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普通小麦(Triticum aestivum L.)中一个控制小穗数目的新基因座的鉴定与验证

Identification and Validation of a Novel Locus Controlling Spikelet Number in Bread Wheat ( L.).

作者信息

Li Tao, Deng Guangbing, Tang Yanyan, Su Yan, Wang Jinhui, Cheng Jie, Yang Zhao, Qiu Xuebing, Pu Xi, Zhang Haili, Liang Junjun, Yu Maoqun, Wei Yuming, Long Hai

机构信息

Triticeae Research Institute, Sichuan Agricultural University, Chengdu, China.

Chengdu Institute of Biology, Chinese Academy of Sciences, Chengdu, China.

出版信息

Front Plant Sci. 2021 Feb 26;12:611106. doi: 10.3389/fpls.2021.611106. eCollection 2021.

Abstract

Spikelet number is an important target trait for wheat yield improvement. Thus, the identification and verification of novel quantitative trait locus (QTL)/genes controlling spikelet number are essential for dissecting the underlying molecular mechanisms and hence for improving grain yield. In the present study, we constructed a high-density genetic map for the Kechengmai1/Chuanmai42 doubled haploid (DH) population using 13,068 single-nucleotide polymorphism (SNP) markers from the Wheat 55K SNP array. A comparison between the genetic and physical maps indicated high consistence of the marker orders. Based on this genetic map, a total of 27 QTLs associated with total spikelet number per spike (TSN) and fertile spikelet number per spike (FSN) were detected on chromosomes 1B, 1D, 2B, 2D, 3D, 4A, 4D, 5A, 5B, 5D, 6A, 6B, and 7D in five environments. Among them, five QTLs on chromosome 2D, 3D, 5A, and 7D were detected in multiple environments and combined QTL analysis, explaining the phenotypic variance ranging from 3.64% to 23.28%. Particularly, for TSN and FSN [phenotypic variation explained (PVE) = 5.97-23.28%, limit of detection (LOD) = 3.73-18.51] is probably a novel locus and located in a 4.5-cM interval on chromosome arm 3DL flanking by the markers and This QTL was further validated in other two populations with different genetic backgrounds using the closely linked Kompetitive Allele-Specific PCR (KASP) marker . The results indicated that significantly increased the TSN (5.56-7.96%) and FSN (5.13-9.35%), which were significantly correlated with grain number per spike (GNS). We also preliminary analyzed the candidate genes within this locus by sequence similarity, spatial expression patterns, and collinearity analysis. These results provide solid foundation for future fine mapping and cloning of . The developed and validated KASP markers could be utilized in molecular breeding aiming to increase the grain yield in wheat.

摘要

小穗数是小麦产量提高的一个重要目标性状。因此,鉴定和验证控制小穗数的新数量性状位点(QTL)/基因对于剖析潜在的分子机制以及提高谷物产量至关重要。在本研究中,我们利用来自小麦55K SNP芯片的13068个单核苷酸多态性(SNP)标记,为科成麦1号/川麦42双单倍体(DH)群体构建了一个高密度遗传图谱。遗传图谱与物理图谱的比较表明标记顺序高度一致。基于该遗传图谱,在五个环境中,于1B、1D、2B、2D、3D、4A、4D、5A、5B、5D、6A、6B和7D染色体上共检测到27个与每穗总小穗数(TSN)和每穗可育小穗数(FSN)相关的QTL。其中,在2D、3D、5A和7D染色体上的5个QTL在多个环境中被检测到,并进行了联合QTL分析,解释的表型变异范围为3.64%至23.28%。特别是,对于TSN和FSN [表型变异解释率(PVE)= 5.97 - 23.28%,检测阈值(LOD)= 3.73 - 18.51]可能是一个新位点,位于3DL染色体臂上4.5 cM区间内,两侧标记为 和 。利用紧密连锁的竞争性等位基因特异性PCR(KASP)标记 在另外两个具有不同遗传背景的群体中进一步验证了该QTL。结果表明, 显著增加了TSN(5.56 - 7.96%)和FSN(5.13 - 9.35%),且与每穗粒数(GNS)显著相关。我们还通过序列相似性、空间表达模式和共线性分析对该位点内的候选基因进行了初步分析。这些结果为未来对 的精细定位和克隆提供了坚实基础。所开发和验证的KASP标记可用于旨在提高小麦籽粒产量的分子育种。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/129d/7952655/a3520ecdea7e/fpls-12-611106-g001.jpg

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