Genome-wide association mapping of phenolic acids in tetraploid wheats     

《Journal of Cereal Science》2017

Phenolic acids are major components of cell walls in wheat and have important implications on human health as antioxidants with anti-tumor activity. Our objectives were to identify phenolic acid genes in wheat by single nucleotide polymorphisms (SNPs) detected within the coding sequences of candidate genes, and to identify chromosomal regions associated with single phenolic acids and total soluble phenolic compounds. A set of candidate genes involved in the biosynthesis of hydroxycinnamic acid derivatives were identified by comparative genomics. SNPs found in the coding sequences of six genes (PAL1, PAL2, C4H, C3H, COMT1 and COMT2) were used to determine their chromosomal location and accurate map position on two reference consensus linkage maps. The genome-wide association study (GWAS), based on genotyping a tetraploid wheat collection with 81,587 gene-associated SNPs, detected 22 quantitative trait loci (QTL) distributed on almost all durum wheat chromosomes. Two QTL for p-coumaric acid were coincident with the phenylalanine ammonia-lyase (PAL2) and p-coumarate 3-hydroxylase (C3H) genes on chromosome arms 2AL and 1AL, respectively. The availability of candidate gene-based markers can allow elucidating the mechanism of phenolic acids accumulation in wheat kernels and exploiting the genetic variability of phenolic acids content for the nutritional improvement of wheat end-products.  相似文献   

Markers, old and new, for examining Phytophthora infestans diversity   总被引：4，自引：1，他引：3  

D. E. L. Cooke†  A. K. Lees 《Plant pathology》2004,53(6):692-704

Late blight, caused by Phytophthora infestans , is an ongoing threat to potato and tomato crop production worldwide and considerable fundamental and applied research is conducted with the long-term aim of improved disease control. Understanding the mechanisms, processes and rates of P. infestans evolution is an important factor in predicting the effectiveness and durability of new management practices. A range of phenotypic and genotypic tests has been applied to achieve this goal, but each has limitations and new methods are sought. Recent progress in P. infestans genomics is providing the raw data for such methods and new high-throughput codominant biomolecular markers are currently being developed that have tremendous potential in the study of P. infestans population biology, epidemiology, ecology, genetics and evolution. This paper reviews some key applications, recommends some changes in approach and reports on the status and potential of new and existing methods for probing P. infestans genetic diversity.  相似文献   

Molecular cloning and variant analysis of the TSHR gene in goose (Anser cygnoides)     

C. Wang  Y. Liu  G. Li  S. Gong  Y. Yang  H. Wang 《British poultry science》2020,61(4):375-381

  相似文献   

猪ECH1基因部分序列的遗传变异分析     

张冬杰  刘娣  汪亮  王文涛  杨国伟 《黑龙江畜牧兽医》2011,(19)

为了进一步研究烯脂酰辅酶A水解酶1(enoyl CoA hydratase,ECH1)基因的生物学功能,研究采用克隆测序结合PCR-RFLP的方法分析了民猪ECH1基因的部分DNA序列,并对其中的1个点突变进行了3个猪种内的基因型频率和基因频率计算。结果表明:研究所检测的ECH1基因序列与网上已有序列相比存在8个单核苷酸多态性(SNPs)位点,其中有2个造成酶切位点的改变;民猪和大白猪在PCR-RFLP-BamHⅠ位点的A、B基因频率均接近0.5,而长白猪B为优势等位基因。  相似文献   

皱皮香猪HAS2基因SNPs的鉴定及生物信息学分析   总被引：1，自引：1，他引：0  

吴行雕  石道宏  黄世会  牛熙  李升  王嘉福  冉雪琴 《畜牧兽医学报》2021,52(12):3390-3402

为了探究皱皮香猪全身性皮肤褶皱是否与透明质酸合成酶2（hyaluronan synthase 2,HAS2）基因变异有关,本研究以普通香猪为对照,采用特异性PCR方法克隆HAS2基因的外显子编码区,应用生物信息学方法分析测定基因编码区的碱基变异,检测变异位点在群体中的分布频率。结果显示,皱皮香猪HAS2基因中检测到4个SNPs位点：位于外显子1的T221A错义突变（导致亮氨酸替换为赖氨酸）和A228G同义突变,位于外显子2的T183C和外显子4的C537T同义突变。生物信息学分析发现,T221A和A228G位点构成4种单倍型,其中T-A为皱皮香猪群体的主要单倍型（27.5%）,且在皱皮香猪群体中紧密连锁（r²=0.253）,而且T221A和A228G突变可引起mRNA自由能和蛋白质结构发生变化,TA组合的自由能为-573.29 kJ·mol^-1,TG组合的自由能为-580.89 kJ·mol^-1,AG组合的自由能为-572.66 kJ·mol^-1;AA组合的自由能为-571.03 kJ·mol^-1;蛋白序列中亮氨酸替换为赖氨酸后,α螺旋由35.52%降为32.97%,自由卷曲由43.17%升至44.51%,同时引起蛋白序列三级结构的改变。位点T221A和A228G在香猪群体中呈现出丰富的多态性,均表现出3种基因型;关联分析结果显示,皱皮香猪T221A位点的A等位基因频率显著高于普通香猪（P<0.05）,A228G位点中皱皮香猪的G等位基因频率极显著高于普通香猪（P<0.01）。T183C位点的C等位基因频率和C537T位点的T等位基因频率在皱皮香猪和普通香猪间未达到显著性差异（P>0.05）。研究结果揭示,HAS2基因的外显子1中发生的两个碱基变异可能影响基因转录后mRNA的稳定性以及蛋白的三维结构,影响HA的合成量,并与皱皮香猪体侧皮肤不均匀增厚且发生褶皱有关。  相似文献   

香猪基因组外显子SNPs检测及繁殖和体型性状候选基因分析     

孙凌翥  冉雪琴  刘畅  牛熙  黄世会  王嘉福 《中国畜牧兽医》2021,48(2):537-553

为从基因组水平上探究香猪性成熟早、产仔数少、体型小的分子机理,本研究下载与香猪在繁殖和体型性状方面有明显差异的梅山猪、杜洛克猪的重测序数据作为参照,对26头香猪、24头梅山猪和24头杜洛克猪的重测序数据进行SNPs检测和等位基因频率差值分析,筛选香猪基因组外显子上与梅山猪、杜洛克猪高度分化的SNPs位点,并使用AS-PCR方法和Sanger测序方法统计其中8个SNPs位点的群体等位基因频率。最后,对含有高度分化SNPs位点的基因进行GO功能富集和KEGG通路分析。结果显示,SNPs检测获得香猪基因组外显子上SNPs共236 710个,包括193个终止密码子丢失、1 238个终止密码子获得、90 945个错义SNPs和144 334个同义SNPs。得到1 046个香猪高度分化SNPs,包括429个错义SNPs、2个终止子丢失、6个终止子获得和609个同义SNPs,影响524个蛋白质编码基因;并发现X染色体上44-58 Mb的一段富含高度分化SNPs的热点区域。群体等位基因频率验证结果与重测序结果一致,鉴定了8个位点均为香猪与梅山猪、杜洛克猪高度分化的SNPs。对524个含有高度分化SNPs的基因进行GO和KEGG分析,富集到卵母细胞减数分裂、雌激素信号途径等繁殖相关通路;GO功能注释到细胞内雌激素受体信号、纤毛运动等繁殖相关条目,骨骼系统形态发生、骨骼发育、成骨细胞分化等体型相关条目。得到含有香猪高度分化SNPs的18个繁殖性状候选基因PTGFR、TRO、DNAH17、PKDREJ、KAT8、DNAI2、VDR、TEX14、QSOX1、AR、WNK3、ADCY3、SPEF1、MIGA2、SLC2A8、PSMF1、TBC1D20、IFT172和7个体型相关基因IBSP、NR6A1、HSPG2、TARS、PDZD2、FGF4、AMER1,可能是决定香猪性成熟早、产仔数少、体型小的关键基因。  相似文献   

哈萨克羊iNOS基因多态性与布鲁氏菌病的相关性分析     

张凡  徐杰  李刚  周永顺  何营  韩凯  陈福龙  高剑峰 《中国畜牧兽医》2021,48(3):1102-1111

试验旨在探讨哈萨克羊诱导型一氧化氮合酶（iNOS）基因多态性与布鲁氏菌病的相关性。使用虎红平板凝集试验（RBPT）方法对231只哈萨克羊血清进行布鲁氏菌病血清学检测,参考GenBank中绵羊iNOS基因序列,针对其第6、7、8外显子及其邻近内含子片段设计引物,利用PCR-SSCP技术和DNA测序技术对231只哈萨克羊的iNOS基因进行多态性检测,分析其SNPs与哈萨克羊布鲁氏菌病易感性的相关性。结果表明,67只哈萨克羊为布鲁氏菌感染阳性,阳性检出率为29.00%。在哈萨克羊iNOS基因的外显子6和8片段上未检测到多态位点,在外显子7片段上检测出F7-T18054C和F7-C18084T 2个多态位点,在F7-T18054C多态位点上检测到3种基因型（TC、TT、CC）,优势等位基因和基因型分别是C型和CT型,其等位基因频率和基因型频率分别是0.660和0.446。在F7-C18084T多态位点上检测到2种基因型（CT、CC）,优势等位基因频率和基因型分别是C和CC型,其等位基因和基因型频率分别是0.946和0.892。F7-C18084T属于低度多态（PIC<0.25）,F7-T18054C属于中度多态（0.25 < PIC < 0.5）。相关性分析表明,F7-T18054C和F7-C18084T多态位点与布鲁氏菌病易感性无显著相关性（P>0.05）。试验结果表明,哈萨克羊iNOS基因F7-T18054C和F7-C18084T多态位点与布鲁氏菌病易感性不存在相关性。  相似文献   

Genomic prediction for meat and carcass traits in Nellore cattle using a Markov blanket algorithm     

Fernando Brito Lopes  Fernando Baldi  Ludmilla Costa Brunes  Marcos Fernando Oliveira e Costa  Eduardo da Costa Eifert  Guilherme Jordão Magalhães Rosa  Raysildo Barbosa Lobo  Cláudio Ulhoa Magnabosco 《Zeitschrift für Tierzüchtung und Züchtungsbiologie》2023,140(1):1-12

This study was carried out to evaluate the advantage of preselecting SNP markers using Markov blanket algorithm regarding the accuracy of genomic prediction for carcass and meat quality traits in Nellore cattle. This study considered 3675, 3680, 3660 and 524 records of rib eye area (REA), back fat thickness (BF), rump fat (RF), and Warner–Bratzler shear force (WBSF), respectively, from the Nellore Brazil Breeding Program. The animals have been genotyped using low-density SNP panel (30 k), and subsequently imputed for arrays with 777 k SNPs. Four Bayesian specifications of genomic regression models, namely Bayes A, Bayes B, Bayes Cπ and Bayesian Ridge Regression methods were compared in terms of prediction accuracy using a five folds cross-validation. Prediction accuracy for REA, BF and RF was all similar using the Bayesian Alphabet models, ranging from 0.75 to 0.95. For WBSF, the predictive ability was higher using Bayes B (0.47) than other methods (0.39 to 0.42). Although the prediction accuracies using Markov blanket of SNP markers were lower than those using all SNPs, for WBSF the relative gain was lower than 13%. With a subset of informative SNPs markers, identified using Markov blanket, probably, is possible to capture a large proportion of the genetic variance for WBSF. The development of low-density and customized arrays using Markov blanket might be cost-effective to perform a genomic selection for this trait, increasing the number of evaluated animals, improving the management decisions based on genomic information and applying genomic selection on a large scale.  相似文献   

鸡GDF-5基因外显子1多态性与鸡骨骼发育性状的相关研究   总被引：1，自引：0，他引：1  

冷丽  李辉  唐志权  王启贵  王桂华  顾志刚 《畜牧兽医学报》2006,37(3):227-231

根据GenBank发表的鸡GDF-5基因的mRNA序列设计引物，以白耳鸡和东北农业大学选育的肉鸡高、低腹脂系第8世代鸡群为试验材料，通过测序和PCR-SSCP的方法进行SNP检测和基因型分析，探讨GDF5基因多态性与鸡生长和骨骼发育性状之间的关系。结果发现在GDF-5基因外显子1的84bp处存在1个C／T的突变位点，对该突变位点在研究群体中进行基因型分析，结果产生3种基因型，AA型个体的基因序列和GenBank（Accession No：AF123389）中的一致为C，而BB型个体的基因序列在84bp处突变为T。基因型与鸡体组成性状的统计分析结果表明，AA基因型个体的跖骨围显著高于AB基因型个体（P〈0．05）；AA基因型和AB基因型个体的跖爪重和跖爪率显著高于BB基因型个体（P〈0．05）；AB基因型个体的股骨长和股骨重显著高于BB基因型个体（P＜0．05）；表明该基因对鸡的骨骼性状有较大的影响或与控制骨骼发育性状的主效基因相连锁。  相似文献   

Analysis of FMO genes and off flavour in pork     

K.L. Glenn  A.M. Ramos  & M.F. Rothschild 《Zeitschrift für Tierzüchtung und Züchtungsbiologie》2007,124(1):35-38

Off flavours in pork sometimes produce tastes such as sourness, fishy, metallic or other non‐typical flavours and are often caused by low pH. Loss of function mutations in flavin containing mono‐oxygenase 3 (FMO3) are known to be associated with a fishy off flavour in both chicken eggs and cow's milk and a similar autosomal recessive disorder is present in humans resulting in a fishy odour. FMO3 is a member of a gene family that is clustered on human chromosome 1. Comparative mapping suggested that FMO3 and the remaining FMO genes (ex. FMO1 and FMO5) might map to the orthologous region on pig chromosome 9 (SSC9) where a quantitative trait locus (QTL) for off flavour was previously identified. Primers were designed to amplify FMO1, FMO3 and FMO5 gene fragments and several SNPs were discovered and genotyping tests developed. The genotypes from the Iowa State University Berkshire × Yorkshire resource population were used to linkage map FMO1 and FMO3 to SSC9 and FMO5 to pig chromosome 4 (SSC4). QTL and associations analyses were performed using the map containing FMO1 and FMO3. Results demonstrated that FMO3 and FMO1 mapped less than 1 cM away from the peak for the off flavour QTL previously detected on SSC9 and provide indications of an association between the FMO3 polymorphism and off flavour in pork.  相似文献