Rapid identification of rice blast resistance gene by specific length amplified fragment sequencing

• Main Authors: Shen Chen, Wen-juan Wang, Jing Su, Cong-ying Wang, Ai-qing Feng, Jian-yuan Yang, Lie-xian Zeng, Xiao-yuan Zhu
• Format: Article
• Language: English
• Published: Taylor & Francis Group 2016-05-01
• Series: Biotechnology & Biotechnological Equipment
• Subjects: rice blast; resistance gene; gene identification; slaf-seq
• Online Access: http://dx.doi.org/10.1080/13102818.2016.1159528

Excavation of resistance genes is one of the most effective and environment-friendly measures to control the devastating rice disease caused by Magnaporthe oryzae. Many resistance genes have been mapped and characterized in the last century. Nevertheless, only a few of the total resistance genes could be really applied in the rice breeding program. Huazhan (HZ) is a new native rice restorer line developed in China and widely used in hybrid rice in recent years. HZ and its crossed combinations usually show a broad spectrum of resistance against rice blast in different rice ecosystems in China. Dissection of the genetic background of HZ is very useful for its further application. In this study, a combined method based on bulked segregation analysis (BSA) and specific length amplified fragment sequencing (SLAF-seq) was used to identify blast resistance gene(s) in HZ. A total of 56,187 SLAFs labels were captured and 9051 polymorphic SLAFs markers were analysed and procured in this study. One trait associated with candidate resistance genes region on chromosome 12 overlapping 10.2–17.6 Mb has been identified, in which 10 NBS-LRR (nucleotide-binding site-leucine-rich repeat) coding genes were used as resistance gene candidates. Our result indicated that SLAF-seq with BSA is a rapid and effective method for initial identification of blast resistance genes. The identification of resistance gene in HZ will improve its molecular breeding and resistance variety application.