Additional file 1: of Application of high-throughput amplicon sequencing-based SSR genotyping in genetic background screening

Autor: Tiantian Li, Zhiwei Fang, Peng, Hai, Junfei Zhou, Pengcheng Liu, Yanyan Wang, Wenhui Zhu, Li, Lun, Quanfang Zhang, Lihong Chen, Li, Lili, Zhihao Liu, Weixiong Zhang, Wenxue Zhai, Lu, Long, Lifen Gao
Rok vydání: 2019
Předmět:
DOI: 10.6084/m9.figshare.8222978.v1
Popis: Figure S1. The sequencing figure shows the mutation patterns of the T0 transgenic lines 3 to 6. + 2, 2 bp insertion; − 10, 10 bp deletion; + 1, 1 bp insertion; − 3, 3 bp deletion. WT, Xa21 wild type; _ indicates inserted bases, and arrows indicate deletion start sites. Figure S2. Expression validation of the genes in which the differential SSRs were distributed. D62B was used as a reference sample, and the rice ubiquitin gene was used as an endogenous control. Figure S3. Development of DXB, DXT and Xa21m. O. longistaminata: Oryza longistaminata, Xa21 donor parent; IR24: Oryza sativa, recurrent parent. MAB: marker-assisted backcrossing. IRBB21, Xa21 donor parent for DXB. D62B, the recipient rice for DXB and DXT; DXB, Xa21 MAB-produced rice; DXT, Xa21 transgenic rice; Xa21m, CRISPR/Cas9-mediated Xa21 mutant rice. (PPTX 98 kb)
Databáze: OpenAIRE