马铃薯紫色胚斑性状的6.49 mb反转

IF 4.6 4区 农林科学 Q1 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Pei Wang, Lin Cheng, Jun Pan, Lianlian Ma, Xiaojing Hu, Zhong Zhang, Dawei Li, Yanhui Zhu, Shiwei Chang, Pingping Yuan, Philip Kear, Ludivine Lassois, Guangtao Zhu, Sanwen Huang, Hui Du, Chunzhi Zhang
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引用次数: 0

摘要

胚胎斑点特征导致胚胎子叶基部呈深紫色或红色,在马铃薯(Solanum tuberosum)种子两侧可见。这一性状长期以来被马铃薯研究者和育种者用作二单倍体诱导过程中的形态标记。胚胎斑点的形成反映了花青素的积累,但这一性状的遗传基础尚不清楚。在本研究中,我们利用斑点与无斑点植物杂交获得的F2群体,将胚胎斑点性状定位到第10染色体末端6.78 mb区域。候选区域的重组率受到严重抑制,这给基础基因的图谱克隆带来了挑战,并提示该区域存在大规模重排。斑点个体的基因组组装和与无斑点马铃薯参考基因组的比较基因组分析显示,斑点植物基因组中存在6.49 mb的反转。这种反转的左断点发生在R2R3 MYB转录因子基因的启动子区域,该基因在斑点胚胎的子叶基部高度表达,而在无斑点胚胎的子叶基部不表达。本研究阐明了马铃薯胚斑形成的遗传基础,为进一步克隆致病基因奠定了基础。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A 6.49-Mb inversion associated with the purple embryo spot trait in potato

The embryo spot trait leads to a deep purple or reddish coloration at the base of the cotyledons of the embryo, visible on both sides of flat potato (Solanum tuberosum) seeds. This trait has long been used by potato researchers and breeders as a morphological marker during dihaploid induction. The formation of embryo spots reflects the accumulation of anthocyanins, but the genetic basis of this trait remains unclear. In this study, we mapped the embryo spot trait to a 6.78-Mb region at the end of chromosome 10 using an F2 population derived from a cross between spotted and spotless plants. The recombination rate in the candidate region is severely suppressed, posing challenges for the map-based cloning of the underlying gene and suggesting large-scale rearrangements in this region. A de novo genome assembly of the spotted individual and a comparative genomic analysis to the reference genome of spotless potato revealed a 6.49-Mb inversion present in the spotted plant genome. The left breakpoint of this inversion occurred in the promoter region of an R2R3 MYB transcription factor gene that is highly expressed in the cotyledon base of spotted embryos but is not expressed in that of spotless embryos. This study elucidated the genetic basis for embryo spot formation in potato and provides a foundation for future cloning of the causative gene.

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CiteScore
7.70
自引率
2.80%
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