Plant Cytogenetics Laboratory, National Institute of Genetics, Mishima, Shizuoka, Japan.
Genetics Course, The Graduate University for Advanced Studies (SOKENDAI), Mishima, Shizuoka, Japan.
Methods Mol Biol. 2025;2869:135-146. doi: 10.1007/978-1-0716-4204-7_14.
Small RNAs are highly abundant and play important roles in plant reproduction. Profiling of small RNAs in reproductive tissues is a critical step in understanding their biology. Here, we describe a protocol for small RNA profiling in rice anthers, with a focus on an abundantly expressed but little-understood reproductive small RNA class named 24-nucleotide phased secondary small interfering RNAs (24-nt phasiRNAs). The protocol details small RNA library preparation steps for high-throughput sequencing, with a subsequent bioinformatic analysis framework. A low-throughput stem-loop reverse transcription PCR protocol for quick semi-quantification of small RNAs is also included as a complementary approach. The collective protocol, although focused on 24-nt phasiRNAs, should be amenable to other small RNA classes in various plant reproductive tissues.
小 RNA 丰度高,在植物繁殖中发挥重要作用。对生殖组织中小 RNA 的分析是了解其生物学功能的关键步骤。本研究描述了一种在水稻花粉中进行小 RNA 分析的方案,重点介绍了一类丰度高但知之甚少的生殖小 RNA 类,即 24 核苷酸相分的次级小干扰 RNA(24-nt phasiRNAs)。该方案详细说明了高通量测序用小 RNA 文库制备步骤,并提供了后续的生物信息学分析框架。还包括一种低通量茎环反转录 PCR 方案,用于快速半定量小 RNA,作为补充方法。虽然该方案侧重于 24-nt phasiRNAs,但应该适用于各种植物生殖组织中的其他小 RNA 类别。