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基于水稻两段式代换系 Z783 开发单片段代换系和精细定位每穗小穗数 和粒宽

Development of Single-Segment Substitution Lines and Fine-Mapping of for Spikelets Per Panicle and for Grain Width Based on Rice Dual-Segment Substitution Line Z783.

机构信息

Rice Research Institute, Academy of Agricultural Science, Engineering Research Center of South Upland Agriculture, Ministry of Education, Southwest University, Chongqing 400715, China.

出版信息

Int J Mol Sci. 2023 Dec 9;24(24):17305. doi: 10.3390/ijms242417305.

Abstract

Single segment substitution line (SSSL) libraries are an ideal platform for breeding by design. To develop SSSLs-Xihui18 covering the whole genome, a novel rice chromosome segment substitution line (CSSL), Z783, carrying two substitution segments (average length of 6.55 Mb) on Chr.4 and Chr.9 was identified, which was a gap in the library previously. Z783 was developed from the progeny of recipient "Xihui18" (an restorer line) and donor "Huhan3" (a cultivar) by advanced backcross combined molecular marker-assisted selection (MAS). It displayed multiple panicles and less spikelets and wide grains. Then, a F population derived from Xihui18/Z783 was used to map quantitative trait loci (QTLs) for yield-related traits by the mixed linear model method. Nine QTLs were detected ( < 0.05). Furthermore, three SSSLs were constructed by MAS, and all 9 QTLs could be validated, and 15 novel QTLs could be detected by these SSSLs by a one-way ANOVA analysis. The genetic analysis showed that for less spikelets and for wide grain all displayed dominant gene action in their SSSLs. Finally, and were fine-mapped to intervals of 2.75 Mb and 1.84 Mb, on Chromosomes 4 and 9, respectively. The results lay a solid foundation for their map cloning and molecular breeding by design.

摘要

单片段代换系(SSSL)文库是设计育种的理想平台。为了开发涵盖整个基因组的 Xihui18 的 SSSL 系,我们鉴定了一个新型的水稻染色体片段代换系(CSSL)Z783,它在第 4 号和第 9 号染色体上携带两个代换片段(平均长度为 6.55 Mb),这是之前文库中的一个缺口。Z783 是由受体“Xihui18”(恢复系)和供体“Huhan3”(品种)的后代通过高级回交与分子标记辅助选择(MAS)相结合开发的。它表现出多穗、少小穗和宽粒。然后,利用 Xihui18/Z783 的 F1 群体,通过混合线性模型方法,对产量相关性状进行数量性状位点(QTL)作图。检测到 9 个 QTL(<0.05)。此外,通过 MAS 构建了 3 个 SSSL,通过单向方差分析(ANOVA)可以验证所有 9 个 QTL,并可以检测到 15 个新的 QTL。遗传分析表明,对于少小穗和宽粒,所有 SSSL 均表现出显性基因作用。最后,将和定位到第 4 号和第 9 号染色体上的 2.75 Mb 和 1.84 Mb 区间内。这些结果为它们的图谱克隆和设计分子育种奠定了坚实的基础。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0b4d/10744095/bcdea650dfd4/ijms-24-17305-g001.jpg

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