Northeast Institute of Geography and Agroecology, Chinese Academy of Sciences, Harbin 150040, China.
Plant Physiol. 2010 May;153(1):198-210. doi: 10.1104/pp.109.150607. Epub 2010 Mar 10.
Classical genetic analysis has revealed that the determinate habit of soybean (Glycine max) is controlled by a recessive allele at the determinate stem (Dt1) locus. To dissect the molecular basis of the determinate habit, we isolated two orthologs of pea (Pisum sativum) TERMINAL FLOWER1a, GmTFL1a and GmTFL1b, from the soybean genome. Mapping analysis indicated that GmTFL1b is a candidate for Dt1. Despite their high amino acid identity, the two genes had different transcriptional profiles. GmTFL1b was expressed in the root and shoot apical meristems (SAMs), whereas GmTFL1a was mainly expressed in immature seed. The GmTFL1b transcript accumulated in the SAMs during early vegetative growth in both the determinate and indeterminate lines but thereafter was abruptly lost in the determinate line. Introduction of the genomic region of GmTFL1b from the indeterminate line complemented the stem growth habit in the determinate line: more nodes were produced, and flowering in the terminal raceme was delayed. The identity between Dt1 and GmTFL1b was also confirmed with a virus-induced gene silencing experiment. Taken together, our data suggest that Dt1 encodes the GmTFL1b protein and that the stem growth habit is determined by the variation of this gene. The dt1 allele may condition the determinate habit via the earlier loss in GmTFL1b expression concomitant with floral induction, although it functions normally under the noninductive phase of flowering. An association test of DNA polymorphisms with the stem growth habit among 16 cultivars suggested that a single amino acid substitution in exon 4 determines the fate of the SAM after floral induction.
经典遗传学分析表明,大豆(Glycine max)的定长习性由位于定长茎(Dt1)基因座的隐性等位基因控制。为了剖析定长习性的分子基础,我们从大豆基因组中分离出豌豆(Pisum sativum)TERMINAL FLOWER1a 的两个同源物 GmTFL1a 和 GmTFL1b。定位分析表明,GmTFL1b 是 Dt1 的候选基因。尽管它们的氨基酸序列高度相似,但这两个基因的转录谱不同。GmTFL1b 在根和茎尖分生组织(SAM)中表达,而 GmTFL1a 主要在未成熟的种子中表达。在定长和不定长系的早期营养生长过程中,GmTFL1b 的转录本在 SAM 中积累,但在定长系中此后突然丢失。从不定长系中引入 GmTFL1b 的基因组区域,补充了定长系的茎生长习性:产生了更多的节点,并且顶端总状花序的开花时间延迟。使用病毒诱导的基因沉默实验也证实了 Dt1 和 GmTFL1b 之间的同一性。综合这些数据,我们认为 Dt1 编码 GmTFL1b 蛋白,茎的生长习性由该基因的变异决定。尽管在开花的非诱导阶段该基因正常发挥作用,但 dt1 等位基因可能通过在花诱导时同时导致 GmTFL1b 表达的早期丢失来决定 SAM 的命运。在 16 个品种中对 DNA 多态性与茎生长习性的关联测试表明,外显子 4 中的单个氨基酸替换决定了花诱导后 SAM 的命运。