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Systematic Perturbation of Thousands of Retroviral LTRs in Mouse Embryos [ChIP-Seq]

ABSTRACT: Systematic Perturbation of Thousands of Retroviral LTRs in Mouse Embryos [ChIP-Seq]

PROVIDER: PRJNA1011394 | ENA |

REPOSITORIES: ENA

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			Action	DRS
	SRR25865022_1.fastq.gz	Fastqsanger.gz
	SRR25865022_2.fastq.gz	Fastqsanger.gz
	SRR25865023_1.fastq.gz	Fastqsanger.gz
	SRR25865023_2.fastq.gz	Fastqsanger.gz
	SRR25865024_1.fastq.gz	Fastqsanger.gz

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Systematic Perturbation of Thousands of Retroviral LTRs in Mouse Embryos

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Systematic Perturbation of Thousands of Retroviral LTRs in Mouse Embryos [ChIP-Seq]

Project description:In mammals, many retrotransposons are de-repressed during zygotic genome activation (ZGA). However, their functions in early development remain elusive largely due to the challenge to simultaneously manipulate thousands of retrotransposon insertions in embryos. Here, we employed epigenome editing to perturb long terminal repeat (LTR) MT2_Mm, a well-known ZGA and totipotency marker that exists in ~2667 insertions throughout the mouse genome. CRISPR interference (CRISPRi) robustly targeted and repressed 2485 (~93%) MT2_Mm insertions and 1090 (~55%) insertions of the closely related MT2C_Mm in 2-cell embryos. Remarkably, such perturbation caused down-regulation of hundreds of ZGA genes at 2C stage and embryonic arrest mostly at morula stage. Mechanistically, MT2_Mm/MT2C_Mm primarily served as alternative ZGA promoters activated by Obox proteins. Thus, through large-scale epigenome editing, we addressed to what extent MT2_Mm/MT2C_Mm regulates ZGA and preimplantation development. Our approach could be adapted to systematically perturb retrotransposons in other mammalian embryos as it doesn’t require transgenic animals.

2023-10-19 | GSE242122 | GEO

Systematic Perturbation of Thousands of Retroviral LTRs in Mouse Embryos [RNA-Seq]

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Systematic perturbation of retroviral LTRs reveals widespread long-range effects on human gene regulation [histone marks]

Project description:Systematic perturbation of retroviral LTRs reveals widespread long-range effects on human gene regulation [histone marks]

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Systematic perturbation of retroviral LTRs reveals widespread long-range effects on human gene regulation [ChIP-seq]

Project description:Systematic perturbation of retroviral LTRs reveals widespread long-range effects on human gene regulation [ChIP-seq]

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Systematic perturbation of retroviral LTRs reveals widespread long-range effects on human gene regulation [RNA-seq]

Project description:Systematic perturbation of retroviral LTRs reveals widespread long-range effects on human gene regulation [RNA-seq]

| PRJNA436643 | ENA

Systematic Perturbation of Thousands of Retroviral LTRs in Mouse Embryos.

Project description:In mammals, many retrotransposons are de-repressed during zygotic genome activation (ZGA). However, their functions in early development remain elusive largely due to the challenge to simultaneously manipulate thousands of retrotransposon insertions in embryos. Here, we employed epigenome editing to perturb the long terminal repeat (LTR) MT2_Mm, a well-known ZGA and totipotency marker that exists in ~2667 insertions throughout the mouse genome. CRISPRi robustly repressed 2485 (~93%) MT2_Mm insertions and 1090 (~55%) insertions of the closely related MT2C_Mm in 2-cell embryos. Remarkably, such perturbation caused down-regulation of hundreds of ZGA genes at the 2-cell stage and embryonic arrest mostly at the morula stage. Mechanistically, MT2_Mm/MT2C_Mm primarily served as alternative ZGA promoters activated by OBOX proteins. Thus, through unprecedented large-scale epigenome editing, we addressed to what extent MT2_Mm/MT2C_Mm regulates ZGA and preimplantation development. Our approach could be adapted to systematically perturb retrotransposons in other mammalian embryos as it doesn't require transgenic animals.

| S-EPMC10541133 | biostudies-literature

Systematic perturbation of retroviral LTRs reveals widespread long-range effects on human gene regulation [RNA-seq]

Project description:Recent work suggests extensive adaptation of transposable elements (TEs) for host gene regulation. However, high numbers of integrations typical of TEs, coupled with sequence divergence within families, have made systematic interrogation of the regulatory contributions of TEs challenging. Here, we employ CARGO, our recent method for CRISPR gRNA multiplexing, to facilitate targeting of LTR5HS, a higher primate-specific class of HERVK (HML-2) LTRs that is active during early development and present in ~700 copies throughout the human genome. We combine CARGO with CRISPR activation or interference to, respectively, induce or silence LTR5HS en masse, and demonstrate that this system robustly targets the vast majority of LTR5HS insertions. Remarkably, activation/silencing of LTR5HS is associated with reciprocal up- and down-regulation of hundreds of human genes. These effects require presence of retroviral sequences, but occur over long genomic distances, consistent with a pervasive function of LTR5HS elements as early embryonic enhancers in higher primates.

2018-08-16 | GSE111332 | GEO

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