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Intersecting impact of CAG repeat and Huntingtin knockout in stem cell-derived cortical neurons [cortical_bulkRNASeq]

ABSTRACT: Intersecting impact of CAG repeat and Huntingtin knockout in stem cell-derived cortical neurons [cortical_bulkRNASeq]

PROVIDER: PRJNA1200684 | ENA |

REPOSITORIES: ENA

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			Action	DRS
	SRR31780640_1.fastq.gz	Fastqsanger.gz
	SRR31780640_2.fastq.gz	Fastqsanger.gz
	SRR31780641_1.fastq.gz	Fastqsanger.gz
	SRR31780641_2.fastq.gz	Fastqsanger.gz
	SRR31780642_1.fastq.gz	Fastqsanger.gz

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Intersecting impact of CAG repeat and Huntingtin knockout in stem cell-derived cortical neurons [cortical]

Project description:Huntington’s Disease (HD) is caused by a CAG repeat expansion in the gene encoding Huntingtin (HTT). While normal HTT function appears impacted by the mutation, the specific pathways unique to CAG repeat expansion versus loss of normal function are unclear. To understand the impact of the CAG repeat expansion, we evaluated biological signatures of HTT knockout (HTT KO) versus those that occur from the CAG repeat expansion by applying multi-omics, live cell imaging, survival analysis and a novel feature- based pipeline to study cortical neurons (eCNs) derived from an isogenic human embryonic stem cell series (RUES2). HTT KO and the CAG repeat expansion influence developmental trajectories of eCNs, with opposing effects on the growth. Network analyses of differentially expressed genes and proteins associated with enriched epigenetic motifs identified subnetworks common to CAG repeat expansion and HTT KO that include neuronal differentiation, cell cycle regulation, and mechanisms related to transcriptional repression and may represent gain-of-function mechanisms that cannot be explained by HTT loss of function alone. A combination of dominant and loss-of-function mechanisms are likely involved in the aberrant neurodevelopmental and neurodegenerative features of HD that can help inform therapeutic strategies.

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Intersecting impact of CAG repeat and Huntingtin knockout in stem cell-derived cortical neurons [cortical]

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Intersecting impact of CAG repeat and Huntingtin knockout in stem cell-derived cortical neurons [ESC]

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Intersecting impact of CAG repeat and Huntingtin knockout in stem cell-derived cortical neurons [cortical_bulkRNASeq]

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Intersecting impact of CAG repeat and Huntingtin knockout in stem cell-derived cortical neurons

Project description:Intersecting impact of CAG repeat and Huntingtin knockout in stem cell-derived cortical neurons

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Intersecting impact of CAG repeat and Huntingtin knockout in stem cell-derived cortical neurons [ESC]

Project description:Intersecting impact of CAG repeat and Huntingtin knockout in stem cell-derived cortical neurons [ESC]

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Intersecting impact of CAG repeat and Huntingtin knockout in stem cell-derived cortical neurons- Cortical Stage

Project description:Huntington Disease (HD) is caused by a CAG repeat expansion in the gene encoding Huntingtin (HTT). While normal HTT function appears impacted by the mutation, the specific pathways unique to CAG repeat expansion versus loss of normal function are unclear. To understand the impact of the CAG repeat expansion, we evaluated biological signatures of HTT knockout (HTT KO) versus those that occur from the CAG repeat expansion by applying multi-omics, live cell imaging, survival analysis and a novel feature-based pipeline to study cortical neurons (eCNs) derived from an isogenic human embryonic stem cell series (RUES2). HTT KO and the CAG repeat expansion influence developmental trajectories of eCNs, with opposing effects on the growth. Network analyses of differentially expressed genes and proteins associated with enriched epigenetic motifs identified subnetworks common to CAG repeat expansion and HTT KO that include neuronal differentiation, cell cycle regulation, and mechanisms related to transcriptional repression and may represent gain-of-function mechanisms that cannot be explained by HTT loss of function alone. A combination of dominant and loss-of-function mechanisms are likely involved in the aberrant neurodevelopmental and neurodegenerative features of HD that can help inform therapeutic strategies.

2024-12-19 | MSV000096707 | MassIVE

Intersecting impact of CAG repeat and Huntingtin knockout in stem cell-derived cortical neurons: Pluripotent stage

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Integrated genomics and proteomics to define huntingtin CAG length-dependent molecular networks in HD mouse brains

Project description:To gain insight into how mutant Huntingtin (mHTT) CAG repeat length may modify Huntington’s disease (HD) pathogenesis, we profiled mRNA in over 600 brain and peripheral tissue samples from HD knock-in mice with increasing CAG repeat length. We find repeat length dependent transcriptional signatures are prominent in the striatum, less so in cortex, and minimal in the liver. Co-expression network analyses reveal 13 striatal and 5 cortical modules that are highly correlated with CAG length and age, and that are preserved in HD models and some in the patients. Top striatal modules implicate mHTT CAG length and age in graded impairment of striatal medium spiny neuron identity gene expression and in dysregulation of cAMP signaling, cell death, and protocadherin genes. Importantly, we used proteomics to confirm 790 genes and 5 striatal modules with CAG length-dependent dysregulation at both RNA and protein levels and validated 21 striatal module genes as modifiers of mHtt toxicities in vivo.

2016-02-16 | PXD003442 | Pride

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