首页|基于BSA-seq技术挖掘番茄耐裂果候选基因

基于BSA-seq技术挖掘番茄耐裂果候选基因

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[目的]明确番茄耐裂基因在染色体上的位置.[方法]以耐裂果番茄14FP5和易裂果番茄14FP26为试材,将二者杂交得到F1代,F1自交得到F2,分别构建2个极端性状的DNA混合池,采用BSA-seq方法进行定位.[结果]利用BSA-seq对F2群体的2个极端混池进行基因组重测序分析,将番茄耐裂基因定位在5号染色体上,位于34140000~38120000 pb,区间大小为3.98 Mb,候选区间内共注释到38个基因,其中非同义突变基因4个.[结论]该研究结果可为番茄耐裂基因的精细定位提供数据支撑,为番茄耐裂分子育种奠定基础.
Extraction of Tomato Cracking Tolerance Candidate Genes Based on BSA-seq Technique
[Objective] To determine the position of tomato crack tolerance gene on chromosome.[Method]Tomato 14FP5 which is resistant to cracking and tomato 14FP26 which is easy to crack are used as test materials,cross the two to get F1 generation, F1 self-cross to get F2 ,DNA mixing pools with two extreme traits were constructed respectively,BSA-seq method was used to locate the location.[Result]BSA-seq was used for genome resequencing analysis of 2 extreme mixed pools of F2 population.The tomato anti-cracking gene was initially located on chromosome 5,located between 34140000 and 38120000 pb,the interval size is 3.98 Mb,a total of 38 genes were annotated in the candidate region,in-cluding 4 non-synonymous mutant genes.[Conclusion]The results provide data support for the fine localization of tomato crack tolerance genes, and lay a foundation for tomato crack tolerance molecular breeding.

TomatoCracking-resistantBSA-seqAssignment of genesCandidate gene

冯汝龙、王彦刚、常晨晨、景涛、冯锡鸿、申太荣、董建力

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宁夏中青农业科技有限公司,宁夏银川750001

宁夏农林科学院农业生物技术研究中心,宁夏银川750002

番茄 耐裂性 BSA-seq 基因定位 候选基因

宁夏回族自治区自然科学基金宁夏回族自治区重大科技项目

2020AAC035082017DC55

2024

安徽农业科学
安徽省农业科学院

安徽农业科学

影响因子:0.413
ISSN:0517-6611
年,卷(期):2024.52(10)
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