Genetics
Study pinpoints why BET inhibitors have underperformed: BRD2 and BRD4 do different jobs in gene activation
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Researchers at the Max Planck Institute of Immunobiology and Epigenetics (MPI-IE) in Freiburg report that a key assumption behind widely used BET-inhibitor drug strategies may be wrong: the BET proteins BRD2 and BRD4 are not interchangeable. The team says BRD2 helps prepare genes for activation while BRD4 acts later to enable productive transcription—differences that could contribute to the modest and unpredictable results seen with drugs that inhibit BET proteins broadly.
A genetic analysis of more than a thousand ancient British genomes shows the Roman conquest left only a small mark on the island's ancestry despite major cultural shifts.
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Researchers comparing appendage regrowth in salamanders, fish and mice report that two related genes, SP6 and SP8, are activated in regenerating skin tissue across species and are required for normal bone regrowth in animal models—findings they say could inform future regenerative-medicine strategies.
Scientists have found genetic evidence that modern humans reached New Guinea and Australia around 60,000 years ago, backing the long chronology over more recent estimates. The international team, led by researchers at the University of Huddersfield and the University of Southampton, analyzed nearly 2,500 mitochondrial DNA genomes from Aboriginal Australians, New Guineans, and Southeast Asian populations. Their work suggests early migrants used at least two routes through Southeast Asia.
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Researchers at Kyoto University and RIKEN report that human cells can detect “non-optimal” synonymous codons—alternative three-letter genetic instructions that encode the same amino acid but are translated less efficiently—and selectively suppress the corresponding mRNAs. In experiments described in Science, the team identifies the RNA-binding protein DHX29 as a central component of this codon-dependent control of gene expression.
Researchers have found that polygenic risk scores, which summarize a person's likelihood of developing diseases like diabetes and cancer, can be reverse-engineered to uncover underlying genetic data. This vulnerability raises privacy concerns, potentially allowing identification through public databases or reconstruction by insurers. The discovery highlights risks in sharing such scores, even anonymously.
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Scientists at EPFL have developed a technique called optovolution, using light to evolve proteins that switch states, sense environments, and perform computations. By engineering yeast cells to survive only if proteins behave dynamically, the method selects optimal variants rapidly. The approach, published in Cell, advances synthetic biology and optogenetics.
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