960 resultados para Genotype


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羊草(Leymus chinensis (Trin.) Tzvel. )又称碱草,隶属禾本科,赖草属,因其营养价值高,富含蛋白质,适口性好,抗旱,耐盐碱,耐贫瘠,抗逆性强,适应性广等优点,对我国发展草原畜牧业和退化草地、荒漠化治理方面具有举足轻重的作用。近年来,由于自然环境变劣,荒漠化加剧,以及过度放牧等不利影响,加之羊草本身固有的“三低”问题(即结实率低、出苗率低、产草量低)已对羊草生物多样性维持构成了严重的威胁,严重限制了我国人工草地建设和天然草地的改良和沙化治理的步伐。加强羊草生物学研究,开展羊草种质生物多样性保护,成为当前研究的紧迫课题。经对国内外相关文献的查新发现:国外发表的文献匮乏,国内的报导大多集中在草原生态等宏观领域,在羊草繁殖生物学方面缺乏系统的研究。本文以本课题组从国内外收集的羊草资源为材料,从以下几个方面进行了初步探索: 一、羊草繁殖性状与遗传多样性分子标记指标的相关分析。利用分子标记与形态标记对随机抽取的17份羊草种质进行了种质评估的比较研究。结果表明:两种方法均在17份供试材料中鉴别出9份羊草种质,说明分子标记方法用于羊草种质资源鉴定是可行的,并具有快速、准确、不受环境条件限制等优点。在40个10 Mer的随机引物当中筛选出21个有效引物,以之对9份羊草材料进行RAPD 分析,共扩增出115条带,其中95条带表现出多态性,多态比率82.61%,并筛选出S1213-900,S1213-1700,S1215-5500, S1396-1370,S1384-900,S1202-5180,S1220-2200,S1381-1580,S1211-1300,S1211-800为羊草种质所具有的10个特异性标记,据此可将羊草种质与披肩草、赖草加以区分。同时在羊草种内亦发现13条可区分供试羊草种质的特有标记。形态标记与分子标记相关性分析结果显示:羊草种质的小穗数,种子千粒重,叶色,有性繁殖量和结实率5个形态学指标与遗传多样性指标---特有带百分率及遗传距离之间,存在一定相关性。同时对羊草种质资源在收集和评价过程中存在的问题进行了探讨。 二、羊草不同基因型无性繁殖特性比较研究。以本课题组从吉林、内蒙古等省份收集的10个基因型羊草为供试材料,在相同的生态因子作用下,以吉生1号羊草为对照,对10个基因型羊草的叶数增量、芽数增量、芽高度、芽间距、芽重量、根量六个无性系形态性状指标进行测评。结果表明:基因型的差异也是影响羊草无性系生长发育的重要影响因子。因此,在今后的羊草无性繁殖生物学研究中,应综合考虑环境因子和基因型因子对羊草无性繁殖生长发育的影响。在所测评的10个基因型中,各基因型的形态性状指标差异很大,栽3基因型较其他基因型优于对照吉生1号,此结论可为今后培育羊草新种提供重要资料。 三、羊草幼穗离体培养方法的建立。其方法是取羊草幼穗为外植体,经0.1%升汞溶液表面消毒后,接种到含2mg/L的2,4-D的MS培养基上,置于恒温25℃条件下诱导愈伤组织。在加有1mg/L2,4-D的MS培养基上继代2次后,转移到含1mg/L KT和0.5mg/LNAA的MS培养基上分化培养得到再生芽。在除去激素后的基本培养基上获得了生根的试管苗。试管苗移栽到温室后生长正常。羊草试管苗的分化因基因型和外源激素条件的不同而异。 四、羊草有性生殖特性的研究。在自然条件下进行了羊草自交、异交结实性实验,采用FDA染色法检测羊草小孢子活性,并观测羊草雌蕊、雄蕊发育的时空特点。结果表明:在大田中羊草异交结实率远大于其自交结实率;成熟花药中有活性的花粉达到92.2%以上;同时,在发育时间顺序和空间结构上,羊草的雌蕊、雄蕊并不妨碍自体授粉。因此,初步结论认为羊草具自交不和性。

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青蒿素是从中药青蒿,学名黄花蒿(Artemisia annua L.)植物地上部分分离出的抗疟疾有效单体,为一种倍半萜内酯类化合物,其生物合成途径属于植物类异戊二烯代谢途径。青蒿素生物合成途径及其调控机制仍不完全清楚,本论文采用GC-MS 和GC×GC-TOFMS 方法对青蒿萜类代谢物谱进行检测,用多维统计学方法对检测结果进行整理和比较分析,研究青蒿素生物合成及其与青蒿中其他萜类代谢的关系,取得了以下结果: 一、通过GC×GC-TOFMS 方法对青蒿挥发油成分进行分析,共鉴定出303 种组分。其中挥发油中相对百分含量大于1%的10 种组分中有9 种为萜类化合物,含量接近总挥发油的50%。在相对百分含量大于0.1%的49 种成分中,有30 种萜类化合物。有27 种相对百分含量大于0.1%的成分首次在青蒿挥发油中报道,其中包括10 种萜类化合物。 二、利用GC-MS 方法分析了青蒿001 和SP18 两个青蒿素高产株系不同生长时期萜类代谢物谱,结果表明:青蒿中萜类化合物在不同时期合成和积累是动态变化的,萜类化合物的种类和数量在营养生长期随生长时间的延长而提高,在营养生长后期和现蕾前期达到最高水平,进入生殖生长后随生长时间的延长而迅速降低。通过多维统计PLS-DA(Partial Leasted Square Discriminant Analysis) 分析,确定001 中有17 个化合物的含量在不同生长时期有明显变化,其中15 个为萜类化合物。SP18 中有18 个化合物的含量在不同生长时期有明显变化,其中16 个为萜类化合物。青蒿素,青蒿酸,二氢青蒿酸,青蒿素B 都是含量变化明显的标记物。其中青蒿酸和二氢青蒿酸含量在营养生长后期达到最高水平,进入生殖生长后迅速下降,而青蒿素和青蒿素B 在整个检测时期含量变化相对较小,在营养生长时期含量已经较高,在现蕾前期含量稍有上升,进入现蕾期后有所下降,本研究确定现蕾前期为代谢物谱分析最佳取样时期,并为药材采收提供指导。 三、不同基因型青蒿代谢物谱研究表明,青蒿素高产株系SP18 和001 代谢物表现出一定的差异,通过多维统计PLS-DA 分析,共找出了22 种在两种基因型中差异明显的化合物,其中包括倍半萜化合物12 种,单萜化合物3 种,三萜化合物4 种。SP18 特征化合物为樟脑和两个未鉴定倍半萜化合物,而001 特征化合物是龙脑和β-法呢烯。另外两种基因型中青蒿素及相关前体化合物的积累模式差异明显,SP18 中二氢青蒿酸和青蒿素含量高,而青蒿酸和青蒿素B 含量极低;001 中二氢青蒿酸和青蒿素含量相对SP18 要低,但青蒿素B 和青蒿酸含量比SP18 要高。该结果表明在青蒿素高产株系中,青蒿素含量与二氢青蒿酸的含量呈正相关,结合Brown 等的活体标记研究结果分析,从二氢青蒿酸到青蒿素的转化可能是青蒿素合成的限速步骤。 四、利用GC×GC-TOFMS 方法对转基因青蒿萜类代谢物谱进行了分析,共对200 个左右化合物峰进行PLS-DA 和OSC-PLS (Orthogonal Signal Correction–Partial leasted Square)多维统计分析,结果表明:青蒿萜类代谢物谱在外源基因转入后发生显著变化,与对照株系相比均呈现显著差异。其中过量表达Amorpha-4,11-diene 合酶基因(ads)株系中青蒿素及相关化合物变化最明显,而过量表达FPP 合酶基因(fps)株系中青蒿素及相关化合物变化相对较小,在受到调控而成为差异标记物的化合物中,70%是倍半萜类化合物。 五、考察了外源茉莉酸甲酯对青蒿素生物合成的影响,结果表明:300 μM 外源茉莉酸甲酯能提高青蒿素含量,在处理后第8 天青蒿素含量提高38%。青蒿萜类代谢物谱研究表明,茉莉酸甲酯不仅可以诱导青蒿中青蒿素的合成,还能诱导很多化合物,特别是倍半萜和三萜类的合成。OSC-PLS 分析结果找出了9 个处理后含量明显提高的标记物,其中6 个倍半萜化合物,3 个三萜化合物。标记物鲨烯含量提高了67%,另一个未鉴定出结构的倍半萜提高了60%,这些化合物可能与青蒿素有着类似的调控机制,而外源喷洒茉莉酸甲酯可以作为提高青蒿素产量的有效途径之一。

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表现型是基因型和环境相互作用的结果,不同环境条件下给定基因型能表达为不同的表型,这是我们所熟知的植物表型可塑性。可塑性一方面帮助植物更好地适应不利环境,但我们也不得不承认可塑性,使得人们难以从表型直接理解基因功能。如今,基因组学快速发展允许解密基因更迅速便捷,甚至发现大量基因。因此,进一步理解可塑性过程的基因背景、理解基因和环境对表型的作用非常必要。由于从基因到表型非线性过程,从而引起基因型和表型差异,期望有效方法或工具能跨越这个横沟。植物生长模型已被开发用来模拟植物响应环境动态关系,并且将参数和环境整合到模型方法中。因此,普遍认为植物生长模型将在探讨复杂可塑性基因功能扮演重要作用。水稻是普遍应用在基因组学和功能基因组学典型的模式植物。水稻分蘖是重要的基因依赖环境敏感的过程,这是农学上非常关注的现象。本文将应用模型方法理解水稻分蘖逆制的可塑性。本研究设计了一个相对优化环境条件下,野生型水稻分蘖逆制试验,该试验有两个处理(1)手工剪切分蘖;(2)一个TDNA突变体,并分别设置对照。本试验在法国国际农业研究发展中心(CIRAD)温室开展,每个试验利用水培方法,培育植株50天左右(营养生长阶段)。在营养生长阶段,定期破坏性测量单个器官的鲜重、干重和单个器官的大小。本文尝试应用两个植物生长模型模拟和解释水稻响应分蘖逆制表型发育。GreenLab是一个植物结构数学模型,已被开发用来模拟植物结构动态和结构功能反馈。植物3D结构决定光捕获和生物产量,然后,生物量分配到新的器官,因此,器官形态结构将发生变化,新阶段的生物量生产将会更新。通过基于最小二乘法的CornerFit软件实现了模型参数优化。另一个模型EcoMeristem,基于作物模型和形态发生概念,用来模拟水稻分生组织活动、器官发生和形态过程等可塑性过程,内部竞争指数Ic主要与环境相关,参数主要描述基因功能。通过植物生长过程模拟与测量的优化,手工提取了模型参数。这两个植物生长模型演示了缩减基因型与表型之间的差距,并实现了水稻响应分蘖完全逆制的可塑性过程。GreenLab模型有一个极好的器官发生基础,但本研究限于单茎拓扑结构。另外,该模型有更长的时间步长,这对描述植物可塑性没有提供足够的分辨能力,这在EcoMeristem模型中得到了解决。很明显,EcoMeristem模型有更弱的结构基础,这可能蕴含了一些可塑性信息的缺失。总体而言,EcoMeristem模型有更专业的可塑性过程、基因环境理解和表达能力。

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mtDNA genotypes of six domestic horses (three adult short horses whose heights are under 1 m and three common domestic horses) from a small region of 15 km(2) in Malipo county of Yunnan province of China were investigated by the technique of restriction fragment length polymorphism (RFLP) with restriction endonucleases which recognize 6-bp sequences. An average of fragments for an individual was obtained. Unlike other domestic animals, this population of horses exhibits high mtDNA genetic diversity. Each of the six horses has a specific mtDNA genotype showing a pattern of multiple maternal origins, as suggested by fossil and literature records. We think the population of horses is an amazing seed-resource pool of horses and hence deserves to be paid more attention from the view of conservation genetics. However it is also remarkable that we did not find any typical mtDNA genetic markers which would discriminate between short horses and common domestic horses.

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In reciprocal mutualism systems, the exploitation events by exploiters might disrupt the reciprocal mutualism, wherein one exploiter species might even exclude other coexisting exploiter species over an evolutionary time frame. What remains unclear is how such a community is maintained. Niche partitioning, or spatial heterogeneity among the mutualists and exploiters, is generally believed to enable stability within a mutualistic system. However, our examination of a reciprocal mutualism between a fig species (Ficus racemosa) and its pollinator wasp (Ceratosolen fusciceps) shows that spatial niche partitioning does not sufficiently prevent exploiters from overexploiting the common resource (i.e., the female flowers), because of the considerable niche overlap between the mutualists and exploiters. In response to an exploiter, our experiment shows that the fig can (1) abort syconia-containing flowers that have been galled by the exploiter, Apocryptophagus testacea, which oviposits before the pollinators do; and (2) retain syconia-containing flowers galled by Apocryptophagus mayri, which oviposit later than pollinators. However, as a result of (2), there is decreased development of adult non-pollinators or pollinator species in syconia that have not been sufficiently pollinated, but not aborted. Such discriminative abortion of figs or reduction in offspring development of exploiters while rewarding cooperative individuals with higher offspring development by the fig will increase the fitness of cooperative pollinating wasps, but decrease the fitness of exploiters. The fig fig wasp interactions are diffusively coevolved, a case in which fig wasps diversify their genotype, phenotype, or behavior as a result of competition between wasps, while figs diverge their strategies to facilitate the evolution of cooperative fig waps or lessen the detrimental behavior by associated fig wasps. In habitats or syconia that suffer overexploitation, discriminative abortion of figs or reduction in the offspring development of exploiters in syconia that are not or not sufficiently pollinated will decrease exploiter fitness and perhaps even drive the population of exploiters to local extinction, enabling the evolution and maintenance of cooperative pollinators through the movement between habitats or syconia (i.e., the metapopulations).

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Physiological functions of human genes may be studied by gene-knockout experiments in model organisms such as the mouse. This strategy relies on the existence of one-to-one gene orthology between the human and mouse. When lineage-specific gene duplication occurs and paralogous genes share a certain degree of functional redundancy, knockout mice may not provide accurate functional information on human genes. Angiogenin is a small protein that stimulates blood-vessel growth and promotes tumor development. Humans and related primates only have one angiogenin gene, while mice have three paralogous genes. This makes it difficult to generate angiogenin-knockout mice and even more difficult to interpret the genotype-phenotype relation from such animals should they be generated. We here show that in the douc langur (Pygathrix nemaeus), an Asian leaf-eating colobine monkey, the single-copy angiogenin gene has a one-nucleotide deletion in the sixth codon of the mature peptide, generating a premature stop codon. This nucleotide deletion is found in five unrelated individuals sequenced, and therefore is likely to have been fixed in the species. Five colobine species that are closely related to the douc langur have intact angiogenin genes, suggesting that the pseudogenization event was recent and unique to the douc langur lineage. This natural knockout experiment suggests that primate angiogenin is dispensable even in the wild. Further physiological studies of douc largurs may offer additional information on the role of this cancer-related gene in normal physiology of primates, including humans. Our findings also provide a strong case for the importance of evolutionary analysis in biomedical studies of gene functions. (C) 2003 Elsevier Science B.V. All rights reserved.

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The human D2 dopamine receptor gene (DRD2) plays a central role in the neuromodulation of appetitive behaviors and is implicated in having a possible role in susceptibility to alcoholism. We genotyped an SNP in DRD2 Exon 8 in 251 nonalcoholic, unrelated, healthy controls and 200 alcoholic Mexican Americans. The DRD2 haplotypes were analyzed using the Exon 8 genotype in combination with five other SNP genotypes, which were obtained from our previous study. The ancestral origins of the DRD2 polymorphisms have been determined by sequencing the homologous region in other higher primates. Twenty DRD2 haplotypes, defined as H1 to H20 based on their frequency from high to low, were obtained in this major minority population. The ancestral haplotype "I-132-G-C-G-A1" and two one-step mutation haplotypes were absent in our study population. The haplotype H1, "I-B1-T-C-A-A1", with the highest frequency in the population, is a three-step mutation from the ancestral form. The first five or eight major haplotypes make up 87% or 95% of the entire population, respectively. The prevalence of the haplotype H1+ (H1/H1 and H1/Hn genotypes) is significantly higher in alcoholics and alcoholic subgroups, including early onset drinkers and benders, than in their respective control groups. The Promoter -141C allele is in linkage disequilibrium (LD) with five other loci in the nonalcoholic group, but not in the alcoholic group. All of the other five loci are in LD in both the alcoholic and control groups. The DRD2 TaqI B allele is in complete LD with the allele located in intron 6. Five SNPs, Promoter -141C, TaqI B (or Intron 6), Exon 7, Exon 8, and TaqI A, are sufficient to define the DRD2 haplotypes in Mexican Americans. Our data indicate that the DRD2 haplotypes are associated with alcoholism in Mexican Americans. (c) 2005 Elsevier Inc. All rights reserved.

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Melanocortin-1 receptor (MC1R) plays a major role in pigmentation in many species. To investigate if the MC1R gene is associated with coat color in water buffalo, the coding region of MC1R gene of 216 buffalo samples was sequenced, which included 49 black river buffalo (Murrah and Nili-Ravi), 136 swamp buffalo (Dehong, Diandongnan, Dechang, Guizhou, and Xilin) with white and gray body, and 31 hybrid offspring of river buffalo Nili-Ravi (or Murrah) and swamp buffalo. Among the three variation sites found, SNP684 was synonymous, while SNP310 and SNP384 were nonsynonymous, leading to p.S104G and p.I128M changes, respectively. Only Individuals carrying homozygote E-BR/E-BR were black. The genotype and phenotype analysis of the hybrid offspring of black river buffalo and gray swamp buffalo further revealed that the river buffalo type allele E-BR or the allele carrying the amino acid p.104S was important for the full function of MC1R. The in silico functional analysis showed that the amino acid substitutions p.G104S and p.M128I had significant impact on the function of MC1R. Above results indicate that the allele E-BR or the allele carrying the amino acid p.104S was associated with the black coat color in buffalo.

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In order to carry out Biometric studies, 75 samples were caught from 3 locations ( Tajan river, Sefidrud and Shirud) using Salic and the length (±1 mm) and weights (± 5 gr) of samples were determined. Using One-way ANOVA by SPPSS software, there wasn’t significant difference between locations in length and fecondity (P ≥0.01(, but there was significant difference between Shirud and tajan samples with sefidrud in weight ) P≤0.01(. In order to carry out genetic variation studies, 210 fish were caught from 3 different regions of the Iranian coastline (Khoshkrud, Tonekabon, Gorganrud) and 1 region in Azerbaijan (Waters of the Caspian Sea close to Kura River mouth) during 2008-2009 . Genomic DNA was extracted of fin using the phenol-chloroform. The quantity and quality of DNA from samples were assessed by spectrophptometer and 1% agarose gel electro-phoresis. PCR was carried out using 15 paired microsatellite primers. PCR products were separated on 8% polyacrylamide gels that were stained using silver nitrate. Molecular weight calculate using UVTech software. The recorded microsatellite genotypes were used as input data for the GENALEX software version 6 package in order to calculate allele and genotype frequencies, observed (Ho) and (He) expected heterozygosities and to test for deviations from Hardy-Weinberg equilibrium. Genetic distance between two populations was estimated from Nei standard genetic distance and genetic similarity index (Nei, 1972). Genetic differentiation between populations was also evaluated by the calculation of pairwise estimates of Fst and Rst values. From 15 SSR markers were used in this investigation, 9 of them were polymorph. Average of expected and observed heterozygosity was 0.54 and 0.49 respectively. Significant deviations from Hardy-Weinberg expectations were observed in all of location except Anzali lagoon- autumn in AF277576 and EF144125, Khoshkrud in EF144125 and Gorganrud and Kura in AF277576. Using Fst and Rst there was significant difference between locations ) P≤0.01(. According to Fst , the highest population differentiation (Fst= 0.217) was between Gorganrud and Khoshkrud that have the lowest Nm and the lowest (Fst= 0.086) was between Gorganrud and Tonekabon that have the highest Nm. Using Rst the highest population differentiation (Rst= 0.271) was between Tonekabon and spring Anzali lagoon and the lowest (Rst= 0.026) was between Tonekabon and Autumn Anzali 159 lagoon. Also the difference between Spring Anzali lagoon and Autumn Anzali lagoon was noticeable (Fst=0.15). AMOVA analysis with consideration of 2 sampling regions (Iran and Azerbaijan) and 7 sampling locations (Iran: Khoshkrud, Tonekabon, Gorganrud, Spring Anzali lagoon and Autumn Anzali lagoon ; Azerbaijan: the Kura mouth) revealed that almost all of the variance in data namely 83% )P≤0.01( was within locations, Genetic variances among locations was 14% )P≤0.01( and among regions was 3% )P≤0.01(. The genetic distance was the highest (0.646) between Gorganrud and Autumn Anzali lagoon populations, whereas the lowest distance (0.237) was between Gorganrud and Tonekabon River. Result obtained from the present study show that at least 2 different population of Rutilus frissi kutum are found in the Caspian sea,which are including the kura river population and the southern Caspian sea samples and it appears that there is more than one population in southern Caspian sea that should be attantioned in artifical reproduction Center and stoke rebilding.

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In one of our recent studies, two HCV genotype 6 variants were identified in patients from Hong Kong and Guangxi in southern China, with injection drug use and HIV-1 co-infection. We report the complete genomic sequences for these two variants: GX004 and

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We identified a new class of human immunodeficiency virus type 1 (HIV-1) recombinants (00CN-HH069 and 00CN-HH086) in which further recombination occurred between two established circulating recombinant forms (CRFs). These two isolates were found among 57 HIV-1 samples from a cohort of injecting drug users in eastern Yunnan Province of China. Informative-site analysis in conjunction with bootscanning plots and exploratory tree analysis revealed that these two strains were closely related mosaics comprised of CRF07_BC and CRF08_BC, which are found in China. The genotype screening based on gag-reverse transcriptase sequences if 57 samples from eastern Yunnan identified 47 CRF08_BC specimens (82.5%), 5 CRF07_BC specimens (8.8%), and 3 additional specimens with the novel recombinant structure. These new "second-generation" recombinants thus constitute a substantial proportion (5 of 57; 8.8%) of HIV-1 strains in this population and may belong to a new but yet-undefined class of CRF. This might be the first example of CRFs recombining with each other, leading to the evolution of second-generation inter-CRF recombinants.

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Molecular epidemiological investigation was conducted among injecting drug users (IDUs) (n = 11) and heterosexuals (n = 15) in Kunming, Yunnan Province of China. HIV-1 genotypes were determined based on the nucleotide sequences of 2.6-kb gag-RT region. The distribution of genotypes among IDUs was as follows: CRF07_BC (5/11) and CRF08_BC (5/11); subtype B' (1/11). Similarly, a majority of Kunming heterosexuals (14/15) were infected with CRF07_BC (4/15), CRF08_BC (6/15), or subtype B' (4/15), known to predominate among IDUs in China. This contrasts with trends in the coastal regions of China and surrounding southeastern Asian countries, where CRF01_AE predominates among heterosexuals. The heterosexual HIV-1 epidemic in Kunming thus appears to derive from the local IDU epidemic. Of note, subtype B' was the most prevalent strain among heterosexuals before 1997, while CRF07_BC and CRF08_BC became predominant in 2002, indicating a transition of HIV-1 genotype distribution between the early and the more recent samples from Kunming heterosexuals.

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Genetic variation at the serotonin transporter-linked polymorphic region (5-HTTLPR) is associated with altered amygdala reactivity and lack of prefrontal regulatory control. Similar regions mediate decision-making biases driven by contextual cues and ambiguity, for example the "framing effect." We hypothesized that individuals hemozygous for the short (s) allele at the 5-HTTLPR would be more susceptible to framing. Participants, selected as homozygous for either the long (la) or s allele, performed a decision-making task where they made choices between receiving an amount of money for certain and taking a gamble. A strong bias was evident toward choosing the certain option when the option was phrased in terms of gains and toward gambling when the decision was phrased in terms of losses (the frame effect). Critically, this bias was significantly greater in the ss group compared with the lala group. In simultaneously acquired functional magnetic resonance imaging data, the ss group showed greater amygdala during choices made in accord, compared with those made counter to the frame, an effect not seen in the lala group. These differences were also mirrored by differences in anterior cingulate-amygdala coupling between the genotype groups during decision making. Specifically, lala participants showed increased coupling during choices made counter to, relative to those made in accord with, the frame, with no such effect evident in ss participants. These data suggest that genetically mediated differences in prefrontal-amygdala interactions underpin interindividual differences in economic decision making.

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Redescription of Balantidium polyvacuolum Li 1963, collected from the hindgut of Xenocypris davidi and Xenocypris argentea, from Niushan Lake Fishery (30A degrees 19' N, 114A degrees 31' E) in Wuhan City, Hubei Province, China in April and June 2007 is presented in this paper to complete Li's description at both light and scanning electronic microscopic levels. The unique body shape of B. polyvacuolum-highly arched dorsal side and flattened ventral surface-as well as its remarkable concave platelet present in the centroventral were well described and compared with other close Balantidium species. Besides, two types of vestibulum shape are observed in our present work, which may suggest the existence of two subspecies or genotype species of these balantidia.

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P>Sex controls have been performed in some farmed fish species because of significant growth differences between females and males. In yellow catfish (Pelteobagrus fulvidraco), adult males are three times larger than female adults. In this study, six Y- and X-linked amplified fragment length polymorphism fragments were screened by sex-genotype pool bulked segregant analysis and individual screening. Interestingly, sequence analysis identified two pairs of allelic genes, Pf33 and Pf62. Furthermore, the cloned flanking sequences revealed several Y- and X-specific polymorphisms, and four Y-linked or X-linked sequence characterized amplified region (SCAR) primer pairs were designed and converted into Y- and X-linked SCAR markers. Consequently, these markers were successfully used to identify genetic sex and YY super-males, and applied to all-male population production. Thus, we developed a novel and simple technique to help commercial production of YY super-males and all-male populations in the yellow catfish.