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番茄抗晚疫病基因Ph-3的分子标记开发及应用
引用本文:胡明瑜,白文钦,潘晓雪,吴红,汝学娟,罗佳,尹贤贵,潘光辉,雷开荣.番茄抗晚疫病基因Ph-3的分子标记开发及应用[J].植物病理学报,2018,48(4):560-566.
作者姓名:胡明瑜  白文钦  潘晓雪  吴红  汝学娟  罗佳  尹贤贵  潘光辉  雷开荣
作者单位:重庆市农业科学院生物技术研究中心/逆境农业研究重庆市重点实验室,重庆 401329;
重庆市农业科学院蔬菜花卉研究所,重庆 401329
基金项目:重庆市科委科技攻关项目“茄果类、瓜类蔬菜抗逆、抗病种质资源精确鉴定及创新”(cstc2015shms-ztzx80008);重庆市科研院所绩效激励引导专项“番茄抗晚疫病基因分子标记及辅助育种技术研究”(cstc2017jxjl80029)
摘    要:正番茄晚疫病由卵菌疫霉属的致病疫霉菌(Phytophthora infestans)侵染引起。病菌对番茄致病性强,侵染寄主后通过气流散发孢子,多次重复侵染植株,引起晚疫病爆发,对番茄生产造成严重危害1]。利用抗晚疫病资源,培育番茄抗病品种是降低晚疫病危害的有效途径。在野生番茄中发现


Analysis of tomato late blight resistance marker based on the analogues of Ph-3 gene
HU Ming-yu,BAI Wen-qin,PAN Xiao-xue,WU Hong,RU Xue-juan,LUO Jia,YIN Xian-gui,PAN Guang-hui,LEI Kai-rong.Analysis of tomato late blight resistance marker based on the analogues of Ph-3 gene[J].Acta Phytopathologica Sinica,2018,48(4):560-566.
Authors:HU Ming-yu  BAI Wen-qin  PAN Xiao-xue  WU Hong  RU Xue-juan  LUO Jia  YIN Xian-gui  PAN Guang-hui  LEI Kai-rong
Institution:Biotechnology research centre of Chongqing academic agricultural science/ Chongqing key laboratory of adversity agriculture, Chongqing 401329, China;
Vegetables and flowers research institution of Chongqing academic agricultural science, Chongqing 401329, China
Abstract:Tomato late blight is caused by Phytophthora infestans, which sends out the spore in airflow and infects plants repeatedly in the field. Under favourable conditions, P. infestans spreads rapidly and the susceptible host will be devastated in few days. Wild tomatoes with resistance genes such as Ph-1, Ph-2, Ph-3, Ph-4, Ph-5-1 and Ph-5-2, are useful germplasm resources to breed late blight-resistant tomatoes. To efficiently introduce the Ph-3 resistance gene, several DNA markers were developed, including RAPD, CAPS etc. Recently, the Ph-3 gene was cloned from CLN2037B, encoding a CC-NBS-LRR protein. In this article, we cloned the Ph-3 analogues from 4 tomato inbred lines (LQH-1, 620-1, 877-1, and QL-1) with sensitive response to late blight. The Ph-3 homology from LQH-1, 620-1, and 877-1 were inserted by a 306 bp fragment, assumably leading to 3 stop codon mutations. The Ph-3 homologous gene from QL-1 encoding an 848 aa protein, was different from the Ph-3 resistance gene in both DNA and protein sequences. Utilizing the DNA differences between Ph-3/ph-3 analogues, we developed DNA markers to facilitate the screening of mass populations for potential resistant tomatoes to late blight.
Keywords:tomato  late blight  Ph-3  DNA marker  
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