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We began analyzing https://link.springer.com/article/10.1007/s44192-023-00034-5, but it redirected us to https://link.springer.com/article/10.1007/s44192-023-00034-5. The analysis below is for the second page.

Title[redir]:
Computational analysis of crosstalk between transcriptional regulators and RNA-binding proteins suggests mutual regulation of polycomb proteins and SRSF1 influencing adult hippocampal neurogenesis | Discover Mental Health
Description:
Background Adult hippocampal neurogenesis (AHN) is a clinically significant neural phenomenon. Understanding its molecular regulation would be important. In this regard, most studies have focused on transcriptional regulators (TRs), epigenetic modifiers, or non-coding RNAs. RNA-binding proteins (RBPs) have emerged as dominant molecular regulators. It would be significant to understand the potential cross-talk between RBPs and TRs, which could influence AHN. Methods The present study employed computational analyses to identify RBPs and TRs regulating AHN, followed by the analysis of their interaction networks and detection of hub proteins. Next, the potential mutual regulation of hub TRs and RBPs was analyzed. Additionally, hippocampal genes differentially expressed upon exercise were analyzed for potential regulation by the identified TRs and RBPs. Results 105 TRs and 26 RBPs were found to influence AHN, which could also form interactive networks. Polycomb complex proteins were among the TR network hubs, while HNRNP and SRSF family members were among the hub RBPs. Further, the polycomb complex proteins and SRSF1 could have a mutual regulatory relationship, suggesting a cross-talk between epigenetic/transcriptional and post-transcriptional regulatory pathways. A number of exercise-induced hippocampal genes were also found to be potential targets of the identified TRs and RBPs. Conclusion SRSF1 may influence post-transcriptional stability, localization, and alternative splicing patterns of polycomb complex transcripts, and the polycomb proteins may in turn epigenetically influence the SRSF1. Further experimental validation of these regulatory loops/networks could provide novel insights into the molecular regulation of AHN, and unravel new targets for disease-treatment.

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Keywords {🔍}

ahn, rbps, genes, trs, srsf, proteins, article, google, scholar, identified, regulation, hub, pubmed, polycomb, neurogenesis, potential, regulatory, adult, gene, regulators, expression, hippocampal, influence, ahnrelated, rnabinding, analysis, found, transcriptional, molecular, potentially, influencing, study, complex, database, involved, neural, protein, factors, present, networks, exerciseinduced, exercise, cell, ezh, central, mango, binding, sites, posttranscriptional, analyzed,

Topics {✒️}

serine/arginine-rich splicing factor exercise-induced differentially-expressed genes rna-binding protein research rna-binding protein signaling rna-binding proteins influencing article google scholar experimentally-validated protein interactors exercise-induced hippocampal genes exercise-induced gene expression cis-regulatory elements significantly higher inter-connections transcription-factor-dependent control maximum neighbourhood component/dmnc maximum neighbourhood component/mnc protein–protein interaction studies exercise-mediated gene expression maximal clique centrality/mcc tri-methylate histone h3 cell-types including neurons post-transcriptional regulatory pathways brain-derived neurotrophic factor article download pdf fragile x-related proteins polycomb complex-encoding transcripts influence post-transcriptional stability rna-binding protein regulating ahn-related genes motor deficits nature rev gene ahn-related genes curated de/ ~ galanisl/mippie/index influence exercise-induced ahn adult hippocampal neurogenesis talent search search bmc syst biol full access protein–protein interactions differentially expressed genes genes differentially expressed influence axon growth forming regulatory loops hippocampal gene expression srsf family members family members formed impaired adult neurogenesis exercise-influenced ahn genes adult mammalian brain rna-binding proteins rna-binding specificities overrepresented binding sites

Schema {🗺️}

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      headline:Computational analysis of crosstalk between transcriptional regulators and RNA-binding proteins suggests mutual regulation of polycomb proteins and SRSF1 influencing adult hippocampal neurogenesis
      description:Adult hippocampal neurogenesis (AHN) is a clinically significant neural phenomenon. Understanding its molecular regulation would be important. In this regard, most studies have focused on transcriptional regulators (TRs), epigenetic modifiers, or non-coding RNAs. RNA-binding proteins (RBPs) have emerged as dominant molecular regulators. It would be significant to understand the potential cross-talk between RBPs and TRs, which could influence AHN. The present study employed computational analyses to identify RBPs and TRs regulating AHN, followed by the analysis of their interaction networks and detection of hub proteins. Next, the potential mutual regulation of hub TRs and RBPs was analyzed. Additionally, hippocampal genes differentially expressed upon exercise were analyzed for potential regulation by the identified TRs and RBPs. 105 TRs and 26 RBPs were found to influence AHN, which could also form interactive networks. Polycomb complex proteins were among the TR network hubs, while HNRNP and SRSF family members were among the hub RBPs. Further, the polycomb complex proteins and SRSF1 could have a mutual regulatory relationship, suggesting a cross-talk between epigenetic/transcriptional and post-transcriptional regulatory pathways. A number of exercise-induced hippocampal genes were also found to be potential targets of the identified TRs and RBPs. SRSF1 may influence post-transcriptional stability, localization, and alternative splicing patterns of polycomb complex transcripts, and the polycomb proteins may in turn epigenetically influence the SRSF1. Further experimental validation of these regulatory loops/networks could provide novel insights into the molecular regulation of AHN, and unravel new targets for disease-treatment.
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