Dataset Information

Fission yeast Caprin protein is required for efficient heterochromatin establishment.

ABSTRACT: Heterochromatin is a key feature of eukaryotic genomes that serves important regulatory and structural roles in regions such as centromeres. In fission yeast, maintenance of existing heterochromatic domains relies on positive feedback loops involving histone methylation and non-coding RNAs. However, requirements for de novo establishment of heterochromatin are less well understood. Here, through a cross-based assay we have identified a novel factor influencing the efficiency of heterochromatin establishment. We determine that the previously uncharacterised protein is an ortholog of human Caprin1, an RNA-binding protein linked to stress granule formation. We confirm that the fission yeast ortholog, here named Cpn1, also associates with stress granules, and we uncover evidence of interplay between heterochromatin integrity and ribonucleoprotein (RNP) granule formation, with heterochromatin mutants showing reduced granule formation in the presence of stress, but increased granule formation in the absence of stress. We link this to regulation of non-coding heterochromatic transcripts, since in heterochromatin-deficient cells, absence of Cpn1 leads to hyperaccumulation of centromeric RNAs at centromeres. Together our findings unveil a novel link between RNP homeostasis and heterochromatin assembly, and implicate Cpn1 and associated factors in facilitating heterochromatin establishment by promoting removal of excess transcripts that would otherwise impair assembly processes.

INSTRUMENT(S): Orbitrap Exploris 480

ORGANISM(S): Schizosaccharomyces Pombe 927

TISSUE(S): Cell Culture

SUBMITTER: Elizabeth Bayne

LAB HEAD: Elizabeth Bayne

PROVIDER: PXD050937 | Pride | 2025-02-14

REPOSITORIES: pride

ACCESS DATA

Dataset's files

Source:

			Action	DRS
	Zhang_etal_2024_Cpn1FLAG_Rep1.7z	Other
	Zhang_etal_2024_Cpn1FLAG_Rep1.raw	Raw
	Zhang_etal_2024_Cpn1FLAG_Rep2.7z	Other
	Zhang_etal_2024_Cpn1FLAG_Rep2.raw	Raw
	Zhang_etal_2024_NoTag_Rep1.7z	Other

Items per page:

1 - 5 of 9

Similar Datasets

Project description:The centromere is defined by the presence of a centromere-specific histone H3 variant, CENH3. Establishment and maintenance of the centromeric chromatin (CEN chromatin) is determined by poorly understood epigenetic mechanisms. Interestingly, CEN chromatin in several eukaryotes showed euchromatic characteristics although being embedded within pericentromeric heterochromatin. Specifically, H3K4me2 appeared to be a unique histone modification mark associated with animal centromeres. We developed a genomic tiling array for four fully sequenced rice centromeres. A ChIP-chip approach was used to study the patterns of several euchromatic histone modification marks, including H3K4me2, H3K4me3, H3K36me3, and H3K4K9a, associated with rice centromeres. We demonstrate that the CENH3 subdomains within the four centromeres are depleted with the four histone H3 marks. The vast majority of the four histone marks were associated with the genes located in the H3 subdomains within the centromeric cores. Genes in the centromeres showed similar histone modification patterns as those located outside of the centromeres. Thus, the euchromatic characteristics of rice CEN chromatin are trademarks of the transcribed sequences embedded in the H3 subdomains of the centromeres. We propose that the constitutively expressed genes located in rice centromeres may provide a barrier for loading of CENH3 into the H3 subdomains. The separation of CENH3 into the H3 subdomains is favorable for the three dimensional structure and its associated function of rice centromeres. We developed a genomic tiling array that covers four rice centromeres (Cen4, Cen5, Cen7, and Cen8) using the NimbleGen 3x720K array based on the NimbleGen HD2 platform. We used four antibodies (H3K4me3, H3K4me2, H3K36me3, H3K4K9ac) to perform ChIP-chip experiments. ChIP was conducted using leaf tissue from two-week old rice seedlings. We have 3 biological replicates for each antibody and 6 technological replicates of hybridization with position exchange on the array. Thus, each histone modification included 18 hybridization experiments.

Dataset Information

Fission yeast Caprin protein is required for efficient heterochromatin establishment.

Dataset's files

Similar Datasets

OmicsDI is part of the ELIXIR infrastructure

Tweets