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Depletion of the RNA-binding protein PURA triggers changes in posttranscriptional gene regulation and loss of P-bodies

ABSTRACT: The RNA-binding protein PURA has been implicated in the rare, monogenetic, neurodevelopmental disorder PURA Syndrome. PURA binds both DNA and RNA and has been associated with various cellular functions. Only little is known about its main cellular functions and the molecular pathways affected upon PURA depletion. Here, we show that PURA is predominantly located in the cytoplasm, where it binds to thousands of mRNAs. Many of these transcripts change abundance in response to PURA depletion. The encoded proteins suggest a role for PURA in immune responses, mitochondrial function, autophagy and processing (P)-body activity. Intriguingly, reduced PURA levels decrease the expression of the integral P-body components LSM14A and DDX6, and strongly affect P-body formation in human cells. Furthermore, PURA knockdown results in stabilization of P-body-enriched transcripts, whereas other mRNAs decrease. Hence, reduced PURA levels, as reported in patients with PURA Syndrome, influence the formation and composition of this phase-separated RNA processing machinery. Our study on PURA provides a blueprint for the comprehensive understanding of the tight connection between P-body-associated RNA regulation and neurodevelopmental disorders.

INSTRUMENT(S): Q Exactive HF

ORGANISM(S): Homo Sapiens (human)

SUBMITTER: Juliane Merl-Pham

LAB HEAD: Dierk Niessing

PROVIDER: PXD030266 | Pride | 2022-12-19

REPOSITORIES: Pride

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			Action	DRS
	MOL13920X002__PURA_KD_1_92-249271.raw	Raw
	MOL13920X003__PURA_KD_2_92-249272.raw	Raw
	MOL13920X005__PURA_KD_4_92-249274.raw	Raw
	MOL13920X006__PURA_KD_5_92-249275.raw	Raw
	MOL13920X008__WT_1_92-249277.raw	Raw

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