作物学报 ›› 2024, Vol. 50 ›› Issue (8): 2143-2156.doi: 10.3724/SP.J.1006.2024.34168
• 研究简报 • 上一篇
肖明昆1(), 严炜1,2,*(
), 宋记明1,2(
), 张林辉1,2, 刘倩1, 段春芳1,2, 李月仙1,2, 姜太玲1,2, 沈绍斌1,2, 周迎春1, 沈正松1,2, 熊贤坤1, 罗鑫1, 白丽娜1, 刘光华3,*(
)
XIAO Ming-Kun1(), YAN Wei1,2,*(
), SONG Ji-Ming1,2(
), ZHANG Lin-Hui1,2, LIU Qian1, DUAN Chun-Fang1,2, LI Yue-Xian1,2, JIANG Tai-Ling1,2, SHEN Shao-Bin1,2, ZHOU Ying-Chun1, SHEN Zheng-Song1,2, XIONG Xian-Kun1, LUO Xin1, BAI Li-Na1, LIU Guang-Hua3,*(
)
摘要:
为解析卷叶木薯叶片异常发育的分子调控机制及代谢通路, 以正常卷叶木薯叶片(JY)、突变株展叶叶片(ZY)和突变株卷叶叶片(BJ)为试验材料, 基于转录组测序(RNA-seq)数据进行生物信息学分析。DESeq差异分析结果显示, ZY vs BJ、JY vs ZY、JY vs BJ分别有327 (255个上调, 72个下调)、1085 (337个上调, 748个下调)、689 (381个上调, 308个下调)个DEGs, 有19个DEGs是3个比较组共同表达的。GO功能分析显示, DEGs在刺激反应、膜的组成部分、跨膜转运蛋白活性等途径差异显著。KEGG富集分析显示, DEGs在苯丙素的生物合成、植物激素信号转导、内质网中的蛋白加工等通路较为活跃。进一步对变异展叶与同株的卷叶和其他植株正常卷叶的DEGs分析发现集中富集到苯丙素的生物合成途径、淀粉和蔗糖代谢、植物激素信号转导, 这可能是展叶突变体形成的关键因子。展叶与卷叶差异基因的主要KEGG代谢通路有9条, 重要差异基因有9个。对不同类型叶片显微分析发现突变后的展叶木薯上表皮细胞层数增加、海绵组织结构变得疏松、维管束细胞减少。研究结果为进一步理解木薯叶片异常发育的分子机制提供了理论指导, 为木薯遗传改良、种质创新挖掘提供基因资源和改良策略。
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