠕虫的群体遗传学研究

寄生蠕虫群体遗传学研究常用的遗传标记有等位酶、线粒体DNA、随机扩增多态性DNA或扩增性片段长度多态性和微卫星DNA等。应用这些遗传标记的研究表明,大多数寄生蠕虫群体遗传结构有不同水平的变异,这些变异的产生主要与寄生虫的生活史和群体生态、宿主的地理分布和环境等因素有关,并因此提出了有关遗传变异的一些假说。本文对寄生蠕虫群体遗传学的研究作一综述。 Abstract:Genetic markers including allozyme,mtDNA,RAPD/RFLP and micro DNA have been used in the research of helminth population genetics.Available data on helminth genetic variability have shown that most helminth populations exhibit different levels of genetic variation resulting mainly from the pattern of life cycle,geographical distribution and parasite-host interaction,and several hypotheses have been proposed to explain the genetic variation.     

家族高发性2型糖尿病的遗传模式研究

对1999～2000年门诊及住院的家族高发性2型糖尿病患者为先证者的136个大家系进行研究,以探讨该病的遗传模式。对家系人群采用Falconer 法估算遗传率,用Penrose法进行多基因分析,并用S.A.G.E-REGD软件拟合A型回归Logistic模型进行复合分离分析的方法,对家族高发性2型糖尿病家系进行研究。结果表明,136个大家系的2型糖尿病遗传率为94.07%±5.84%,提示在这些家系中可能有显性主基因存在。多基因分析研究表明,在该人群中,2型糖尿病因性别不同而存在两种遗传模式。复合分离分析拒绝单纯环境模型、非传递模型、共显性模型,接受隐性模型和显性模型,但隐性模型为最佳遗传模式。因此,2型糖尿病具有高度的遗传性和遗传异质性,总体表现为多因子遗传,在部分遗传背景较一致的家系人群中可能存在由主要基因决定的常染色体显性遗传。 Abstract:This study is to explore the genetic model of type 2 diabetes mellitus (type 2 DM) among the hereditary family.One hundred and thirty-six pedigrees of familial type 2 DM were studied.The heritability of type 2 DM was estimated according to Falconer's method and the multi-factorial inheritance analyzed according to Penrose's method.Complex segregation analysis was performed using S.A.G.E-REGD.The heritability of familial type 2 DM was 9407%±5.84%.Dominant major gene might influence the genesis of type 2 DM.Analysis of multi-factorial inheritance indicated that there be two genetic patterns respectively in male and female populations.By complex segregation analysis,environment,non-transmitted and co-dominant inheritance were rejected.Autosomal dominant (AD) inheritance and autosomal recessive (AR) inheritance was accepted but AR inheritance was the best pattern.This study suggested that type 2 DM had significant heritability and genetic heterogeneity,which appeared to be a disease of multi-factorial inheritance generally and autosomal dominant (AD) inheritance in part of pedigrees.     

昆明城郊中国树鼩群体线粒体DNA遗传多样性

由于树鼩是灵长类动物的近亲,且具有体型小、繁殖周期短、饲养管理成本低等优点,长期以来被认为有望替代灵长类动物用于人类疾病的动物模型研究.然而,目前对树鼩的群体遗传结构还知之甚少,这极大地限制了其在疾病动物模型研究的应用,也是其品系资源创制的瓶颈.本研究通过分析80只采自于云南省昆明周边地区的野生树鼩(Tupaia belangeri chinensis)线粒体DNA(mtDNA)多态性,结合国外报道的2个树鼩(Tupaia belangeri)序列比较后发现,在604 bp的mtDNA控制区片段中兵检测到29个核苷酸替代变异,这些变异共界定了13种单倍型,表现较高的群体遗传多样度.另外,昆明地区的树鼩与国外报道的2个树鼩间存在较大的遗传分化,mtDNA控制区单倍型之间的核苷酸替换数大于18个,远高于昆明地区树鼢群体内部不同单倍型之间的差异.选择含有代表性的mtDNA控制区单倍型的17个昆明地区树鼩个体进一步测定了细胞色素b基因片段(1134 bp),结合前人报道的数据分析,结果进一步支持mtDNA控制区数据反映的遗传格局及揭示的昆明地区树询与国外报道树鼩之间的明显差异.本研究结果提示,昆明地区树鼩与国外树鼩之间存在较大遗传差异,在将树鼩用于人类疾病动物模型研究中要注意这些遗传差别.昆明城郊的树鼩群体具有较高的遗传多样度,在开展近交系建立等工作时须考虑选取群体内部具有代表性的mtDNA世系.

Abstract：

Due to their special phylogenetic position in the Euarchontoglires and close affinity to primates, tree shrews have been proposed as an alternative experimental animal to primates in biomedical research. However, the population genetic structure of tree shrews has largely remained unknown and this has hindered the development of tree shrew breeding and selection. Here we sampled 80 Chinese tree shrews (Tupaia belangeri chinensis) in Kunming, China, and analyzed partial mtDNA control region sequence variation. Based on our samples and two published sequences from northern tree shrews (T. belangeri), we identified 29 substitutions in the mtDNA control region fragment (～ 604 bp)across 82 individuals and defined 13 hapiotypes. Seventeen samples were selected for sequencing of the cytochrome b (Cyt b; 1134 bp) gene based on control region sequence variation and were analyzed in combination with 34 published sequences to solidify the phylogenetic pattern obtained from control region data. Overall, tree shrews from Kunming have high genetic diversity and present a remarkable long genetic distance to the two reported northern tree shrews outside China. Our results provide some caution when using tree shrews to establish animal models because of this apparent genetic difference. In addition, the high genetic diversity of Chinese tree shrews inhabiting Kunming suggests that systematic genetic investigations should be conducted before establishing an inbred strain for medical and biological research.     

A behavioral paradigm to study the persistence of reward memory extinction in Drosophila

<正>Drosophila has been proven to be a powerful animal model to study genetic mechanisms underlying different behaviors and diseases (Sokolowski,2001;Bier,2005).Extinction is a process that repeated presentation of a conditioned stimulus without reinforcement results in decreased conditioned responses (Bouton,2004) and receives increasing attention for treating its related diseases such as post-traumatic stress disorder (PTSD) and addiction     

混合线性模型下猪群间遗传联系的度量

采用关联指数(IC)和决定系数(CD)两种方法,度量混合线性模型遗传评估下 猪群体间的遗传关联性。结果表明,加拿大安大略省的大约克夏猪、长白猪、杜洛克猪和汉普夏猪4个主要品种群体间具有良好的遗传联系。CD法既组合了数据结构和信息量,又考虑了预测误差方差和遗传变异性,是一个选择判断遗传评估精度的好方法。 Abstract:Two criteria for the measures of genetic connectedness in mixed linear model of genetic evaluation are used:the degree of connectedness(IC)and the generalized coefficient of determination(CD).The results indicated that the data of four dominant swine breeds:Yorkshire,Landrace,Duroc and Hampshire in Ontario,Canada are well connected.The CD,which combines data structure and amount of information and also accounts for both prediction error variance and genetic variability,is a good method to select for judging the precision of a genetic evaluation.     

14种多基因、疑为多基因遗传病的遗传率研究

本文采用Falconer法和其修正法计算了14种多基因疾病的遗传率（h2）。研究结果表明：脑性瘫痪、先天性耳廓畸形、原因不明精神发育迟滞、脊柱侧弯或瑚突有明显遗传倾向（h2>0.75）; 共转性内斜视、唇裂±腭裂、先天性髋关节关节脱位、多指（趾）症、腹股沟斜疝、银屑病（牛皮癣）及原发性癫痫有遗传倾向（0.60< h2<0.75）; 而共转性外斜视、精索静脉曲张、隐睾症以及先天性心脏病（各型）受遗传因素的作用相对较小（h2<0.60）。Abstract: An epidemiologic survey of genetic diseases was carried out in general population from 11 areas, 42 survey sites, 126876 people of Sichuan. With the stratified cluster random samping method, 150 kinds ofgenetic diseases were found according to the diagnostic strandard. And the heritabilities of 14 kinds of polygenic or polygenic-doubted diseases were estimated. The results showed that the contribution of genetic factors to aetiology is greater in cerebral paisy, congenital ear deformity, mental retardation of unknown actiology and scoliosis (h2>0.75). The congenital of genetic factors is moderate in con.comitant esotropia, cleft lip±cleft palate, congenital dislocation of the hip, Polydactyly, inguinal oblique hernia, psoriasis as well as idiopatic epilepsy (0.60< h2<0.75). The contribution of genetic factors is relatively little in concomitant exotropia, varicocele, enorchia and congenital heart disease (various types)( h2<0.60).     

动物遗传标记辅助选择研究及其应用

随着分子数量遗传学及其相关学科的发展,有关动物遗传标记辅助选择方面的研究也在不断深入,且已经在动物遗传改良中有了一些成功应用的示例。就如何综合利用表型、系谱和遗传标记信息进行育种值估计的统计学方法研究方面,目前已基本形成了较为完善的统计学方法。同时,在标记辅助选择相对效率及其影响因素,以及标记辅助选择实施方案的研究上也取得了不少喜人的成果。本文综述了动物遗传标记辅助选择研究的一些进展,并对标记辅助选择在动物遗传改良中应用的有关问题进行了讨论。 Abstract:With the development of molecular and quantitative genetics and its related subjects,it made a great progress on the research about animal genetic marker-assisted selection (MAS).There were also some successful examples on the application of MAS to animal genetic improvement.The statistical method which using phenotypic,pedigree and genetic marker information to predict individual breeding values has already been developed.Many achievements were obtained from the researches,which carried on MAS relative efficiency and its affecting factors and selection schemes.The present paper reviewed some progresses of MAS research and discussed some problems about MAS application to animal breeding.     

畜禽遗传评定方法的研究进展

畜禽遗传评定是畜禽育种的重要内容。目前畜禽遗传评定方法中应用最广的是基于表型信息的BLUP动物模型。基因组学的发展和应用产生了大量分子遗传标记,结合分子遗传标记信息的遗传评定方法MBLUP随之产生。MBLUP将成为一种快速有效的畜禽遗传评定方法。本文主要介绍了畜禽遗传评定方法的研究进展和发展趋势。 Abstract:Genetic evaluation is one of the most important components in livestock breeding program.Best linear unbiased prediction (BLUP) Animal Model,which based on phenotypic information,has become the most widely accepted method for genetic evaluation of domestic livestock.Large numbers of molecular genetic markers have been discovered as the development and application of genomics.Some new methods (Marked Assisted BLUP,MBLUP) for genetic evaluation have being developed,which incorporating molecular genetic markers information into genetic evaluation.MBULP will be a rapid and efficient method for genetic evaluation of domestic livestock.The aim of the paper is to introduce the development and current situation of the methods for livestock genetic evaluation.     

分子系统学研究中分子位点数与遗传差异信息可靠性的关系

用桑蚕(包括不同生态地理品种59个及野桑蚕)和桑属植物(包括12个种和2个变种)两类截然不同的材料,探讨了分子系统学研究中RAPD分子位点数与遗传差异信息可靠性间的关系。发现:(1)所分析的位点数多少与所能提供系统信息的量及可靠性之间有明显的关系;(2)当位点数在20以下时,得到的遗传差异的结果极不可靠,随着位点数的增加所提供的信息量及可靠性增加。当位点数超过70个时,所提供的信息可靠性趋于稳定;(3)对桑蚕和桑属植物两种截然不同的材料的分析,均得相似结果。由此推论:在用RAPD进行生物系统学研究中,以分析70个左右位点数为好;这一结论受研究对象的影响小,在其它类似的研究中或许具有一定的参考价值。 Abstract:We studied the correlation between the number of RAPD-loci investigated and the reliability of the information on genetic variation analysis using quite different two-kind materials,silkworms(including 59 geographic varieties of Bombyx mori belonging to different ecotype,as well as Bombyx mandarina M.)and mulberries(including 12 species and 2 varieties).The results showed as follows:(1)There was obvious correlation between the numbers of RAPD-loci investigated and the reliability of the information on genetic variation analysis.(2)The data were not suitable for the genetic variation analysis when the number of RAPD-loci in vestigated was smaller than 20.The more RAPD loci were analyzed,the more accurate genetic diversity would be identified when the number of the locus was varied from 20 to 70.Furthermore,the stable information to be available is shown when the number exceeded 70.(3)The similar regularities mentioned above were observed in both silkworm and mulberry.In order to get reliable information of genetic variation in molecular phylogenetic studies,at least 70 RPD loci would be investigated.And the results obtained in this study might be referential for AFLP and RFLP analysis.     

群体遗传不平衡条件下的结构基因遗传共适应特性

本研究以柴达木山羊、柴达木绒山羊和辽宁绒山羊三个群体共147只山羊为材料,利用聚丙烯酰胺凝胶电泳（PAGE）技术检测了5种血液蛋白质（酶）基因座的遗传多态性,并进行了结构基因遗传共适应的研究,结果发现：45个基因座组合中有10个基因座组合处于遗传不平衡状态,并且这些遗传不平衡皆单纯由遗传共适应差异造成;除辽宁绒山羊Tf-PA-3组合的遗传不平衡包含非等位基因间的遗传共适应差异外,其他基因座组合的遗传不平衡皆由等位基因间的共适应差异,即单基因座的遗传不平衡造成;LAP-EsD组合的共适应差异在群体间有遗传传递现象。 Abstract:With the technology of PAGE,the genetic polymorphism of blood protein and enzyme was investigated,and genetic co-adaptability among structural genes was studied in three goat populations(147 goats) including Chaidamu goat(CS),Chaidamu Cashmere goat(CRS) and Liaoning Cashmere goat(LRS) in Qinghai Province,China.The results were showed that the genetic disequilibrium of 10 locus combinations was found among 45 locus combinations in the three goat populations,and these genetic disequilibria were caused only by the difference of genetic co-adaptability among genes,because there didn′t exist the linkage disequilibrium among non-allelic genes.The genetic disequilibrium including the difference of genetic co-adaptability between non-allelic genes was only found at Tf-PA-3 locus combinations in LRS population,the other ones were all caused by the genetic disequilibrium at a single locus.The difference of genetic co-adaptability of LAP-EsD locus combinations could be messaged among different populations.     

注意植物迁地保护中的遗传风险

稀有濒危植物迁地保护的长期目标之一就是要保护物种的遗传多样性和进化潜力。介绍了稀有濒危植物在植物园迁地保护过程中存在的一系列遗传风险。由于引种或取样的不足,容易导致被保存的物种缺乏足够的遗传代表性;盲目的引种、不合理的定植以及材料的来源不清则会导致稀有濒危植物的遗传混杂、近交衰退或杂交衰退;人为选择和生长环境的改变也容易造成濒危物种对迁地保护的遗传适应。在实际的迁地保护工作中,这些遗传风险往往被忽视。植物迁地保护中遗传风险将严重影响稀有濒危物种的回归和恢复。植物园应当重视濒危植物的遗传管理,以降低或避免迁地保护中的遗传风险。Abstract: Conserving genetic diversity of rare and endangered species and their evolutionary potential is one of the long-term goals of ex-situ conservation. Some potential genetic risks in ex-situ conservation in botanical gardens are presented. The preserved species may lack genetic representativity because of poor sampling. Inappropriate plantations, inadequate records and unclear kinships jeopardize endangered species to genetic confusion, inbreeding depression or outbreeding depression. Artificial selection and habitat conversion also potentially result endangered plants in adapting to ex-situ conservation, which had been usually overlooked. All the genetic risks can decrease the success of reintroduction and recovery. Therefore, appropriate genetic management should be carried out in botanical gardens to decrease or avoid genetic risks in ex-situ conservation.     

群体遗传结构中的基因流

群体遗传结构上的差异是遗传多样性的一种重要体现,对群体遗传结构的研究已有较久的历史,而其中的基因流研究近些年来越来越受到重视。它对群体遗传学、进化生物学、保护生物学、生态学有着极其重要的作用。虽然传统的群体遗传学能估测基因流大小,但它的精确性还有很大局限性。随着生物技术的进步,对基因流的研究逐渐向分子水平过渡,应用蛋白质电泳技术、分子标记技术(RAPD、RFLP、VNTR、ISSR、DNA测序等)方法对群体间基因流的流动水平进行了深入细致的研究。本文综述了群体遗传结构的几种模式：陆岛模式、海岛模式、阶石模式、距离隔离模式、层次模式,以及在群体遗传结构的几种模式基础上的基因流的研究方法、作用、地位和近些年来研究者的研究成果,并指出了这些方法的局限性。Abstract: The difference of population genetic structure is one of the important embodiments of genetic diversity. There is a long history of the study of population genetic structure, and the study of gene flow of population genetic structure is aroused more and more importance. It has an important effect on population genetics, evolution biology, conservation biology and ecology. Although the level of gene flow is estimated by traditional population genetics, there is a large restriction in its precision. With the development of biological technology, the methods of the research on gene flow reach the molecular level. Methods of protein electrophoresis and molecular markers (RAPD, RFLP, VNTR, ISSR and mitochondrial DNA) are used to research gene flow among populations. This paper introduces not only some models of population genetic structure: Continent-Island Model, Island Model, Stepping-Stone Model, Isolation-By-Distance Model and Hierarchical Model; but also the study methods, function and role of gene flow is based on models of population genetic structure, research achievements in recent years and the restriction of the methods.     

RAPD分析在绢丝昆虫亲缘关系研究中的应用Ⅱ.柞蚕品种间的遗传差异

采用RAPD技术,对5个柞蚕品种的遗传差异进行比较研究.结果表明,所采用的40个随机引物中,有27个引物扩增谱带清晰且重复性较好,扩增总片段数253条,单个引物的扩增片段数在4～16之间,片段大小在0.33～3.0kb之间.不同柞蚕品种间的遗传差异较小,遗传距离(D)在0.066～0.1659之间,根据D值,由UPGMA聚类分析软件绘制了它们的分子进化树。 Abstract:Random amplified Polymorphic DNA (RAPD) was used to analyze the genetic diversity among Antheraea pernyi.The genetic variance of five Antheraea pernyi was studied.The result showed that:27 of 40 arbitrary primers could amplify clear and repeating bands.A total of 262 fragments were obtained.Each primer gave 4~16 bands and the average was 9.7.The length of the band was 0.33~3.0kb.The D value between different breeds of Antheraea pernyi was 0.066~0.1659.The D value was used to construct a dendrogram by UPGMA.     

波尔山羊及其杂交改良后代群体遗传结构与亲缘关系研究

利用RAPD标记和POPGENE、PHYLIP及SPSS等统计分析软件,研究了波尔山羊及其杂交改良后代群体的遗传结构及遗传亲缘关系。结果表明,波尔山羊与其杂交改良后代间特别是高代杂种间具有相似的多态基因座百分率、等位基因数和基因多样性。随着级进杂交改良代数的递增,高代杂种之间以及与改良亲本之间的群体遗传结构的差异逐渐缩小,群体间的基因分化降低,基因流动和遗传相似度增加,遗传距离缩小,高代杂种与波尔山羊间具有更近的遗传亲缘关系。 Abstract:The genetic structure and relationship of Boer goat and its upgrading offspring to Tangshan Diary goat were studied using the RAPD marker and some statistical program,such as POPGENE,PHYLIP and SPSS.The results indicated that there were the similar percentage of polymorphic loci,observed and effective number of alleles,gene diversity between Boer goat and its upgrading offspring,especially higher upgrading offspring.With the increasing of upgrading,the difference of population structure decreased as well as the genetic distance and differentiation among higher upgrading offspring and their improving parental,but gene flow and genetic identity increased.There was a close genetic relationship between higher upgrading offspring and Boer goat.     

松属植物遗传多样性研究进展

研究松属遗传多样性的方法涉及表型、同工酶、染色体、DNA等多层面。 松树表型性状变异广泛,其不同树种不同性状的遗传力（或遗传率）均存在差异。到目前为止,同工酶仍是检测松树遗传多样性的最常用方法,一般而言,松属树种群体内等位酶多样性程度高,群体间分化较低,但各树种的情形也不尽相同。松属树种染色体水平的变异很低,其核型高度一致。核DNA组较一般阔叶树大,遗传多样性丰富,但叶绿体等质体DNA则多样性较低。影响遗传多样性的因素很多,其中自身的交配系统和外部的生长环境是影响它的两个主要因素。最后,回顾了松树的起源及其遗传多样性保护策略等方面的研究。 Abstract:The ways of probing genetic diversity of pines involve many aspects,such as morphology,chromosome,isozyme,DNA,etc.The phenotypic characteristics in pines vary widely and the differences of inheritability(h2) are obvious among characteristics and among species.Up to now,isozyme is still the most common means to measure genetic diversity of pines.Generally,there are high allozyme diversity within populations and low differentiation coefficient among populations,but differences exist between species in Pinus.The variations of chromosome among pines are very low and the karyotypes of pines are consentaneous,but the genomes of pines in cell nucleus are much larger than that of broadleaves.Diversity of pines are abundant at nucleus DNA level but are poor at plastid DNA level,such as ctDNA.There are many factors that will affect genetic diversity of pines,in which mating system and environment are two main factors.Finally,we reviewed the research on origin of Pinus and conservation strategy of genetic diversity,etc.