Keep Current with the Latest in Cell Biology Research
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A Genome-Wide Screen Identifies Runx2 As a Novel Regulator of Hematopoietic Stem Cell Expansion and T-Cell Commitment
[Blood] Scientists performed a genome-wide CRISPR knockout screen in primary mouse hematopoietic stem and progenitor cells to discover novel regulators of ex vivo expansion. The screen identified Runx2 as a strong negative regulator of HSC expansion.
CRISPR-Engineered Human GATA2 Deficiency Model Uncovers Mitotic Dysfunction and Premature Aging in HSPCs, Impairing Hematopoietic Fitness
[Leukemia] Researchers developed a novel humanized model using CRISPR/Cas9 technology to knock-in GATA2-R398W variant in primary cord blood CD34⁺ cells.
Somatic mtDNA Mutations at Intermediate Levels of Heteroplasmy Are a Source of Functional Heterogeneity among Primary Leukemic Cells
[Science Advances] Bulk whole-genome sequencing of 637 matched tumor-normal samples from the Pediatric Cancer Genome Project revealed an enrichment of functionally impactful mitochondrial DNA variants in specific pediatric leukemia subtypes.
The Mitochondrial Protease ClpP Is a Metabolic Vulnerability and an Immunogenic Trigger against Multiple Myeloma
[Blood] Researchers showed that the mitochondrial protease caseinolytic peptidase P (ClpP) is both a cell-intrinsic metabolic vulnerability and an actionable immunogenic trigger in multiple myeloma.
Transposable Elements As Novel Therapeutic Targets for PARPi-Induced Synthetic Lethality in PcG-Mutated Blood Cancer
[Blood] Investigators showed that genetic inactivation of additional sex combs like 1 and enhancer of zeste homolog 2 in murine hematopoietic stem/progenitor cells results in highly penetrant hematological malignancies as observed in corresponding human diseases.
Molecular Insights into the Pathophysiology of Dysregulated Erythropoiesis: The Crucial Role of Iron Homeostasis
[Molecular and Cellular Biology] The authors summarize the current understanding of the mechanisms by which iron imbalance contributes to erythropoietic failure and highlight BACH1 as a potential integrative regulator in the pathophysiology of anemia in both iron-overload and iron-deficient states.
World’s First AI-Designed Viruses a Step Towards AI-Generated Life
[Nature] Scientists used AI to write coherent viral genomes, using them to synthesize bacteriophages capable of killing resistant strains of bacteria.
Enterobactin: A Key Player in Bacterial Iron Acquisition and Virulence and Its Implications for Vaccine Development and Antimicrobial Strategies
[Virulence] The authors explore the biosynthesis and regulation of enterobactin, highlighting its contribution to bacterial pathogenesis and immune evasion
Differential Response of Human Plasmacytoid Pre-Dendritic Cells to SARS-CoV-2 Variants
[iScience] Researchers investigated the ability of primary plasmacytoid pre-dendritic cells, type 2 dendritic cells, and monocytes isolated from healthy donors to respond to SARS-CoV-2 variants.
Virion Proteomics of Genetically Intact HCMV Reveals a Regulator of Envelope Glycoprotein Composition That Protects against Humoral Immunity
[Proceedings of the National Academy of Sciences of the United States of America] Scientists conducted proteomic analysis of a clinical human cytomegalovirus strain virion. This revealed 18 novel components, including the viral protein gpUL141, which is recognized as an NK immune-evasin that targets several host proteins when expressed within the cell.
Myeloperoxidase Transforms Chromatin Into Neutrophil Extracellular Traps
[Nature] Investigators show how myeloperoxidase, a highly expressed neutrophil protein, disassembles nucleosomes, thereby facilitating neutrophil extracellular traps (NETs) formation, yet also binds stably to NETs extracellularly.
Genetic and Epigenetic Screens in Primary Human T Cells Link Candidate Causal Autoimmune Variants to T Cell Networks
[Nature Genetics] Researchers tested >18,000 autoimmune disease-associated variants for allele-specific effects on expression using massively parallel reporter assays in primary human CD4+ T cells.