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Immunohistochemical analysis demonstrated that DTX3L was highly expressed in the glioma tissues and its level was correlated with the grade of malignancy. Multivariate analysis revealed the association between high expression of DTX3L and the poor prognosis of glioma patients. In addition, knockdown of DTX3L by siRNA transfection increased glioma cell apoptosis.
Dtx3L heterodimerization with Parp9 enables NAD(+) and poly(ADP-ribose) regulation of E3 activity.
we also found that DTX3L expression was regulated by focal adhesion kinase. Taken together, the results of this study show that DTX3L plays an important role in the proliferation and cell adhesion-mediated drug resistance of multiple myeloma cells and as such may play a key role in the development of multiple myeloma.
A novel role for the really interesting new gene-domain E3 ubiquitin ligase (显示 MUL1 抗体) deltex-3-like (DTX3L) in regulating CXCR4 (显示 CXCR4 抗体) sorting from endosomes to lysosomes.
The present study further suggests that the combined targeted inhibition of STAT1 (显示 STAT1 抗体), ARTD8 (显示 PARP14 抗体), ARTD9 (显示 PARP9 抗体) and/or DTX3L could increase the efficacy of chemotherapy or radiation treatment in prostate and other high-risk tumor types with an increased STAT1 (显示 STAT1 抗体) signaling.
Data establish that BAL1 and BBAP are bona fide members of a DNA damage response pathway and are directly associated with PARP1 activation, BRCA1 recruitment, and double-strand break repair.
we report the high-resolution crystal structure of this previously uncharacterized C-terminal domain of human DTX3L, which we term the Deltex (显示 DTX1 抗体) C-terminal domain.
BAL1 and BBAP are located on chromosome 3q21 in a head-to-head orientation and are regulated by a IFN-gamma (显示 IFNG 抗体)-responsive bidirectional promoter.
Overexpression of DTX3L, PIK3R4, ATP2C1, and SLC25A36, all located at 3q21.1-23 are associated with cervical cancer.
Data directly implicate BBAP in the monoubiquitylation and additional posttranslational modification of histone H4 and an associated DNA damage response.
Data indicate that PARP (显示 PARP1 抗体) polymerase PARP9 (显示 PARP9 抗体)-E3 ligase DTX3L interacts with STAT1 (显示 STAT1 抗体) transcription factor and enhances translocation of STAT1 (显示 STAT1 抗体) to the nucleus.
DTX3L functions as an E3 ubiquitin ligase (Takeyama et al., 2003
B-lymphoma- and BAL-associated protein
, E3 ubiquitin-protein ligase DTX3L
, rhysin 2
, deltex 3-like (Drosophila)
, protein deltex-3-like
, E3 ubiquitin-protein ligase DTX3L-like
, e3 ubiquitin-protein ligase DTX3L-like