Weier Guo, Héloïse Bastiaanse, Julin N Maloof, Luca Comai, Isabelle M Henry
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引用次数: 0
摘要
许多植物性状的基因控制可能非常复杂。等位基因变异(序列变化)和剂量变异(拷贝数变化)都会对植物的表型产生影响。虽然有许多研究调查了等位基因或剂量变异的影响,但很少有研究记录了同一系统中的这两种变异,因此它们对表型效应的相对贡献尚不清楚。杨树基因组具有高度多态性,而且杨树对基因剂量变异具有相当的耐受性。在这里,我们利用以前建立的杨树杂交 F1 群体,评估并比较了自然等位基因变异和诱导剂量变异对生物量、物候学和叶片形态特征的影响。我们确定了其中许多性状的 QTLs,但结果表明,与天然等位基因变异和诱导剂量变异相关的 QTLs 重叠有限。此外,整合等位基因变异和剂量变异的数据后,我们发现了一组更大的 QTLs,它们共同解释了更大比例的表型变异。最后,我们的研究结果表明,大嵌合体的效应可能会掩盖等位基因 QTLs 的效应。我们的研究有助于澄清等位基因和剂量变异之间的关系及其对数量性状的影响。
Induced and natural variation affect traits independently in hybrid Populus
The genetic control of many plant traits can be highly complex. Both allelic variation (sequence change) and dosage variation (copy number change) contribute to a plant’s phenotype. While numerous studies have investigated the effect of allelic or dosage variation, very few have documented both within the same system, leaving their relative contribution to phenotypic effects unclear. The Populus genome is highly polymorphic, and poplars are fairly tolerant of gene dosage variation. Here, using a previously established Populus hybrid F1 population, we assessed and compared the effect of natural allelic variation and induced dosage variation on biomass, phenology and leaf morphology traits. We identified QTLs for many of these traits, but our results indicate limited overlap between the QTLs associated with natural allelic variation and induced dosage variation. Additionally, the integration of data from both allelic and dosage variation identifies a larger set of QTLs that together explain a larger percentage of the phenotypic variance. Finally, our results suggest that the effect of the large indels might mask that of allelic QTLs. Our study helps clarify the relationship between allelic and dosage variation and their effects on quantitative traits.
期刊介绍:
G3: Genes, Genomes, Genetics provides a forum for the publication of high‐quality foundational research, particularly research that generates useful genetic and genomic information such as genome maps, single gene studies, genome‐wide association and QTL studies, as well as genome reports, mutant screens, and advances in methods and technology. The Editorial Board of G3 believes that rapid dissemination of these data is the necessary foundation for analysis that leads to mechanistic insights.
G3, published by the Genetics Society of America, meets the critical and growing need of the genetics community for rapid review and publication of important results in all areas of genetics. G3 offers the opportunity to publish the puzzling finding or to present unpublished results that may not have been submitted for review and publication due to a perceived lack of a potential high-impact finding. G3 has earned the DOAJ Seal, which is a mark of certification for open access journals, awarded by DOAJ to journals that achieve a high level of openness, adhere to Best Practice and high publishing standards.