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Plant Mobile Domain protein-DNA motif modules counteract Polycomb silencing to stabilize gene expression

ABSTRACT: Plant Mobile Domain protein-DNA motif modules counteract Polycomb silencing to stabilize gene expression

PROVIDER: PRJNA1167782 | ENA |

REPOSITORIES: ENA

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Plant Mobile Domain protein-DNA motif modules counteract Polycomb silencing to stabilize gene expression

Project description:In plants and animals, Polycomb group (PcG) proteins are crucial for development, regulating gene expression through H3K27me3 deposition and subsequent gene silencing. While Polycomb silencing target specification is increasingly understood, it remains unclear how certain genes with apparent silencing-attracting features escape this process. Here, we show that the plant mobile domain C (PMD-C) containing proteins MAINTENANCE OF MERISTEMS (MAIN), MAIN-LIKE 1 (MAIL1) and MAIL2 oppose Polycomb silencing at numerous actively transcribed genes in Arabidopsis. Mutations in MAIN, MAIL1 or MAIL2 result in PcG-dependent ectopic H3K27me3 deposition, often associated with transcriptional repression. We show that MAIL1, which functions in concert with MAIN, and MAIL2 target distinct gene sets and associate with chromatin at specific DNA sequence motifs. We demonstrate that the integrity of these motif sequences is essential for promoting expression and antagonizing H3K27me3 deposition. Our results unveil a novel system opposing Polycomb silencing involving PMD-C protein-DNA motif modules, expanding our understanding of eukaryotic gene regulation mechanisms.

2025-09-02 | GSE278560 | GEO

Boundary Formation is an Inherent Property of Mobile Small RNA Gradients

Project description:Small RNAs recently emerged as a new class of mobile instructive signals in development. Here, we investigate their mechanism of action and show that the gradients formed by mobile small RNAs generate sharply defined domains of target gene expression. By modulating the source of artificial miRNAs we show that boundary formation is an inherent property of the small RNA gradient itself. The threshold-based readout of such gradients is highly sensitive to small RNA levels at the source, allowing plasticity in the positioning of a target gene expression boundary. In addition to generating sharp expression domains of their immediate targets, the readouts of opposing small RNA gradients enable formation of stable and uniformly positioned developmental boundaries. These novel patterning properties of small RNAs are reminiscent of those of morphogens in animal systems. However, their exceptionally high specificity, direct mode of action, and the fully intrinsic nature of their gradients, distinguish mobile small RNAs from classical morphogens. Our findings present mobile small RNAs and their targets as highly portable and evolutionarily-tractable regulatory modules through which to create pattern in development and beyond.

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Knockdown specificity of Mobile-CRISPRi system targeting chromosomal mRFP

Project description:The Mobile CRISPRi system with and without mRFP-targeting sgRNA was engineered into Pseudomonas aeruginosa PA14 strain with chromosomally encoded mRFP. RNA was isolated from these strains, and the corresponding cDNA library was synthesized and sequenced in 150 bp paired-end reads. Approximately 1,000,000 reads were collected for each of the two samples, with ~94% alignment to PA14 WT by Bowtie254, and transcripts were counted with HTSeq55. Only genes with a non-normalized read count greater than 1 in both samples were included in analysis, with a coverage of 1286 genes (~20% genome). This data shows that the Mobile CRISPRi system is selective for sgRNA-guided knockdown of mRFP.

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