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piRNAs 的克隆、测序和连锁分析。

Cloning, Sequencing, and Linkage Analysis of piRNAs.

机构信息

The John Curtin School of Medical Research, Australian National University, Acton, ACT, Australia.

出版信息

Methods Mol Biol. 2022;2509:107-133. doi: 10.1007/978-1-0716-2380-0_7.

Abstract

Piwi-interacting RNAs (piRNAs) are 25- to 32-nucleotide-long small RNAs that silence transposable elements (transposons) in animal gonads. piRNAs have a large sequence diversity (over one million different sequences per organism) to target a variety of transposon sequences. This is achieved by flexible and distinct biogenesis pathways that are evolutionarily conserved. In this chapter, I describe a detailed method of purifying and cloning piRNAs from freshly dissected tissue samples, such as fruit fly ovaries, for the high-throughput sequencing. I also describe how to computationally process the sequencing data and interrogate the characteristic pattern of piRNA biogenesis, including ping-pong amplification and head-to-tail phasing.

摘要

Piwi 相互作用 RNA (piRNA) 是 25-32 个核苷酸长的小 RNA,可在动物生殖腺中沉默转座元件 (转座子)。piRNA 具有很大的序列多样性(每个生物体超过一百万种不同的序列),可以靶向各种转座子序列。这是通过灵活和独特的生物发生途径来实现的,这些途径在进化上是保守的。在本章中,我描述了一种从新鲜解剖组织样本(如果蝇卵巢)中纯化和克隆 piRNA 的详细方法,以便进行高通量测序。我还描述了如何计算处理测序数据,并探究 piRNA 生物发生的特征模式,包括乒乓扩增和头尾相位。

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