Literature DB >> 19433866

Rrs1 is involved in endoplasmic reticulum stress response in Huntington disease.

Alisia Carnemolla1, Elisa Fossale, Elena Agostoni, Silvia Michelazzi, Raffaella Calligaris, Luca De Maso, Giannino Del Sal, Marcy E MacDonald, Francesca Persichetti.   

Abstract

The induction of Rrs1 expression is one of the earliest events detected in a presymptomatic knock-in mouse model of Huntington disease (HD). Rrs1 up-regulation fulfills the HD criteria of dominance, striatal specificity, and polyglutamine dependence. Here we show that mammalian Rrs1 is localized both in the nucleolus as well as in the endoplasmic reticulum (ER) of neurons. This dual localization is shared with its newly identified molecular partner 3D3/lyric. We then show that both genes are induced by ER stress in neurons. Interestingly, we demonstrate that ER stress is an early event in a presymptomatic HD mouse model that persists throughout the life span of the rodent. We further show that ER stress also occurs in postmortem brains of HD patients.

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Year:  2009        PMID: 19433866      PMCID: PMC2709382          DOI: 10.1074/jbc.M109.018325

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


  32 in total

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Journal:  Hum Mol Genet       Date:  2002-03-15       Impact factor: 6.150

Review 5.  Molecular genetics: unmasking polyglutamine triggers in neurodegenerative disease.

Authors:  J F Gusella; M E MacDonald
Journal:  Nat Rev Neurosci       Date:  2000-11       Impact factor: 34.870

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Authors:  A Wyttenbach; J Swartz; H Kita; T Thykjaer; J Carmichael; J Bradley; R Brown; M Maxwell; A Schapira; T F Orntoft; K Kato; D C Rubinsztein
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  68 in total

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9.  Small molecule modulator of protein disulfide isomerase attenuates mutant huntingtin toxicity and inhibits endoplasmic reticulum stress in a mouse model of Huntington's disease.

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10.  Huntingtin interacts with the cue domain of gp78 and inhibits gp78 binding to ubiquitin and p97/VCP.

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