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Transcript profiling and identification of molecular markers for early microspore embryogenesis in Brassica napus

机译:甘蓝型油菜早期小孢子胚胎发生的转录谱分析和分子标记物的鉴定

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Isolated microspores of Brassica napus are developmentally programmed to form gametes; however, microspores can be reprogrammed through stress treatments to undergo appropriate divisions and form embryos. We are interested in the identification and isolation of factors and genes associated with the induction and establishment of embryogenesis in isolated microspores. Standard and normalized cDNA libraries, as well as subtractive cDNA libraries, were constructed from freshly isolated microspores (0 h) and microspores cultured for 3, 5, or 7 d under embryogenesis-inducing conditions. Library comparison tools were used to identify shifts in metabolism across this time course. Detailed expressed sequence tag analyses of 3 and 5 d cultures indicate that most sequences are related to pollen-specific genes. However, semiquantitative and real-time reverse transcription-polymerase chain reaction analyses at the initial stages of embryo induction also reveal expression of embryogenesis-related genes such as BABYBOOM1, LEAFY COTYLEDON1 (LEC1), and LEC2 as early as 2 to 3 d of microspore culture. Sequencing results suggest that embryogenesis is clearly established in a subset of the microspores by 7 d of culture and that this time point is optimal for isolation of embryo-specific expressed sequence tags such as ABSCISIC ACID INSENSITIVE3, ATS1, LEC1, LEC2, and FUSCA3. Following extensive polymerase chain reaction-based expression profiling, 16 genes were identified as unequivocal molecular markers for microspore embryogenesis in B. napus. These molecular marker genes also show expression during zygotic embryogenesis, underscoring the common developmental pathways that function in zygotic and gametic embryogenesis. The quantitative expression values of several of these molecular marker genes are shown to be predictive of embryogenic potential in B. napus cultivars (e. g. 'Topas' DH4079, 'Allons,' 'Westar,' 'Garrison').
机译:甘蓝型油菜的分离小孢子经过发育程序形成配子。但是,可以通过应力处理对小孢子进行重新编程,以进行适当的分裂并形成胚胎。我们对与分离的小孢子中诱导和建立胚发生有关的因子和基因的鉴定和分离感兴趣。从新鲜分离的小孢子(0 h)中构建标准和标准化的cDNA文库,以及减法cDNA文库,并在诱导胚胎发生的条件下培养3、5或7 d的小孢子。库比较工具用于确定该时间过程中新陈代谢的变化。对3d和5d培养物的详细表达序列标签分析表明,大多数序列与花粉特异性基因有关。然而,在胚胎诱导的初始阶段进行的半定量和实时逆转录聚合酶链反应分析也揭示了与胚胎发生相关的基因(如BABYBOOM1,LEAFY COTYLEDON1(LEC1)和LEC2)的表达早在小孢子的2-3天文化。测序结果表明,到培养7 d时,在小孢子的一个子集中就清楚地建立了胚胎发生,并且这个时间点是分离胚胎特异性表达序列标签(如ABSCISIC ACID INSENSITIVE3,ATS1,LEC1,LEC2和FUSCA3)的最佳选择。经过广泛的基于聚合酶链反应的表达谱分析,确定了16个基因作为油菜小孢子胚胎发生的明确分子标记。这些分子标记基因还在合子胚发生期间显示表达,强调了在合子和配子胚发生中起作用的常见发育途径。这些分子标记基因中的几个的定量表达值显示出可预测甘蓝型油菜品种的胚发生潜能(例如,“ Topas” DH4079,“ Allons”,“ Westar”,“ Garrison”)。

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