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Whole-Genome Re-Sequencing of Corylus heterophylla Blank-Nut Mutants Reveals Sequence Variations in Genes Associated With Embryo Abortion

机译:Corylus heterophylla Blank-ubly突变体的全基因组重新测序显示出与胚胎流产相关的基因的序列变化

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摘要

Yield loss in the economically important hazelnut (Corylus spp.) occurs through the frequent formation of blank nuts. Although the condition is associated with embryo abortion, we have not yet identified the regulatory genes involved. Therefore, this study aimed to determine the genes related to embryo abortion in hazel. We performed whole-genome re-sequencing and single-nucleotide polymorphism (SNP) analysis on four mutant hazelnut trees (Empty1 to Empty4, C. heterophylla) bearing blank nuts and four wild-type trees (Full1 to Full4, C. heterophylla). A paired comparison of Empty1 vs. Full1, Empty2 vs. Full2, Empty3 vs. Full3, and Empty4 vs. Full4, along with the intersection of Empty1 to Empty4, revealed 3 081 common SNPs in the four blank-nut mutants. Of these, 215 synonymous SNPs in exonic regions were distributed across 178 candidate genes. Heterozygosity analysis showed that average homozygous and heterozygous SNP ratios were respectively 0.409 and 0.591 in the samples. According to Gene Ontology classification, candidate genes were enriched in the categories of binding, catalysis, molecular transducer, transporter, and molecular function regulator. Among these, 18 of 178 genes had homozygous SNPs in Empty1–4. Cis elements in the promoter region of starch synthase 4 (SS4) contain the RY-element, implying seed-specific expression. Starch granules were absent from Empty1–4 cotyledon cells, but abundantly present in Full1–Full4 cotyledon cells. The blank-nut phenotype has heavier nut shells. Overall, we conclude that single-nucleotide variants of Acetyl-CoA carboxylase 1 (ACC1), intracellular sodium/hydrogen exchanger 2 (NHX2), UDP-glycosyltransferase 74E2 (UGT74E2), DEFECTIVE IN MERISTEM SILENCING 3 (DMS3), DETOXIFICATION 43 (FRD3), and SS4 may induce embryo abortion, leading to blank-nut formation. Our results will benefit future research on how the gain or loss of candidate genes influences seed development. Moreover, our study provides novel prospects for seedless cultivar development.
机译:经济上重要的榛子(Corylus SPP)中的产量损失通过频繁形成空质螺母而发生。虽然病症与胚胎流产有关,但我们尚未确定涉及的调节基因。因此,本研究旨在确定榛子中胚胎流产有关的基因。我们对四个突变榛子树(空1至空4,C. heterophylla)进行了全基因组重新测序和单核苷酸多态性(SNP)分析,横螺母和四个野生型树(Full1至Full4,C. heterophylla)。 Ampty1与Full1,Empty2与Full2,Empty3与Full3和Empty4与Full4的配对比较,以及Empty1到Empty4的交叉点显示了四个空白突变体中的3 081常见SNP。其中,在178个候选基因上分布了215个中的同义SNP。杂合性分析表明,平均纯合和杂合的SNP比率分别为0.409和0.591。根据基因本体类别分类,候选基因富含结合,催化,分子传感器,转运蛋白和分子功能调节剂的类别。其中,178个基因中的18个中有纯合子SNPS在空1-4中。淀粉合酶4(SS4)启动子区域中的顺式元素含有Ry元素,暗示特异性表达。淀粉颗粒不存在于空1-4个子叶细胞中,但在全1 - 全4个子叶细胞中大量存在。空白表型具有较重的坚果壳。总体而言,我们得出结论,乙酰-CoA羧基酶1(ACC1),细胞内钠/氢气交换器2(NHX2),UDP-糖基转移酶74E2(UGT74E2)的单核苷酸变体,在单位沉默3(DMS3)中有缺陷,排毒43(FRD3 ),SS4可以诱导胚胎流产,导致空白形成。我们的结果将使未来研究候选基因的增益或丧失影响种子发展的研究。此外,我们的研究为无籽品种发育提供了新的前景。

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