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Nature. 2017 Jan 5;541(7635):92-95. doi: 10.1038/nature20610. Epub 2016 Dec 21.
2
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J Zhejiang Univ Sci B. 2016;17(12):905-915. doi: 10.1631/jzus.B1600125.
3
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Highly efficient de novo mutant identification in a Sorghum bicolor TILLING population using the ComSeq approach.利用ComSeq方法在双色高粱TILLING群体中高效鉴定从头突变体
Plant J. 2016 May;86(4):349-59. doi: 10.1111/tpj.13161.
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DHPLC technology for high-throughput detection of mutations in a durum wheat TILLING population.用于高通量检测硬粒小麦TILLING群体中突变的变性高效液相色谱技术
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基于高分辨率熔解曲线的γ射线诱导水稻突变体的 TILLING。

High-resolution melting-based TILLING of γ ray-induced mutations in rice.

机构信息

National Key Laboratory of Rice Biology, Institute of Crop Sciences, Zhejiang University, Hangzhou 310058, China.

Institute of Nuclear Agricultural Sciences, Zhejiang University, Hangzhou 310029, China.

出版信息

J Zhejiang Univ Sci B. 2018;19(8):620-629. doi: 10.1631/jzus.B1700414.

DOI:10.1631/jzus.B1700414
PMID:30070085
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6102187/
Abstract

Targeting Induced Local Lesions IN Genomes (TILLING) is a reverse genetics strategy for the high-throughput screening of induced mutations. γ radiation, which often induces both insertion/deletion (Indel) and point mutations, has been widely used in mutation induction and crop breeding. The present study aimed to develop a simple, high-throughput TILLING system for screening γ ray-induced mutations using high-resolution melting (HRM) analysis. Pooled rice (Oryza sativa) samples mixed at a 1:7 ratio of Indel mutant to wild-type DNA could be distinguished from the wild-type controls by HRM analysis. Thus, an HRM-TILLING system that analyzes pooled samples of four M plants is recommended for screening γ ray-induced mutants in rice. For demonstration, a γ ray-mutagenized M rice population (n=4560) was screened for mutations in two genes, OsLCT1 and SPDT, using this HRM-TILLING system. Mutations including one single nucleotide substitution (G→A) and one single nucleotide insertion (A) were identified in OsLCT1, and one trinucleotide (TTC) deletion was identified in SPDT. These mutants can be used in rice breeding and genetic studies, and the findings are of importance for the application of γ ray mutagenesis to the breeding of rice and other seed crops.

摘要

靶向诱导基因组局部突变(TILLING)是一种高通量筛选诱导突变的反向遗传学策略。γ 射线常用于插入/缺失(Indel)和点突变的诱导,已被广泛应用于诱变和作物育种。本研究旨在开发一种简单、高通量的 TILLING 系统,用于使用高分辨率熔解(HRM)分析筛选γ射线诱导的突变。通过 HRM 分析,可以将 Indel 突变体与野生型 DNA 以 1:7 比例混合的 pooled 水稻(Oryza sativa)样品与野生型对照区分开来。因此,建议使用分析 4 个 M 植株 pooled 样品的 HRM-TILLING 系统筛选水稻中的γ射线诱导突变体。为了验证这一方法,我们使用该 HRM-TILLING 系统对一个经γ射线诱变的 M 水稻群体(n=4560)中的两个基因 OsLCT1 和 SPDT 进行了突变筛选。在 OsLCT1 中鉴定到一个单核苷酸替换(G→A)和一个单核苷酸插入(A)突变,在 SPDT 中鉴定到一个三核苷酸(TTC)缺失突变。这些突变体可用于水稻的育种和遗传研究,对于γ射线诱变在水稻和其他种子作物的育种中的应用具有重要意义。