Datasheet H3K9me3 sp056 DATASHEET Datasheet description | Download |
Datasheet H3K9me3 C15410056 DATASHEET Polyclonal antibody raised in rabbit against the region of histone H3 containing the trimethylate... | Download |
Synthetic peptide derived from the N-terminal domain of human histone H3 containing the trimethylated lysine 9.
This peptide was used as immunogen to raise the ChIP-grade Diagenode antibody directed against H3K9me3 (purified antibody: Cat. No. pAb-056-050; crude serum: Cat. No. CS-056-050). The same peptide can be used to block this antibody in negative control experiments.
For more information about H3K9me3: see overview in the Technical Data Sheet of the ChIP-grade Diagenode antibody directed against H3K9me3 (Cat. No. pAb-056-050).
Datasheet H3K9me3 sp056 DATASHEET Datasheet description | Download |
Datasheet H3K9me3 C15410056 DATASHEET Polyclonal antibody raised in rabbit against the region of histone H3 containing the trimethylate... | Download |
How to properly cite this product in your workDiagenode strongly recommends using this: H3K9me3 peptide (Diagenode Cat# C16000056). Click here to copy to clipboard. Using our products in your publication? Let us know! |
Single amino-acid mutation in a Drosoph ila melanogaster ribosomalprotein: An insight in uL11 transcriptional activity. |
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In addition, no mutant for uL11 is available suggesting that this gene is haplo-insufficient as many other Ribosomal Protein Genes (RPGs). We have previously shown that overexpression of Drosophila melanogaster uL11 enhances the transcription of many RPGs and Ribosomal Biogenesis genes (RiBis) suggesting that uL11 might globally regulate the level of translation through its transcriptional activity. Moreover, uL11 trimethylated on lysine 3 (uL11K3me3) interacts with the chromodomain of the Enhancer of Polycomb and Trithorax Corto, and both proteins co-localize with RNA Polymerase II at many sites on polytene chromosomes. These data have led to the hypothesis that the N-terminal end of uL11, and more particularly the trimethylation of lysine 3, supports the extra-ribosomal activity of uL11 in transcription. To address this question, we mutated the lysine 3 codon using a CRISPR/Cas9 strategy and obtained several lysine 3 mutants. We describe here the first mutants of D. melanogaster uL11. Unexpectedly, the uL11K3A mutant, in which the lysine 3 codon is replaced by an alanine, displays a genuine Minute phenotype known to be characteristic of RPG deletions (longer development, low fertility, high lethality, thin and short bristles) whereas the uL11K3Y mutant, in which the lysine 3 codon is replaced by a tyrosine, is unaffected. In agreement, the rate of translation decreases in uL11K3A but not in uL11K3Y. Co-immunoprecipitation experiments show that the interaction between uL11 and the Corto chromodomain is impaired by both mutations. However, Histone Association Assays indicate that the mutant proteins still bind chromatin. RNA-seq analyses from wing imaginal discs show that Corto represses RPG expression whereas very few genes are deregulated in uL11 mutants. 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