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We thus identified a previously unrecognized role of DOT1L in regulating protein production. Decreased translation was one of the earliest effects measurable after DOT1L inhibition and specific to KMT2A-rearranged cell lines. H3K79me2 chromatin immunoprecipitation sequencing patterns over ribosomal genes were similar to those of the canonical KMT2A-fusion target genes in primary AML patient samples. The effects of DOT1L inhibition on ribosomal gene expression prompted us to evaluate the combination of EPZ5676 with a protein translation inhibitor. EPZ5676 was synergistic with the protein translation inhibitor homoharringtonine (omacetaxine), supporting further preclinical/clinical development of this combination. In summary, we discovered a novel epigenetic regulation of a metabolic process-protein synthesis-that plays a role in leukemogenesis and affords a combinatorial therapeutic opportunity.Background Dimethyl fumarate (DMF) is the active ingredient of Skilarence™ and Tecfidera™ which are used for the treatment of psoriasis and multiple sclerosis, respectively. check details Various immunomodulatory mechanisms of action have been identified for DMF; however, it is still unclear what effects DMF exerts in vivo in psoriasis patients. Aim In this study we examined the effects of DMF, both in vivo and in vitro, on T cells which play a key role in the pathogenesis of psoriasis. Methods The frequency of T cell subsets was examined by flow cytometry in untreated psoriasis patients or those treated with DMF. The effects of DMF in vitro on T cell survival, activation and proliferation and cell surface thiols were assessed by flow cytometry. Results In psoriasis patients treated with DMF we observed an increase in the frequency of Treg cells and a decrease in Th17 lineage cells and associated cytokines IL-17, IL-22 and GM-CSF. T cells cultured in vitro with DMF exhibited reduced viability and inhibition of activation and proliferation in response to stimulation due to the oxidative effects of DMF. However, the frequency of Treg cells increased in the presence of DMF due to their heightened ability to resist DMF-induced oxidative stress. Conclusions DMF enhanced the ratio of TregTh17 cells both in psoriasis patients, multiple sclerosis patients and in vitro. Furthermore, our data suggest that this is at least in part as a result of the differential effects of DMF on Treg compared with T conventional cells.As of 17th May, 2020 the number of patients infected by coronavirus disease 2019 (COVID-19) worldwide has exceeded 4.5 million (WHO 2020). A subgroup of patients with COVID-19 pneumonia develop a hyperinflammatory syndrome which has a similar cytokine release profile to secondary haemophagocytic lymphohistiocytosis (HLH) (Huang, et al 2020). Immunomodulatory drugs are hypothesised to abrogate the dysfunctional immune response in hyperinflammatory COVID-19 and are currently being investigated in clinical trials. IL-1 blockage with anakinra has been shown to be safe and is associated with clinical improvement in patients with hyperinflammatory COVID-19 (Cavalli, et al 2020).Eating out of phase with the biological clock induces circadian misalignment in peripheral organs and impairs glucose tolerance in preclinical models. Time-restricted eating (TRE) is a dietary approach that consolidates energy intake to 6 to 10 hours during the biologically active phase of the day, without necessarily altering diet quality and quantity. TRE induces pleiotropic metabolic benefits in mice, flies, and humans. Most studies have initiated TRE early in the biological morning. This perspective discusses the potential challenges in translating early TRE to the community and considers the potential metabolic consequences of delaying TRE.Reconstruction of one thalamic neuron, mapping hundreds of presynaptic inputs and postsynaptic outputs, reveals diverse types of interaction in a neural microcircuit.How do we learn in the absence of direct experience? In this issue of Neuron, Charpentier et al. (2020) proposes a new computational account of observational learning, which arbitrates between choice imitation and goal emulation.Due to the Raman signal coexists with other scatter spectra which leads to the low ratio of the wanted signal and high background, the appropriate method should be applied to enhance this ratio. The nature of raw spectra is a multi-source system, so its determinacy must be ensured by multi-input. Besides, the faithfulness of output should be provided. Then, the huge fall within the frequencies of Raman and background almost satisfies separating demand for independent component analysis (ICA), and this analysis can give help to the achievement of the two type signals classing and estimate the optimal number of source and match ICA output signals to Raman or background. Thus, based on ICA and the mixing-entropy criteria, the background and Raman adapting calibration kit (BRACK) method is proposed, which is a kind of multiple raw spectral inputs and multiple output (MIMO) method. This method firstly divides the raw data into two parts of Raman and background by ICA, identifies Raman signal by entropy criterion, then restores the part of Raman signal. BRACK method obtains several advantages, for instance, well-adapted, no need for any additional option or extra-intervention, high fidelity, and no unwanted external information. In principle, the correction of background and Raman signals can be expected to be completed by BRACK method.Rearrangements involving the mixed lineage leukemia gene (MLL) are found in the majority of leukemias that develop within the first year of age, known as infant leukemias, and likely originate during prenatal life. MLL rearrangements are also present in about 10% of other pediatric and adult acute myeloid leukemia (AML) and acute lymphoid leukemia (ALL). These translocations and others occurring in early life are associated with a dismal prognosis compared with adult leukemias carrying the same translocations. This observation suggests that infant and adult leukemias are biologically distinct but the underlying molecular mechanisms for these differences are not understood. In this work, we induced the same MLL chromosomal translocation in the embryo at the time of fetal liver hematopoiesis and in the adult hematopoietic tissues to develop disease models in mice that recapitulate human infant and adult leukemias, respectively. We successfully obtained myeloid leukemia in adult mice after MLL-ENL recombination induction using the interferon inducible Mx1-Cre line.