Sandhu Devinder, Ghosh Jayadri, Johnson Callie, Baumbach Jordan, Baumert Eric, Cina Tyler, Grant David, Palmer Reid G, Bhattacharyya Madan K
USDA-ARS, US Salinity Laboratory, Riverside, CA, United States of America.
Department of Agronomy, Iowa State University, Ames, IA, United States of America.
PLoS One. 2017 Aug 10;12(8):e0180732. doi: 10.1371/journal.pone.0180732. eCollection 2017.
In soybean, variegated flowers can be caused by somatic excision of the CACTA-type transposable element Tgm9 from Intron 2 of the DFR2 gene encoding dihydroflavonol-4-reductase of the anthocyanin pigment biosynthetic pathway. DFR2 was mapped to the W4 locus, where the allele containing Tgm9 was termed w4-m. In this study we have demonstrated that previously identified morphological mutants (three chlorophyll deficient mutants, one male sterile-female fertile mutant, and three partial female sterile mutants) were caused by insertion of Tgm9 following its excision from DFR2. Analyses of Tgm9 insertion sites among 105 independent mutants demonstrated that Tgm9 hops to all 20 soybean chromosomes from its original location on Chromosome 17. Some genomic regions are prone to increased Tgm9-insertions. Tgm9 transposed over 25% of the time into exon or intron sequences. Tgm9 is therefore suitable for generating an indexed insertional mutant collection for functional analyses of most soybean genes. Furthermore, desirable Tgm9-induced stable knockout mutants can be utilized in generating improved traits for commercial soybean cultivars.
在大豆中,花色斑驳可由编码花青素色素生物合成途径中二氢黄酮醇 - 4 - 还原酶的DFR2基因内含子2中的CACTA型转座元件Tgm9的体细胞切除引起。DFR2被定位到W4位点,其中含有Tgm9的等位基因被称为w4 - m。在本研究中,我们证明了先前鉴定的形态突变体(三个叶绿素缺乏突变体、一个雄性不育 - 雌性可育突变体和三个部分雌性不育突变体)是由Tgm9从DFR2切除后插入引起的。对105个独立突变体中Tgm9插入位点的分析表明,Tgm9从其在17号染色体上的原始位置跳跃到所有20条大豆染色体上。一些基因组区域易于发生Tgm9插入增加。Tgm9超过25%的时间转座到外显子或内含子序列中。因此,Tgm9适用于生成用于大多数大豆基因功能分析的索引插入突变体文库。此外,理想的Tgm9诱导的稳定敲除突变体可用于为商业大豆品种培育改良性状。