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Journal ArticleDOI

Mutations in the DJ-1 Gene Associated with Autosomal Recessive Early-Onset Parkinsonism

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TLDR
It is shown that DJ-1 mutations are associated with PARK7, a monogenic form of human parkinsonism, and these findings indicate that loss ofDJ-1 function leads to neurodegeneration.
Abstract
The DJ-1 gene encodes a ubiquitous, highly conserved protein. Here, we show that DJ-1 mutations are associated with PARK7, a monogenic form of human parkinsonism. The function of the DJ-1 protein remains unknown, but evidence suggests its involvement in the oxidative stress response. Our findings indicate that loss of DJ-1 function leads to neurodegeneration. Elucidating the physiological role of DJ-1 protein may promote understanding of the mechanisms of brain neuronal maintenance and pathogenesis of Parkinson's disease.

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Journal ArticleDOI

Neuroimmune Connections in Aging and Neurodegenerative Diseases.

TL;DR: This review focuses on the impact of CNS-resident cells of the innate immune system for the development of neurodegenerative diseases, review immune pathway genes that have been identified, and discuss the vicious cycle between inflammation and Neurodegeneration.
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DJ-1, a cancer and Parkinson's disease associated protein, regulates autophagy through JNK pathway in cancer cells.

TL;DR: It is shown that knockdown of DJ-1 induces autophagy through activating JNK pathway to promote Beclin 1 transcription, whereas overexpression ofDJ-1 inhibits these processes.
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Glucocerebrosidase and Parkinson Disease: Molecular, Clinical, and Therapeutic Implications:

TL;DR: The main features of GBA-PD are summarized, the implications of glucocerebrosidase modulation on PD pathogenesis are discussed and cell and animal models suggest that increasing GBA enzyme activity can reduce alpha-synuclein levels.
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Mitochondrial dysfunction in genetic animal models of Parkinson's disease.

TL;DR: The evidence for mitochondrial dysfunction in genetic animal models of Parkinson's disease is critically discussed, and whether abnormal mitochondrial function represents a cause or consequence of disease pathogenesis is evaluated.
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Mitochondrial Dysfunction: The Road to Alpha-Synuclein Oligomerization in PD

TL;DR: This paper highlights some of the findings that provide proof of evidence for a mitochondrial metabolism control in Parkinson's disease, namely, mitochondrial regulation of microtubule-dependent cellular traffic and autophagic lysosomal pathway.
References
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Journal ArticleDOI

WHAT IF: A molecular modeling and drug design program

TL;DR: The menu-driven operation of WHAT IF, combined with the use of default values wherever user input is required, makes it very easy to use for a novice user while keeping full flexibility for more sophisticated studies.
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Twilight zone of protein sequence alignments.

TL;DR: All findings are applicable to automatic database searches and using intermediate sequences for finding links between more distant families was almost as successful: pairs were predicted to be homologous when the respective sequence families had proteins in common.
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Increasing the precision of comparative models with YASARA NOVA--a self-parameterizing force field.

TL;DR: An all‐atom force field aimed at protein and nucleotide optimization in vacuo (NOVA), which has been specifically designed to avoid this problem and can be applied to modeling applications as well as X‐ray and NMR structure refinement.
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DJ-1, a novel oncogene which transforms mouse NIH3T3 cells in cooperation with ras.

TL;DR: DJ-1 showed a cooperative transforming activity with H-Ras, more than 3 times as strong as the activity of ras/myc combination and is suggested to be a novel mitogen-dependent oncogene product involved in a Ras-related signal transduction pathway.
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