McCallum John, Laing William, Bulley Sean, Thomson Susan, Catanach Andrew, Shaw Martin, Knaebel Mareike, Tahir Jibran, Deroles Simon, Timmerman-Vaughan Gail, Crowhurst Ross, Hilario Elena, Chisnall Matthew, Lee Robyn, Macknight Richard, Seal Alan
New Cultivar Innovation, The New Zealand Institute for Plant & Food Research Limited, Private Bag 4704, Christchurch 8140, New Zealand.
Biochemistry Department, University of Otago, Dunedin 9054, New Zealand.
Plants (Basel). 2019 Jul 22;8(7):237. doi: 10.3390/plants8070237.
During analysis of kiwifruit derived from hybrids between the high vitamin C (ascorbic acid; AsA) species and , we observed bimodal segregation of fruit AsA concentration suggesting major gene segregation. To test this hypothesis, we performed whole-genome sequencing on pools of hybrid genotypes with either high or low AsA fruit. Pool-GWAS (genome-wide association study) revealed a single Quantitative Trait Locus (QTL) spanning more than 5 Mbp on chromosome 26, which we denote as qAsA26.1. A co-dominant PCR marker was used to validate this association in four diploid ( × ) × backcross families, showing that the allele at this locus increases fruit AsA levels by 250 mg/100 g fresh weight. Inspection of genome composition and recombination in other genetic maps confirmed that the qAsA26.1 region bears hallmarks of suppressed recombination. The molecular fingerprint of this locus was examined in leaves of backcross validation families by RNA sequencing (RNASEQ). This confirmed strong allelic expression bias across this region as well as differential expression of transcripts on other chromosomes. This evidence suggests that the region harbouring qAsA26.1 constitutes a supergene, which may condition multiple pleiotropic effects on metabolism.
在对源自高维生素C(抗坏血酸;AsA)品种与 杂交种的猕猴桃进行分析时,我们观察到果实AsA浓度呈双峰分离,表明存在主基因分离。为了验证这一假设,我们对高AsA果实或低AsA果实的杂交基因型池进行了全基因组测序。池基因组全关联研究(Pool-GWAS)揭示了26号染色体上一个跨越超过5兆碱基对的单一定量性状位点(QTL),我们将其命名为qAsA26.1。使用共显性PCR标记在四个二倍体( × )× 回交家系中验证了这种关联,结果表明该位点的 等位基因使果实AsA水平提高了250毫克/100克鲜重。对其他 遗传图谱中的基因组组成和重组进行检查证实,qAsA26.1区域具有重组受抑制的特征。通过RNA测序(RNASEQ)在回交验证家系的叶片中检查了该位点的分子指纹。这证实了该区域存在强烈的等位基因表达偏差以及其他染色体上转录本的差异表达。这些证据表明,包含qAsA26.1的区域构成了一个超级基因,它可能对代谢产生多种多效性影响。