Fied DNA was performed using PCR Master MIX (Promega). Amplicons were

Fied DNA was performed using PCR Master MIX (Promega). Pleuromutilin site Amplicons were gel purified and cloned into pGEM-T vector (Promega), followed by sequencing at least 7 clones of each sample. For each DNA sample, the number of cytosine residues that remained as “C” was counted, and converted to a percentageof the total 30 CpGs presented in 487 bp region of the CMV promoter.Statistical AnalysisStatistical analysis were performed with the SPSS 13.0 software. Values were shown as Mean6SD and subjected to correlation analysis of Pearson. P value less than 0.05 was considered as statistically significant.Generation of Transgenic Sheep by LentivirusResults Generation of EGFP Transgenic SheepTotal of 46 zygotes were collected from FSH stimulated donors after artificial HIF-2��-IN-1 insemination. One or two cell stage embryos were injected with lentivirus (3.76109 IU/mL) into perivitelline space. The injected embryos were then transferred to 22 hormonally synchronized recipients. In order to increase the productivity, all recipients were transferred with two embryos and resulted in the birth of 13 lambs from 9 pregnant ewes. Of the 13 newborn lambs, eight transgenic sheep were identified by PCR (Fig. 1A) and southern blotting (Fig. 2A and 2B). The rate of transgenic sheep to total of new born lambs and to embryos were 61.5 (8/13) and 17.4 (8/46) respectively. Except two lambs (#4 and #12) died after birth, the other 6 lambs survive normally. There was obvious variation of 18325633 congenital malformation in dorsal keel of #4 lamb with death at birth. The other died lamb #12 displayed the anorexia and diarrhea before death, no other developmental abnormality was observed. Transgenic sheep mortality is 25 (2/ 8), which is the same as that of normal lamb of 25 (9/36). For the two died transgenic lambs, the genomic DNAs extracted from heart, liver, spleen, lung and kidney were subjected to PCR screening. The integration of transgene was observed in all tested tissues (Fig. 1B). The results inferred that the integration of lentiviral transgenesis may exist in all the tissues.from tail tips of all transgenic sheep and inner organs from two died lambs to perform Western blotting. Expression of GFP was detected in tail tips of eight transgenic lambs (Fig. 3B), which indicated that GFP transgene expressed in all transgenic founders. The relative quantification of western blot showed that the levels of GFP expression of #7 and #8 were much higher than that of other founders. Consistent with green fluorescent intensity in inner organs of #12 lamb, the level of GFP protein measured by western blotting was highest in liver and lowest in lung, no GFP was detected in spleen (Fig. 4E, right panel). The expression of GFP in lamb #4 indicated that the expression of GFP was highest in tail and lower in lung and kidney, and no expression was detected in spleen and liver (Fig. 4E, left panel). These data indicated the disparity of transgene expression in different individuals and tissues.Status of Promoter Methylation and Influence on Transgene ExpressionPrevious studies documented that transgene could be methylated in transgenic animals and resulted in repression of expression [23,24]. To investigate the methylation status and its influence on transgene expression in lentiviral-mediated transgenic sheep, we examined the methylation density of 487-bp region of the CMV promoter containing one CpG island with 30 CpGs in individuals and tissues. Firstly, CMV promoter methylation status in all tr.Fied DNA was performed using PCR Master MIX (Promega). Amplicons were gel purified and cloned into pGEM-T vector (Promega), followed by sequencing at least 7 clones of each sample. For each DNA sample, the number of cytosine residues that remained as “C” was counted, and converted to a percentageof the total 30 CpGs presented in 487 bp region of the CMV promoter.Statistical AnalysisStatistical analysis were performed with the SPSS 13.0 software. Values were shown as Mean6SD and subjected to correlation analysis of Pearson. P value less than 0.05 was considered as statistically significant.Generation of Transgenic Sheep by LentivirusResults Generation of EGFP Transgenic SheepTotal of 46 zygotes were collected from FSH stimulated donors after artificial insemination. One or two cell stage embryos were injected with lentivirus (3.76109 IU/mL) into perivitelline space. The injected embryos were then transferred to 22 hormonally synchronized recipients. In order to increase the productivity, all recipients were transferred with two embryos and resulted in the birth of 13 lambs from 9 pregnant ewes. Of the 13 newborn lambs, eight transgenic sheep were identified by PCR (Fig. 1A) and southern blotting (Fig. 2A and 2B). The rate of transgenic sheep to total of new born lambs and to embryos were 61.5 (8/13) and 17.4 (8/46) respectively. Except two lambs (#4 and #12) died after birth, the other 6 lambs survive normally. There was obvious variation of 18325633 congenital malformation in dorsal keel of #4 lamb with death at birth. The other died lamb #12 displayed the anorexia and diarrhea before death, no other developmental abnormality was observed. Transgenic sheep mortality is 25 (2/ 8), which is the same as that of normal lamb of 25 (9/36). For the two died transgenic lambs, the genomic DNAs extracted from heart, liver, spleen, lung and kidney were subjected to PCR screening. The integration of transgene was observed in all tested tissues (Fig. 1B). The results inferred that the integration of lentiviral transgenesis may exist in all the tissues.from tail tips of all transgenic sheep and inner organs from two died lambs to perform Western blotting. Expression of GFP was detected in tail tips of eight transgenic lambs (Fig. 3B), which indicated that GFP transgene expressed in all transgenic founders. The relative quantification of western blot showed that the levels of GFP expression of #7 and #8 were much higher than that of other founders. Consistent with green fluorescent intensity in inner organs of #12 lamb, the level of GFP protein measured by western blotting was highest in liver and lowest in lung, no GFP was detected in spleen (Fig. 4E, right panel). The expression of GFP in lamb #4 indicated that the expression of GFP was highest in tail and lower in lung and kidney, and no expression was detected in spleen and liver (Fig. 4E, left panel). These data indicated the disparity of transgene expression in different individuals and tissues.Status of Promoter Methylation and Influence on Transgene ExpressionPrevious studies documented that transgene could be methylated in transgenic animals and resulted in repression of expression [23,24]. To investigate the methylation status and its influence on transgene expression in lentiviral-mediated transgenic sheep, we examined the methylation density of 487-bp region of the CMV promoter containing one CpG island with 30 CpGs in individuals and tissues. Firstly, CMV promoter methylation status in all tr.