Ontology highlight
ABSTRACT:
PROVIDER: PRJNA837973 | ENA |
REPOSITORIES: ENA
Dataset's files
| Action | DRS | |||
|---|---|---|---|---|
| SRR19237562_1.fastq.gz | Fastqsanger.gz | |||
| SRR19237562_2.fastq.gz | Fastqsanger.gz | |||
| SRR19237563_1.fastq.gz | Fastqsanger.gz | |||
| SRR19237563_2.fastq.gz | Fastqsanger.gz | |||
| SRR19237564_1.fastq.gz | Fastqsanger.gz |
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Project description:Formalin induces inter- and intra-molecular crosslinks within exposed cells. This cross-linking can be exploited to characterise chromatin state as in the FAIRE (Formaldehyde-Assisted Isolation of Regulatory Elements) and MNase (micrococcal nuclease) assays. Our team aims to optimise these assays for application in museum preserved formalin-exposed specimens. To do so, we first sought to understand the effect of prolonged formalin fixation on the read alignment signatures resulting from FAIRE and MNase treatment. Here we cultured yeast (Saccharomyces cerevisiae) under normal and heat-shock conditions then fixed the cells with formalin for 15 minutes, 1 hour, 6 hours, and 24 hours. We found that heavy formalin fixation modulates rather than eliminates signatures of differential chromatin accessibility and enables semi-quantitative estimates of relative gene expression in this yeast model.
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