Cloned (Comment) | Organism |
---|---|
phr1 fragment subcloned between the HindIII and BamHI sites located downstream of the Orgyia pseudotsugata multiple NPV immediate early 2 promoter and upstream of the EGFP reporter gene in the vector PIZ-EGFP-N3 to generate PIZ-phr1-EGFP. Coding region of the phr2 gene flanked by EcoRI and BamHI restriction sites amplified and cloned into PIZ-EGFP-N3 between the corresponding restriction sites to give PIZ-phr2-EGFP. Complete ORF of phr2 with stop codon and flanked by EcoRI sites recloned from a phr2-containing pGEM-T Easy vector into the EcoRI site of PIZ/HIS-V5. Expression of phr2-egfp and non-fused phr2 in transfected Trichoplusia ni High Five cells | Chrysodeixis chalcites nucleopolyhedrovirus |
Localization | Comment | Organism | GeneOntology No. | Textmining |
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cytoplasm | non-fused PHR1-EGFP is distributed homogeneously over the cytoplasm and the nucleus at all time points analysed, as shown for 96 h post-transfection. PHR2-EGFP fusion protein is distributed over the cytoplasm and nucleus but, over time, it becomes localized predominantly in the nucleus | Chrysodeixis chalcites nucleopolyhedrovirus | 5737 | - |
additional information | both PHR-EGFP fusion proteins strongly colocalize with chromosomes and spindle, aster and midbody structures during host-cell mitosis. When PHR2-EGFP-transfected cells are superinfected with Autographa californica multiplenucleocapsid NPV, the protein colocalizes with virogenic stroma, the replication factories of baculovirus DNA | Chrysodeixis chalcites nucleopolyhedrovirus | - |
- |
nucleus | PHR1-EGFP fusion is localized predominantly in the nucleus from 28 h until 120 h post-transfection. Non-fused PHR1-EGFP is distributed homogeneously over the cytoplasm and the nucleus at all time points analysed, as shown for 96 h post-transfection. In the early phase of Autographa californica multiplenucleocapsid NPV infection (4 h post-infection), the PHR1-EGFP fusion protein shows a nuclear localization similar to that at 28 h post-transfection without infection. At 24 h post infection, when virogenic stroma appears in the centre of the nucleus of infected cells, fluorescence is present uniformly in the cytoplasm as well as in the nucleus. At 48 and 72 h post-transfection, many viral occlusion bodies or polyhedra are seen in the nucleus of infected cells and fluorescence is seen in both the cytoplasm and nucleus. PHR2-EGFP fusion protein is distributed over the cytoplasm and nucleus but, over time, it becomes localized predominantly in the nucleus. Early after transfection, non-fused PHR2 is already present mainly in the nucleus, suggesting that the fusion of PHR2 to EGFP hinders its nuclear import | Chrysodeixis chalcites nucleopolyhedrovirus | 5634 | - |
Molecular Weight [Da] | Molecular Weight Maximum [Da] | Comment | Organism |
---|---|---|---|
53000 | - |
non-fused PHR2, Western blot analysis | Chrysodeixis chalcites nucleopolyhedrovirus |
83000 | - |
PHR2-EGFP fusion protein, Western blot analysis | Chrysodeixis chalcites nucleopolyhedrovirus |
Organism | UniProt | Comment | Textmining |
---|---|---|---|
Chrysodeixis chalcites nucleopolyhedrovirus | - |
- |
- |
Synonyms | Comment | Organism |
---|---|---|
class II CPD photolyase | - |
Chrysodeixis chalcites nucleopolyhedrovirus |
CPD photolyase | - |
Chrysodeixis chalcites nucleopolyhedrovirus |
cyclobutane pyrimidine dimer photolyase | - |
Chrysodeixis chalcites nucleopolyhedrovirus |
DNA photolyase | - |
Chrysodeixis chalcites nucleopolyhedrovirus |
PHR1 | - |
Chrysodeixis chalcites nucleopolyhedrovirus |
PHR2 | - |
Chrysodeixis chalcites nucleopolyhedrovirus |
General Information | Comment | Organism |
---|---|---|
physiological function | PHR2 protein plays a role in baculovirus DNA repair | Chrysodeixis chalcites nucleopolyhedrovirus |