鲤低氧适应性状的全基因组关联分析

低氧适应是水产养殖物种的重要性状,筛选用于改良低氧适应性状的分子标记及候选基因有助于鱼类耐低氧品种选育.在数量性状和质量性状的遗传研究中,全基因组关联分析(GWAS)广泛应用于性状相关标记和基因的发掘.本研究对鲤(Cyprinus carpio)养殖群体开展了低氧胁迫实验,选取了低氧敏感和低氧耐受的极端性状个体作为研究...     

Development and Validation of Single‐nucleotide Polymorphism Markers in the Pacific Oyster,Crassostrea gigas,Using High‐resolution Melting Analysis

High‐resolution melting (HRM) has been considered as a fast and simple single‐nucleotide polymorphism (SNP) scanning and genotyping method for identifying differences in the shapes of melting curves between different genotypes. Fifty‐six SNPs were developed in the Pacific oyster, Crassostrea gigas by mining expressed sequence tags database, using the HRM method. The frequency of the SNPs was estimated at 1 per 113 bp of contig sequences. Analysis of segregation in a full‐sib family showed that 28 SNPs were polymorphic, with 15 in accordance to expected Mendelian ratios. Linkage grouping of the 28 markers resulted in six linkage groups. The combined power of exclusion of the 42 SNPs, which conformed to Hardy–Weinberg equilibrium, was greater than 99.98%, while the average polymorphic information content was 0.2223. The simulation results showed that the success rate of parentage analysis could be 97% with the 42 SNPs. These SNPs will be useful for pedigree analysis, association studies, and marker‐associated selection of this species .     

Characterization of single‐nucleotide polymorphism markers in the Mediterranean mussel,Mytilus galloprovincialis

The Mediterranean mussel, Mytilus galloprovincialis, is one of the most important aquaculture species in Europe. Appropriate molecular markers are required to evaluate genetic resources and to trace genealogies in breeding programmes for improving mussel culture. Microsatellites have been commonly applied to this purpose in other species. However, Mediterranean mussel microsatellites have demonstrated high frequencies of null alleles that hamper accurate estimates of population parameters and confident parentage inferences. As alternative markers, we have characterized in silico 25 potential single‐nucleotide polymorphism (SNP) markers in the Mediterranean mussel from expressed sequence tag (EST) public databases. The genotyping of SNPs was performed using a single‐base extension approach. Their polymorphism was evaluated in 47 individuals from an Atlantic population. Out of the 25 potential SNPs tested, 12 were technically feasible (producing a single amplicon) and polymorphic. All were biallelic and had an unbiased heterozygosity ranging from 0.160 to 0.504. One SNP was from a mitochondrial gene. The combined potential of nuclear SNPs for parentage assignment gave an exclusion probability of a false couple of parents of 0.9471. These markers will be useful for evaluating resources and tracing genealogies in genetic breeding programmes implemented to solve the main problems of mussel culture.     

Identification,Characterization, and Evaluation of Polymorphic Microsatellite Markers for Parentage Assignment in Pinctada fucata

Parentage analysis is a useful tool for establishing pedigree relationships in selective breeding. In this study, 31 microsatellite markers were tested, and 13 loci were subsequently used to identify parenthood in Pinctada fucata. According to simulation analysis, the power of nine loci to exclude false parents was 99.94%, and that of 10 loci was 99.95%. Moreover, using 10 loci and known parental and filial information, the cumulative assignment success rate to one true parental pair was as high as 99%. Of the 120 progeny tested, 93.3% were exclusively assigned to their parental pairs in mixed pedigrees. These results suggested that these microsatellite markers can be used for rapid and effective parentage assignment and contribute to the selective breeding of P. fucata.     

Use of Microsatellite DNA Profiling to Identify Japanese Flounder,Paralichthys olivaceus of Hatchery Origin

Japanese flounder, Paralichthys olivaceus, is an economically important marine fish species in Asia. A suite of 18 microsatellite markers chosen from published genetic linkage maps was used to carry out parentage assignments of 188 hatchery‐reared juveniles from a small number of breeders. The probabilities of exclusion for the 18 microsatellite markers were 0.604–0.913, and the effectiveness of combined probability of exclusion reached 100% when using the eight microsatellite markers with higher Excl 1 probabilities. The cultured and wild stocks (WSs) were differentiated in a release‐recapture population based on these markers. Of the 321 recaptured offspring, 28.34% were assigned to their parental pairs in our broodstock, whereas the remaining offspring could not be traced back to a possible sire or dam. Significant reduction in genetic diversity of the cultured stock (CS) had not been found compared with that of the WS. The results suggest that CSs released into the wild will not adversely affect the genetic structure of natural populations. Our results demonstrate that these markers provide an efficient tool for parentage assignments and genetic analysis of Japanese flounder.     

Application of microsatellite DNA parentage markers in the swimming crab Portunus trituberculatus

Microsatellites have been a powerful genetic tool in determining pedigree relationships among individuals. A microsatellite marker suite can be used to reliably assign parentage in the Portunus trituberculatus selective breeding programs. Thirty published microsatellites were screened for their suitability to be included in a DNA parentage marker suite. Nineteen microsatellite markers that exhibited significant stutter, poor allele resolution, null allele, and significant deviation from Mendelian expectations were eliminated from the marker suite, and the left eleven markers were ranked by PIC. Six most polymorphic markers with mean He?=?0.928 and PIC?=?0.901 from the original eleven were further assessed for the efficiency of pedigree identification. Total predicted power of the markers to exclude false parents was higher than 99%. Both simulations and real data analysis confirmed the high statistical power of six microsatellites suite in parentage exclusion, which permit us to trace back all offspring to single pairs of parents.     

凡纳滨对虾SNP标记开发与家系亲缘关系验证分析

本研究基于转录组序列开发了37个SNP标记,并对22个凡纳滨对虾(Litopenaeus vannamei)家系进行了遗传多样性、家系聚类和亲子鉴定分析,探讨SNP标记在对虾家系选择育种中的应用途径。结果显示,37个SNP位点在凡纳滨对虾22个家系中的平均期望杂合度(He)和平均观测杂合度(Ho)分别为0.38和0.34;平均多态信息含量(PIC)为0.30,属于中度多态性(0.25相似文献   

Practical Considerations of Molecular Parentage Analysis in Fish

Pedigree information is important in selective breeding programs and hatchery management of aquaculture. However, in aquaculture species, tagging of young fish with physical tags is very difficult. Molecular parentage analyses have been used in reconstructing pedigrees in aquaculture species since the 1990s. Some studies have been carried out to optimize every step to reduce the cost and improve the efficiency of molecular parentage analysis. However, molecular parentage analysis of a large number of individuals is still too expensive because some steps of molecular parentage analysis are very cost‐intensive. In this review, we have summarized the techniques of major steps in parentage analysis, and provided a guide for aquaculture scientists on how to cost‐effectively and rapidly extract DNA from a large number of samples, select the right types of DNA markers, optimize multiplex polymerase chain reaction, and select appropriate methods and software to analyze the genotyping data for reconstructing pedigrees. In addition, we discuss the challenges and future directions of molecular parentage analysis in aquaculture species.     

斑马鱼微卫星分子标记检测鲤鱼种间多态性

用6072对斑马鱼（Danio rerio）微卫星引物对黑龙江鲤（Cyprinus carpio haematopterus Temminck et Schlegel）、荷包红鲤（Cyprinus carpio var．wuyuanensis）和柏氏鲤（Cyprinus pellegrini Tchang）进行种间遗传差异分析，共发现563个斑马鱼微卫星标记在鲤鱼种间表现出多态性。从中随机抽选25个标记，对斑马伍和3种鲤鱼的遗传多样性进行分析，使用Phylip3．63软件按照Nei氏标准遗传距离计算种间遗传距离，再用MEGA3．0软件绘制NJ系统发生树，并进行1000次bootstrap检验系统树。结果显示，黑龙江鲤与荷包红鲤首先聚类，然后是柏氏鲤、斑马鱼。这些具有多态性的斑马鱼微卫星标记可用于鲤鱼种间种质鉴定，同时，借用模式生物斑马鱼的丰富遗传标记资源，增加同科的鲤鱼遗传连锁图谱上遗传标记的密度，必将对鲤鱼遗传育种进入分子育种时代起到促进作用。     

Multiplex microsatellite PCR sets for parentage assignment of grass carp (Ctenopharyngodon idella)

Pedigree information is essential for the genetic improvement of traits of interests in breeding programs. In this study, twelve microsatellite loci were selected to optimize three multiplex PCR protocols for parentage assignment in grass carp (Ctenopharyngodon idella). One hundred and fifty adult fish and 252 progenies produced from three pilot groups (P1, P2, and P3) were used to examine the power of the three multiplex microsatellite PCR sets for parentage analysis. The average number of alleles (Na) per locus, observed heterozygosity (Ho), expected heterozygosity (He), and polymorphism (PIC) were 21.83, 0.883, 0.882, and 0.869, respectively. The combined exclusion power using all loci was greater than 99.99 %. Simulation analysis revealed a high assignment success rate (100 %). Parentage analysis of real offspring demonstrated that 99.6 % of all offspring were unambiguously allocated to single pairs of parents. Our results indicate that these three multiplex PCR sets could be used in pedigree reconstruction for grass carp breeding.     

异源四倍体鲫鲤及其原始亲本遗传变异的RAPD分析

在优化RAPD检测条件的基础上，从100个随机引物中筛选出60个扩增较好的引物对异源四倍体鲫鲤及其原始亲本红鲫和湘江野鲤相互间扩增DNA片段的异同性进行比较研究。结果显示，60个引物共产生1554条带，单一引物扩增的DNA片段数在6～20条之间，片段大小在200～3500bp之间。遗传相似率分析表明，异源四倍体鲫鲤与其原始母本红鲫的相似率为69．41％，与其原始父本野鲤的相似率为64．47％，说明异源四倍体鲫鲤接受原始母本红鲫的遗传物质要多一些；而红鲫和野鲤之间的相似率为42．18％，说明两者的基因组成有较大的相似性，从分子水平证实了红鲫和野鲤的远缘杂交具有较大的亲和性。在分析中，还发现异源四倍体鲫鲤有4条非亲本带，非亲本带谱率达0．72％，这些非亲本带可以作为异源四倍体鲫鲤特异性的分子标记。     

基于黄河鲤新品系IGF2b基因SNPs获取体系的建立及在该品系选育中的应用

为了建立鲤 IGF2b (insulin-like growth factor 2)基因全基因组信息 SNPs (single nucleotide polymorphism)的获取体系,并验证该获取体系在黄河鲤新品系选育中运用的适用性,本研究首先对 10个不同鲤品种的 33个鲤个体重测序数据进行分析,整体上了解 IGF2b 基因的单核苷酸位点及其在基因组上的分布情况。然后在基因组 DNA 水平上分段获取 IGF2b 基因的 SNPs 信息,并以不同的鲤品种验证引物的适用性,最后在黄河鲤新品系中检测其应用。研究结果:获得 8 对聚合酶链式反应(polymerase chain reaction, PCR)引物进行分段克隆的结果,并通过直接测序和限制性片段长度多态性来获取相应的 SNPs。经过直接测序,本文对黄河鲤、建鲤、黄河鲤和建鲤的正反交后代进行 PCR 检测发现条带单一,目地片段正确;结合黄河鲤新品系的体重数据,本文又以 IGF2b3#引物检测到一个与体重明显相关的 SNPs,同时检测到一个与该基因表达量相关的另一个 SNPs。本研究的方法能够在该基因全基因组范围内开展鲤分子育种中 SNPs 的检测,并验证发现黄河鲤新品系 IGF2b3#引物 227 号位点处,出现的突变位点使体重降低,且有一处 SNPs 与其表达量有关。这将为其他物种、其他功能基因的多态性分子标记研究提供思路。     

Comparison of microsatellite and SNP DNA markers for pedigree assignment in Black Tiger shrimp,Penaeus monodon

Custom‐built single‐nucleotide‐polymorphism (SNP) marker systems that are compatible with Sequenom^® chemistry are compared with a general purpose microsatellite marker system in their ability to accurately assign Black Tiger shrimp parentage. The microsatellite system consisted of 13 markers, while the SNP systems comprised of 63 (SNPa), 59 (SNPb) or 122 markers (SNPab). Comparisons were made using animals from commercial breeding lines with thresholds for assignment derived using simulated genotypes. Pedigree assignment for commercial lines was highest when panel SNPab was used. Panel SNPa, panel SNPb and Msat functioned with an overall similar level of power for pedigree assignment, however, for some families, the Msat panel was not as powerful. Pedigree assignment for the simulated diploid genotypes was higher for all SNP panels compared with Msat. Overall the three SNP panels provided parentage assignment rates suitable for commercial shrimp breeding programs with assignment rates in the simulated genotypes greater than 96.8% and correct assignments greater than 99.3%. Compared with the microsatellite panel, custom‐built SNP panels, whether they operate as single panels, or as a combined panel, have improved power to perform dam and sire assignment to progeny and provide faster turnaround time as they are compatible with Sequenom^® chemistry.     

Evaluation of a novel pentaplex microsatellite marker system for paternity studies in Atlantic cod (Gadus morhua L.)

Five Atlantic cod (Gadus morhua L.) microsatellites (Gmo8, Gmo19, Gmo35, Gmo37 and Tch11) were selected for parentage assignment. All markers were co‐amplified using dye‐labelled primers and sized by automated sample processing in a 3130xl Genetic Analyser. The genotyping of samples was reproducible and alleles from all loci could be genotyped confidently (precision and accuracy above 99.7 and 99.1% respectively). The number of alleles, observed allelic and genotypic frequencies were calculated. A population database was established for fish originating from randomly selected wild‐caught Norwegian coastal‐ and North‐East Arctic cod. Combined paternity exclusion and the probability of match were 99.97 and 1.5 × 10^?9 respectively. The multiplex assay system was used successfully for parental assignment of 2336 juveniles from different mass spawning breeding tanks. Of all offspring, 91.2% were assigned to a single parental pair. In total, 523 different matings were recorded, and 69 of 70 dams and all of the 30 sires contributed to the offspring.     

Application of high‐throughput single nucleotide polymorphism genotyping for assessing the origin of Engraulis encrasicolus eggs

1. Single nucleotide polymorphism (SNP) markers in anchovy (Engraulis encrasicolus) egg samples were analysed to detect their origin on a small spatial scale (200 km) by assigning genotypes to adult anchovy stocks. The novelty of this work is the application of a rapid high‐throughput method for genotyping each single anchovy egg, in a single execution, using a set of 96 genome‐wide SNPs in a dynamic array system with microfluidic technology (Fluidigm 96.96).
2. The existence of two ecotypes in E. encrasicolus had already been identified based on SNP polymorphism in the Atlantic Ocean and in the Mediterranean Sea, showing that habitat type (offshore versus coastal/estuarine) is the most important component of genetic differentiation among populations of anchovy.
3. In this work, anchovy egg genotypes from areas of the Western Mediterranean were assigned to adult populations. Only two localities in which adult anchovies were sampled represented donor populations for the coastal/estuarine egg genotypes. Although some degree of mixing among the hauls could exist, the assignment of egg groups to adult populations led to distinguishing the contributions of distinct ecotypes to new wild generations. We can conclude that the high rate of egg dispersion caused by marine currents and the different degrees of local retention could explain the genetic heterogeneity observed in the adult populations, where eggs from neighbouring spawning sites tend to mix.
4. The results highlight that this technique represents a new and useful tool for addressing evolutionary questions, breed recognition, assignment, and connectivity assessment of individual eggs, and anchovy population dynamics, for the management of stocks.

     

牙鲆家系亲权鉴定的微卫星DNA标记分析

为准确进行不同家系的亲权鉴定,筛选具有高亲本排除概率的微卫星DNA标记,从牙鲆选育基础群体中挑选性腺发育良好的雌雄亲本各10尾建立全同胞家系10个,从独立饲养的每个家系中随机选取30尾个体组成系谱结构已知的家系群体,从混合培育的子代群体中随机选取200尾个体组成系谱结构未知的混合群体。48个微卫星DNA标记选自牙鲆第二代遗传连锁图谱,且均匀分布于24个连锁群上,每个连锁群2个标记。家系群体的遗传分析结果发现,10个拥有丰富遗传多态性的微卫星DNA标记表现出高的亲本排除概率,其Excl1和Excl2的范围分别为0.655~0.719和0.792~0.837。随鉴定所用微卫星DNA标记数目的增加,累计排除概率逐步升高。当使用8个微卫星DNA标记鉴定时,累计排除概率达到100%。利用这些标记开展混合群体的亲权鉴定,显示共有13个雌雄个体参与繁殖过程,不同亲本配组产生的后代数量存在差异,亲本与后代群体之间的各项遗传学统计指标不存在明显差异。研究表明,筛选出具有高亲本排除概率的微卫星DNA标记能够有效进行牙鲆家系的亲权鉴定,可以作为今后开展家系选育与DNA分子标记联合育种的候选标记。     

基于微卫星标记对长江江苏段鳙增殖放流效果评估

为评估长江江苏段鳙(Aristichthys nobilis)增殖放流效果,本研究基于微卫星标记的亲子鉴定技术,选用 10对扩增效果稳定的微卫星荧光标记引物,结合毛细管电泳对江苏省内良种场 563 尾鳙亲鱼和长江江苏段 687 尾回捕鳙进行基因分型,并对位点多态性及亲子鉴定结果进行了分析。结果表明,各位点等位基因介于 19~55 之间,其观测杂合度为 0.530~0.909(平均值为 0.748),期望杂合度为 0.818~0.929 (平均值为 0.882),多态性信息含量为0.797~0.924 (平均值为 0.871);Cervus3.0 模拟结果显示,当双亲未知且置信度为 95%时, 10 个微卫星位点的累积非亲权排除率为 99.996%。亲子鉴定结果发现,所有回捕鳙中有 42 尾与亲本之间存在亲子关系,被确认来源于鳙增殖放流群体,并由此推算此次评估亲本的放流子代对长江江苏段野生群体的贡献率为 6.11%。结果显示该研究进行的鳙亲子鉴定技术可为长江鳙增殖放流效果评估工作提供可靠的数据支撑,为长江渔业资源管理提供参考资料。     

基于微卫星标记评估凡纳滨对虾收获体长、体质量以及抗WSSV性状的遗传参数

为更加准确地评估凡纳滨对虾体长、体质量以及抗WSSV性状的遗传参数,实验利用8个微卫星位点对凡纳滨对虾69个家系母本和子代进行基因分型,并利用分型信息进行系谱重构和分子亲缘关系相关度的计算,以重构系谱、分子亲缘关系度以及物理系谱分别构建加性遗传相关矩阵,进而对体长、体质量和抗WSSV性状的遗传参数进行评估.最终通过交叉...     

Parentage determination of the mud crab Scylla paramamosain using microsatellite markers

This study evaluated the properties of nine Scylla paramamosain microsatellite loci screened by us previously for inclusion in a parentage assignment marker suite. These nine highly polymorphic markers (mean He=0.847 and PIC=0.830) were determined as being suitable for parentage assignment. Simulations based on allele frequency data from 15 known maternal families (165 individuals) demonstrated that at least four loci were required to assign >95% of offspring to maternal parents with 95% confidence. In actual parentage assignments, all progenies were assigned to the maternal parents with six or more loci, which was similar to the simulation predictions. Our results suggest that this set of microsatellites provide a powerful and efficient tool for identifying pedigree information for selective breeding programmes of S. paramamosain.     

凡纳滨对虾(Litopenaeus vannamei)微卫星多重PCR体系的建立及其在家系亲权鉴定中的应用

为了在遗传分析研究中提高效率并节约成本,本研究从已报道的凡纳滨对虾(Litopenaeus vannamei)微卫星位点中选取多态性较高的位点,基于各位点的扩增片段大小及退火温度等因素进行微卫星位点的组合.通过不断优化位点组合、反应体系及反应程序,成功建立了1个五重、2个四重和1个三重PCR反应体系,并将其应用于11个凡纳滨对虾家系的亲权鉴定.结果显示,四组多重PCR体系中的16个微卫星位点在11个凡纳滨对虾家系中的平均等位基因数(Na)为6,平均多态信息含量(PIC)为0.5813,平均观测杂合度(Ho)为0.513,平均期望杂合度(He)为0.636.利用Cervus3.0软件,对已知系谱关系的11个凡纳滨对虾家系进行亲权分析,其第一亲本累积排除率(CE-1P)、第二亲本累积排除率(CE-2P)和双亲累积排除率(CE-PP)分别为0.99525487、0.99990862和0.99999986.进一步分析表明,当同时使用四组多重PCR体系进行亲权分析时,其模拟配对率和亲权鉴定准确率均为100％,全同胞和半同胞家系鉴别效果良好,表现出准确的鉴别能力.本研究所建立的四组凡纳滨对虾微卫星多重PCR体系均可为后续的凡纳滨对虾遗传多样性分析和亲权鉴定提供高效、准确的检测手段.