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一种新颖且普遍存在的 miRNA 参与的调控模块确保了 RNA 聚合酶 II 的精确磷酸化和适当的转录。

A novel and ubiquitous miRNA-involved regulatory module ensures precise phosphorylation of RNA polymerase II and proper transcription.

机构信息

China Agricultural University, Beijing, China.

Sanya Institute of China Agricultural University, Sanya, China.

出版信息

PLoS Pathog. 2024 Apr 19;20(4):e1012138. doi: 10.1371/journal.ppat.1012138. eCollection 2024 Apr.

DOI:10.1371/journal.ppat.1012138
PMID:38640110
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11062530/
Abstract

Proper transcription orchestrated by RNA polymerase II (RNPII) is crucial for cellular development, which is rely on the phosphorylation state of RNPII's carboxyl-terminal domain (CTD). Sporangia, developed from mycelia, are essential for the destructive oomycetes Phytophthora, remarkable transcriptional changes are observed during the morphological transition. However, how these changes are rapidly triggered and their relationship with the versatile RNPII-CTD phosphorylation remain enigmatic. Herein, we found that Phytophthora capsici undergone an elevation of Ser5-phosphorylation in its uncanonical heptapeptide repeats of RNPII-CTD during sporangia development, which subsequently changed the chromosomal occupation of RNPII and primarily activated transcription of certain genes. A cyclin-dependent kinase, PcCDK7, was highly induced and phosphorylated RNPII-CTD during this morphological transition. Mechanistically, a novel DCL1-dependent microRNA, pcamiR1, was found to be a feedback modulator for the precise phosphorylation of RNPII-CTD by complexing with PcAGO1 and regulating the accumulation of PcCDK7. Moreover, this study revealed that the pcamiR1-CDK7-RNPII regulatory module is evolutionarily conserved and the impairment of the balance between pcamiR1 and PcCDK7 could efficiently reduce growth and virulence of P. capsici. Collectively, this study uncovers a novel and evolutionary conserved mechanism of transcription regulation which could facilitate correct development and identifies pcamiR1 as a promising target for disease control.

摘要

RNA 聚合酶 II(RNPII)介导的转录是细胞发育所必需的,这依赖于 RNPII 的羧基末端结构域(CTD)的磷酸化状态。孢子囊是从菌丝体发育而来的,是破坏性卵菌植物病原菌的重要组成部分,在形态转变过程中观察到显著的转录变化。然而,这些变化是如何迅速触发的,以及它们与多功能 RNPII-CTD 磷酸化的关系仍然是个谜。在这里,我们发现辣椒疫霉在孢子囊发育过程中,其 RNPII-CTD 的非典型七肽重复序列中的 Ser5 磷酸化水平升高,随后改变了 RNPII 的染色体占据,并主要激活了某些基因的转录。一种细胞周期蛋白依赖性激酶 PcCDK7 在这个形态转变过程中高度诱导并磷酸化 RNPII-CTD。在机制上,我们发现了一种新型的 DCL1 依赖性 microRNA pcamiR1,它作为一个反馈调节剂,通过与 PcAGO1 结合来精确调控 RNPII-CTD 的磷酸化,并调节 PcCDK7 的积累。此外,这项研究还揭示了 pcamiR1-CDK7-RNPII 调控模块在进化上是保守的,并且 pcamiR1 和 PcCDK7 之间平衡的破坏可以有效地降低辣椒疫霉的生长和毒力。总之,这项研究揭示了一种新的、进化上保守的转录调控机制,这有助于正确的发育,并确定 pcamiR1 是一种有前途的疾病控制靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bff2/11062530/ee28c86e53ed/ppat.1012138.g010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bff2/11062530/f2d00eb0af32/ppat.1012138.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bff2/11062530/c64ea2ac4d32/ppat.1012138.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bff2/11062530/9bb904d6d4b9/ppat.1012138.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bff2/11062530/e78d640f61f2/ppat.1012138.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bff2/11062530/b00b36a7c210/ppat.1012138.g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bff2/11062530/a90b85afd0f7/ppat.1012138.g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bff2/11062530/d62c630cc07c/ppat.1012138.g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bff2/11062530/44bad6abcc90/ppat.1012138.g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bff2/11062530/0852997de4d0/ppat.1012138.g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bff2/11062530/ee28c86e53ed/ppat.1012138.g010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bff2/11062530/f2d00eb0af32/ppat.1012138.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bff2/11062530/c64ea2ac4d32/ppat.1012138.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bff2/11062530/9bb904d6d4b9/ppat.1012138.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bff2/11062530/e78d640f61f2/ppat.1012138.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bff2/11062530/b00b36a7c210/ppat.1012138.g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bff2/11062530/a90b85afd0f7/ppat.1012138.g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bff2/11062530/d62c630cc07c/ppat.1012138.g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bff2/11062530/44bad6abcc90/ppat.1012138.g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bff2/11062530/0852997de4d0/ppat.1012138.g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bff2/11062530/ee28c86e53ed/ppat.1012138.g010.jpg

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