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利用QTL定位、BSE-Seq和候选基因分析对小麦条锈病抗性基因QYrXN3517-1BL进行高密度定位

High density mapping of wheat stripe rust resistance gene QYrXN3517-1BL using QTL mapping, BSE-Seq and candidate gene analysis.

作者信息

Huang Shuo, Zhang Yibo, Ren Hui, Zhang Xin, Yu Rui, Liu Shengjie, Zeng Qingdong, Wang Qilin, Yuan Fengping, Singh Ravi P, Bhavani Sridhar, Wu Jianhui, Han Dejun, Kang Zhensheng

机构信息

State Key Laboratory of Crop Stress Biology for Arid Areas, Plant Protection, Northwest A&F University, Yangling, 712100, Shaanxi, People's Republic of China.

State Key Laboratory of Crop Stress Biology for Arid Areas, College of Agronomy, Northwest A&F University, Yangling, 712100, Shaanxi, People's Republic of China.

出版信息

Theor Appl Genet. 2023 Mar 10;136(3):39. doi: 10.1007/s00122-023-04282-5.

Abstract

Fine mapping of a major stripe rust resistance locus QYrXN3517-1BL to a 336 kb region that includes 12 candidate genes. Utilization of genetic resistance is an effective strategy to control stripe rust disease in wheat. Cultivar XINONG-3517 (XN3517) has remained highly resistant to stripe rust since its release in 2008. To understand the genetic architecture of stripe rust resistance, Avocet S (AvS) × XN3517 F RIL population was assessed for stripe rust severity in five field environments. The parents and RILs were genotyped by using the GenoBaits Wheat 16 K Panel. Four stable QTL from XINONG-3517 were detected on chromosome arms 1BL, 2AL, 2BL, and 6BS, named as QYrXN3517-1BL, QYrXN3517-2AL, QYrXN3517-2BL, and QYrXN3517-6BS, respectively. Based on the Wheat 660 K array and bulked segregant exome sequencing (BSE-Seq), the most effective QTL on chromosome 1BL is most likely different from the known adult plant resistance gene Yr29 and was mapped to a 1.7 cM region [336 kb, including twelve candidate genes in International Wheat Genome Sequencing Consortium (IWGSC) RefSeq version 1.0]. The 6BS QTL was identified as Yr78, and the 2AL QTL was probably same as QYr.caas-2AL or QYrqin.nwafu-2AL. The novel QTL on 2BL was effective in seedling stage against the races used in phenotyping. In addition, allele-specifc quantitative PCR (AQP) marker nwafu.a5 was developed for QYrXN3517-1BL to assist marker-assisted breeding.

摘要

将一个主要的条锈病抗性位点QYrXN3517 - 1BL精细定位到一个336 kb的区域,该区域包含12个候选基因。利用遗传抗性是控制小麦条锈病的有效策略。品种西农3517(XN3517)自2008年发布以来一直对条锈病保持高度抗性。为了解条锈病抗性的遗传结构,在五个田间环境中评估了Avocet S(AvS)×XN3517 F重组自交系群体的条锈病严重程度。利用GenoBaits小麦16K芯片对亲本和重组自交系进行基因分型。在1BL、2AL、2BL和6BS染色体臂上检测到来自西农3517的四个稳定QTL,分别命名为QYrXN3517 - 1BL、QYrXN3517 - 2AL、QYrXN3517 - 2BL和QYrXN3517 - 6BS。基于小麦660K芯片和混合分离群体外显子测序(BSE - Seq),1BL染色体上最有效的QTL很可能与已知的成株抗性基因Yr29不同,并被定位到一个1.7 cM的区域[336 kb,包括国际小麦基因组测序联盟(IWGSC)RefSeq版本1.0中的12个候选基因]。6BS QTL被鉴定为Yr78,2AL QTL可能与QYr.caas - 2AL或QYrqin.nwafu - 2AL相同。2BL上的新QTL在苗期对表型分析中使用的小种有效。此外,还开发了针对QYrXN3517 - 1BL的等位基因特异性定量PCR(AQP)标记nwafu.a5,以辅助标记辅助育种。

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