SH3GL3 associates with the Huntingtin exon 1 protein and promotes the formation of polygln-containing protein aggregates (Q28288296)

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S Wälter

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N Wedemeyer

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R Hasenbank

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E Scherzinger

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H Eickhoff

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G P Bates

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E E Wanker

HAP1-huntingtin interactions do not contribute to the molecular pathology in Huntington's disease transgenic mice

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language of work or name

English

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publication date

October 1998

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published in

Molecular Cell

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volume

2

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issue

4

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page(s)

427-36

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cites work

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Huntingtin and DRPLA proteins selectively interact with the enzyme GAPDH.

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Formation of neuronal intranuclear inclusions underlies the neurological dysfunction in mice transgenic for the HD mutation

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Subcellular localization of the Huntington's disease gene product in cell lines by immunofluorescence and biochemical subcellular fractionation

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Huntingtin is a cytoplasmic protein associated with vesicles in human and rat brain neurons

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Aggregation of huntingtin in neuronal intranuclear inclusions and dystrophic neurites in brain

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A novel SH3-containing human gene family preferentially expressed in the central nervous system

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Identification and localization of huntingtin in brain and human lymphoblastoid cell lines with anti-fusion protein antibodies

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A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes.

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Suppression of aggregate formation and apoptosis by transglutaminase inhibitors in cells expressing truncated DRPLA protein with an expanded polyglutamine stretch.

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Peptides containing glutamine repeats as substrates for transglutaminase-catalyzed cross-linking: relevance to diseases of the nervous system

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HIP1, a human homologue of S. cerevisiae Sla2p, interacts with membrane-associated huntingtin in the brain

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The scanning model for translation: an update

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A huntingtin-associated protein enriched in brain with implications for pathology

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Exon 1 of the HD gene with an expanded CAG repeat is sufficient to cause a progressive neurological phenotype in transgenic mice

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Length of huntingtin and its polyglutamine tract influences localization and frequency of intracellular aggregates

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The cerebellar leucine-rich acidic nuclear protein interacts with ataxin-1

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Interaction of Grb2 via its Src homology 3 domains with synaptic proteins including synapsin I

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Intranuclear inclusions of expanded polyglutamine protein in spinocerebellar ataxia type 3.

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Protein modules and signalling networks

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Glutamine repeats and inherited neurodegenerative diseases: molecular aspects

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The SH3p4/Sh3p8/SH3p13 protein family: binding partners for synaptojanin and dynamin via a Grb2-like Src homology 3 domain

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When more is less: pathogenesis of glutamine repeat neurodegenerative diseases

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Identification of an HD patient with a (CAG)180 repeat expansion and the propagation of highly expanded CAG repeats in lambda phage

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Huntingtin-encoded polyglutamine expansions form amyloid-like protein aggregates in vitro and in vivo

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High efficiency transformation of intact yeast cells using single stranded nucleic acids as a carrier

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Widespread expression of Huntington's disease gene (IT15) protein product

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Alternative splicing of exon 14 determines nuclear or cytoplasmic localisation of fmr1 protein isoforms

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Ataxin-1 with an expanded glutamine tract alters nuclear matrix-associated structures

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Cloning of ligand targets: systematic isolation of SH3 domain-containing proteins

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Cellular localization of the Huntington's disease protein and discrimination of the normal and mutated form

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HIP-I: a huntingtin interacting protein isolated by the yeast two-hybrid system

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