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R-loop dependent promoter-proximal termination ensures genome stability [ChIP-seq]

ABSTRACT: Precise regulation of transcription is essential to maintain genome integrity, yet key mechanisms coordinating transcription, genome stability and downstream cellular functions remain incomplete. Here we report the identification of SOSS-INTAC, a stable association of the genome stability regulator Sensor of Single-stranded DNA (ssDNA) (SOSS) complex and transcription regulator Integrator-PP2A (INTAC). Via SSB1-mediated ssDNA recognition at its targets, SOSS-INTAC stimulates early termination of transcription and thus attenuates paused Pol II-induced formation of R-loops to prevent its aberrant accumulation that has the risk of increasing chromatin accessibility and compromising genome stability. SOSS-INTAC-mediated attenuation of R-loops is greatly enhanced by SSB1's unique property of forming liquid-like condensates. In contrast, preventing SSB1 condensation through deletion or cancer-associated mutation within its intrinsically disordered region (IDR) leads to pervasive accumulation of R-loops at a genome-wide level. Thus, our study highlights the genomic surveillance function of SOSS-INTAC that enables timely transcriptional termination to constrain aberrant R-loop accumulation and ensure genomic stability.

ORGANISM(S): Homo sapiens

PROVIDER: GSE223994 | GEO | 2023/06/20

REPOSITORIES: GEO

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R-loop dependent promoter-proximal termination ensures genome stability [CUT&Tag]

Project description:Precise regulation of transcription is essential to maintain genome integrity, yet key mechanisms coordinating transcription, genome stability and downstream cellular functions remain incomplete. Here we report the identification of SOSS-INTAC, a stable association of the genome stability regulator Sensor of Single-stranded DNA (ssDNA) (SOSS) complex and transcription regulator Integrator-PP2A (INTAC). Via SSB1-mediated ssDNA recognition at its targets, SOSS-INTAC stimulates early termination of transcription and thus attenuates paused Pol II-induced formation of R-loops to prevent its aberrant accumulation that has the risk of increasing chromatin accessibility and compromising genome stability. SOSS-INTAC-mediated attenuation of R-loops is greatly enhanced by SSB1's unique property of forming liquid-like condensates. In contrast, preventing SSB1 condensation through deletion or cancer-associated mutation within its intrinsically disordered region (IDR) leads to pervasive accumulation of R-loops at a genome-wide level. Thus, our study highlights the genomic surveillance function of SOSS-INTAC that enables timely transcriptional termination to constrain aberrant R-loop accumulation and ensure genomic stability.

2023-06-20 | GSE223993 | GEO

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Ssb1 and Ssb2 have essential and overlapping functions in adult stem cell homeostasis - granulocyte-macrophage progenitor data.

Project description:The single-stranded DNA binding proteins SSB1 and SSB2 are crucial regulators of the DNA damage response, however the overlapping functions of these related proteins is incompletely understood. We generated mice where both Ssb1 and Ssb2 were constitutively or conditionally deleted. Constitutive Ssb1/Ssb2 double knockout (DKO) caused early embryonic lethality, while conditional Ssb1/Ssb2 double knockout (cDKO) in adult mice resulted in acute lethality due to bone marrow failure and intestinal atrophy featured by stem and progenitor cell depletion. cDKO cells exhibited increased replication stress, R-loop accumulation, genome wide double strand breaks and cytosolic single-stranded DNA. Transcriptional profiling of cDKO cells revealed activation of p53 DNA damage and interferon responses. Hematopoietic stem and progenitor cells in cDKO mice showed enforced cell cycling, with subsequent apoptotic cell death. Collectively, these results demonstrate that Ssb1 and Ssb2 have compensatory functions in maintaining genomic stability and are collectively necessary for adult stem cell homeostasis. Single colour, Illumina MouseRef-8 v2.0 Beadarrays.

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Ssb1/2-IntS complexes maintain splicing integrity and genomic stability through regulating RNA Polymerase II mediated snRNA levels

Project description:Ssb1(NABP2/OBFC2A) and Ssb2 (NABP1/OBFC2B) are two closely related proteins that show functional redundancies supported by their existence in two separate subcomplexes with identical proteins. Ssb1 knockout causes perinatal lethality in mice, Ssb2 knockout does not associate with any observable phenotypes, however, double knockout of both Ssb1/2 causes embryonically lethality. Notably, conditional loss of both in adult mice leads to acute lethality due to bone marrow and gut failure. Here, we further demonstrate that the overlapping essential function of both Ssb1/2 is through their prime binding partner IntS3, a member of the multiprotein complex called the Integrator. The Integrator complex interacts with the largest subunit of RNA Polymerase II and is required for processing and termination of small nuclear RNAs (snRNAs). Here, we provide a firsthand evidence that the stability of the Integrator complex is compromised in mouse-embryonic fibroblasts (MEFs) with compound loss of both Ssbs. We further demonstrate that these MEFs show overexpression of unprocessed snRNAs which forces the cells to express alternative spliced variants of genes that are required for transcription and cell cycle regulation. This phenotype closely phenocopies loss of core integrator subunit, IntS11 as well as splicing components B and C. Interestingly, the phenotype gets partially restored by overexpression of wildtype Ssb1 but not by the Ssb-mutant defective in binding integrator subunit, IntS3, demonstrating the essential roles of Ssb1/2 in the maintenance of the Integrator complex and thereby, genomic stability.

2022-03-11 | GSE155240 | GEO

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Project description:R-loops impact transcription and genome stability and are related to human diseases. Genome-wide R-loop mapping typically uses the S9.6 antibody or inactive RNase H, both requiring a large number of cells with varying results observed depending on the approach applied. Here, we present strand-specific KAS-seq (spKAS-seq) to map R-loops by taking advantage of the presence of a single-stranded DNA (ssDNA) in the triplex structure. We show that spKAS-seq detects R-loops and their dynamics at coding sequences, enhancers, and other intergenic regions with as few as 50,000 cells and eliminates potential bias towards open chromatin and RNase H-sensitive regions. A joint analysis of R-loops and chromatin-bound RNA-binding proteins (RBPs) suggested that R-loops can be RBP-binding hotspots on the chromatin.

2022-06-06 | GSE192822 | GEO

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