Plant Stress and Germplasm Development Unit, Cropping Systems Research Laboratory, U.S. Department of Agriculture-Agricultural Research Service, Lubbock, TX 79415, USA.
Cold Spring Harbor Laboratory, Cold Spring Harbor, New York, NY 11724, USA.
Int J Mol Sci. 2019 Oct 28;20(21):5359. doi: 10.3390/ijms20215359.
Grain number per panicle is an important component of grain yield in sorghum ( (L.)) and other cereal crops. Previously, we reported that mutations in multi-seeded 1 ( and genes result in a two-fold increase in grain number per panicle due to the restoration of the fertility of the pedicellate spikelets, which invariably abort in natural sorghum accessions. Here, we report the identification of another gene, which is also involved in the regulation of grain numbers in sorghum. Four bulked F populations from crosses between BTx623 and each of the independent mutants p6, p14, p21, and p24 were sequenced to 20× coverage of the whole genome on a HiSeq 2000 system. Bioinformatic analyses of the sequence data showed that one gene, Sorbi_3001G407600, harbored homozygous mutations in all four populations. This gene encodes a plastidial ω-3 fatty acid desaturase that catalyzes the conversion of linoleic acid (18:2) to linolenic acid (18:3), a substrate for jasmonic acid (JA) biosynthesis. The mutants had reduced levels of linolenic acid in both leaves and developing panicles that in turn decreased the levels of JA. Furthermore, the panicle phenotype was reversed by treatment with methyl-JA (MeJA). Our characterization of and now demonstrates that JA-regulated processes are critical to the phenotype. The identification of the gene reveals a new target that could be manipulated to increase grain number per panicle in sorghum, and potentially other cereal crops, through the genomic editing of functional orthologs.
每穗粒数是高粱((L.))和其他谷类作物产量的重要组成部分。此前,我们报道称,多粒 1(和基因的突变导致每穗粒数增加一倍,这是由于不育小穗的育性恢复,而不育小穗在自然高粱品系中总是败育的。在这里,我们报告了另一个基因的鉴定,该基因也参与了高粱的粒数调控。BTx623 和每个独立的突变体 p6、p14、p21 和 p24之间杂交的四个混池 F 群体,在 HiSeq 2000 系统上进行了全基因组 20×覆盖测序。对序列数据的生物信息学分析表明,四个群体中都有一个基因 Sorbi_3001G407600 发生了纯合突变。该基因编码质体 ω-3 脂肪酸去饱和酶,催化亚油酸(18:2)转化为亚麻酸(18:3),这是茉莉酸(JA)生物合成的底物。突变体叶片和发育中的小穗中的亚麻酸水平降低,从而降低了 JA 水平。此外,茉莉酸甲酯(MeJA)处理逆转了突变体的小穗表型。我们对突变体的鉴定和现在的鉴定表明,JA 调节的过程对突变体表型至关重要。鉴定基因揭示了一个新的目标,通过对功能性同源物进行基因组编辑,可以在高粱中增加每穗粒数,并可能在其他谷类作物中增加每穗粒数。