scholarly journals Transcriptome Analysis of Gene Expression Patterns of Populus tomentosa in Response to Oxidative Stress

2018 ◽  
Vol 07 (02) ◽  
pp. 186-195
Author(s):  
嘉鑫 李
2017 ◽  
Vol 40 (3) ◽  
pp. 253-263 ◽  
Author(s):  
Li Bian ◽  
Changlin Liu ◽  
Siqing Chen ◽  
Fazhen Zhao ◽  
Jianlong Ge ◽  
...  

2010 ◽  
Vol 109 (5) ◽  
pp. 1404-1415 ◽  
Author(s):  
Kimberly A. Reich ◽  
Yi-Wen Chen ◽  
Paul D. Thompson ◽  
Eric P. Hoffman ◽  
Priscilla M. Clarkson

Although short-term disuse does not result in measurable muscle atrophy, studies suggest that molecular changes associated with protein degradation may be initiated within days of the onset of a disuse stimulus. We examined the global gene expression patterns in sedentary men ( n = 7, mean age ± SD = 22.1 ± 3.7 yr) following 48 h unloading (UL) via unilateral lower limb suspension and 24 h reloading (RL). Biopsy samples of the left vastus lateralis muscle were collected at baseline, 48 h UL, and 24 h RL. Expression changes were measured by microarray and gene clustering; identification of enriched functions and canonical pathways were performed using the Database for Annotation, Visualization and Integrated Discovery (DAVID) and Ingenuity Pathway Analysis (IPA). Four genes were validated with quantitative RT-PCR (qRT-PCR), and protein levels were measured with Western blot. Of the upregulated genes after UL, the most enriched functional group and highest ranked canonical pathway were related to protein ubiquitination. The oxidative stress response pathway was the second highest ranked canonical pathway. Of the downregulated genes, functions related to mitochondrial metabolism were the most highly enriched. In general, gene expression patterns following UL persisted following RL. qRT-PCR confirmed increases in mRNA for ubiquitin proteasome pathway-related E3 ligase Atrogin1 (but not accompanying increases in protein products) and stress response gene heme oxygenase-1 (HMOX, which showed a trend toward increases in protein products at 48 h UL) as well as extracellular matrix (ECM) component COL4A3. The gene expression patterns were not reversed on RL, suggesting that molecular responses to short-term periods of skeletal muscle inactivity may persist after activity resumes.


2020 ◽  
Author(s):  
Gang Xue ◽  
Gang Wang ◽  
Qianqian Shi ◽  
Hui Wang ◽  
Bo-Min Lv ◽  
...  

AbstractAchieving an improved understanding of the temporal sequence of factors involved in Parkinson’s disease (PD) pathogenesis may accelerate drug discovery. In this study, we performed a longitudinal transcriptome analysis to identify associated genes underlying the pathogenesis of PD at three temporal phases. We firstly found that multiple initiator genes, which are related to processes of olfactory transduction and stem cell pluripotency, indicate PD risk to those subjects at the prodromal phase. And many facilitator genes involved in calcium signaling and stem cell pluripotency contribute to PD onset. We next identified 325 aggravator genes whose expression could lead to disease progression through damage to dopaminergic synapses and ferroptosis via an integrative analysis with DNA methylation. Last, we made a systematic comparison of gene expression patterns across PD development and accordingly provided candidate drugs at different phases in an attempt to prevent the neurodegeneration process.


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