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Biology subjects

Bunel, B.

Publications and source records attributed to Bunel, B..

2 recordsLinked to original sources

Uneven mitochondrial segregation during embryonic neurogenesis

Asymmetric divisions of vertebrate neural progenitors are critical for generating neurons while preserving the stem cell pool, ensuring proper central nervous system development. It was previously shown that the post-mitotic remodeling of mitochondrial activity in daughter cells influences neural fates. In this study, we demonstrate that unequal distribution of mitochondria during asymmetric mitosis plays a decisive role in triggering this differentiation process. Using live imaging to monitor mitochondrial segregation in individual progenitors and track their progenys fate within embryonic neural tissue, we show that daughter cells inheriting fewer mitochondria consistently differentiate into neurons, whereas their sibling receiving more mitochondria retains the progenitor status. Furthermore, experimental displacement of mitochondria during mitosis to force their unequal inheritance was sufficient to drive premature neuronal differentiation. Our findings establish a direct causal relationship between unequal mitochondrial inheritance and the asymmetric fate of sister cells in vivo, uncovering a key mechanism in neural development.

developmental biology↗

A tunable and versatile chemogenetic near infrared fluorescent reporter

Near-infrared (NIR) fluorescent reporters provide additional colors for highly multiplexed imaging of cells and organisms, and enable imaging with less toxic light and higher contrast and depth. Here, we present the engineering of nirFAST, a small tunable chemogenetic NIR fluorescent reporter that is brighter than top-performing NIR fluorescent proteins in cultured mammalian cells. nirFAST is a small genetically encoded protein of 14 kDa that binds and stabilizes the fluorescent state of synthetic, highly cell-permeant, fluorogenic chromophores (so-called fluorogens) that are otherwise dark when free. Engineered to emit NIR light, nirFAST can also emit far-red or red lights through change of chromophore. nirFAST allows the imaging of proteins in live cultured mammalian cells, chicken embryo tissues and zebrafish larvae. Its near infrared fluorescence provides an additional color for high spectral multiplexing. We showed that nirFAST is well-suited for stimulated emission depletion (STED) nanoscopy, allowing the efficient imaging of proteins with subdiffraction resolution in live cells. nirFAST enabled the design of a chemogenetic green-NIR fluorescent ubiquitination-based cell cycle indicator (FUCCI) for the monitoring of the different phases of the cell cycle. Finally, bisection of nirFAST allowed the design of a fluorogenic chemically induced dimerization technology with NIR fluorescence readout, enabling the control and visualization of protein proximity.

cell biology↗