Dataset Information

Parkinson's Disease Mouse Model Brain LC-MS/MS

ABSTRACT: Brains of a transgenic Parkinson's Disease Mouse Model were used to investigate proteomics using LC-MS/MS. The Model has the human alpha-synuclein expression under the Control of CamkIIa promotor and a DOX system, making the expression inducible. Data includes aging, long expression, short expression, no expression as conditions

INSTRUMENT(S):

ORGANISM(S): Mus Musculus (mouse)

TISSUE(S): Brain

DISEASE(S): Parkinson's Disease

SUBMITTER: Jaehyun Lee

LAB HEAD: Karin M. Danzer

PROVIDER: PXD069528 | Pride | 2025-12-09

REPOSITORIES: Pride

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			Action	DRS
	004_3237_F1_2ug-3_8ul.raw	Raw
	005_1955_F2_1_5ug_3_0ul.raw	Raw
	005_3198_F1_2ug_2_2ul.raw	Raw
	005_3198_F3_1_5ug_4_3ul.raw	Raw
	005_3210_F1_2ug-3_2ul.raw	Raw

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Project description:Fungal fruiting body size and form are influenced by the ecology of the species, including diverse environmental stimuli. Accordingly, nutritional resources available to the fungus during development can be vital to successful production of fruiting bodies. To investigate the effect of nutrition, perithecial development of N. crassa was induced on two different media, a sparsely nutritive Synthetic Crossing Medium (SCM) and a natural Carrot Agar (CA). Protoperithecia were collected before crossing, and perithecia were collected at 2, 24, 48, 72, 96, 120, and at full maturity 144 hours after crossing. No differences in fruiting body morphology were observed between the two media at any time point. A circuit of microarray hybridizations comparing cDNA from all neighboring stages was performed. For a majority of differentially expressed genes, expression was higher in SCM than in CA, and expression of core metabolic genes was particularly affected. Effects of nutrition were highest in magnitude before crossing, lowering in magnitude during early perithecial development. Interestingly, metabolic effects of the media were also large in magnitude during late perithecial development, at which stage the lower expression in CA presumably reflected the continued intake of diverse complex initial compounds, diminishing the need for expression of anabolic pathways. However, for genes with key regulatory roles in sexual development, including pheromone precursor ccg-4 and poi2, expression patterns were similar between treatments. When possible, a common nutritional environment is ideal for comparing transcriptional profiles between different fungi. Nevertheless, the observed consistency of the developmental program across media, despite considerable metabolic differentiation is reassuring. This result facilitates comparative studies that will require different nutritional resources for sexual development in different fungi. Neurospora crassa mat A FGSC#2489 and mat-a FGSC 4200: Eight perithecial developmental stages, 0hr, 2 hr, 24 hr, 48 hr, 72 hr, 96 hr, 120 hr, and 144 hr were sampled and compared

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Parkinson's Disease Mouse Model Brain LC-MS/MS

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