We've posted a preprint: "Early-peaking caspase-7 activity at the plasma membrane drives apoptotic phosphatidylserine exposure” — the culmination of my 12-year journey and love for caspase, with incredible efforts by Yusuke Taira in Masayuki Miura lab.
https://t.co/QKLmh4TifZ
Excited to share that our work from RIKEN is now published in Nature! 🎉
We uncovered how protein intake during development shapes lifespan and identified a mechanism that transmits a “nutritional memory” into adulthood.
https://t.co/Kz8VVxsCv9
Today, I’m starting my own lab as a professor at Nagoya University!
By a wonderful coincidence, my lab is located in the very same place where my graduate lab once stood.
I’m excited to devote myself to research and education, and to advancing the field of insect endocrinology!
Our new paper is out in @ScienceMagazine! We developed mice with reversible control of autophagy, and showed that restoring this pathway after its suppression reverses neuronal abnormalities and brain dysfunction, demonstrating the resilience of neurons. https://t.co/kegmU08mcY
Happy 30th birthday, Pokémon! Since 1996, the Japanese media sensation has inspired generations of researchers in fields as diverse as evolution, biodiversity and research integrity. https://t.co/xDkf4D7VyT
Building on our previous finding that Drosophila caspase Dcp-1 promotes tissue growth in a non-lethal manner, we identify regulatory factors, including the giant IAP Bruce, that shape this non-lethal activity using TurboID and AlphaFold3 in collaboration with @YHama0105.
I am happy to announce that our “Reviewed Preprint” has been published in
@elife: Bruce suppresses autophagy-regulated caspase activity and wing tissue growth in Drosophila
https://t.co/oDv6e17eNW
New work describes our efforts to achieve CRISPR editing of the mitochondrial genome.
https://t.co/8Jc51WnEmg
The CRISPR toolbox has revolutionized the study of nuclear DNA, but the mitochondrial genome (mtDNA) has remained out of reach, mainly because there are no known ways to deliver sgRNAs across both outer and inner mitochondrial membranes.
Yet many organisms have evolved mechanisms to transport RNAs across their mitochondrial membranes. Trypanosomes, for example, do not encode any tRNAs in their mtDNA, and must import all of them from the cytosol to support intra-mitochondrial protein translation.
We started with yeast. We engineered a strain that must repair a STOP codon in mtDNA (an arginine biosynthesis gene) to survive. After screening a library of sgRNA import sequences, we identified one that enables a small degree of functional CRISPR editing in mitochondria.
Graduate student Sifei Yin obtained these exciting results several years ago, and spent the intervening time understanding how sgRNA import works, and how to make it better. Read the paper to learn what she uncovered!
We are happy to announce that the first paper from the Najafov Lab has been published in @Nature! In this study, we identified SIGLEC12 as a mediator of plasma membrane rupture (PMR) for necroptotic cell death using a genome-wide CRISPR-based systematic approach. @UTSWMedCenter@UTSWScience@UTSWNews@UTSWInternalMed@CRI_UTSW #necroptosis #MLKL
https://t.co/nB2yHIRUEi
Our new paper is out in Nature! We discovered that the neuroendocrine peptide Capa acts as a calcium-mobilizing hormone in the fruit flies, showing that even boneless insects have a vertebrate PTH-like endocrine system for calcium homeostasis.
https://t.co/d2la76xu89