Literature DB >> 24145027

Presenilins regulate neurotrypsin gene expression and neurotrypsin-dependent agrin cleavage via cyclic AMP response element-binding protein (CREB) modulation.

Angels Almenar-Queralt1, Sonia N Kim, Christopher Benner, Cheryl M Herrera, David E Kang, Ivan Garcia-Bassets, Lawrence S B Goldstein.   

Abstract

Presenilins, the catalytic components of the γ-secretase complex, are upstream regulators of multiple cellular pathways via regulation of gene transcription. However, the underlying mechanisms and the genes regulated by these pathways are poorly characterized. In this study, we identify Tequila and its mammalian ortholog Prss12 as genes negatively regulated by presenilins in Drosophila larval brains and mouse embryonic fibroblasts, respectively. Prss12 encodes the serine protease neurotrypsin, which cleaves the heparan sulfate proteoglycan agrin. Altered neurotrypsin activity causes serious synaptic and cognitive defects; despite this, the molecular processes regulating neurotrypsin expression and activity are poorly understood. Using γ-secretase drug inhibitors and presenilin mutants in mouse embryonic fibroblasts, we found that a mature γ-secretase complex was required to repress neurotrypsin expression and agrin cleavage. We also determined that PSEN1 endoproteolysis or processing of well known γ-secretase substrates was not essential for this process. At the transcriptional level, PSEN1/2 removal induced cyclic AMP response element-binding protein (CREB)/CREB-binding protein binding, accumulation of activating histone marks at the neurotrypsin promoter, and neurotrypsin transcriptional and functional up-regulation that was dependent on GSK3 activity. Upon PSEN1/2 reintroduction, this active epigenetic state was replaced by a methyl CpG-binding protein 2 (MeCP2)-containing repressive state and reduced neurotrypsin expression. Genome-wide analysis revealed hundreds of other mouse promoters in which CREB binding is similarly modulated by the presence/absence of presenilins. Our study thus identifies Tequila and neurotrypsin as new genes repressed by presenilins and reveals a novel mechanism used by presenilins to modulate CREB signaling based on controlling CREB recruitment.

Entities:  

Keywords:  CREB; Chromatin Immunoprecipitation (ChIP); Drosophila Larval Brains; GSK3; MEFs; Neurotrypsin; Presenilin; Promoters; Secretases; Tequila

Mesh:

Substances:

Year:  2013        PMID: 24145027      PMCID: PMC3853272          DOI: 10.1074/jbc.M113.513705

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  83 in total

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Journal:  Science       Date:  2002-11-29       Impact factor: 47.728

Review 2.  The presenilin hypothesis of Alzheimer's disease: evidence for a loss-of-function pathogenic mechanism.

Authors:  Jie Shen; Raymond J Kelleher
Journal:  Proc Natl Acad Sci U S A       Date:  2006-12-29       Impact factor: 11.205

3.  PTH induction of transcriptional activity of the cAMP response element-binding protein requires the serine 129 site and glycogen synthase kinase-3 activity, but not casein kinase II sites.

Authors:  Darren R Tyson; John T Swarthout; Stephen C Jefcoat; Nicola C Partridge
Journal:  Endocrinology       Date:  2002-02       Impact factor: 4.736

4.  Nicastrin is required for gamma-secretase cleavage of the Drosophila Notch receptor.

Authors:  Yue Hu; Yihong Ye; Mark E Fortini
Journal:  Dev Cell       Date:  2002-01       Impact factor: 12.270

Review 5.  Cistrome plasticity and mechanisms of cistrome reprogramming.

Authors:  Ivan Garcia-Bassets; Dong Wang
Journal:  Cell Cycle       Date:  2012-08-16       Impact factor: 4.534

6.  Neurotrypsin, a novel multidomain serine protease expressed in the nervous system.

Authors:  T P Gschwend; S R Krueger; S V Kozlov; D P Wolfer; P Sonderegger
Journal:  Mol Cell Neurosci       Date:  1997       Impact factor: 4.314

7.  A map of the cis-regulatory sequences in the mouse genome.

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8.  Neural progenitor cells do not differentiate prematurely in presenilin-1 null mutant mice.

Authors:  Paul H Wen; Rita De Gasperi; Miguel A Gama Sosa; Gregory A Elder
Journal:  Neurosci Lett       Date:  2004-11-23       Impact factor: 3.046

Review 9.  WNT and beta-catenin signalling: diseases and therapies.

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Review 3.  Vasculogenic mimicry signaling revisited: focus on non-vascular VE-cadherin.

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Journal:  Mol Cancer       Date:  2017-03-21       Impact factor: 27.401

Review 4.  Presenilins as Drug Targets for Alzheimer's Disease-Recent Insights from Cell Biology and Electrophysiology as Novel Opportunities in Drug Development.

Authors:  R Scott Duncan; Bob Song; Peter Koulen
Journal:  Int J Mol Sci       Date:  2018-05-31       Impact factor: 5.923

Review 5.  Nerve, Muscle, and Synaptogenesis.

Authors:  Lauren Eric Swenarchuk
Journal:  Cells       Date:  2019-11-16       Impact factor: 6.600

6.  Chromatin establishes an immature version of neuronal protocadherin selection during the naive-to-primed conversion of pluripotent stem cells.

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Journal:  Nat Genet       Date:  2019-11-18       Impact factor: 38.330

7.  Seasonal variation in UVA light drives hormonal and behavioural changes in a marine annelid via a ciliary opsin.

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8.  Analysis of Brugada syndrome loci reveals that fine-mapping clustered GWAS hits enhances the annotation of disease-relevant variants.

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Journal:  Cell Rep Med       Date:  2021-04-20

9.  Identification of in vivo roles of ErbB4-JMa and its direct nuclear signaling using a novel isoform-specific knock out mouse.

Authors:  Robert Doherty; Brenna L MacLeod; Megan M Nelson; Mostafa M H Ibrahim; Beatriz C Borges; Nada W Jaradat; Matthew C Finneran; Roman J Giger; Gabriel Corfas
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  9 in total

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