摘要
通过对籼稻黄华占EMS(甲磺酸乙酯)诱变,筛选得到一隐性核不育的水稻雄性不育突变体osms55,遗传分析表明该突变体为单基因控制的隐性核不育,采用高通量的Illumina Infinium iSelect SNP(50 K)芯片检测技术鉴定该突变体的遗传背景,确认该突变体的遗传背景与黄华占一致。文章利用改进的MutMap方法成功克隆该雄性不育基因,突变位点与突变表型的共分离分析表明LOC_Os02g40450(MER3)是控制osms55突变体雄性不育的基因,该基因的剪切识别位点发生变异后导致剪切异常,造成第5外显子缺失15个碱基,从而产生雄性不育。改进的MutMap方法无需精确组装的野生型基因组序列作对照,而是通过将定位群体中有突变表型植株的DNA pool和野生型植株DNA的重测序结果分别与日本晴参考基因组进行比对,然后再比较突变体和野生型的差异SNP来确定候选基因,该方法大大降低了野生型基因组测序和组装成本,进一步扩大了MutMap方法的应用范围。
A pollen defective male sterile rice mutant, osms55, was isolated from an elite indica eultivar HI-IZ using EMS （ethyl methanesulfonate） mutagenesis strategy. Genetic analysis showed that osms55 was controlled by a single reces sive gene. Genome-wide SNP analysis using the high-throughput Illumina Infinium iSelect SNP （50 K） microarray tech nology indicated that the genetic makeup ofosms55 is the same as wild type （WT） HHZ. Using a modified MutMap method, we successfully identified a mutation in the LOC_Os02g40450 （MER3） gene that is co-segregated with the male sterilityphenotype. The mutation is located at the intron splice-recognition site, leading to a 15 nucleotide deletion in the fifth exon. Different from the published MutMap method that aligns the mutant pool DNA sequence with the assembled WT genome, the method used in this study was to align the re-sequencing data of the mutant pool DNA and WT HHZ with the Nipponbare reference genome. The resulting SNPs of mutant/Nipponbare and WT HHZ/Nipponbare were further compared to determine the candidate mutant gene. This modified method does not need an assembled WT genome as reference and thus is more cost-effective and widely applicable.
出处
《遗传》
CAS
CSCD
北大核心
2014年第1期85-93,共9页
Hereditas（Beijing)
基金
国家自然科学基金项目(编号:31110103917)
广东省引进创新科研团队计划资助项目(编号:201001S0104725509)
深圳市科创委基础研究重点项目(编号:JC201005280655A)资助
