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利用大规模平行测序和茎环反转录 PCR 技术对水稻花药中 24 核苷酸 phasiRNAs 的分析。

Profiling of 24-nt phasiRNAs in Rice Anther by Massively Parallel Sequencing and Stem-Loop Reverse Transcription PCR.

机构信息

Plant Cytogenetics Laboratory, National Institute of Genetics, Mishima, Shizuoka, Japan.

Genetics Course, The Graduate University for Advanced Studies (SOKENDAI), Mishima, Shizuoka, Japan.

出版信息

Methods Mol Biol. 2025;2869:135-146. doi: 10.1007/978-1-0716-4204-7_14.

Abstract

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.

摘要

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。

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