In order to discover the mechanism of cold stress and identify differentially expressed genes in hypothalamus during cold stress, 4 weeks of age Huainan partridge chickens, Chinese indigenous breed, were chosen for 24 h cold stress and then hypothalamus were isolated and labeled by reverse transcription reaction for cDNA. Labeled cDNA were hybridized with cDNA microarray. After scanning and image processing, the different gene expression profiling of hypothalamus and normal control was investigated. The differentially expressed genes included 334 down-regulated genes and 543 up-regulated genes. In these differentially regulated genes, myosin heavy chain polypeptide 11 (MYH11), light chain polypeptide 9 (MYL9) and tenascin-Y (TNXB), etc., which involved in muscle activity were significantly down-regulated. Genes like cholecystokinin (CCK), neuropeptide Y (NPY), neuropeptide Y receptor 5 (NPY5R), hypocretin receptor 2 (HCRTR2) and hypocretin neuropeptide precursor (HCRT) which responsible for regulation of feeding behavior were significantly up-regulated. In addition, genes responsible for lipid synthesis, like apolipoprotein (APOB) and agouti related protein homolog (AGRP), were also up-regulated. Through pathway analysis using the Kyoto Encyclopedia of Gene and Genomics, during 24 h cold stress, the neuroactive ligand-receptor interaction was firstly initiated in chickens for stimulation of central nervus for feed intake. Adipocytokine signaling pathway was in high activation for supplementation of body energy. Jak-STAT, Ca(2+) signaling pathway and other biological reactions were also initiated in response to cold stress. The biological pathways participated in cold stress would provide important information for clarify the mechanism of cold stress and the differentially expressed genes would give much help for screening of candidate genes in breeding of cold stress resistant lines.
With 300 Gy of [ 60Co] γ-ray radiation of dry wheat seeds of Vortex 9722, the protein content, wet gluten content, sedimentation value, and hardness variation were analyzed in 341 lines in M4. Using over population mean ± 2X standard deviation as the screening standard, 8 lines with higher protein and wet gluten content and 4 lines with lower protein and wet gluten content were selected. In the M5 generation, the quality traits -silty parameters and high molecular weight glutenin subunits (HMW-GS) -were further analyzed in these 12 lines. The results showed that in the M5 generation, the quality traits in some variants were significantly different from those in the parents; the farinograms varied greatly. Eleven variants had significantly different HMW-GS bands compared to their parents. The parents had a HMW-GS composition of 5 + 14 + 15 + 12 + 9, and the variants had HMW-GS of 11 + 5 + 7 + 9 + 12 subunits or 1 + 5 + 7 + 8 + 12 subunits, indicating that the glutenin loci of these lines were mutated.
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