Перегляд вихідного коду сторінки Stated Viral Buzz Regarding BI 2536

Disruption of 5�� tRNA processing has previously been shown to stimulate translation of GCN4, the yeast equivalent of ATF4, although in a p-eIF2��-independent manner (Qiu et al., 2000). To explore whether ATF4 activation may be induced by unprocessed n-Tr20 generated from the B6J allele, we generated transgenic B6N mice that expressed the mutant n-Tr20 gene (B6N-Tg-nTr20mut) at levels 6-fold above that observed in B6J brain (Figure 4��figure supplement 1). Quantitative PCR using cerebellar cDNA from B6N and B6N-Tg-nTr20mut mice was performed for the ATF4 target genes that showed highest fold expression changes between the B6J and B6J-Gtpbp2nmf205-/- cerebellum. As shown in Figure 4C, overexpression of the unprocessed n-Tr20 did not result in upregulation of these genes. To determine if ATF4 activation was influenced by interaction between overexpression of the unprocessed tRNA and loss of Gtpbp2, we crossed B6N mice (wild type for n-Tr20) that transgenically [https://en.wikipedia.org/wiki/BML-190 BML-190] overexpress mutant n-Tr20 (B6N-Tg-n-Tr20mut) mice to B6J.B6Nn-Tr20-Gtpbp2nmf205-/- mice (wildtype for n-Tr20, mutant for Gtpbp2). RT-qPCR for the ATF4-target genes analyzed above was performed on cerebella from 3-week-old B6J.B6Nn-Tr20-Gtpbp2nmf205-/- with, and without, the mutant transgene, and B6J.B6Nn-Tr20 (n-Tr20 wild type), B6J (n-Tr20 mutant) and B6J-Gtpbp2nmf205-/- (mutant for n-Tr20; Gtpbp2-/-) mice. As expected, the expression of ATF4 target genes was dramatically upregulated in the B6J-Gtpbp2nmf205-/- cerebellum relative to the [http://www.selleckchem.com/products/Cyclopamine.html Selleck Cyclopamine] other strains. However, the expression of the mutant n-Tr20 transgene, even in the presence of the Gtpbp2 mutation, did not alter expression of ATF4 target genes (Figure 4D). Together, these results suggest that the induction of ATF4 target gene expression in B6J-Gtpbp2nmf205-/- is not due to expression of the unprocessed n-Tr20 tRNA. For further evidence that loss of mature n-Tr20 causes GCN2 activation in the absence of Gtpbp2, we generated B6J mice in which the n-Tr20 gene was deleted by homologous recombination (B6J-n-Tr20-/-; Figure 4��figure supplement 2). Mice heterozygous or homozygous for this deletion were born at expected [http://www.selleckchem.com/products/BI-2536.html BI 2536 order] Mendelian ratios. However when these mice were crossed with Gtpbp2nmf205-/- mice, mice that were homozygous for both the n-Tr20 deletion and the nmf205 mutation died shortly after birth, demonstrating that residual levels of aminoacylated n-Tr20 in the B6J brain allows postnatal survival of B6J-Gtpbp2nmf205-/- mice. RT-qPCR for the 10 most highly induced ATF4-target genes were performed on cDNA generated from the brain of P0 B6J, B6J-Gtpbp2nmf205-/-, B6J-n-Tr20-/-, and B6J-n-Tr20-/-; Gtpbp2nmf205-/- mice (Figure 4E). Overall, these genes were expressed at higher levels in the B6J-Gtpbp2nmf205-/- brain relative to that of B6J mice (p