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在 a 中,核糖体 RNA 前体在初级 P 位点切割后,热应激处理会损害成熟 rRNA 的形成。

Upon heat stress processing of ribosomal RNA precursors into mature rRNAs is compromised after cleavage at primary P site in a.

机构信息

CNRS, Laboratoire Génome et D#x0E9;veloppement des Plantes (LGDP), UMR 5096, 66860 Perpignan, France.

Univ. Perpignan Via Domitia, LGDP, UMR 5096, Perpignan, France.

出版信息

RNA Biol. 2022;19(1):719-734. doi: 10.1080/15476286.2022.2071517. Epub 2021 Dec 31.

DOI:10.1080/15476286.2022.2071517
PMID:35522061
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9090299/
Abstract

Transcription and processing of 45S rRNAs in the nucleolus are keystones of ribosome biogenesis. While these processes are severely impacted by stress conditions in multiple species, primarily upon heat exposure, we lack information about the molecular mechanisms allowing sessile organisms without a temperature-control system, like plants, to cope with such circumstances. We show that heat stress disturbs nucleolar structure, inhibits pre-rRNA processing and provokes imbalanced ribosome profiles in plants. Notably, the accuracy of transcription initiation and cleavage at the primary P site in the 5'ETS (5' External Transcribed Spacer) are not affected but the levels of primary 45S and 35S transcripts are, respectively, increased and reduced. In contrast, precursors of 18S, 5.8S and 25S RNAs are rapidly undetectable upon heat stress. Remarkably, nucleolar structure, pre-rRNAs from major ITS1 processing pathway and ribosome profiles are restored after returning to optimal conditions, shedding light on the extreme plasticity of nucleolar functions in plant cells. Further genetic and molecular analysis to identify molecular clues implicated in these nucleolar responses indicate that cleavage rate at P site and nucleolin protein expression can act as a checkpoint control towards a productive pre-rRNA processing pathway.

摘要

45S rRNAs 的转录和加工是核糖体生物发生的关键。虽然这些过程在多种物种中受到压力条件的严重影响,主要是在暴露于热时,但我们缺乏有关允许没有温度控制系统的固着生物(如植物)应对这种情况的分子机制的信息。我们表明,热应激会破坏核仁结构,抑制 pre-rRNA 加工,并在植物中引发不平衡的核糖体谱。值得注意的是,转录起始的准确性和在 5'ETS(5' 外部转录间隔区)中的主要 P 位的切割不受影响,但初级 45S 和 35S 转录本的水平分别增加和减少。相比之下,18S、5.8S 和 25S RNA 的前体在热应激时迅速无法检测到。值得注意的是,核仁结构、主要 ITS1 加工途径的 pre-rRNAs 和核糖体谱在返回最佳条件后得到恢复,这揭示了植物细胞中核仁功能的极端可塑性。进一步的遗传和分子分析以鉴定涉及这些核仁反应的分子线索表明,P 位的切割率和核仁蛋白表达可以作为一种检查点控制,以实现有效的 pre-rRNA 加工途径。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/da49/9090299/1f4af96ae48d/KRNB_A_2071517_F0007_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/da49/9090299/a0671f9124e9/KRNB_A_2071517_F0001_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/da49/9090299/377013c6f6b2/KRNB_A_2071517_F0002_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/da49/9090299/b85ee92ddd79/KRNB_A_2071517_F0003_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/da49/9090299/98ea3ec3aa2b/KRNB_A_2071517_F0004_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/da49/9090299/e078f579a5c6/KRNB_A_2071517_F0005_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/da49/9090299/52f35b7fb74a/KRNB_A_2071517_F0006_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/da49/9090299/1f4af96ae48d/KRNB_A_2071517_F0007_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/da49/9090299/a0671f9124e9/KRNB_A_2071517_F0001_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/da49/9090299/377013c6f6b2/KRNB_A_2071517_F0002_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/da49/9090299/b85ee92ddd79/KRNB_A_2071517_F0003_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/da49/9090299/98ea3ec3aa2b/KRNB_A_2071517_F0004_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/da49/9090299/e078f579a5c6/KRNB_A_2071517_F0005_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/da49/9090299/52f35b7fb74a/KRNB_A_2071517_F0006_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/da49/9090299/1f4af96ae48d/KRNB_A_2071517_F0007_OC.jpg

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