Although many genes have been identified using high throughput technologies in endometriosis (ES), only a small number of individual genes have been analyzed functionally. This is due to the complexity of the disease that has different stages and is affected by various genetic and environmental factors. Many genes are upregulated or downregulated at each stage of the disease, thus making it difficult to identify key genes. In addition, little is known about the differences between the different stages of the disease. We assumed that the study of the identified genes in ES at a system-level can help to better understand the molecular mechanism of the disease at different stages of the development. We used publicly available microarray data containing archived endometrial samples from women with minimal/mild endometriosis (MMES), mild/severe endometriosis (MSES) and without endometriosis. Using weighted gene co-expression analysis (WGCNA), functional modules were derived from normal endometrium (NEM) as the reference sample. Subsequently, we tested whether the topology or connectivity pattern of the modules was preserved in MMES and/or MSES. Common and specific hub genes were identified in non-preserved modules. Accordingly, hub genes were detected in the non-preserved modules at each stage. We identified sixteen co-expression modules. Of the 16 modules, nine were non-preserved in both MMES and MSES whereas five were preserved in NEM, MMES, and MSES. Importantly, two non-preserved modules were found in either MMES or MSES, highlighting differences between the two stages of the disease. Analyzing the hub genes in the non-preserved modules showed that they mostly lost or gained their centrality in NEM after developing the disease into MMES and MSES. The same scenario was observed, when the severeness of the disease switched from MMES to MSES. Interestingly, the expression analysis of the new selected gene candidates including CC2D2A, AEBP1, HOXB6, IER3, and STX18 as well as IGF-1, CYP11A1 and MMP-2 could validate such shifts between different stages. The overrepresented gene ontology (GO) terms were enriched in specific modules, such as genetic disposition, estrogen dependence, progesterone resistance and inflammation, which are known as endometriosis hallmarks. Some modules uncovered novel co-expressed gene clusters that were not previously discovered.
In recent years, drought-induced tree mortality has occurred in the oak forests of the Zagros Mountains (western Iran). The impacts of climate change induced by drought stress have been most acutely experienced by two populations of Persian oaks (Quercus brantii Lindl) grown in the western provinces (Ilam and Lorestan) of the Zagros region. We surveyed growth, physiological, and biochemical responses of one-year-old Persian oak seedlings from Melasyah (Ilam) and Chegeni (Lorestan) provenances, which were subjected to three watering regimes (100%, 40%, and 20% of field capacity) in a greenhouse. The severe drought stress decreased the diameter and height growth, total biomass, net photosynthesis, gas exchange, xylem water potential, maximum Rubisco activity (Vcmax) as well as the maximum PSII photochemical efficiency of the oak seedlings in both populations, but the rate of decrease was greater in Chegeni seedlings as compared to Melasyah seedlings. Although proline and soluble sugar contents significantly increased in response to drought in both populations under stress, the rate of increase was higher in Melasyah seedlings as compared to Chegeni seedlings. In addition, the activities of peroxidase, superoxide dismutase, catalase, and ascorbic peroxidase as well as that of phenylalanine ammonia lyase were promoted in both populations under drought stress. However, the incremental rate was higher in the Melasyah population than in the Chegeni population. Under severe drought stress, the MDA content, electrolyte leakage, the content of hydrogen peroxide, and superoxide radical significantly increased in both the populations. The rate of increase, however, was higher in the Chegeni population. Under drought stress, the total phenol and flavonoid contents of Melasyah seedlings were higher than those of Chegeni seedlings. The results showed that Chegeni seedlings are more sensitive than Melasyah seedlings when exposed to a water limitation stress. Our findings suggest that the climate conditions of the Persian oak stands should be considered by nursery managers while creating establishment and restoration programs.
Long non-coding RNAs (lncRNAs) are transcribed RNA molecules >200 nucleotides in length that do not encode proteins and serve as key regulators of diverse biological processes. Recently, thousands of long intergenic non-coding RNAs (lincRNAs), a type of lncRNAs, have been identified in mammalians using massive parallel large sequencing technologies. The availability of the genome sequence of sheep (Ovis aries) has allowed us genomic prediction of non-coding RNAs. This is the first study to identify lincRNAs using RNA-seq data of eight different tissues of sheep, including brain, heart, kidney, liver, lung, ovary, skin, and white adipose. A computational pipeline was employed to characterize 325 putative lincRNAs with high confidence from eight important tissues of sheep using different criteria such as GC content, exon number, gene length, co-expression analysis, stability, and tissue-specific scores. Sixty-four putative lincRNAs displayed tissues-specific expression. The highest number of tissues-specific lincRNAs was found in skin and brain. All novel lincRNAs that aligned to the human and mouse lincRNAs had conserved synteny. These closest protein-coding genes were enriched in 11 significant GO terms such as limb development, appendage development, striated muscle tissue development, and multicellular organismal development. The findings reported here have important implications for the study of sheep genome.
Although the female gametophyte in angiosperms consists of just seven cells, it has a complex biological network. In this study, female gametophyte microarray data from Arabidopsis thaliana were integrated into the Arabidopsis interactome database to generate a putative interaction map of the female gametophyte development including proteome map based on biological processes and molecular functions of proteins. Biological and functional groups as well as topological characteristics of the network were investigated by analyzing phytohormones, plant defense, cell death, transporters, regulatory factors, and hydrolases. This approach led to the prediction of critical members and bottlenecks of the network. Seventy-four and 24 upregulated genes as well as 171 and 3 downregulated genes were identified in subtracted networks based on biological processes and molecular function respectively, including novel genes such as the pathogenesis-related protein 4, ER type Ca2+ ATPase 3, dihydroflavonol reductase, and ATP disulfate isomerase. Biologically important relationships between genes, critical nodes, and new essential proteins such as AT1G26830, AT5G20850, CYP74A, AT1G42396, PR4 and MEA were found in the interactome's network. The positions of novel genes, both upregulated and downregulated, and their relationships with biological pathways, in particular phytohormones, were highlighted in this study.
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