Yin Lu, Karn Avinash, Cadle-Davidson Lance, Zou Cheng, Underhill Anna, Atkins Paul, Treiber Erin, Voytas Daniel, Clark Matthew
Department of Horticultural Science, University of Minnesota, Twin Cities, MN, United States.
Institute of Biotechnology, Bioinformatics Facility, Cornell University, Ithaca, NY, United States.
Front Plant Sci. 2021 Mar 3;12:587640. doi: 10.3389/fpls.2021.587640. eCollection 2021.
Segregation for leaf trichome density was observed in a cold-hardy hybrid grape population GE1025 ( = ∼125, MN1264 × MN1246) that was previously used to detect a quantitative trait locus (QTL) underlying foliar phylloxera resistance on chromosome 14. Our hypothesis was that high trichome density was associated with resistance to phylloxera. Existing literature found trichome density QTL on chromosomes 1 and 15 using a hybrid grape population of "Horizon" × Illinois 547-1 and suggested a few candidate genes. To validate the reported QTL and our hypothesis, interval mapping was conducted in GE1025 with previous genotyping-by-sequencing (GBS) single nucleotide polymorphism (SNP) genotype data and phenotypic scores collected using a 0-6 trichome density scale at several leaf positions. Evaluations were done on replicated forced dormant cuttings in 2 years and on field-grown leaves in 1 year. There was no strong relationship between trichome density and phylloxera resistance except for a Pearson's correlation (r) of about -0.2 between a few trichome density traits and phylloxera severity traits at 2 and 3 weeks after infestation. Two genetic regions were repeatedly detected for multiple trichome density traits: from 10 to 20.7 Mbp (∼10 Mbp) on chromosome 1 for ribbon and simple density traits and from 2.4 to 8.9 Mbp on chromosome 10 for ribbon density traits, explaining 12.1-48.2 and 12.6-27.5% of phenotypic variation, respectively. To fine map, we genotyped a larger population, GE1783 ( = ∼1,023, MN1264 × MN1246), with conserved rhAmpSeq haplotype markers across multiple species and phenotyped 233 selected potential recombinants. Evaluations were conducted on field-grown leaves in a single year. The QTL for ribbon trichome density on adaxial vein and adaxial leaf and simple density on abaxial vein was fine mapped to 12.63-13.38 Mbp (747 kb) on chromosome 1. We found variations of MN1264 and MN1246 at candidate genes NAC transcription factor 29, EF-hand protein, and MYB140 in this region and three other surrounding candidate genes proposed previously. Even though no strong relationship between foliar phylloxera resistance and trichome density was found, this study validated and fine mapped a major QTL for trichome density using a cold-hardy hybrid grape population and shed light on a few candidate genes that have implications for different breeding programs.
在一个抗寒杂交葡萄群体GE1025(约125株,MN1264×MN1246)中观察到叶片毛状体密度的分离现象,该群体先前被用于检测14号染色体上叶瘿蚊抗性的数量性状位点(QTL)。我们的假设是高毛状体密度与对叶瘿蚊的抗性相关。现有文献利用“Horizon”×伊利诺伊547 - 1的杂交葡萄群体在1号和15号染色体上发现了毛状体密度QTL,并提出了一些候选基因。为了验证报道的QTL和我们的假设,在GE1025中利用先前通过测序基因分型(GBS)获得的单核苷酸多态性(SNP)基因型数据以及在几个叶片位置使用0 - 6毛状体密度量表收集的表型评分进行区间作图。在两年内对重复的强迫休眠插条以及一年内对田间生长的叶片进行了评估。除了在侵染后2周和3周时,一些毛状体密度性状与叶瘿蚊严重程度性状之间的皮尔逊相关性(r)约为 -0.2外,毛状体密度与叶瘿蚊抗性之间没有很强的关系。在两个遗传区域反复检测到多个毛状体密度性状:1号染色体上10至20.7兆碱基对(约10兆碱基对)处的带状和简单密度性状,以及10号染色体上2.4至8.9兆碱基对处的带状密度性状,分别解释了12.1 - 48.2%和12.6 - 27.5%的表型变异。为了进行精细定位,我们对一个更大的群体GE1783(约1023株,MN1264×MN1246)进行基因分型,使用跨多个物种保守的rhAmpSeq单倍型标记,并对233个选定的潜在重组体进行表型分析。在一年中对田间生长的叶片进行了评估。1号染色体上叶正面叶脉和叶正面的带状毛状体密度以及叶背面叶脉的简单密度的QTL被精细定位到12.63 - 13.38兆碱基对(747千碱基对)处。我们在该区域以及先前提出的其他三个周围候选基因中发现了MN1264和MN1246在候选基因NAC转录因子29、EF - 手型蛋白和MYB140上的变异。尽管未发现叶瘿蚊抗性与毛状体密度之间有很强的关系,但本研究利用抗寒杂交葡萄群体验证并精细定位了毛状体密度的一个主要QTL,并揭示了一些对不同育种计划有影响的候选基因。