勐养保护区亚洲象微卫星位点筛选及种群遗传多样性分析

本文以亚洲象肌肉样品提出的DNA为模板,从非洲象31个微卫星位点和5个已知亚洲象微卫星位点中筛选勐养亚洲象的微卫星位点,进而对在西双版纳勐养保护区3年采集到的191 份亚洲象粪便样品中提出的DNA进行特异性PCR扩增、基因分型、检测位点信息和遗传多样性分析.结果表明:36个位点中有14个位点能在亚洲象肌肉样品提出的DNA中成功扩增,且经测序证实为微卫星位点.其中9个多态位点能在185份粪便样品DNA中稳定扩增.勐养种群中,3个位点可能偏离Hardy Weubberg平衡,至少8个位点间无明显连锁存在,平均等位基因数3.78±1.72,平均期望杂和度0.32 ± 0.06,平均观察杂和度0.36±0.02,平均多态信息含量0.28 ,说明这9个位点适用于勐养亚洲象的遗传学研究.根据微卫星位点的杂合度和等位基因频率,相比于其他亚洲象种群,勐养亚洲象种群遗传多样性较低且等位基因频率具有特异性.     

无特定病原体金定鸭微卫星DNA遗传多样性分析

目的利用微卫星标记对无特定病原体金定鸭群进行遗传多样性分析。方法采用微卫星标记,对SPF金定鸭种群中71个个体进行遗传多样性分析。结果 SPF金定鸭种群中17个位点上共检测到119个等位基因,每个微卫星上等位基因数介于3~13;该SPF金定鸭群体中有13个位点(PIC0.5)呈现出高度多态,平均杂合度为(0.5816±0.0142),其他位点均呈现出中度多态。仅有5个位点处于Hardy-Weinberg平衡状态,其余12个位点显著偏离Hardy-Weinberg平衡,达到极显著水平(P0.01)。结论该SPF金定鸭群体内均存在丰富的遗传多样性,满足建立封闭群的遗传特征,可以利用该群体继续开展无特定病原体金定鸭封闭群的建立。     

喜马拉雅旱獭种群微卫星变异及遗传多样性

为了解不同地理种群喜马拉雅旱獭(Marmota himalayana)的种群数量变化并探讨其内在的遗传学机制,通过构建部分基因组文库的方法筛选出8个高变异微卫星位点,根据微卫星位点的测序结果设计相应引物,PCR扩增检测了青藏高原4个地理种群(德令哈、乌兰、沱沱河、安多)喜马拉雅旱獭的遗传多态性及其种群结构.研究结果显示:8个位点在喜马拉雅旱獭种群中均为高度多态,观察等位基因数、有效等位基因数、多态信息含量分别为4.75、3.033 2、0.610 2;喜马拉雅旱獭种群总的期望杂合度和观察杂合度分别为0.670、0.699;3个喜马拉雅旱獭种群显著(P＜0.05)或极显著(P＜0.01)偏离H-W平衡状态,且这些偏离平衡的位点均由杂合过度导致(FIS＜0);喜马拉雅旱獭种群的部分位点已经偏离了突变-漂移平衡.结论:筛选出的8个微卫星位点适合于喜马拉雅旱獭种群遗传多样性的研究,所研究的喜马拉雅旱獭种群有较高的遗传多样性,安多地理种群在近期可能经历过瓶颈效应,种群数量曾经下降.     

基于转录组测序的大熊猫多态性微卫星标记筛选

结合已公布的大熊猫Ailuropoda melanoleuca基因组和本实验室所测6只大熊猫的转录组数据,筛选多态性微卫星位点并分析其组成及特征。结果显示:共获得326个多态性微卫星位点,其中二碱基多态性微卫星最多,共228个,占69.93%;三、四、五、六碱基所占比例分别为9.51%、14.11%、5.21%、1.22%。根据分析结果中缺失率与标准差2项指标以及位点序列长度,选取20个多态性二碱基微卫星位点,用于25只大熊猫个体血液DNA进行PCR验证并做后续分析。结果表明:不同位点的等位基因数为2~8,平均等位基因数为3.70,观测杂合度、期望杂合度分别为0~1.000、0.280~0.784,平均值分别为0.472和0.532。在Bonferroni校正后,证实4个位点显著偏离哈迪-温伯格平衡,所有位点未观察到显著连锁不平衡(P>0.01)。20个位点多态信息含量(PIC)在0.246~0.734,其中具有高度多态性的位点9个(PIC>0.50),11个位点呈中度多态性(0.25相似文献   

应用微卫星标DNA记对三个封闭群兔遗传分析

目的检测国内Et本大耳白兔、青紫蓝兔、新西兰白兔的遗传背景及遗传结构,为封闭群兔遗传检测方法建立和标准化提供基础资料。方法应用18个微卫星标记及荧光标记一半自动基因分型技术对三个群体95个个体进行Hardy．Weinberg检测,统计每个位点等位基因频率、杂合度、F值、遗传距离等信息。结果三个种群平均等位基因观测数为3．167、4．556、3．444,平均观测杂合度为0．444、0．5230、0．4976。18个位点平均多态信息含量（PIC）为0．410、0．549、0．470,日本大耳白兔6个位点HWE检验（P〈0．05）,显著偏离Hardy—Weinberg平衡,并在Satl3,INRCCDDV0088位点基因型完全纯和,新西兰白兔和青紫蓝兔分别有2个位点显著偏离Hardy—Weinberg平衡。三个种群遗传距离：青紫蓝兔与新西兰白兔遗传距离最近,为0．124,与日本大耳白兔遗传关系最远,为0．320;新西兰白兔与日本大耳白兔较远,为0：10。结论三个种群有各自不同遗传特征,遗传多样性较高,种群间分化明显。个别位点偏离遗传平衡,推测人工繁育过程中存在一定问题。     

微卫星标记对WHBE兔封闭群、日本大耳白兔和新西兰兔的遗传分析

目的分析比较大耳白黑眼兔（WHBE兔）封闭群与日本大耳白兔（Jw兔）、新西兰兔（NZW兔）基因组存在的微卫星结构,研究WHBE兔封闭群的微卫星多态性。方法利用21个微卫星位点,通过微卫星分子标记技术对WHBE兔封闭群、Jw兔和NZW兔进行遗传多样性检测和对比。结果根据初步结果,在21对微卫星引物中筛选出扩增产物稳定并且具有多态性的11对引物。WHBE兔封闭群在每个位点上的等位基因数为3～8个不等,11个位点的平均有效等位基因数为2．0402个,平均杂合度为0．4810;Jw兔在每个位点上的等位基因数为2～8个不等,11个位点的平均有效等位基因数为3．6077个,平均杂合度为0．5039;NZW兔在每个位点上的等位基因数为3～9个不等,11个位点的平均有效等位基因数为2．6537个,平均杂合度为0．5334。WHBE兔封闭群在11个微卫星位点上的平均多态信息含量（PIC）为0．6005,多位点累积个体识别率达到100％,多位点累积非父排除概率（CPE）在双亲信息都是未知情况下的为0．9613,而在得知任一亲本信息的情况下,CPE值高达0．9973。在11个微卫星座位中,9个位点上出现了WHBE兔封闭群特有等位基因,其中在Sat2、Sat5、Sat7、Sat12、Sat13、Sat16、S0144和INRACCDDV0003八个位点上WHBE兔封闭群的特有等位基因为一个,在sat8位点上为两个。结论WHBE兔8个位点的平均杂合度、平均有效等位基因数均比JW兔及NZW兔低,说明WHBE兔群体的基因纯合度高于其他两个品系,具有更优的遗传稳定性。9个WHBE兔特有的等位基因可作为区分WHBE兔封闭群和其它两个品系实验兔的分子标记。     

白颈长尾雉微卫星多态性的遗传学分析

采用7个微卫星位点遗传标记,对白颈长尾雉(Syrnaticus ellioti)4个地理种群105个个体进行了种群遗传分析。研究发现4个地理种群均偏离Hardy-Weinberg平衡,共检测到62个等位基因,平均等位基因数目为8.86;大多数微卫星位点的观察杂合度值较低,平均为0.504,要明显低于期望杂合度。7个位点的多态信息含量为0.549～0.860,平均为0.712。用无限等位基因模型、逐步突变模型和双相突变模型对4个地理种群的种群瓶颈效应检测,发现各种群近期内都经历过瓶颈效应的影响。地理种群之间的Fst值表明,贵州与湖南地理种群间的分化达到了极显著水平(P<0.001);由Nei氏的无偏遗传距离所构建的邻接树显示,贵州地理种群与湖南地理种群的遗传关系较远。微卫星对不同地理种群的分层分子变异分析(贵州地理种群对其他地理种群)发现:来自地理种群间和组群间的遗传变异量相对较小;而同一地理种群内个体之间的变异量较大(92.84%),且达到显著水平。     

长江下游地区夜鹭种群微卫星变异及遗传多样性

利用微卫星位点对长江下游地区夜鹭3个地方种群的遗传多样性及其种群结构进行了分析。研究结果表明:除了Ah526位点外,其他7个位点在夜鹭种群中均为高度多态。在3个地方种群中,6个微卫星位点中经Bonferroni校正后南京大校场种群和芜湖四褐山种群中分别有2个及3个位点显示杂合不足,显著偏离了哈迪-温伯平衡,这可能与夜鹭繁殖后个体的扩散能力较强及长江下游地区夜鹭存在着替代型迁徙现象有关。突变-漂移平衡分析表明,长江下游地区夜鹭种群显著具有杂合过剩的位点,这表明长江下游地区夜鹭种群已偏离了突变-漂移平衡,近期可能经历了瓶颈效应,种群数量曾经下降。地方种群间Fst分析表明,长江下游地区夜鹭地方种群间遗传分化程度较低,并没有形成显著的遗传结构,在保护与管理上可以作为同一个保护单元(或管理)单元     

长江中上游两个鲢群体遗传变异的微卫星分析

对长江中上游2个鲢群体使用39个微卫星标记进行了遗传多样性分析, 计算并统计了平均观测等位基因数、平均有效等位基因数、多态信息含量、遗传杂合度、Hardy-Weinberg平衡偏离指数、遗传相似系数、遗传距离等遗传参数。结果表明: 万州鲢和监利鲢群体所检测微卫星位点的平均观测等位基因数分别为6.128和4.974; 平均有效等位基因数分别为4.107和3.395; 多态位点百分率分别为100和94.87; 39个微卫星标记共有等位基因259个, 173个等位基因为两群体所共有; 多态微卫星位点的PIC在0.077~0.865之间变动,平均为0.617; 两群体所检测位点平均观测杂合度为0.834和0.775, 平均期望杂合度为0.713和0.623; 两个群体间的遗传相似系数为0.618, 群体间的遗传距离为0.482。结果显示长江中上游两个鲢群体间存在显著遗传分化, 应隶属于不同的种群。     

我国新引进吉富品系尼罗罗非鱼群体的遗传多样性分析

选取罗非鱼(Oreochromis spp.)第二代遗传连锁图谱中的26个微卫星位点,对淡水渔业研究中心引进的、由60个家系组成的吉富品系尼罗罗非鱼(O.niloticus)群体进行遗传结构分析。结果显示,26个微卫星位点在吉富罗非鱼群体中共检测到124个等位基因,各位点的等位基因数为3～7个,平均4.8个。片段长度104～322 bp,平均杂合度观测值为0.622 1,平均杂合度期望值为0.642 3,平均多态信息含量(PIC)为0.633 4。所检测的26个位点中,有25个位点属于高度多态位点(PIC0.5),占所检测位点的96.15%;1个位点属于中度多态位点。结果表明,该吉富罗非鱼群体多态信息含量丰富,遗传多样性水平较高。因而该群体仍然具有较大的选育潜力,可以作为选育的基础群体开展进一步的选育工作。     

Isolation and characterization of microsatellite markers from the limpet Cellana grata

This note describes the development of nine polymorphic microsatellite loci in the limpet Cellana grata to investigate population structure and cohort variation in this species. The number of alleles ranged from seven to 22 and observed heterozygosity ranged from 0.62 to 0.95. Deviation from the Hardy-Weinberg equilibrium was detected in two loci, both as a result of heterozygote deficiency. Null alleles were detected in one of these loci. These genetic markers will be used to investigate the genetic structure of C. grata populations, as well as variation among cohorts of this common intertidal species.     

PERMANENT GENETIC RESOURCES: Development of microsatellite markers for two nonviviparous mangrove species, Acanthus ilicifolius and Lumnitzera racemosa

Eight and nine of microsatellite loci were isolated from two nonviviparous mangrove species, Acanthus ilicifolius and Lumnitzera racemosa, respectively. The number of alleles per locus ranged from two to eight in A. ilicifolius and two to nine in L. racemosa. The observed heterozygosities ranged from 0.200 to 0.875 in A. ilicifolius and from 0.025 to 0.350 in L. racemosa. These loci would be effective for analysing genetic diversity and population genetic structure of these two mangrove species.     

Characterization of microsatellite markers in the shea tree (Vitellaria paradoxa C. F Gaertn) in Mali

In order to study the genetic diversity and structure in the population of Vitellaria paradoxa, we characterized eight polymorphic microsatellite loci. Primers to amplify these loci were tested on 169 individual trees representing a sample of the population of shea tree in Mali. The loci were all polymorphic with a number of alleles between three to nine and with observed level of heterozygosity ranging from 0.035 to 0.507. These markers will be useful for genetic and ecological studies of this species.     

Microsatellite primers in the endangered quillwort Isoetes hypsophila (Isoetaceae) and cross-amplification in I. sinensis

? Premise of the study: The first microsatellite primers were developed for Isoetes hypsophila, an endangered quillwort species endemic to the Qinghai-Tibetan Plateau in China, to further describe its genetic variability and population structure. We also examined their cross-amplification in a congeneric species, I. sinensis. ? Methods and Results: Using the Fast Isolation by AFLP of Sequences COntaining Repeats (FIASCO) protocol, nine microsatellite loci were isolated and characterized in 32 samples from four natural populations of I. hypsophila. The primers amplified di- and hexanucleotide repeats with three to 11 alleles per locus. Seven of nine primers were cross-amplified in I. sinensis with two to seven alleles per locus. ? Conclusion: The microsatellite loci primers will be useful for studies of genetic diversity and gene flow in natural populations of Isoetes species.     

Development and characterization of the first microsatellite markers in the mangrove species Pelliciera rhizophorae Triana & Planchon

Pelliciera rhizophorae is a unique Neotropical mangrove species belonging to Pelliciera genus. We isolated eight microsatellite loci from this species. All loci were polymorphic and showed three to nine alleles per locus in Colombian Pacific and Caribbean populations. Polymorphic information content ranged from 0.46 to 0.69. Two loci (PeRh‐14 and PeRh‐19) showed null alleles on the Caribbean coast, which suggest genetic differentiation between Pacific and Caribbean populations of P. rhizophorae. Development of these microsatellite loci constitutes a new molecular tool to carry out studies in the genome of the species and to evaluate its population dynamics.     

Allozyme differentiation and genetic structure of the Lady's slipper (Cypripedium calceolus) island populations in north-east Poland

The population genetic structure in the rare and endangered perennial plant, Cypripedium calceolus , from north-east Poland was investigated. A total of 11 loci were analysed, of which five were polymorphic for the species and in every population. The 11 loci resolved gave a total of 19 alleles with the mean number of 1.73 alleles per locus. The proportion of polymorphic loci (P) was the same for the species and in every population, 45.5%. The average observed and expected heterozygosities for the total Lady's slipper data set were 0.156 and 0.184, respectively. The average expected heterozygosity for the populations under study ranged from 0.176 to 0.188 and did not differ significantly among populations. Genetic diversity within C. calceolus populations from the Biebrza Valley is relatively high compared with rare taxa and taxa with similar life histories. The genetic diversity among populations of C. calceolus studied ( F _ST = 0.016) is much smaller than the genetic diversity within populations. In the species studied, there was no significant correlation between genetic and geographical distances ( r = −0.73, Mantel test). This may indicate the relatively recent origin of the populations studied, or a high level of gene flow among populations. © 2002 The Linnean Society of London, Botanical Journal of the Linnean Society , 2002, 138 , 433–440.     

Low level of genetic variability in European bisons (Bison bonasus) from the Bialowieza National Park in Poland

Nuclear DNA markers (microsatellites) were used to screen the genetic variability in the European bison population of the Bialowieza National Park, Poland. The species is listed as endangered and the Bialowieza population is the largest one worldwide. Many other herds were founded by individuals from Bialowieza. Out of 18 microsatellites, nine were polymorphic, five were found to be homozygous, and four loci did not amplify. No significant deviation from Hardy–Weinberg-equilibrium (HWE) was observed, and the average number of alleles was 2.3 per locus. Thus, the European bison is characterized by a very low level of genetic diversity, most likely resulting from the population decline in the nineteenth century. Nevertheless, allelic variability derived from the nine polymorphic loci established in this study allowed to identify each individual by its genotypic profile. This data is valuable for conservation plans of this impressive species, especially for the control of breeding success in these animals.     

Informative microsatellites for genetic population studies of black-faced lion tamarins (Leontopithecus caissara)

Leontopithecus caissara is a critically endangered primate species from the Brazilian Atlantic Forest. Nineteen microsatellite loci, previously developed for congeneric species, were tested with 34 L. caissara individuals from Superagüi Island. Of the 19 loci, 17 (89.4%) produced robust alleles, nine (47.4%) of these proved to be polymorphic, with a total of 23 alleles and an average of 2.56 alleles per locus. Expected and observed heterozygosity averaged 0.483 and 0.561, respectively. The exclusion power for identifying the first parent of an arbitrary offspring was 0.315 over all loci. The results thus indicate both the usefulness and limitations of these nine microsatellite loci in the genetic analysis of L. caissara, as well as their potentiality for genetic investigation in other congeneric species.     

Characterization of 22 microsatellites loci from the endangered Houbara bustard (Chlamydotis undulata undulata)

Here we present a new set of 22 microsatellite loci isolated from Chlamydotis undulata undulata, an endangered Houbara bustard found across North Africa. The number of alleles per locus ranged from one to nine, and heterozygosities ranged from 0.167 to 0.944. Total exclusionary probabilities using these loci for the first and the second parent were 0.992932 and 0.999915, respectively. Successful cross‐amplification was observed in eight other Otididae species (12–22 of the 22 loci). These microsatellite markers are powerful tools for genetic identification, paternity assignment and population genetic studies.     

Development of microsatellite markers in Fosterella rusbyi (Bromeliaceae) using 454 pyrosequencing

? Premise of the study: Polymorphic microsatellite markers were developed for Fosterella rusbyi (Bromeliaceae) to evaluate the population genetic structure and genetic diversity of natural populations of F. rusbyi and other Fosterella species in Bolivia. ? Methods and Results: 454 pyrosequencing technology was used to generate 73027 sequence reads from F. rusbyi DNA, which together contained 2796 perfect simple sequence repeats (SSRs). Primer pairs were designed for 30 loci, of which 15 were used to genotype 30 F. rusbyi plants from two geographical areas in Bolivia. All markers were polymorphic, with two to nine alleles in the overall sample. Cross-species amplification was tested in 10 additional Fosterella species. Seven loci showed consistent amplification in six or more species. ? Conclusions: The 15 SSR markers developed for F. rusbyi are promising candidates for population genetic analyses within F. rusbyi and other species of Fosterella.