multi-locus GWAS

  • 文章类型: Journal Article
    籽粒相关性状在水稻种植中至关重要,影响产量和消费者偏好。这些特征的复杂遗传,涉及促成其表达的多个等位基因,对育种提出了挑战。为了应对这些挑战,我们利用35,286个高质量单核苷酸多态性(SNPs)进行了多基因座全基因组关联研究(ML-GWAS).我们的研究利用了一个关联小组,该小组包括来自东北核心组的483个水稻基因型和从印度各个地区收集的地方品种组。鉴定了40个数量性状核苷酸(QTNs),与四个籽粒相关性状相关:籽粒长度(GL),晶粒宽度(GW),谷物香气(阿罗),和长宽比(LWR)。值得注意的是,使用两种ML-GWAS方法同时鉴定了16种QTNs,分布在多个染色体上。在16个显著的QTNs附近发现了近258个基因。基因注释研究表明,这些基因中有60个在特定组织中表现出升高的表达水平,并且与影响谷物品质的途径有关。基因本体论(GO),特质本体论(TO),和富集分析确定了60个富含相关GO术语的候选基因(CGs)。其中,LOC_Os05g06470、LOC_Os06g06080、LOC_Os08g43470和LOC_Os03g53110被确认为GL的主要贡献者,GW,阿罗,和LWR。来自QTNs和CGs的见解阐明了水稻性状调控和遗传联系,为未来的研究提供潜在的目标。
    Grain-related traits are pivotal in rice cultivation, influencing yield and consumer preference. The complex inheritance of these traits, involving multiple alleles contributing to their expression, poses challenges in breeding. To address these challenges, a multi-locus genome-wide association study (ML-GWAS) utilizing 35,286 high-quality single-nucleotide polymorphisms (SNPs) was conducted. Our study utilized an association panel comprising 483 rice genotypes sourced from a northeast core set and a landraces set collected from various regions in India. Forty quantitative trait nucleotides (QTNs) were identified, associated with four grain-related traits: grain length (GL), grain width (GW), grain aroma (Aro), and length-width ratio (LWR). Notably, 16 QTNs were simultaneously identified using two ML-GWAS methods, distributed across multiple chromosomes. Nearly 258 genes were found near the 16 significant QTNs. Gene annotation study revealed that sixty of these genes exhibited elevated expression levels in specific tissues and were implicated in pathways influencing grain quality. Gene ontology (GO), trait ontology (TO), and enrichment analysis pinpointed 60 candidate genes (CGs) enriched in relevant GO terms. Among them, LOC_Os05g06470, LOC_Os06g06080, LOC_Os08g43470, and LOC_Os03g53110 were confirmed as key contributors to GL, GW, Aro, and LWR. Insights from QTNs and CGs illuminate rice trait regulation and genetic connections, offering potential targets for future studies.
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  • 文章类型: Journal Article
    新生儿腹泻是一个重要的全球性挑战,由于其多因素的病因,导致高发病率和死亡率,和巨大的经济损失。虽然对农场动物的遗传弹性/新生儿腹泻易感性的分子水平研究很少,先前的观察表明有希望的研究方向。因此,本研究利用了两种全基因组关联方法,pKWmEB和传销,探索卡拉卡比美利诺羔羊先天免疫遗传变异与新生儿腹泻之间的潜在联系。分析707只羔羊,包括180例病例和527例对照,显示总体患病率为25.5%。pKWmEB分析鉴定出13个超过≥LOD3阈值的显著SNP。此外,MLM在SLC22A8基因中检测到一个SNP(s61781.1)(p值,1.85eE-7),这两种方法都有共同检测。进行McNemar测试作为最终评估,以鉴定在检测的SNP中是否存在任何主要的有效标记。结果表明,四个标记-oar3_OAR1_12235257,OAR17_77709936.1,oar3_OAR18_17278638和s61781.1-对新生儿腹泻患病率有重大影响(比值比:2.03至3.10;统计功效:0.88至0.99)。因此,我们提出了带有三个相关标记的注释基因,TIAM1,YDJC,和SLC22A8,作为选择性育种抗新生儿腹泻的候选主要基因。
    Neonatal diarrhea presents a significant global challenge due to its multifactorial etiology, resulting in high morbidity and mortality rates, and substantial economic losses. While molecular-level studies on genetic resilience/susceptibility to neonatal diarrhea in farm animals are scarce, prior observations indicate promising research directions. Thus, the present study utilizes two genome-wide association approaches, pKWmEB and MLM, to explore potential links between genetic variations in innate immunity and neonatal diarrhea in Karacabey Merino lambs. Analyzing 707 lambs, including 180 cases and 527 controls, revealed an overall prevalence rate of 25.5%. The pKWmEB analysis identified 13 significant SNPs exceeding the threshold of ≥ LOD 3. Moreover, MLM detected one SNP (s61781.1) in the SLC22A8 gene (p-value, 1.85eE-7), which was co-detected by both methods. A McNemar\'s test was conducted as the final assessment to identify whether there are any major effective markers among the detected SNPs. Results indicate that four markers-oar3_OAR1_122352257, OAR17_77709936.1, oar3_OAR18_17278638, and s61781.1-have a substantial impact on neonatal diarrhea prevalence (odds ratio: 2.03 to 3.10; statistical power: 0.88 to 0.99). Therefore, we propose the annotated genes harboring three of the associated markers, TIAM1, YDJC, and SLC22A8, as candidate major genes for selective breeding against neonatal diarrhea.
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  • 文章类型: Journal Article
    结论:通过GWAS阐明了菊花开花时间的动态遗传结构。在稳定的QTNs和QEI周围确定了36个已知基因和14个候选基因,其中ERF-1突出显示。花时间(FT)适应是菊花的主要育种目标之一,多用途观赏植物。为了揭示菊花FT的动态遗传结构,在2个环境中的169个条目中对10个FT相关性状进行了表型调查。五个非条件FT性状的广义遗传力,即,出芽(FBD),可见着色(VC),早期开放(EO),盛开(OF)和衰变期(DP),从56.93到84.26%,高于五个衍生条件FT性状(38.51-75.13%)。OF_EO和DP_OF的表型变异系数相对较大,范围为30.59%至36.17%。基于375,865个SNP,压缩方差分量混合线性模型3VmrMLM应用于多基因座全基因组关联研究(GWAS).因此,在单环境分析中,为非条件FT性状鉴定了313个数量性状核苷酸(QTNs),而在多环境分析中确定了119个QTNs和67个QTN-by-environment交互作用(QEI)。至于条件特征,在单环境分析中检测到343例QTNs,在多环境分析中确定了119个QTNs和83个QEI。在稳定QTNs和QEI周围的基因中,36个是拟南芥和其他植物中已知FT基因的直向同源物;通过结合转录组学数据和功能注释,包括ERF-1、ACA10和FOP1。此外,ERF-1的单倍型分析显示有六个极端FBD的精英种质。我们的发现有助于理解FT的动态遗传结构,并为未来的菊花分子育种计划提供宝贵的资源。
    CONCLUSIONS: The dynamic genetic architecture of flowering time in chrysanthemum was elucidated by GWAS. Thirty-six known genes and 14 candidate genes were identified around the stable QTNs and QEIs, among which ERF-1 was highlighted. Flowering time (FT) adaptation is one of the major breeding goals in chrysanthemum, a multipurpose ornamental plant. In order to reveal the dynamic genetic architecture of FT in chrysanthemum, phenotype investigation of ten FT-related traits was conducted on 169 entries in 2 environments. The broad-sense heritability of five non-conditional FT traits, i.e., budding (FBD), visible coloring (VC), early opening (EO), full-bloom (OF) and decay period (DP), ranged from 56.93 to 84.26%, which were higher than that of the five derived conditional FT traits (38.51-75.13%). The phenotypic variation coefficients of OF_EO and DP_OF were relatively large ranging from 30.59 to 36.17%. Based on 375,865 SNPs, the compressed variance component mixed linear model 3VmrMLM was applied for a multi-locus genome-wide association study (GWAS). As a result, 313 quantitative trait nucleotides (QTNs) were identified for the non-conditional FT traits in single-environment analysis, while 119 QTNs and 67 QTN-by-environment interactions (QEIs) were identified in multi-environment analysis. As for the conditional traits, 343 QTNs were detected in single-environment analysis, and 119 QTNs and 83 QEIs were identified in multi- environment analysis. Among the genes around stable QTNs and QEIs, 36 were orthologs of known FT genes in Arabidopsis and other plants; 14 candidates were mined by combining the transcriptomics data and functional annotation, including ERF-1, ACA10, and FOP1. Furthermore, the haplotype analysis of ERF-1 revealed six elite accessions with extreme FBD. Our findings contribute to the understanding of dynamic genetic architecture of FT and provide valuable resources for future chrysanthemum molecular breeding programs.
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  • 文章类型: Journal Article
    由PucciniapolysoraUnderw引起的南方玉米锈病(SCR)是导致中国夏玉米带严重产量损失的主要疾病。使用六种多位点GWAS方法,我们从中国夏玉米带收集的140个自交系的多样性小组中确定了一组SCR抗性QTNs。将染色体1、2、4、5、6和8上的13个QTNs分为三种类型的等位基因效应,并通过GWAS病例对照采样验证了它们与SCR表型的关联。等位基因/单倍型效应分析。从单个QTN和QTN-QTN组合中估计了适应其近交携带者的相对抗性(RRR)和相对敏感性(RR),并估计了QTN-QTN组合的认识论效应。通过转录组学注释,预测一组候选基因参与转录调控(S5_145,Zm00001d01613,转录因子GTE4),磷酸化(S8_123,Zm00001d010672,Pgk2-磷酸甘油酸激酶2),和温度胁迫响应(S6_164a/S6_164b,Zm00001d038806、hsp101和S5_211、Zm00001d017978、纤维素酶25)。讨论了上述发现的育种意义。
    Southern corn rust (SCR) caused by Puccinia polysora Underw is a major disease leading to severe yield losses in China Summer Corn Belt. Using six multi-locus GWAS methods, we identified a set of SCR resistance QTNs from a diversity panel of 140 inbred lines collected from China Summer Corn Belt. Thirteen QTNs on chromosomes 1, 2, 4, 5, 6, and 8 were grouped into three types of allele effects and their associations with SCR phenotypes were verified by post-GWAS case-control sampling, allele/haplotype effect analysis. Relative resistance (RRR) and relative susceptibility (RRs) catering to its inbred carrier were estimated from single QTN and QTN-QTN combos and epistatitic effects were estimated for QTN-QTN combos. By transcriptomic annotation, a set of candidate genes were predicted to be involved in transcriptional regulation (S5_145, Zm00001d01613, transcription factor GTE4), phosphorylation (S8_123, Zm00001d010672, Pgk2- phosphoglycerate kinase 2), and temperature stress response (S6_164a/S6_164b, Zm00001d038806, hsp101, and S5_211, Zm00001d017978, cellulase25). The breeding implications of the above findings were discussed.
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  • 文章类型: Journal Article
    硬粒小麦基因组数据的最新提升(Triticumturgidumsubsp。durum)提供了更好地了解育种对调节农艺性状表达的遗传结构的影响的机会。此外,鉴定可用于标记辅助选择的DNA标记还可以提高用于品种保护和注册的技术方案的可靠性.
    在这种动机背景下,123种硬粒小麦,分为三组:地方品种(LR),古代(OC)和现代品种(MC),在两个地点进行了评估,34个农艺性状,包括UPOV描述符,评估现代育种过程中发生的变化的影响。
    关联映射分析,用4,241个SNP标记和六个多基因座GWAS模型进行,揭示了与植物形态和籽粒相关性状相关的28个可靠的定量性状核苷酸(QTNs)。控制开花时间和植物高度的一些重要基因与本研究中确定的QTNs处于连锁不平衡(LD)衰变中。在6A号染色体上发现了黄莓的强关联(Q.Yb-6A)在包含nadh-泛醌氧化还原酶亚基的区域中,参与淀粉代谢的基因。Q.Kcp-2A具有PPO位点,与Ppo-A1和Ppo-A2在LD衰变中的相关标记(Ku_c13700_1196)。有趣的是,由RAC875_c34512_685确定的Q.FGSGls-2B.1,用于旗叶白度,从白斑的上位性抑制剂(Iw1)中映射小于1Mb,因此代表了用分子标记支持形态DUS性状的良好候选者。LD单倍型阻断方法显示出更高的多样性,MC中单倍体的丰富度和长度比OC和LR(LR中580,OC为585,MC为612),表明育种程序可能对与农艺性状相关的基因组区域产生影响。
    我们的发现通过使用一组与UPOV描述符相关的成本效益SNP标记,为支持品种注册所需的表型表征铺平了新的道路。此外,相关SNP组可能代表了在硬粒小麦育种和遗传学中使用的有利等位基因库。
    UNASSIGNED: The recent boosting of genomic data in durum wheat (Triticum turgidum subsp. durum) offers the opportunity to better understand the effects of breeding on the genetic structures that regulate the expression of traits of agronomic interest. Furthermore, the identification of DNA markers useful for marker-assisted selection could also improve the reliability of technical protocols used for variety protection and registration.
    UNASSIGNED: Within this motivation context, 123 durum wheat accessions, classified into three groups: landraces (LR), ancient (OC) and modern cultivars (MC), were evaluated in two locations, for 34 agronomic traits, including UPOV descriptors, to assess the impact of changes that occurred during modern breeding.
    UNASSIGNED: The association mapping analysis, performed with 4,241 SNP markers and six multi-locus-GWAS models, revealed 28 reliable Quantitative Trait Nucleotides (QTNs) related to plant morphology and kernel-related traits. Some important genes controlling flowering time and plant height were in linkage disequilibrium (LD) decay with QTNs identified in this study. A strong association for yellow berry was found on chromosome 6A (Q.Yb-6A) in a region containing the nadh-ubiquinone oxidoreductase subunit, a gene involved in starch metabolism. The Q.Kcp-2A harbored the PPO locus, with the associated marker (Ku_c13700_1196) in LD decay with Ppo-A1 and Ppo-A2. Interestingly, the Q.FGSGls-2B.1, identified by RAC875_c34512_685 for flag leaf glaucosity, mapped less than 1 Mb from the Epistatic inhibitors of glaucousness (Iw1), thus representing a good candidate for supporting the morphological DUS traits also with molecular markers. LD haplotype block approach revealed a higher diversity, richness and length of haploblocks in MC than OC and LR (580 in LR, 585 in OC and 612 in MC), suggesting a possible effect exerted by breeding programs on genomic regions associated with the agronomic traits.
    UNASSIGNED: Our findings pave new ways to support the phenotypic characterization necessary for variety registration by using a panel of cost-effectiveness SNP markers associated also to the UPOV descriptors. Moreover, the panel of associated SNPs might represent a reservoir of favourable alleles to use in durum wheat breeding and genetics.
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  • 文章类型: Journal Article
    背景:叶绿素含量(CC)是影响玉米光合效率和最终产量的关键因素。然而,其遗传基础尚不清楚。统计方法的发展使研究人员能够设计和应用各种GWAS模型,包括传销,MLMM,超级,FarmCPU,BLINK和3VmrMLM。对其结果进行比较分析可以更有效地挖掘关键基因。
    结果:CC的遗传力为0.86。六个统计模型(MLM,BLINK,MLMM,FarmCPU,超级,和3VmrMLM)和125万个SNP用于GWAS。共检测到140个数量性状核苷酸(QTNs),3VmrMLM和MLM检测到最多(118)和最少(3)QTNs,分别。QTNs与481个基因相关,解释了0.29-10.28%的表型变异。此外,通过至少两种不同的模型或方法检测到10个共定位的QTNs,在至少两种不同的环境中确定了三个位于同一地点的QTNs,在不同的环境中,通过不同的模型或方法检测到6个共定位的QTNs。此外,基于B73(RefGen_v2)基因组筛选这些稳定QTNs内或附近的69个候选基因。GRMZM2G110408(ZmCCS3)由多个模型和多个环境中识别。该基因的功能表征表明编码的蛋白质可能有助于叶绿素的生物合成。此外,CC在该基因中显著QTN的单倍型之间存在显着差异,单倍型1的CC较高。
    结论:这项研究的结果拓宽了我们对CC遗传基础的理解,挖掘与CC相关的关键基因,可能与基于意识形态的高光合效率玉米新品种育种有关。
    BACKGROUND: The chlorophyll content (CC) is a key factor affecting maize photosynthetic efficiency and the final yield. However, its genetic basis remains unclear. The development of statistical methods has enabled researchers to design and apply various GWAS models, including MLM, MLMM, SUPER, FarmCPU, BLINK and 3VmrMLM. Comparative analysis of their results can lead to more effective mining of key genes.
    RESULTS: The heritability of CC was 0.86. Six statistical models (MLM, BLINK, MLMM, FarmCPU, SUPER, and 3VmrMLM) and 1.25 million SNPs were used for the GWAS. A total of 140 quantitative trait nucleotides (QTNs) were detected, with 3VmrMLM and MLM detecting the most (118) and fewest (3) QTNs, respectively. The QTNs were associated with 481 genes and explained 0.29-10.28% of the phenotypic variation. Additionally, 10 co-located QTNs were detected by at least two different models or methods, three co-located QTNs were identified in at least two different environments, and six co-located QTNs were detected by different models or methods in different environments. Moreover, 69 candidate genes within or near these stable QTNs were screened based on the B73 (RefGen_v2) genome. GRMZM2G110408 (ZmCCS3) was identified by multiple models and in multiple environments. The functional characterization of this gene indicated the encoded protein likely contributes to chlorophyll biosynthesis. In addition, the CC differed significantly between the haplotypes of the significant QTN in this gene, and CC was higher for haplotype 1.
    CONCLUSIONS: This study\'s results broaden our understanding of the genetic basis of CC, mining key genes related to CC and may be relevant for the ideotype-based breeding of new maize varieties with high photosynthetic efficiency.
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  • 文章类型: Journal Article
    油菜(甘蓝型油菜),第三大油料作物,是世界植物油和生物燃料的重要来源。虽然育种和产量得到了提高,与其他主要作物相比,油菜的产量仍然最低。因此,提高油菜籽产量对于植物油和优质蛋白质的高需求至关重要。每个工厂的Silique编号(SN),每荚种子(SP),1000粒重(SW)是影响油菜种子产量的三个重要因素。一些产量相关性状,包括植物高度(PH),开花时间(FT),初枝数(BN)和每花序角果数(SI)也会影响单株产量(YP)。使用六种多基因座全基因组关联研究(ML-GWAS)方法,基于全基因组测序,在由403个油菜籽核心种质组成的小组中,共鉴定出908个产量相关的数量性状核苷酸(QTNs).ML-GWAS与转录组分析的整合,79个候选基因,包括BnaA09g39790D(RNA解旋酶),BnaA09g39950D(脂肪酶)和BnaC09g25980D(SWEET7),进一步鉴定,并通过qRT-PCR验证了12个基因对油菜中的SW或SP的影响。在20个优质油菜品种中,来自19个稳定QTNs的优良等位基因的分布表明,高产品种包含更多的优良等位基因。这些结果将有助于进一步了解产量相关性状的遗传基础,并可用于油菜的作物改良。
    Rapeseed (Brassica napus L.), the third largest oil crop, is an important source of vegetable oil and biofuel for the world. Although the breeding and yield has been improved, rapeseed still has the lowest yield compared with other major crops. Thus, increasing rapeseed yield is essential for the high demand of vegetable oil and high-quality protein for live stocks. Silique number per plant (SN), seed per pod (SP), and 1000-seed weight (SW) are the three important factors for seed yield in rapeseed. Some yield-related traits, including plant height (PH), flowering time (FT), primary branch number (BN) and silique number per inflorescence (SI) also affect the yield per plant (YP). Using six multi-locus genome-wide association study (ML-GWAS) approaches, a total of 908 yield-related quantitative trait nucleotides (QTNs) were identified in a panel consisting of 403 rapeseed core accessions based on whole-genome sequencing. Integration of ML-GWAS with transcriptome analysis, 79 candidate genes, including BnaA09g39790D (RNA helicase), BnaA09g39950D (Lipase) and BnaC09g25980D (SWEET7), were further identified and twelve genes were validated by qRT-PCRs to affect the SW or SP in rapeseed. The distribution of superior alleles from nineteen stable QTNs in 20 elite rapeseed accessions suggested that the high-yielding accessions contained more superior alleles. These results would contribute to a further understanding of the genetic basis of yield-related traits and could be used for crop improvement in B. napus.
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  • 文章类型: Journal Article
    镰刀菌枯萎病(FHB),由真菌镰刀菌Schwabe引起的小麦是一种重要的疾病,会导致严重的产量损失以及严重的质量问题。结合来自任一野生亲戚的宿主抵抗,地方品种,或异国情调的材料仍然具有挑战性,并显示出有限的成功。因此,更好地了解硬质冬小麦(HWW)中天然FHB抗性的遗传基础,并将其与主要数量性状基因座(QTL)结合使用,可以促进抗FHB品种的发展。在这项研究中,我们评估了来自南达科他州立大学(SDSU)育种计划的257个育种系,以揭示美国硬冬小麦中本地FHB抗性的遗传基础。我们进行了多基因座全基因组关联研究(ML-GWAS)与9,321个高质量的单核苷酸多态性(SNP)。在包括2A在内的五个不同染色体上,针对FHB疾病指数(DIS)总共鉴定了六个不同的标记-性状关联(MTA)。2B,3B,4B,和7A。Further,在包括3B,5A,6B,6D,7A,7B在14个重要的MTA中,在以前报道的不同小麦类别的FHB抗性区域附近发现了10个,并在HWW中进行了验证,而四个MTA代表FHB抗性的可能新基因座。报道的MTA的有利等位基因的积累导致显著较低的平均DIS和FDK评分,证明了FHB抗性等位基因的加性效应。两个重要的MTA的候选基因分析确定了几个具有假定的目的蛋白的基因;然而,需要进一步研究这些区域以鉴定赋予FHB抗性的基因。当前的研究揭示了美国HWW种质中天然FHB抗性的遗传基础,本研究中鉴定的抗性系和MTA将是通过标记辅助选择进行FHB抗性育种的有用资源。
    Fusarium head blight (FHB), caused by the fungus Fusarium graminearum Schwabe is an important disease of wheat that causes severe yield losses along with serious quality concerns. Incorporating the host resistance from either wild relatives, landraces, or exotic materials remains challenging and has shown limited success. Therefore, a better understanding of the genetic basis of native FHB resistance in hard winter wheat (HWW) and combining it with major quantitative trait loci (QTLs) can facilitate the development of FHB-resistant cultivars. In this study, we evaluated a set of 257 breeding lines from the South Dakota State University (SDSU) breeding program to uncover the genetic basis of native FHB resistance in the US hard winter wheat. We conducted a multi-locus genome-wide association study (ML-GWAS) with 9,321 high-quality single-nucleotide polymorphisms (SNPs). A total of six distinct marker-trait associations (MTAs) were identified for the FHB disease index (DIS) on five different chromosomes including 2A, 2B, 3B, 4B, and 7A. Further, eight MTAs were identified for Fusarium-damaged kernels (FDK) on six chromosomes including 3B, 5A, 6B, 6D, 7A, and 7B. Out of the 14 significant MTAs, 10 were found in the proximity of previously reported regions for FHB resistance in different wheat classes and were validated in HWW, while four MTAs represent likely novel loci for FHB resistance. Accumulation of favorable alleles of reported MTAs resulted in significantly lower mean DIS and FDK score, demonstrating the additive effect of FHB resistance alleles. Candidate gene analysis for two important MTAs identified several genes with putative proteins of interest; however, further investigation of these regions is needed to identify genes conferring FHB resistance. The current study sheds light on the genetic basis of native FHB resistance in the US HWW germplasm and the resistant lines and MTAs identified in this study will be useful resources for FHB resistance breeding via marker-assisted selection.
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  • 文章类型: Journal Article
    结论:关联遗传分析使我们能够识别形态生理自然变异的候选基因,抗氧化剂,和大麦籽粒产量相关性状。鉴定并解剖了新的有趣的基因组区域。盐度胁迫是影响生理形态的非生物胁迫之一,抗氧化剂,和作物植物的产量相关性状。在生殖阶段,在田间条件下暴露于盐胁迫后,分析了138种不同大麦品种的核心植物。然后使用19,276个单核苷酸多态性(SNP)进行全基因组关联扫描(GWAS),以揭示形态生理和谷物相关性状的遗传基础。在当前的研究中,探索了种质对盐胁迫的广泛响应。GWAS检测到263个与抗氧化剂显著相关的SNP,K+/Na+含量比,和农艺性状。五个基因组区域在LD±1.2Mbp内含有有趣的推定候选基因。Choromosome2H包含许多与抗氧化剂抗坏血酸(AsA)和谷胱甘肽(GSH)相关的候选基因,如超氧化物歧化酶(SOD),抗坏血酸过氧化物酶(APX),和谷胱甘肽还原酶(GR),盐胁迫下。很明显,染色体7H上153,773,211bp的A:CSNP位于HORVU基因内部。莫雷克斯.r3.7HG0676830(153,772,300-153,774,057bp),注释为L-古洛内酯氧化酶,调节SOD_S和APX_S的自然变异该SNP的等位基因变异揭示了携带C等位基因的种质的阴性选择,主要发现于起源于Far-的六行春季地方品种中,近东,和中亚携带光周期敏感等位基因,酶促抗氧化剂活性较低。在当前研究中检测到的SNP性状关联构成了开发用于大麦中抗氧化剂化合物选择的分子选择工具的基准。
    CONCLUSIONS: Association genetic analysis empowered us to identify candidate genes underlying natural variation of morpho-physiological, antioxidants, and grain yield-related traits in barley. Novel intriguing genomic regions were identified and dissected. Salinity stress is one of the abiotic stresses that influence the morpho-physiological, antioxidants, and yield-related traits in crop plants. The plants of a core set of 138 diverse barley accessions were analyzed after exposure to salt stress under field conditions during the reproductive phase. A genome-wide association scan (GWAS) was then conducted using 19,276 single nucleotide polymorphisms (SNPs) to uncover the genetic basis of morpho-physiological and grain-related traits. A wide range of responses to salt stress by the accessions was explored in the current study. GWAS detected 263 significantly associated SNPs with the antioxidants, K+/Na+ content ratio, and agronomic traits. Five genomic regions harbored interesting putative candidate genes within LD ± 1.2 Mbp. Choromosome 2H harbored many candidate genes associated with the antioxidants ascorbic acid (AsA) and glutathione (GSH), such as superoxide dismutase (SOD), ascorbate peroxidase (APX), and glutathione reductase (GR), under salt stress. Markedly, an A:C SNP at 153,773,211 bp on chromosome 7H is located inside the gene HORVU.MOREX.r3.7HG0676830 (153,772,300-153,774,057 bp) that was annotated as L-gulonolactone oxidase, regulating the natural variation of SOD_S and APX_S. The allelic variation at this SNP reveals a negative selection of accessions carrying the C allele, predominantly found in six-rowed spring landraces originating from Far-, Near-East, and central Asia carrying photoperiod sensitive alleles having lower activity of enzymatic antioxidants. The SNP-trait associations detected in the current study constitute a benchmark for developing molecular selection tools for antioxidant compound selection in barley.
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  • 文章类型: Journal Article
    早期开花,成熟,和株高是亚麻籽适合水稻休耕的重要性状,对于雨养农业,为了经济上可行的种植。这里,多基因座全基因组关联研究(ML-GWAS)在131个种质的关联映射面板中进行,使用通过测序方法进行基因分型鉴定的68,925个SNP进行基因分型。使用包括3年和两个地点的五个环境的表型评估数据。GWAS进行了三个开花时间性状,包括天数到5%,50%,95%开花,天成熟,通过采用五种ML-GWAS方法:FASTmrEMMA,FASTmrMLM,ISISEM-BLASSO,mrMLM,和pLARmEB。在五个环境中,共有335个独特的QTNs被鉴定为五个性状。109个QTNs在≥2种方法和/或环境中观察到稳定,解释高达36.6%的表型变异。对于三个开花时间性状,天成熟,和植物高度,53、30和27个稳定的QTNs,分别,已确定。在花中发挥作用的候选基因,花粉,胚胎,种子和果实发育,木质部/韧皮部组织发生已经确定。使用早熟品种Sharda(IC0523807)的转录组研究了开花和植物高度候选基因的基因表达。本研究揭示了复杂开花的QTNs/候选基因,天成熟,亚麻籽的株高性状。
    Early flowering, maturity, and plant height are important traits for linseed to fit in rice fallows, for rainfed agriculture, and for economically viable cultivation. Here, Multi-Locus Genome-Wide Association Study (ML-GWAS) was undertaken in an association mapping panel of 131 accessions, genotyped using 68,925 SNPs identified by genotyping by sequencing approach. Phenotypic evaluation data of five environments comprising 3 years and two locations were used. GWAS was performed for three flowering time traits including days to 5%, 50%, and 95% flowering, days to maturity, and plant height by employing five ML-GWAS methods: FASTmrEMMA, FASTmrMLM, ISIS EM-BLASSO, mrMLM, and pLARmEB. A total of 335 unique QTNs have been identified for five traits across five environments. 109 QTNs were stable as observed in ≥2 methods and/or environments, explaining up to 36.6% phenotypic variance. For three flowering time traits, days to maturity, and plant height, 53, 30, and 27 stable QTNs, respectively, were identified. Candidate genes having roles in flower, pollen, embryo, seed and fruit development, and xylem/phloem histogenesis have been identified. Gene expression of candidate genes for flowering and plant height were studied using transcriptome of an early maturing variety Sharda (IC0523807). The present study unravels QTNs/candidate genes underlying complex flowering, days to maturity, and plant height traits in linseed.
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