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Identification of proteins and miRNAs that specifically bind an mRNA in vivo [total RNA]

ABSTRACT: Identification of proteins and miRNAs that specifically bind an mRNA in vivo [total RNA]

PROVIDER: PRJNA541233 | ENA |

REPOSITORIES: ENA

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			Action	DRS
	SRR9016770.fastq.gz	Fastqsanger.gz
	SRR9016771.fastq.gz	Fastqsanger.gz
	SRR9016772.fastq.gz	Fastqsanger.gz
	SRR9016773.fastq.gz	Fastqsanger.gz
	SRR9016774.fastq.gz	Fastqsanger.gz

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Identification of proteins and miRNAs that specifically bind an mRNA in vivo

Project description:Identification of proteins and miRNAs that specifically bind an mRNA in vivo

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Identification of proteins and miRNAs that specifically bind an mRNA in vivo [small RNA]

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Identification of proteins and miRNAs that specifically bind an mRNA in vivo [total RNA]

Project description:Understanding regulation of an mRNA requires knowledge of its regulators. However, methods for reliable de-novo identification of proteins binding to a particular RNA are scarce and were so far only successfully applied to abundant noncoding RNAs in cell culture. Here, we present vIPR, an RNA-protein crosslink, RNA pulldown, and shotgun proteomics approach to identify proteins bound to a selected mRNA in C. elegans. Applying vIPR to the germline-specific transcript gld-1 led to enrichment of known and novel interactors. By comparing enrichment upon gld-1 and lin-41 pulldown, we demonstrate that vIPR recovers both common and specific RNA-binding proteins, and we validate DAZ-1 as a novel and specific gld-1 regulator. Finally, combining vIPR with small RNA sequencing, we recover known and biologically important transcript-specific miRNA interactions, and we identify miR-84 as a specific interactor of the gld-1 transcript. We envision that vIPR provides a platform for investigating RNA in vivo regulation in diverse biological systems.

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Identification of proteins and miRNAs that specifically bind an mRNA in vivo.

Project description:Understanding regulation of an mRNA requires knowledge of its regulators. However, methods for reliable de-novo identification of proteins binding to a particular RNA are scarce and were thus far only successfully applied to abundant noncoding RNAs in cell culture. Here, we present vIPR, an RNA-protein crosslink, RNA pulldown, and shotgun proteomics approach to identify proteins bound to selected mRNAs in C. elegans. Applying vIPR to the germline-specific transcript gld-1 led to enrichment of known and novel interactors. By comparing enrichment upon gld-1 and lin-41 pulldown, we demonstrate that vIPR recovers both common and specific RNA-binding proteins, and we validate DAZ-1 as a specific gld-1 regulator. Finally, combining vIPR with small RNA sequencing, we recover known and biologically important transcript-specific miRNA interactions, and we identify miR-84 as a specific interactor of the gld-1 transcript. We envision that vIPR will provide a platform for investigating RNA in vivo regulation in diverse biological systems.

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Identification of proteins and miRNAs that specifically bind an mRNA in vivo [small RNA]

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miRNAs specifically bound by PrPc during C2C12 cell differentiation

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identify the possible proteins that specifically bind to the 59-bp nucleotide sequence containing rs2280381

Project description:we performed DNA-affinity precipitation assay (DAPA) followed by mass spectrometry to identify the possible proteins that specifically bind to the 59-bp nucleotide sequence containing rs2280381 using U-937 cell nuclear extracts.

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Identification of proteins and miRNAs that specifically bind an mRNA in vivo

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