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单核 RNA 测序和 mRNA 杂交表明在荔枝花转变过程中芽事件的关键以及 LcFT1 和 LcTFL1-2 mRNA 的可运输性。

Single-nucleus RNA sequencing and mRNA hybridization indicate key bud events and LcFT1 and LcTFL1-2 mRNA transportability during floral transition in litchi.

机构信息

Guangdong Laboratory for Lingnan Modern Agriculture/Key Laboratory of Biology and Genetic Improvement of Horticultural Crops-South China, College of Horticulture, South China Agricultural University, Guangzhou, China.

Becton Dickinson Medical Devices (Shanghai) Co., Ltd, Guangzhou, Guangdong, 510180, China.

出版信息

J Exp Bot. 2023 Jun 27;74(12):3613-3629. doi: 10.1093/jxb/erad103.

Abstract

In flowering plants, floral induction signals intersect at the shoot apex to modulate meristem determinacy and growth form. Here, we report a single-nucleus RNA sequence analysis of litchi apical buds at different developmental stages. A total of 41 641 nuclei expressing 21 402 genes were analyzed, revealing 35 cell clusters corresponding to 12 broad populations. We identify genes associated with floral transition and propose a model that profiles the key events associated with litchi floral meristem identity by analyzing 567 identified floral meristem cells at single cell resolution. Interestingly, single-nucleus RNA-sequencing data indicated that all putative FT and TFL1 genes were not expressed in bud nuclei, but significant expression was detected in bud samples by RT-PCR. Based on the expression patterns and gene silencing results, we highlight the critical role of LcTFL1-2 in inhibiting flowering and propose that the LcFT1/LcTFL1-2 expression ratio may determine the success of floral transition. In addition, the transport of LcFT1 and LcTFL1-2 mRNA from the leaf to the shoot apical meristem is proposed based on in situ and dot-blot hybridization results. These findings allow a more comprehensive understanding of the molecular events during the litchi floral transition, as well as the identification of new regulators.

摘要

在开花植物中,花诱导信号在茎尖相交,以调节分生组织的确定性和生长形式。在这里,我们报告了荔枝顶端芽在不同发育阶段的单细胞 RNA 序列分析。共分析了 41641 个表达 21402 个基因的核,揭示了 35 个细胞簇对应于 12 个广泛的群体。我们鉴定了与花转变相关的基因,并提出了一个模型,通过分析 567 个鉴定的花分生组织细胞的单细胞分辨率,描绘了与荔枝花分生组织身份相关的关键事件。有趣的是,单细胞 RNA-seq 数据表明,所有假定的 FT 和 TFL1 基因在芽核中均未表达,但通过 RT-PCR 在芽样品中检测到显著表达。基于表达模式和基因沉默结果,我们强调了 LcTFL1-2 在抑制开花中的关键作用,并提出 LcFT1/LcTFL1-2 表达比可能决定花转变的成功。此外,根据原位杂交和斑点杂交的结果,提出了 LcFT1 和 LcTFL1-2 mRNA 从叶到茎尖分生组织的运输。这些发现使我们能够更全面地了解荔枝花转变过程中的分子事件,并鉴定新的调节剂。

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