Ansgenic founders was measured (Fig. 5B). The average methylation levels ranged

Ansgenic founders was measured (Fig. 5B). The average methylation levels ranged from 37.6 to 79.1 in transgenic individuals (Fig. 5D, middle panel). Then the promoter methylation status in different tissues was measured (Fig. 5C) and the methylated CpG rate ranged from 34.7 to 93.3 (Fig. 5E and 5F, middle panels). Analysis of the correlation of methylation level with GFP expression in individuals (Fig. 5D, low panel) and tissues (Fig. 5E and 5F, low panels) revealed that the expression of GFP expression was inversely correlated with methylation status (r = 0.6591 for individules, p,0.05; r = 20.9685 for #4 tissues, p,0.05; r = 20.8782 for #12 tissues, p,0.05). The lowest GFP expression (Fig. 5D, up panel) was observed in the transgenic sheep with the highest methylation level (79.1 , transgenic sheep #9). On the contrary, the lowest promoter methylation level was corresponding to the highest GFP expression level (transgenic sheep #8). In tissues, the highest methylation level was found in spleen of #4 lamb with 93.3 (Fig. 5E, middle panel), at which little GFP expression was detected (Fig. 5E, up panel), whereas the highest expression of GFP was found in liver of #12 lamb (Fig. 5F, up panel), in concomitant with the lowest methylation density (34.7 ) (Fig. 5F, middle panel).Analysis of the Transgene Essed between all patients (groups HAT-1 and HAT-2) and the control IntegrationIn order to analyze transgene integration and copy numbers, southern blot assay was carried out with genomic DNA digested with EcoRI or double-digested with SfiI and HpaI. In EcoRI digested genomic DNA samples, the number of integrants were visualized ranging from 2 to 6 copies and for most individuals with 2 to 3 copies (Fig. 2A). To exactly quantify the copy number of each transgenic sheep, we performed the southern blot with double-digested genomic DNA and quantified the copy number by standard curve. The standard curve was generated with pLEXEGFP plasmid by concentration gradient southern blot, which was performed in parallel with double-digested genomic DNA derived from transgenic lambs (Fig. 2B). The copy number of each doubledigested plasmid with serial dilution was linearly matched to the plasmid concentration (Fig. 2C and 2D). The copy number for each blot of transgenic lamb was calculated based on standard curve (Table.1). The highest copy number was identified in #12 lamb with 6 copies, followed by #5 lamb with 5 copies. The copy numbers of other transgenic sheep were around 2 to 3. Copy number derived from these two approaches was consistent (Fig. 2A).Analysis of EGFP Expression in Transgenic LambsThe expression of EGFP transgene was analyzed by direct fluorescence observation and Western blotting. At first, we observed embryos injected with EGFP lentivirus in blastula stage 23977191 under fluorescent microscope (Fig. 3A, left panels). Approximately 80 embryos subjected to injection of lentiviral transgene were presented green fluorescence. Further, we observed green fluorescence in hoof, lip and horn of newborn transgenic lambs (Fig. 3A, middle panels) and continuously to maturity (Fig. 3A, right panels), which suggested that the GFP could be N-related peptides and their receptors elicit profound scratching like morphine in expressed persistently in transgenic sheep. Additionally, we anatomized the died lamb (#4 and #12) to investigate the distribution of GFP expression in inner organs (Fig. 4A). Notably, the most intense GFP fluorescence was observed in liver (Fig. 4B) and then in kidney (Fig. 4C), weak GFP fluorescence was observed in lung of #12 lamb (Fig. 4D). To further analyze the GFP expression,.Ansgenic founders was measured (Fig. 5B). The average methylation levels ranged from 37.6 to 79.1 in transgenic individuals (Fig. 5D, middle panel). Then the promoter methylation status in different tissues was measured (Fig. 5C) and the methylated CpG rate ranged from 34.7 to 93.3 (Fig. 5E and 5F, middle panels). Analysis of the correlation of methylation level with GFP expression in individuals (Fig. 5D, low panel) and tissues (Fig. 5E and 5F, low panels) revealed that the expression of GFP expression was inversely correlated with methylation status (r = 0.6591 for individules, p,0.05; r = 20.9685 for #4 tissues, p,0.05; r = 20.8782 for #12 tissues, p,0.05). The lowest GFP expression (Fig. 5D, up panel) was observed in the transgenic sheep with the highest methylation level (79.1 , transgenic sheep #9). On the contrary, the lowest promoter methylation level was corresponding to the highest GFP expression level (transgenic sheep #8). In tissues, the highest methylation level was found in spleen of #4 lamb with 93.3 (Fig. 5E, middle panel), at which little GFP expression was detected (Fig. 5E, up panel), whereas the highest expression of GFP was found in liver of #12 lamb (Fig. 5F, up panel), in concomitant with the lowest methylation density (34.7 ) (Fig. 5F, middle panel).Analysis of the Transgene IntegrationIn order to analyze transgene integration and copy numbers, southern blot assay was carried out with genomic DNA digested with EcoRI or double-digested with SfiI and HpaI. In EcoRI digested genomic DNA samples, the number of integrants were visualized ranging from 2 to 6 copies and for most individuals with 2 to 3 copies (Fig. 2A). To exactly quantify the copy number of each transgenic sheep, we performed the southern blot with double-digested genomic DNA and quantified the copy number by standard curve. The standard curve was generated with pLEXEGFP plasmid by concentration gradient southern blot, which was performed in parallel with double-digested genomic DNA derived from transgenic lambs (Fig. 2B). The copy number of each doubledigested plasmid with serial dilution was linearly matched to the plasmid concentration (Fig. 2C and 2D). The copy number for each blot of transgenic lamb was calculated based on standard curve (Table.1). The highest copy number was identified in #12 lamb with 6 copies, followed by #5 lamb with 5 copies. The copy numbers of other transgenic sheep were around 2 to 3. Copy number derived from these two approaches was consistent (Fig. 2A).Analysis of EGFP Expression in Transgenic LambsThe expression of EGFP transgene was analyzed by direct fluorescence observation and Western blotting. At first, we observed embryos injected with EGFP lentivirus in blastula stage 23977191 under fluorescent microscope (Fig. 3A, left panels). Approximately 80 embryos subjected to injection of lentiviral transgene were presented green fluorescence. Further, we observed green fluorescence in hoof, lip and horn of newborn transgenic lambs (Fig. 3A, middle panels) and continuously to maturity (Fig. 3A, right panels), which suggested that the GFP could be expressed persistently in transgenic sheep. Additionally, we anatomized the died lamb (#4 and #12) to investigate the distribution of GFP expression in inner organs (Fig. 4A). Notably, the most intense GFP fluorescence was observed in liver (Fig. 4B) and then in kidney (Fig. 4C), weak GFP fluorescence was observed in lung of #12 lamb (Fig. 4D). To further analyze the GFP expression,.

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